A clathrin coat assembly role for the muniscin protein central linker revealed by TALEN-mediated gene editing

Clathrin-mediated endocytosis is an evolutionarily ancient membrane transport system regulating cellular receptivity and responsiveness. Plasmalemma clathrin-coated structures range from unitary domed assemblies to expansive planar constructions with internal or flanking invaginated buds. Precisely how these morphologically-distinct coats are formed, and whether all are functionally equivalent for selective cargo internalization is still disputed. We have disrupted the genes encoding a set of early arriving clathrin-coat constituents, FCHO1 and FCHO2, in HeLa cells. Endocytic coats do not disappear in this genetic background; rather clustered planar lattices predominate and endocytosis slows, but does not cease. The central linker of FCHO proteins acts as an allosteric regulator of the prime endocytic adaptor, AP-2. By loading AP-2 onto the plasma membrane, FCHO proteins provide a parallel pathway for AP-2 activation and clathrin-coat fabrication. Further, the steady-state morphology of clathrin-coated structures appears to be a manifestation of the availability of the muniscin linker during lattice polymerization. DOI: http://dx.doi.org/10.7554/eLife.04137.001


Introduction
The precise purpose of clathrin-coated vesicles was correctly deduced 50 years ago from thin-section electron micrographs (Roth and Porter, 1964). Noticing the very close apposition of a compacted lumenal protein load and a cytosol-oriented 'bristle' coat on opposite faces of striking membrane invaginations, it was astutely reasoned that the bulbous plasmalemma structures ferry macromolecules into the cell interior in a highly selective manner. While it was soon clear clathrin-mediated endocytosis is a rapid activity (Brown and Goldstein, 1976), and is importantly involved in many fundamental cellular processes (McMahon and Boucrot, 2011;Brodsky, 2012;Kirchhausen et al., 2014), the regularity of the static coated structures in micrograph views masks the true underlying molecular dynamics and complexity. It is also challenging to identify the very earliest stages of clathrin coat assembly in thin sections because of the restricted size, ill-defined morphological features, and a lack of prominent membrane curvature. With the recent live-cell clarification of the linked temporal steps that define clathrin-coated structure initiation, growth, invagination and scission (Kaksonen et al., 2003;Taylor et al., 2011), it is clear that a large number of gene products are involved. The choreographed arrival and departure of these numerous proteins matches well their defined biochemical activities and the morphological progression of the bud (Taylor et al., 2011). Yet, what exactly defines a restricted plasma membrane zone that is destined to become a clathrin-coated bud remains elusive. In this regard, the clathrin coats at the cell surface are distinct from many other intracellular cargo sorting coats in that the selected assembly site is not demarcated by deposition of a GTP-bound small GTPase (Ren et al., 2013). The lipid phosphatidylinositol 4,5-bisphosphate (PtdIns(4,5)P 2 ) is required for clathrin assembly (Boucrot et al., 2006;Zoncu et al., 2007;Nunez et al., 2011), but this phosphoinositide is broadly distributed over the inner leaflet of the plasma membrane. Ordered polymerization of a clathrin patch in fact appears to be a variable and probabilistic process (Ehrlich et al., 2004;Taylor et al., 2011;Cocucci et al., 2012;Brach et al., 2014). The nucleation stage displays the widest temporal variation and likely involves the largest number of protein cofactors (Taylor et al., 2011). While the principal heterotetameric cargo-selective adaptor, designated AP-2, is certainly important (Mitsunari et al., 2005;Cocucci et al., 2012;Aguet et al., 2013), its initial occurrence at inchoate bud sites is paralleled by a sizable suite of early-arriving pioneers, including eps15, intersectin, epsin, Fcho1 and Fcho2, CALM (Taylor et al., 2011) and Necap 1 (Ritter et al., 2013). The Fcho family (Fer/Cip4 homology only proteins), collectively termed the muniscins , is posited to act as internalization site founders on the basis of the biochemical properties of the proteins and the endocytic consequences of RNAi-mediated transcript silencing (Henne et al., 2010). Here we show that munsicins are indeed consequential endocytic pioneers, but that clathrin-mediated endocytosis still persists in their absence (Uezu et al., 2011;Mulkearns and Cooper, 2012;Mayers et al., 2013;Brach et al., 2014). We delineate a key biochemical aspect of the early operation of these endocytic proteins that regulates the rate and extent of clathrin-lattice fabrication at the cell surface.

Results
FCHO1 (KIAA0290; located on chromosome 19) and FCHO2 (on chromosome 5) display ∼50% overall amino acid identity and a similar domain organization ( Figure 1A; Katoh, 2004). Both are EFC domain proteins (Shimada et al., 2007) characterized by a C-terminal μ-homology domain (μHD), distantly related in primary sequence but with an analogous fold to the cargo-engaging μ2 subunit of the heterotetrameric AP-2 clathrin adaptor . This combination of an EFC domain (alternatively designated the F-BAR domain [Frost et al., 2008;Heath and Insall, 2008]) with a μHD is unique, and eLife digest Cells can take proteins and other molecules that are either embedded in, or attached to, their surface membrane and move them inside via a process called endocytosis. This process often involves a protein called clathrin working together with numerous other proteins. Early on, a complex of four proteins, called the adaptor protein-2 complex, interacts with both the 'cargo' molecules that are to be taken into the cell, and the cell membrane. Clathrin molecules then assemble into an ordered lattice-like coat, on top of the adaptor protein complex layer. This deforms a small patch of the cell membrane and curves it inwards. The clathrin molecules coat this pocket as it grows in size, until it engulfs the cargo. The pocket quickly pinches off from the membrane to form a bubble-like structure called a vesicle, which is brought into the cell.
A family of proteins termed Muniscins were thought to be involved in the early stages of endocytosis and have to arrive at the membrane before the adaptor protein-2 complex and clathrin. But experiments to test this idea-that reduced, or 'knocked-down', the production of Muniscinshad given conflicting results. As such, it remained unclear how the small patches of membrane carrying cargo molecules are marked as being destined to become clathrin-coated vesicles. Now Umasankar et al. have studied the role that these proteins play in the early stages of endocytosis in human cells grown in a laboratory. A gene-editing approach was used to precisely disrupt a gene that codes for a Muniscin protein called FCHO2. Umasankar et al. observed that these 'edited' cells formed clathrin coats that were more irregular compared with those that form in normal cells. Nevertheless, clathrin-mediated vesicles still formed when this protein was absent, though the process of endocytosis was slower.
Similar results were seen when Umasankar et al. used the same approach to disrupt the gene for a related protein called FCHO1 in the same cells. A short fragment of the Muniscin proteins, called the linker, was shown to bind to, and activate, the adaptor protein-2 complex. The linker then recruits this complex to the specific regions of the cell membrane where clathrin-coated vesicles will form. Several dozen other proteins also accumulate where clathrin pockets form; as such, one of the next challenges will be to investigate if this mechanism of locally activating the cargo-gathering machinery is common in living cells. these paralogous proteins have orthologues in chordates, arthropods and nematodes (Katoh, 2004;Umasankar et al., 2012;Mayers et al., 2013), as well as in unicellular eukaryotes (Boettner et al., 2009;Reider et al., 2009;Stimpson et al., 2009). In the budding yeast Saccharomyces cerevisiae, Syp1p has an analogous architecture to FCHO1/2 despite limited (<20%) overall primary sequence identity ( Figure 1A). Phylogenetic dendrograms (TreeFam TF328986) (Ruan et al., 2008) show that a third chordate member, Sgip1, is more closely related to FCHO2 than to FCHO1, but this neuronal protein, while containing a modular C-terminal μHD, lacks the folded N-terminal helical EFC domain ( Figure  1A; Uezu et al., 2007;Dergai et al., 2010). At steady state, endogenous FCHO2 (Henne et al., 2010;Umasankar et al., 2012) and both transfected FCHO1 Taylor et al., 2011;Umasankar et al., 2012) and Sgip1 (Uezu et al., 2007;Stimpson et al., 2009) colocalize extensively with clathrin-coated structures, unlike several other EFC domain proteins (Cip4/Fbp17/Pacsin) implicated in endocytosis (Modregger et al., 2000;Kamioka et al., 2004;Taylor et al., 2011).
After selection, an AseI resistant ∼650-bp PCR fragment, in addition to the wild-type 351-, and 294bp cleavage products, is evident in six representative HeLa TALEN clones ( Figure 1D). The digests of the individual clones are similar to the PCR products seen in the initial TALEN-transfected population pool. Although this pattern suggests only heterozygosity, sequencing of the PCR amplified alleles discloses several homozygous gene-disrupted HeLa lines ( Figure 1E); some of the small deletions, although producing frame-shifted nonsense mutations, regenerate an AseI restriction site ( Figure 1E). One of the expanded clones (#52) contains four distinct disrupted alleles, indicating a mixed cell population. Immunoblotting verifies the genotype of the clones (Figure 2A).
Following RNAi, the phenotype typical of FCHO2-depleted HeLa cells is a reduced surface clathrin density and apparently enlarged or clustered clathrin-coated structures ( Figure 2B,C) (Mulkearns and Cooper, 2012;Umasankar et al., 2012;but see Cocucci et al., 2012;Henne et al., 2010). Confocal optical sections of the FCHO2-disrupted clones illustrate that a very similar phenotype is evident in gene-edited cells. Compared with the control HeLa cells ( Figure 2D), four of the edited lines (clones #6, 27, 52 and 64) have a clearly abnormal arrangement of AP-2 and EPS15-positive clathrin-coated structures ( Figure 2E-I). The exceptions ( Figure 2J,K) are clone #68 and #71, which contains one undisrupted allele ( Figure 1E), illustrating that there is no apparent gene dosage effect (Henne et al., 2010). and genomic organization of the FCHO2 gene with pertinent details of TALEN design. The repeat variable di-residues (RVD) selective for the different deoxyribonucleotides are color-coded (single letter amino acid notation). The endogenous AseI recognition sequence within the targeted exon is boxed (yellow). (C) Gene-specific RT-PCR analysis of various endocytic protein and control mRNA transcripts in the parental HeLa SS6 and neuroblastoma SH-SY5Y cells. HC; heavy chain. (D) AseI restriction enzyme digestion of FCHO2 gene-specific PCR amplicons from genomic DNA extracted from wild-type (WT) and TALEN-treated clones. The undigested parental (HeLa) PCR product and digested PCRs are shown. The 'pool' designates a PCR reaction from a genomic DNA sample of TALEN-transfetced HeLa cells prior to clone selection. The AseI nuclease generates three PCR DNA fragments; the 55-bp band is not visible on these gels but causes the shift in the singly-cleaved product to 645 bp. (E) Genomic sequence analysis of TALEN clones. TALEN generated insertions (lower case letters) and deletions are indicated in relation to the WT nucleotide and amino acid sequences. AseI restriction sites are boxed (yellow) and in-frame stop codons are highlighted (red) and identified with a red asterisk. DOI: 10.7554/eLife.04137.003

Figure 1. Continued
We selected clone #64 for further detailed analysis as this cell has two distinct 4-bp deletions, each leading to an immediate in-frame stop codon (Q97X) terminating the FCHO1 polypeptide within the EFC domain ( Figure 1E). RT-PCR shows a strong qualitative decrease in FCHO2 mRNA abundance in clone #64 cells ( Figure 3A), presumably due to nonsense-mediated decay. In these FCHO2-null cells, the relative levels of numerous other endocytic and some unrelated cellular proteins are essentially unaltered ( Figure 3B). Notably, FCHO1, undetectable by immunoblotting in HeLa cells (Uezu et al., 2011;Umasankar et al., 2012; Figure 3B) does not show a compensatory increase in clone #64 cells, either at the RNA or protein level, clearly dissimilar to the counteracting expression reported in BS-C-1 cells (Nunez et al., 2011). Endogenous FCHO1 is readily detectable, along with FCHO2, in K562 erythroleukemia cells. RNA-seq results indicate an eightfold higher FCHO1 expression in K562 cells compared with HeLa Uhlen et al., 2010). Moreover, RT-PCR fails to detect evidence of the SGIP1 transcript in either HeLa or clone #64 cells ( Figure 3A). Indeed, SGIP1 is essentially a neuronally-expressed protein (Trevaskis et al., 2005;Uezu et al., 2007), with RT-PCR HeLa SS6 cells and TALEN clones #6, #27, #52, #64, #68 and #71 were analyzed by SDS-PAGE. Duplicate immunoblots were probed with polyclonal antibodies directed against FCHO2, the AP-2 μ2 subunit and epsin 1. (B and C) Selected but representative confocal optical sections of HeLa SS6 cells either mock transfected (B) or transfected with FCHO2 transcript-targeting siRNA oligonucleotides (Umasankar et al., 2012) (C). Fixed cells were stained with a mAb directed against the AP-2 α subunit (AP.6, green) and affinity purified antibodies against DAB2 (red). (D-K) HeLa SS6 cells (D) or the indicated TALEN-treated clones (E-K) were fixed and stained with mAb AP.6 (green) and affinity purified antibodies directed EPS15 (red). Colorseparated channels from a portion of the micrograph of clone #64 cells (H) are presented (I). Scale bar: 10 μm. DOI: 10.7554/eLife.04137.004  Figure 1C were used. HC; heavy chain. (B) Whole cell lysates from HeLa SS6, clone #64 and K562 cells were resolved by SDS-PAGE and either stained with Coomassie blue or transferred to nitrocellulose. Replicate blots were probed with antibodies specific for the indicated proteins. Positions of the molecular mass standards (in kDa) are indicated on the left. (C and D). After incubation at 37°C for 60 min in serum-free medium, cover slip-attached HeLa SS6 (C) or clone #64 cells (D) were pulsed for 10 min with Alexa Fluor488-labelled transferrin (green). After chilling on ice and washing with ice-cold PBS, the cells were fixed and stained for AP-2 (red) with the α-subunit specific mAb AP.6. Representative single confocal optical sections focused on a medial region, rich in transferrin-positive endosomal structures, are shown, with color-separated channels of the boxed regions shown below. Scale bar: 10 μm. DOI: 10.7554/eLife.04137.005 ( Figure 1C) and RNA-seq Uhlen et al., 2010) indicating >30-fold higher transcript abundance in SH-SY5Y neuroblastoma cells vs HeLa cells.

Research article
The spatial reconfiguration of clathrin-coated structures in clone #64 cells is accompanied with altered kinetics of transferrin receptor internalization. 10 min after addition of fluorescent transferrin, bright juxtanuclear clusters of recycling endosomes are present in the parental HeLa SS6 cells ( Figure 3C). At this juncture, little of the transferrin colocalizes with AP-2. By contrast, after 10 min of identical treatment, there is still residual overlap between the added transferrin and surfaceassociated AP-2 in the clone #64 cells, while the intensity of transferrin within endosomes is obviously diminished and occurs in a more peripheral early endosome compartment ( Figure 3D). These results concur that internalization is obviously rate limiting in these edited cells (Uezu et al., 2011;Mulkearns and Cooper, 2012) and a diffuse pool of surface receptors not clustered within clathrin-coated structures is evident after a brief pulse of labeled transferrin. Cessation of receptor-mediated endocytosis (Henne et al., 2010) is not, however, apparent.
While clone #64 cells closely resemble FCHO2 + FCHO1 gene-silenced HeLa cells (Mulkearns and Cooper, 2012;Umasankar et al., 2012), the presence of the appropriate FCHO1 PCR product ( Figures 1C and 3A) is consistent with full-length cDNA clones (CR597235, CR620485, and CR625849) isolated from HeLa cells, and also with the identification of FCHO1-and FCHO2-derived peptides in proteomic analysis of HeLa cell extracts (Beausoleil et al., 2006). Although transcript silencing of FCHO1 alone has little effect on surface clathrin coat organization in HeLa SS6 cells ( Figure 4-figure supplement 1), it is possible that the residual clathrin-coated structures present in clone #64 could be due to the expression of FCHO1.
Stable clathrin assemblies at the plasma membrane of FCHO1 + FCHO2 gene-edited cells An iterative TALEN-based approach to disrupt the FCHO1 gene in clone #64 cells was therefore used. A tract within exon 5, encoding residues Lys24-Ser29 on the predicted EFC domain α2 helix (Henne et al., 2007) and housing an internal ApaI site, was selected for disruption ( Figure 4A). Similar to the FCHO2 TALEN lesions, the selected clones display an ApaI-resistant band(s) in addition to the two 387-and 150-bp cleavage products of the 537-bp PCR amplicon ( Figure 4B). Also, parallel AseI digests confirm retention of the disrupted FCHO2 alleles ( Figure 4C). Sequencing of a representative clone (#64/45F1), uncovers three differently disrupted and a single wild-type FCHO1 allele. Yet this does not represent a mixed cell population, as three independent subclones derived from this line all display the identical genotype ( Figure 4D). Because HeLa cells are aneuploid (Bottomley et al., 1969), and chromosome 19 is duplicated in some HeLa lines (Adey et al., 2013;Landry et al., 2013), we interpret this to be TALEN-mediated disruption of three of the four FCHO1 alleles in HeLa SS6 cells. We used clone #64/1.E (designated clone 1.E cells) for all further analysis. More generally, our results highlight potential complications when using gene editing on cultured cell lines with non-diploid genomes.
Genotype-phenotype analysis corroborates diminished steady-state mRNA levels for both FCHO1 and FCHO2 ( Figure 3A). Biochemical pull-down assays further reveal exceptionally low levels of FCHO1 protein in clone 1.E cells compared with K562, which normally express this protein. Despite typical enrichment of cytosolic munsicins by affinity isolation on immobilized GST-EPS15 (595-889) (Umasankar et al., 2012), there is no immunoreactivity for either protein in the TALEN-edited cells ( Figure 5A). Still, the AP-2 in each of the cell extracts binds avidly to the GST-EPS15, while EPS15R remains within the supernatant fractions. These results thus resemble (neuronal) dynamin 1 expression in SK-MEL-2 cells; despite mRNA recognition there is no immunodetectable protein and this GTPase is ∼70-fold less abundant than the ubiquitious dynamin 2 (Grassart et al., 2014). Yet, if ectopically expressed, either GFP-tagged full-length FCHO1 or Sgip1 are readily detectable in whole HeLa clone 1.E cell lysates ( Figure 5B). By contrast, AP-2 and numerous other endocytic and trafficking proteins are present in equivalent amounts in HeLa and clone 1.E cells ( Figure 5B).
Not surprisingly, the overall disposition of AP-2-positive endocytic structures in the clone 1.E cells ( Figure 5D) differs from HeLa SS6 cells ( Figure 5C) and resembles closely the clone #64 cells, from which they were derived ( Figure 2H). And the clathrin-coated regions in the clone 1.E cells are populated with a full cohort of early-arriving clathrin coat pioneers despite the abnormal surface arrangement. At steady state, surface deposited AP-2 and clathrin are accompanied by CALM, DAB2, intersectin 1, EPS15 and HRB ( Figure 5C-J), all members of the pioneer module of endocytic proteins (Taylor et al., 2011) and found in HeLa cell clathrin-coated vesicles (Borner et al., 2012). Thus, in obvious contrast to other observations (Henne et al., 2010), neither clathrin nor AP-2 is completely soluble in the clone 1.E cells in spite of the extremely low level of muniscins compared with unedited cells. Further, these results demonstrate plainly that congregation of EPS15/EPS15R and intersectin 1 at bud zones does not depend upon stoichiometric FCHO1/2 (Henne et al., 2010). Our findings are congruent with results with yeast (Boettner et al., 2009;Reider et al., 2009;Stimpson et al., 2009) and nematode (Mayers et al., 2013) model systems that show deletion of the single muniscin expressed in these organisms is not lethal.
Comparative quantitative analysis of the distribution of AP-2 in HeLa SS6 and the clone 1.E cells indicates a sharp increase in the very smallest (<60 nm 2 ) coated structures on the ventral surface. In the parental cells, these account for <25% of the AP-2 signal while in the FCHO1/2-depleted cells these small puncta represent almost 45% of the total AP-2. There is also an increase in the largest (>600 nm 2 )    prebound to glutathione-Sepharose beads were incubated with cell lysates from HeLa SS6, clone #64, clone #64/1.E and K562 cells. After washing, aliquots of the supernatant (S) and pellet (P) fractions were resolved by SDS-PAGE and stained with Coomassie blue or replicates transferred to nitrocellulose. Positions of the molecular mass standards (in kDa) are shown. Results from both an anti-FCHO1 mAb directed against the μHD and an affinity-purified polyclonal raised against the EFC domain and weakly cross-reactive with FCHO2 are shown. (B) Parental HeLa SS6 or clone #64/1.E cells, mock transfected or transfected with plasmid DNA encoding GFP-FCHO1 or GFP-Sgip1 as indicated, were collected after 16 hr and whole cell lysates subject to SDS-PAGE Figure 5. Continued on next page clathrin assemblages, as previously seen in FCHO2 silenced HeLa cells (Mulkearns and Cooper, 2012;Umasankar et al., 2012). After disruption of the FCHO1 and FCHO2 genes, 46% of membraneassociated AP-2 is present in structures >600 nm 2 while only 29% of AP-2 occurs within this size category in the HeLa SS6 cells. Analogous results are obtained upon measuring the distribution of EPS15 in the two cell types. Engineered loss of muniscins therefore shifts the equilibrium of clathrin lattices at the cell surface to the very small and the largest forms.
The ultrastructural basis for the altered surface distribution of clathrin assemblies in clone 1.E cells can be appreciated in deep-etch EM replicas ( Figure 6). At steady state, the ventral surface of the parental HeLa SS6 cell line typically exhibits a range of clathrin-coated assemblies and invaginated buds ( Figure 6A,B). Both solitary coated buds and spherical coated invaginations adjacent to regions of planar clathrin lattice are regularly dispersed over the membrane. By contrast, conspicuous expanses of plasma membrane devoid of polyhedral clathrin typify the clone 1.E cells, and overall the number of deeply invaginated buds is reduced ( Figure 6C-E). Whereas abutting planar assemblages are abundant, individual, spatially isolated de novo forming coated buds are present in clone 1.E cells, as well as small patches of flat polygonal assemblies ( Figure 6C,D). Beside the spatial effects of FCHO1/2 gene disruption, structural alterations within the assembled clathrin layer are also apparent. Higher magnification views reveal that, in contrast to the well ordered, principally hexagonal flat sheets in control HeLa cells ( Figure 6B, Figure 6-figure supplement 1), the clone 1.E cells display geometrically poorly ordered lattices ( Figure 6E, Figure 6-figure supplement 1). So, despite having a complement of co-assembled AP-2, EPS15, DAB2, CALM, intersectin 1 and HRB, the lattices do not appear to assemble as regularly as in control HeLa cells.

Clathrin-mediated cargo internalization in clone 1.E cells
A two-minute pulse of fluorescent transferrin at 37°C labels surface AP-2 puncta and peripheral early endosomes in control HeLa cells ( Figure 7A), as the unsynchronized ligand fluxes through the cell surface into the endosomal compartment. The clone 1.E cells have the larger, less regular clathrincoated structures also labeled with transferrin at 2 min, although a diffuse pool of unclustered receptors is clearly evident on the cell surface ( Figure 7B). This confirms endocytic entry is rate limiting in FCHO1/2-depleted cells (Uezu et al., 2011;Mulkearns and Cooper, 2012). A buildup of transferrin receptors at the cell surface may be explained, in part, by lattice defects and a reduced number of invaginated buds. After 10 min, the bulk of transferrin is within endosomes in both the control ( Figure 7C) and clone 1.E cells, but residual transferrin at the enlarged clathrin-coated structures and on the plasma membrane in the edited cells is apparent. (Figure 7D).
Given the coat protein densities within the aberrant clathrin-coated structures typical of clone 1.E cells, and the accumulation of transferrin receptors at the cell surface, the extent of transferrin clustering is reduced relative to the HeLa cell control line. Because the transferrin receptor has a YXXØ-type YTRF internalization signal that depends on AP-2 for uptake (Hinrichsen et al., 2003;Motley et al., 2003;Huang et al., 2004), our results suggest that AP-2 cargo capture may be compromised in the clathrin assemblies in clone 1.E cells. The disparity in transferrin sequestration between steady-state clone 1.E and ordinary clathrin-coated structures is better appreciated by transfecting GFP-tagged full-length FCHO1 into the gene-edited cells ( Figure 7E-L). Forced reexpression of FCHO1 normalizes the AP-2 arrangement on the ventral surface ( Figure 7F). A 2-min pulse of transferrin concentrates the ligand near these AP-2/FCHO1-positive spots ( Figure 7E-H). Adjacent untransfected clone 1.E cells have the characteristic dispersed transferrin signal over the plasma membrane, and even strongly AP-2-positive structures do not concentrate transferrin similar to relatively dimmer AP-2 puncta in the transfected cells ( Figure 7E). Further analysis of transferrin binding to GFP-FCHO1-transfected HeLa clone 1.E cells by total internal reflection microscopy ( Figure 7-figure supplement 1) corroborates the defect in transferrin clustering in the clone 1.E cell line.
analysis. Gels were either stained with Coommassie blue or transferred to nitrocellulose. Duplicate blots were probed with designated antibodies. Positions of the molecular mass standards (in kDa) are shown. (C-J) Representative images of HeLa SS6 (C, E, G, I) or HeLa clone #64/1.E (D, F, H, J) cells after immunolabeling with anti-AP-2 mAb AP.6, affinity-purified anti-CALM antibodies, anti-clathrin heavy chain (HC) mAb X22, affinity purified anti-DAB2 antibodies, anti-intersectin 1 mAb , affinity-purified anti-EPS15 antibodies, and anti-HRB serum. Arrows indicate the Golgi/endosomal population of clathrin present in both control and clone #64/1.E HeLa cells. Scale bar: 10 μm. DOI: 10.7554/eLife.04137.008 After a 10-min pulse of transferrin, medial plane confocal optical sections illustrate that both the clone 1.E cells and neighboring GFP-FCHO1-transfected cells accumulate the ligand in perinuclear endosomes ( Figure 7I-L), albeit internalization is more efficient in the presence of expressed FCHO1. Stalled ligand-bound receptor still persists at the surface of the clone 1.E cells. Overall, the data obtained from the TALEN-edited cells are fully consistent with the siRNA results in HeLa cells (Mulkearns and Cooper, 2012;Uezu et al., 2012;Umasankar et al., 2012). We conclude that clathrin-coat assembly and endocytosis does not cease entirely when cellular levels of muniscin proteins are extremely low. These proteins also do not appear obligatory for sustained clathrin lattice growth (Cocucci et al., 2012), but rather impact the fidelity of the polyhedral construction.

Muniscin-dependent restoration of a regular clathrin coat distribution in clone 1.E cells
Transiently expressed GFP-FCHO1 clusters at surface puncta and changes the general AP-2 configuration compared with the surrounding non-transfected clone 1.E cells ( Figure 7F,G, 8B,B′ and Figure  8-figure supplement 1). By contrast, transfected GFP alone is diffusely cytosolic, and has no effect on the abnormal clathrin patches in the gene-edited cells ( Figure 8A,A′). This effect of FCHO1 on clathrin coat arrangement is not restricted to gene-edited lines. The native topology of surface clathrin lattices in cultured MCF-7 cells, a breast adenocarcinoma, is even more exaggerated and extensively abutting than the gene-edited clone 1.E cells (Figure 8-figure supplement 2). A considerable size distribution of clathrin assemblies can thus occur naturally in different cell types (Maupin and Pollard, 1983;Akisaka et al., 2003;Ehrlich et al., 2004;Grove et al., 2014;Sochacki et al., 2014). Strikingly, temporary introduction of GFP-FCHO1 (or GFP-FCHO2) into MCF-7 cells switches the AP-2 assemblies to considerably smaller puncta (Figure 8-figure supplement 2). Because the altered clathrin distribution in the clone 1.E (and MCF-7) cells is extremely penetrant and robust, we used complementation transfection experiments to delineate the domain(s) of FCHO1 required to revert the morphology to the wild-type pattern.
On expressing alone the lipid-binding EFC domain (Henne et al., 2007;Edeling et al., 2009) in clone 1.E cells, while membrane associated, it neither clusters at clathrin-coated structures nor modifies their appearance ( Figure 8C,C′). By contrast, the GFP-μHD does concentrate at plasma membrane clathrin assemblages, because the domain functions as an interaction hub Dergai et al., 2010;Henne et al., 2010;Mulkearns and Cooper, 2012;Umasankar et al., 2012) but, again, does not refashion these atypical coated zones ( Figure 8D,D′). Yet expression of proteins containing the polypeptide stretch linking the EFC domain to the μHD reestablishes a more regular arrangement of AP-2-positive sites in clone 1.E cells ( Figure 8E-G′, Figure 8-figure supplement 1). Systematic truncation and deletion experiments better pinpoints the active region of the FCHO1 linker ( Figure 8I). In various proteins, inclusion of FCHO1 residues 339-416 promotes the redistribution of AP-2 into more a uniform and evenly dispersed form over the ventral plasma membrane. Deletion of residues 316-467 from full-length GFP-tagged FCHO1 prevents complementation of the clathrin distribution despite deposition of the transfected protein at clathrin pincta ( Figure 8H,H′). The linker section of FCHO1, but neither the EFC domain nor μHD, also repatterns the bulky clathrin in MCF-7 cells to more regularly dispersed arrays (Figure 8-figure supplement 2). Forced expression of the N-terminal linker-containing segment of Sgip1 (residues 1-514) has a similar consequence in clone 1.E cells, in spite of the absence of an EFC domain ( Figure 8J,J′).
Together, these experiments show that the central linker in FCHO1, FCHO2 and Sgip1, despite likely being intrinsically disordered, is required to revert the organization of clathrin-coated structures to the more uniform format typical of control cells. A remarkable aspect of this activity is that at very low expression levels, the linker can alter the steady-state organization of coated regions without being enriched at assembly zones, and can even operate when expressed as a soluble protein.  The linker tract is the most divergent portion of the muniscin family members, with generally <25% identity overall. Yet alignments of this region of Fcho1, Fcho2, Sgip1 (Katoh, 2004) reveal they share small blocks of phylogenetically conserved residues, particularly rich in acidic side chains and phospho-modifiable residues ( Figure 9A). As the linker regions from FCHO1, FCHO2 and Sgip1 can each correct the HeLa clone 1.E cell coat morphology, it seems likely that these blocks of common residues are functionally important. In fact, post-translational phosphorylation events are enriched at proteinprotein interaction surfaces (Nishi et al., 2011), and high-throughput mass spectrometry identifies numerous phosphosites within the shared region of the linker domain ( Figure 9A).
Several distinct lines of evidence indicate that the central linker acts with AP-2: First, the anomalous transferrin clustering at coated patches noted in clone 1.E cells indicates muniscins could impact AP-2 cargo engagement. Second, in GST pull-down assays, the minimal FCHO1 linker (residues 316-467) binds physically to cytosolic AP-2 ( Figure 9B). All four subunits of the heterotetramer sediment with the GST-FCHO1 linker, but engagement of AP-2 is not as efficient as the C-terminal portion of the cargo-selective monomeric adaptor ARH that binds directly to the β2 subunit appendage (He et al., 2002;Mishra et al., 2005), and clathrin binding is limited. We find no evidence for the linker polypeptide engaging lipid modifying enzymes (PIP5KIγ [ Figure 9B], PLD, DGKδ1 [not shown]) that could, in principal, affect clathrin coat assembly without physically being enriched at coat assembly zones. Fused to GST, the conserved central segments of FCHO2 (residues 314-444) and Sgip1 (residues 77-214) also bind to cytosolic AP-2, although the interaction with FCHO2 is comparatively weaker (Figure 9-figure supplement 1A).
The independently folded αand β2-subunit appendages of AP-2 ( Figure 9C) can engage FCHO1 (Umasankar et al., 2012). Yet titrating an excess of α appendage into pull-down assays does not alter the extent of soluble AP-2 heterotetramer engagement, so the major contact surface for the AP-2 on the FCHO1 linker tract does not appear to interact with the α appendage ( Figure 9-figure supplement 1B). In the same experiment, the added α appendage does bind to the C-terminal region of EPS15 and concomitantly diminish cytosolic AP-2 association, in a dose-dependent manner (Figure 9figure supplement 1B).
Binary interaction assays reveal that the purified tetrameric core of AP-2 binds physically to the linker regions of FCHO1, FCHO2 and Sgip1 ( Figure 9D), with relative affinities similar to interactions with intact cytosolic AP-2 (Figure 9-figure supplement 1A). The sequence-related linkers of the muniscin members thus contact the AP-2 core directly. The other currently known interaction partner for the FCHO1/2 linker segment is Necap 1 (Ritter et al., 2013). Soluble Necap 1 in brain cytosol binds only very weakly to the GST-FCHO1 linker and not to the analogous portions of FCHO2 and Sgip1 (Figure 9-figure supplement 1A). However, when this association is assayed using immobilized GST-Necap 1 PHear domain (residues 1-133) and K562 cell lysates, a strong interaction with FCHO1 is apparent (Figure 9-figure supplement 1C). This suggests either that Necap 1 in brain cytosol is in an inhibited conformation or that the optimal binding site upon the FCHO1 linker lies outside of the minimal region (residues 316-467) necessary for correction of the clone 1.E cell clathrin phenotype.
A clue to the mechanistic connection between FCHO1/2 and AP-2 comes from additional biochemical studies. The muniscin μHD is a densely wired endocytic interaction hub, physically contacting the pioneer proteins Eps15/R, intersectin, Dab2, Hrb and CALM Henne et al., 2010;Mulkearns and Cooper, 2012;Umasankar et al., 2012). The C-terminal portion of EPS15 is the highest affinity μHD binding partner ( Figure 5A). A limited sequence tract between residues 595 and 636 represents the principal interaction region in EPS15 (Umasankar et al., 2012). Deletion of part of AP-2 with mAb AP.6 (blue). A cell in each field is outlined (orange) and a low GFP-FCHO1 expressing cell (arrow) and adjacent untransfected FCHO1/2depleted cells (asterisks) are indicated. Scale bar (for E-L): 10 μm. (I-L) Medial plane optical section of GFP-FCHO1 (1-889) transfected HeLa clone #64/1.E cells following a 10-min pulse of transferrin. The perimeter of a non-complemented clone #64/1.E cell is indicated (orange). DOI: 10.7554/eLife.04137.011 The following figure supplement is available for figure 7:   H and H′). Fixed cells were stained for AP-2 using the anti-AP-2 α-subunit mAb AP.6. Merged channel images (A-H) and the corresponding AP-2 α subunit channel alone (A′-H′) are shown. Transgene-dependent refashioning of the irregular 1.E cell clathrin-coated structures to a more uniformly dispersed pattern is indicated (arrows). Scale bar for all panels: 10 μm. (I) Cartoon diagram of the overall domain organization of FCHO1 with the relative locations of the various N-terminally-tagged truncation and deletion constructs tested shown schematically. The minimal region Figure 8. Continued on next page this region (residues 617-636) within the GST-EPS15 (595-896) fusion protein has a strong inhibitory effect on both FCHO1 and FCHO2 interactions from K562 cell lysates ( Figure 9E). AP-2 also binds to the C-terminal third of EPS15 ( Figure 5, Figure 9-figure supplement 1B), but with lower apparent affinity and utilizing the tandemly arrayed Asp-Pro-Phe (DPF) tripeptide repeats positioned distal to the μHD-binding region (Benmerah et al., 1996;Iannolo et al., 1997). Consequently, the association of cytosolic AP-2 with the GST-EPS15 (Δ617-636) is not different from the binding to the whole GST-EPS15 ( Figure 9E). Yet there is a strong decrease in the amount of clathrin associated with the immobilized Δ617-636 fusion, which parallels the diminished engagement of FCHO1 and FCHO2. The majority of the soluble clathrin remains in the Δ617-636 assay supernatant fractions. Because AP-2 cannot engage clathrin trimers productively without undergoing allosteric activation (Kelly et al., 2014), it is as if FCHO1/2 promote conformational rearrangement of AP-2 to facilitate clathrin binding.

Functional linkage between the muniscin linker polypeptide and AP-2
The role of the FCHO1 linker polypeptide was further explored using a tailored fusion to the cytosolic aspect of Tac (CD25), a type I transmembrane protein (Uchiyama et al., 1981). Transient expression of Tac in HeLa SS6 cells leads to surface accumulation because this α chain of the IL-2 receptor is poorly internalized (Humphrey et al., 1993). At steady state, individual low-level-expressing cells have a prominent surface pool of Tac and an internal population that overlaps partly with the Golgi-region marker GPP130 (Linstedt et al., 1997) and with the trans-Golgi network (TGOLN2/TGN46). The intracellular population in these cells thus represents primarily the biosynthetic trafficking of new Tac molecules en route to the surface ( Figure 10A,A′). Cells expressing high levels of the Tac transgene have, in addition, a second internal accumulation of Tac, which colocalizes well with a pulse of internalized transferrin ( Figure 10A). Switching a Tac-linker (FCHO1 residues 265-609) hybrid-encoding plasmid for Tac leads to similar but not identical expression and spread in HeLa SS6 cells ( Figure 10B-B″). Increased localization of Tac-linker with the transferrin endocytic marker indicates that this customized fusion is more rapidly internalized from the cell surface than the native Tac protein. Analogous results are obtained upon expressing a Tac-FCHO1 μHD (residues 609-889) hybrid ( Figure 10C,C′). Consequently, we find that ectopic Tac and Tac-fusion proteins display a dichotomous distribution of surface and internal pools, the composition of the latter differing depending on the level of Tac protein driven by the transfected plasmid DNA and on the amino acid sequence of the cytosolic portion.
Two conspicuous changes in clathrin coat organization occur when just the full FCHO1 linker is expressed in HeLa SS6 cells in a membrane-tethered form. First, assembled AP-2, normally restricted entirely to puncta on the inner leaflet of the plasma membrane, becomes mistargeted to juxtanuclear regions ( Figure 11A-A″), located similarly to the Golgi and endosome compartment markers that overlap with intracellular Tac. The ectopic AP-2 is accompanied by colocalized EPS15 ( Figure 11A). We infer that the high local density of the Tac-FCHO1 linker, as it traverses the biosynthetic pathway following ER export or concentrates on maturing endosomes, promotes anomalous recruitment of AP-2. Yet, when a corresponding Tac fusion with the FCHO1 μHD (residues 609-889) is transfected, very strong EPS15 and intersectin 1 (not shown) deposition on the Golgi/endosome region occurs, but strikingly this is not paralleled by AP-2 binding ( Figure 11B-B″). The effect of overexpression of a Taclinker + μHD (FCHO1 residues 316-889) hybrid appears similar to the linker alone, albeit with more robust EPS15 binding accompanying juxtanuclear AP-2 ( Figure 11C-C″). Visualizing the Tac-FCHO1 fusion-expressing cells with an anti-Tac mAb ( Figure 11D-D″) clarifies that the juxtanuclear pool of endocytic proteins is indeed recruited to Tac-positive internal structures. Thus, EPS15 (and intersectin 1) recruited by the Tac-anchored FCHO1 μHD concentrated on Golgi/endosome membranes does not  Figure 9. Continued on next page attract cytosolic AP-2, but AP-2 associated with these compartments through the membrane-linked linker polypeptide results in deposition of EPS15. Impressively, the massing of AP-2 and EPS15 upon perinuclear biosynthetic and endocytic organelles in Tac-FCHO1 linker ( Figure 12A-C) or Tac-FCHO1 linker + μHD ( Figure 12D-F) expressing cells occurs in the absence of any conspicuous PtdIns(4,5)P 2 enrichment in these compartments, as judged by a GFP-tagged PLCδ1 PH domain sensor selective for PtdIns(4,5)P 2 .
Second, the Tac-linker fusion, when located on the plasma membrane, reconfigures the apparent dimensions of the clathrin-coated structures on the ventral surface relative to adjacent untransfected HeLa SS6 cells ( Figures 11C and 12A). This overall shift to small, more uniformly grouped puncta also happens with transfection of the Tac-linker + μHD ( Figures 11D″ and 12D), but not with the Tac-μHD fusion ( Figure 11B″), even though the relocation of EPS15 is so dramatic in these cells that the protein becomes depleted from the surface AP-2-positive clathrin assemblies.
The phenotypic consequence of forced expression of the tailored Tac-FCHO1 chimeras is even more notable in the muniscin-depleted clone 1.E cells. While Tac alone has no noticeable effect on the characteristic distribution of AP-2 and EPS15 in these cells ( Figure 13A-D), the Tac-FCHO1 linker promotes deposition of a fraction of these proteins onto juxtanuclear membranes and remodels the abnormal surface clathrin patches into more homogenous and regularly scattered assemblies ( Figure  13E-H). By contrast, the Tac-FCHO1 μHD gives rise to noteworthy sequestration of EPS15 on juxtanuclear structures, as occurs in the parental HeLa SS6 cells, but again without accompanying AP-2 recruitment or refashioning of the surface clathrin structures in the clone 1.E cells ( Figure 13I-L). Transient expression of the Tac-FCHO1 linker + μHD amalgamates the separate effects of the Taclinker and Tac-μHD proteins, with marked AP-2 and EPS15 intracellular congregation and a drop in the dimensions of clathrin-coated puncta on the plasma membrane ( Figure 13M-P). Parallel experiments utilizing the variously transfected HeLa clone 1.E cells and stained for Tac expression (Figure 13-figure supplement 1) recapitulate all these findings. That the ectopic transmembrane anchored FCHO1 linker alters the morphologic characteristics of surface clathrin patches toward uniform small puncta strengthens the proposition that enlarged coats in the clone 1.E cells originate directly from limiting cellular muniscin concentrations.
Crucially, the discrete clathrin/AP-2 surface assemblies that arise in Tac-linker-expressing cells are operational. Live-cell imaging of a HeLa SS6 cells stably transfected with a YFP-tagged AP-2 β2 subunit (β2-YFP) (Keyel et al., 2008) shows that forced expression of the Tac-FCHO1 linker (residues 265-609) in these cells again reconfigures the overall arrangement of clathrin-coated structures ( Figure 14A). Using total internal reflection fluorescence microscopy, the more uniform and evenly spread β2-YFP puncta at the ventral surface of Tac-linker-containing cells differ from the adjacent untransfected cells ( Figure 14A). After 2 min at 37°C, added fluorescent transferrin rapidly clusters at the β2-YFPcontaining structures ( Figure 14B) but, again, the relative ratio of transferrin to YFP differs between the Tac-linker producing and untransfected cells ( Figure 14A vs Figure 14B), suggesting that the AP-2 spots in the Tac-FCHO1 linker-expressing cells are better able to concentrate transferrin receptors.
In the time-lapse data set, comparing the initial (2 min) transferrin signal (pseudocolored green) with a frame acquired 10 min later (colored blue) illustrates that the Tac-transfected cells, have more dynamic clathrin-coated vesicle uptake ( Figure 14C). Numerous green or blue puncta are present in the transfected cells ( Figure 14C-E), indicating that these transferrin-laden structures ,  or GST-Sgip1 (77-214) immobilized on glutathione-Sepharose were used in pull-down assays with the purified AP-2 heterameric core complex as in (B). The identity of the large subunit trunk polypeptides (α and β2 subunits) and the myc-tagged μ2 subunit is confirmed on immunoblots with mAb clone 8, mAb 100/1 and mAb clone 31, respectively. (E) Aliquots of 100 μg of GST or either 25 μg or 100 μg of  or GST-EPS15 (595-896/Δ617-636) immobilized on glutathione-Sepharose were incubated with soluble lysate from K562 cells. After washing, portions of the supernatant and pellet fractions were analyzed as in (B). FCHO1 antibody 1 is a mAb while antibody 2 is an affinity-purified antibody that also recognizes FCHO2 weakly. Non-specific cross-reactive bands are indicated with asterisks; reactivity of the GST-EPS15 fusion proteins with the anti-FCHO1 and anti-FCHO2 antibody preparations is also indicated with asterisks. Notice the decreased FCHO1 and FCHO2 binding upon deletion of the minimal μHD sequence within the EPS15 C-terminal region that correlates with reduced clathrin association. DOI: 10.7554/eLife.04137.016 The following figure supplement is available for figure 9:  Figure 14F). Also, at this time point transferrin concentrated within endosomes is evident in the evanescent field. We conclude that the linker polypeptide in munsicin proteins affects the operation of AP-2 on the cell surface; the linker facilitates the production of more numerous cargo-filled clathrin-coated structures.

Discussion
The polyhedrally interdigitated outer lattice is emblematic of the extensive protein-protein interactions that underpin the formation of a clathrin-coated vesicle. Yet perhaps the most impressive array of protein contacts occurs at the outset of clathrin polymerization on the limiting cell membrane. The early module of proteins implicated in the nucleation of surface clathrin coats is very highly interconnected Fixed cells were stained with anti-AP-2 α subunit mAb AP.6 (green) and affinity purified anti-EPS15 antibodies (red) and mounted in Hoechst 33342 to label DNA (blue) prior to imaging. Aberrant accumulation of AP-2 and EPS15 adjacent to the nucleus (arrows) in Tac-transfected cells (asterisks) correlates with smaller clathrin-coated puncta in the basal optical section of the same cell population (A″). Scale bar (for A-C″): 10 μm. (B-C″) Chosen middle (B, B′, C and C′) or maximal projection (B″ and C″) optical sections of HeLa SS6 cells transfected with Tac-FCHO1 μHD (residues 609-889) or Tac-FCHO1 linker + μHD (residues 265-889) and prepared analogously to (A-A″). The Tac-fused μHD produces dramatic relocalization of EPS15 (B), diminishing this protein in surface AP-2-positive puncta (B″) yet AP-2 does not relocate similarly. With ectopic expression of the FCHO linker + μHD, prominent accumulation of irregular intracellular AP-2 and EPS15 in a juxtanuclear locations again correlates with diminished surface clathrin spots, which are again relatively deficient in EPS15 because of the massive deposition of this endocytic pioneer Figure 11. Continued on next page (McMahon and Boucrot, 2011;Reider and Wendland, 2011); microscopic temporal connections (Taylor et al., 2011) are enabled by nanoscopic macromolecular associations. The principal interaction hub is undoubtedly AP-2, which can, through the independently folded α and β2 appendages, bind to >20 other endocytic factors utilizing four separate contact interfaces (Traub, 2009;Kelly and Owen, 2011;McMahon and Boucrot, 2011). Numerous other pioneer proteins bind physically to PtdIns(4,5) P 2 , similar to AP-2 (Höning et al., 2005;Jackson et al., 2010), and some contain EH and SH3 domains, producing a densely populated interactome to coordinate membrane remodeling, coat biogenesis and cargo selection. The inherent redundancy and functional overlap between several of these earlyarriving proteins is responsible for the robust nature of clathrin-mediated endocytosis.
For example, CALM, a PtdIns(4,5)P 2 binding clathrin-associated sorting protein for the R-SNAREs VAMP2, -3 and -8 (Koo et al., 2011;Miller et al., 2011;Sahlender et al., 2013), interacts with the μHD of FCHO1 (Henne et al., 2010;Umasankar et al., 2012). CALM also contains an FXDXF-type interaction motif that engages directly the PHear domain of Necap 1 (Ritter et al., 2007), has several component upon intracellular membranes. (D-D″) Single ventral optical section of HeLa SS6 cells transfected with Tac-FCHO1 linker + μHD (residues 265-889) and stained with anti-Tac mAb (7 G7B6; green) and affinity-purified anti-EPS15 antibodies (red). Relocalization of EPS15 occurs only in Tac overexpressing cells (arrows), and the dose-dependent massing of EPS15 in the perinuclear region limits the amount of EPS15 present in surface clathrin-coated structures. The limiting membrane of the Tac-expressing cells is delineated (orange). Scale bar: 10 μm. DOI: 10.7554/eLife.04137.019 Figure 11. Continued DXF-and FXSXF-based AP-2-associating peptide sequences (Meyerholz et al., 2005), and can interact physically with clathrin (Tebar et al., 1999;Meyerholz et al., 2005). The protein also has two NPF tripeptide motifs that bind to EH domains , as found in Eps15/R and intersectins. Yet CALM knock-out mice are born, and mouse embryonic fibroblasts can be cultured and analyzed (Scotland et al., 2012;Suzuki et al., 2012). In fact, a considerable number of clathrin coat components and ancillary proteins have been experimentally deleted or incapacitated without complete disruption of clathrin-dependent internalization (Garcia et al., 2001;Kang-Decker et al., 2001;Morris et al., 2002;Kamikura and Cooper, 2003;Holmes et al., 2007;Koh et al., 2007;Wang et al., 2008;Chen et al., 2009;Mullen et al., 2012;Pozzi et al., 2012;Scotland et al., 2012;Suzuki et al., 2012;Umasankar et al., 2012;Kononenko et al., 2013;Tsushima et al., 2013;Alazami et al., 2014). Although Fcho1 and Fcho2 were proposed to be all-important (Henne et al., 2010), we have carefully evaluated the overall veracity of this provocative idea. HeLa cells with undetectable levels of FCHO1 and FCHO2 still fabricate clathrin lattices and internalize clathrin-dependent transmembrane cargo. We have maintained these muniscin-depleted cells in culture for many months. Color channel separated total internal reflection images of HeLa SS6 cells stably expressing β2-YFP (A) and pulsed for 2 min with 25 μg/ml Alexa Fluor647 transferrin (B). The cells were previously transfected with Tac-FCHO1 linker (265-609) and Tac-expressing cells are indicated (asterisks). (C) Comparison of individual frames from the transferrin channel at 2 min and 12 min by pseudocoloring the initial fame green and overlaying the last frame colored blue. The Tac-expressing cells with the rearranged β2-YFP spots are indicated (asterisks). (D and E) Enlarged, color-channel separated views of the labeled boxed regions in (C). (F) After completion of time-resolved image acquisition, Alexa Fluor546-conjugated anti-Tac mAb 7 G7B6 was added to identify unambiguously the Tac-transfected cells. Following incubation with the anti-Tac, a final image was collected. Internalized transferrin within endosomes visible in the total internal reflection field is indicated (arrows). Scale bar: 10 μm. DOI: 10.7554/eLife.04137.023 That is not to say that these proteins are insignificant. The cellular concentration of muniscins regulates clathrin-coated structure organization and dynamics and, thereby, the efficiency of cargo internalization. Clearly, this underscores the importance of these particular pioneers in clathrin lattice biogenesis and function. The enlarged clustered clathrin assemblies characteristic of essentially-munsicin-null HeLa cells appear to be linked to physiological compensation. Operationally, they resemble hot spots, areas of repeated vesicle budding from non-terminal clathrin puncta within a spatially restricted area (Nunez et al., 2011). Hot spots were actually reported the first time GFP-tagged clathrin-coated structures were visualized live . Endocytic activity at hot spots is more resistant to perturbations in the levels AP-2 and PtdIns(4,5)P 2 , so-called nucleation factors (Nunez et al., 2011). Thus, the extended long-lived lattices are likely better adapted to coupled budding events to conserve and reuse limiting factors and maintain steady, but slowed, clathrin-mediated endocytosis.
The reduced capacity to sequester transferrin (receptors) within the clathrin-coated structures that we note in clone 1.E cells could indicate that the unstructured linker domain of FCHO1/2 stabilizes the activated, open form of AP-2 to bias cargo capture. This idea is in line with the increased abundance of the smallest population of coated structures in the clone 1.E (and clone #64) cells, presumably abortive structures because of the overall reduced rate of transferrin uptake in these cells. However, livecell imaging discloses that FCHO1/2 arrive at nascent clathrin bud sites on the cell surface with or before AP-2 (Henne et al., 2010;Taylor et al., 2011), and current copy number estimates suggest that AP-2 outnumbers FCHO2 in HeLa cells by an order of magnitude and FCHO1 by at least a factor of 1000 (Kulak et al., 2014). So the interaction between AP-2 and FCHO1/2 is unlikely to be stoichiometric within the lattice, as borne out by proteomic analysis (Borner et al., 2012). An obvious question, though, is why AP-2 is not able to properly engage the transferrin receptor YTFR sorting signal despite being positioned in the surface lattices of clone 1.E cells. As indicated above, it is well established that the heterotetramer displays multiple modes of attachment to membrane-apposed clathrin. In addition to four spatially discrete PtdIns(4,5)P 2 binding sites Jackson et al., 2010), AP-2 has at least two dedicated cargo-specific interactions surfaces (Jackson et al., 2010), a clathrin box (Shih et al., 1995) to contact the clathrin heavy chain terminal domain β-propeller (ter Haar et al., 2000), as well as a second site in the β2 subunit appendage (Edeling et al., 2006) that binds to the extended α-solenoid region of the clathrin heavy chain designated the ankle (Knuehl et al., 2006). Both the αand β2-subunit appendages interact with a large overlapping set of earlyarriving clathrin-associated sorting and accessory proteins. The appendages do not depend on allosteric changes within the core to promote binding because AP-2 can be quantitatively affinity purified with immobilized appendage binding motifs or immunoprecipitated with mAb AP.6 (Chin et al., 1989), which binds to the platform interaction site of the α appendage. We suspect that the wide range of interaction possibilities allows deposition of some incompletely rearranged AP-2 at clathrin lattices formed in the absence of muniscins. AP-2 can transition between metastable states; a partially open form bound to the dileucine sorting signal has been characterized (Kelly et al., 2008). An incomplete conformational transition in all membrane-associated AP-2 in the clone 1.E cells may also be linked to the alterations in lattice arrangement we see. Using synthetic liposome templates, AP-2 driven clathrin-coated buds are spherical (Kelly et al., 2014) while clathrin coats nucleated by a monomeric clathrin binding domain are flat but stabilize membrane remodeling induced by thermal fluctuations (Dannhauser and Ungewickell, 2012).
The crescent-shaped EFC domain in the FCHO proteins prompted the conjecture that initial dimpling of a spherical membrane patch defined a bud site (Henne et al., 2010). Further, if the munsicins, and their pioneer binding partners collectively assembled into a circumferential rim defining the outer edge of the indented membrane, they could stabilize nascent buds possibly by preventing lateral diffusional escape of phosphoinositides (Zhao et al., 2013) necessary for successful placement of incoming inner layer coat constituents. Yet two lines of evidence argue against this notion: First, the linker region alone is able to correct or remodel the abnormal distribution of clathrin structures, even when not directly membrane associated. Second, the Tac-linker + μHD chimera, while membrane spanning, is unlikely to similarly remodel membrane topology adjacent to the linker, but it is still able to restore the organization of surface clathrin in clone #64/1.E cells. Instead, the unstructured linker tract between the folded EFC and μHD domains in FCHO1, and the sequence-related portion of Sgip1, are able to drive membrane deposition of AP-2 and partner engagement. In this sense, muniscins could operate in a conceptually analogous manner to the small GTPase Arf1 activating the structurally and functionally related heterotetrameric AP-1 clathrin adaptor (Ren et al., 2013).
Our findings allow us to rationalize a number of recent studies with an integrated model for the biogenesis of clathrin lattices at the cell surface. We concur that both AP-2 and Fcho1/2 are central regulators during clathrin coat initiation; both are clearly core members of the pioneer module of endocytic components (Henne et al., 2010;Taylor et al., 2011;Cocucci et al., 2012). A pivotal assembly step involves the conformational rearrangement of AP-2 (Collins et al., 2002;Höning et al., 2005;Kelly et al., 2008;Jackson et al., 2010;Cocucci et al., 2012;Kelly et al., 2014). This shift in the equilibrium from the closed cytosolic basal conformation to the open, assembly-competent form of AP-2 can be regulated synergistically by PtdIns(4,5)P 2 and tyrosine (YXXØ)-or dileucine ([DE] XXXL[LIM]-based internalization signals). Reorganization of AP-2 by these allosteric regulators could account for the reported minimal stoichiometry of two AP-2 heterotetramers and one or two clathrin trimers to nucleate a clathrin-coated structure (Cocucci et al., 2012). Indeed targeted gene disruption of the AP-2 μ2 subunit is pre-implantation lethal in mice (Mitsunari et al., 2005). But in C. elegans and S. cerevisae, AP-2 is dispensable (Huang et al., 1999;Yeung et al., 1999;Mayers et al., 2013). In yeast, seven early module (pioneer) proteins can be deleted without fully disrupting clathrin-dependent internalization (Brach et al., 2014). As noted above, loss of numerous mammalian pioneer factors (Eps15, CALM, Hrb, epsin, Dab2, intersectin, Necap 1) similarly does not terminate clathrin-mediated endocytosis. One interpretation of these results is that there are several parallel pathways to arrive at an internalization competent clathrin assemblage at the plasma membrane. However, extinguishing the muniscins has a more severe effect than loss of a set of pioneers that physically engage the μHD. This is plainly apparent in cells expressing the tailored Tac-μHD protein-despite massive misrouting of EPS15 (and EPS15R and intersectin) to the juxtanuclear region, AP-2-positive puncta at the cell surface persist. Our findings indicate that FCHO1, and specifically the linker segment, interacts with AP-2 and can promote membrane deposition of the heterotetramer in the absence of elevated levels of PtdIns(4,5)P 2 . Further, because AP-2 cannot bind productively to clathrin in the closed basal conformation (Kelly et al., 2014), our biochemical experiments showing that FCHO1 can modulate the clathrin binding properties of EPS15-bound AP-2 suggest that FCHO1 can provide an alternative pathway to rearrange AP-2 to promote cargo capture, clathrin lattice assembly and budding. The remarkable effect that a membrane-attached FCHO1 linker has on the disposition of surface clathrin structures supports this idea. The appearance of expanded planar clathrin sheets, which often contain assembly defects in cells depleted of muniscins (FCHO2 principally), argues additionally for an important role of these proteins in overseeing swift and regular polymerization of the clathrin coat. Necap 1 also exerts a regulatory input on AP-2 by competitively engaging several binding surfaces on the heterotetramer (Ritter et al., 2013). As FCHO1 and Necap 1 associate with each other, whether the effect of the FCHO1 linker directly involves Necap 1 will be important to establish. Finally, our results defining regulation of overall size of clathrin-coated buds raise the possibility that kinetic uncoupling between the outer and inner layer components of other vesicular coats could also alter the morphology of the forming tubulovesiclular carrier to accommodate variably sized cargo.

Construction of TALEN gene-edited cells
All TALENs were designed using open-access software (Mojo Hand; http://www.talendesign.org) as described (Bedell et al., 2012). The repeat variable di-peptide (RVD)-containing units for FCHO2 TAL-1 (NG NN NN NI NG HD NG NG NN NG NG NI NN NI NI NI) and FCHO2 TAL-2 (NI HD NG NG HD NG NN NI NI HD NG NG HD HD NG NG) or FCHO1 TAL-1 (HD HD NG NN NG NI HD HD NI HD NI NN HD NN NG NN NI) and FCHO1 TAL-2 (HD HD NN HD HD NI NN HD NG HD HD NG NG NN NN NG NN) were assembled using the Golden Gate approach (Cermak et al., 2011). After assembly, the RVDs were cloned into the pC-Goldy TALEN destination vector (Bedell et al., 2012;Carlson et al., 2012) suitable for expression in mammalian cells (Addgene, Boston, MA).
For TALEN transfections, equal amounts of each pair of TALENs were introduced into a HeLa cells grown in a 35 × 10 mm tissue culture dish using Lipofectamine 2000 (Invitrogen/Life Technologies, Grand Island, NY). Transfected cells were cultured 3 days at 30°C, before splitting for indel analysis and plating for clone selection. Individual clones were collected by a standard limiting dilution approach in 96-well plates. Clonal populations were expanded and screened by SDS-PAGE and immunoblotting with antibodies specific for human FCHO2. To confirm gene disruption in FCHO1 mutants, genomic DNA was isolated from individual clonal populations or from the transfected-cell pool using DNeasy Blood and Tissue kit (Qiagen, Valencia, CA). The genomic region surrounding the target site was PCR amplified with human FCHO1 locus specific primers using the genomic DNA template obtained from each clone. PCR amplicons were initially digested with appropriate restriction enzymes and the mutations were assessed by loss of restriction enzyme digestion. Then the poly-allelic mixture of the individual clones was ligated to TOPO-TA vector (Invitrogen) and analyzed by sequencing.
Cells were transfected with plasmids using Lipofectamine 2000 (Invitrogen) or with siRNA oligonucleotides using Oligofectamine (Invitrogen) according to the manufacturer's recommendations (Umasankar et al., 2012). After 18-24 hr, cells were fixed with 4% paraformaldehyde in PBS (pH 8.0) and quenched and permeabilized with a mixture of 75 mM NH 4 Cl, 20 mM glycine and 0.1% Triton X-100. The cells were blocked in 5% normal goat serum diluted in PBS/fish skin gelatin/saponin mixture and stained with various antibodies. For fluorescent transferrin binding and uptake assays, cells were preincubated in DMEM, 25 mM Hepes, 0.5% BSA at 37°C for 1 hr to remove bound transferrin.

GST pull-down assays and immunoblotting
The purification of GST, various GST-fusion proteins, and the preparation of rat brain cytosol for GST-based pull-down assays have been thoroughly described previously (Umasankar et al., 2012). The lysates from parental HeLa SS6, HeLa clone #64 or HeLa clone #64/1.E cells were prepared from cells detached with Cellstripper (Cellgro/Mediatech, Manassas, VA). K562 cells grown in suspension were pelleted directly. After washing, cell pellets were solubilized on ice for 30 min in 25 mM Hepes-KOH pH 7.2, 125 mM potassium acetate, 5 mM magnesium acetate, 2 mM EDTA, 2 mM EGTA, and 2 mM dithiothreitol (assay buffer) supplemented with 1% Triton X-100, 1 mM PMSF and complete protease inhibitor cocktail (Roche, Indianapolis, IN). Lysates were centrifuged at 20,000×g before use in binding assays. Assays were in assay buffer, usually in a final volume of 300 μl. After incubation at 4°C for 1-2 hr, glutathione-Sepharose beads were sedimented and washed four times with ice-cold PBS. Aliquots of the supernatant and washed pellet factions were resolved by SDS-PAGE and either stained with Coomassie blue or transferred to nitrocellulose for immunoblotting. Detection was with enhanced chemiluminescence and X-ray film. The heterotetrameric core of AP-2 was produced in Escherichia coli BL21 (DE3) pLysS after transfection with two bicistronic plasmids encoding the β2-subunit trunk and myc-tagged μ2 subunits (Amp r ) and the GST-αsubunit trunk and σ2 subunit (Kan r ) generously provided by David Owen. Purification was exactly as described (Collins et al., 2002;Kelly et al., 2008;Jackson et al., 2010). For the binary interaction assays, a modified assay buffer composed of 25 mM Hepes-KOH pH 7.2, 25 mM Tris-HCl, 125 mM potassium acetate, 5 mM magnesium acetate, 2 mM EDTA, 2 mM EGTA, 10 mM dithiothreitol, 0.2% Igepal CA-630 (Nonidet P40 substitute) and 0.1 mg/ml BSA was used. After incubation of immobilized GST-fusion proteins with 20 μg/ml purified AP-2 core in modified assay buffer for 60 min at 4°C, the glutathione-Sepharose beads were recovered at 1000 × g for 1 min. Following a first wash in ice-cold modified assay buffer and centrifugation at 1000×g for 1 min, the beads were washed two additional times with ice-cold PBS and centrifugation at 10,000×g for 1 min.

Microscopy and live-cell imaging
Confocal fluorescence images were collected on an Olympus Fluoview FV1000 microscope as described previously Umasankar et al., 2012). The z-stacks were collected with a 0.25-µm step size between optical sections and the stacks were deconvolved using the blind Research article deconvolution algorithm within Autoquant X3 (Media Cybernetics, Rockville, MD). Quantitation of objects in fluorescent images was with the Nikon Elements software (version 4.30,Nikon,Melville,NY).
For three-color total internal reflection fluorescence microscopy, adherent cells were imaged on a Nikon Eclipse Ti inverted microscope with a 60 × 1.49 NA oil-immersion objective. Cells were maintained in DMEM supplemented with 10% fetal calf serum and 25 mM HEPES, pH 7.2 at 37°C on MatTek dishes (MatTek Corporation, Ashland, MA) and imaged continuously at 5 s/frame. GFP/YFP was excited with a 488 nm laser, Alexa Fluor546 conjugated anti-Tac mAb with a 561 nm laser, and transferrin-Alexa 647 (Molecular Probes/Life Technologies, Grand Island, NY) with a 647 nm laser line. Images were collected using an Andor (Belfast, Ireland) Xyla 5.5 camera; at full resolution under these conditions the pixel size with a 1 × coupler matches Nyquist sampling (120 nm xy exactly). Data sets were acquired acquired using Nikon Elements.

Electron microscopy
Adherent plasma membrane from parental HeLa SS6 and clone #64/1.E cells were prepared for rapid-freeze, deep-etch electron microscopy as described previously (Heuser, 2000). Briefly, cells grown on oriented pieces of glass cover slip were disrupted by sonication and fixed in a glutaraldehyde and paraformaldehyde mixture before flash freezing in liquid helium .