Gap junctions deliver malonyl-CoA from soma to germline to support embryogenesis in Caenorhabditis elegans

Gap junctions are ubiquitous in metazoans and play critical roles in important biological processes, including electrical conduction and development. Yet, only a few defined molecules passing through gap junction channels have been linked to specific functions. We isolated gap junction channel mutants that reduce coupling between the soma and germ cells in the Caenorhabditis elegans gonad. We provide evidence that malonyl-CoA, the rate-limiting substrate for fatty acid synthesis (FAS), is produced in the soma and delivered through gap junctions to the germline; there it is used in fatty acid synthesis to critically support embryonic development. Separation of malonyl-CoA production from its site of utilization facilitates somatic control of germline development. Additionally, we demonstrate that loss of malonyl-CoA production in the intestine negatively impacts germline development independently of FAS. Our results suggest that metabolic outsourcing of malonyl-CoA may be a strategy by which the soma communicates nutritional status to the germline.


Introduction
Gap junctions are clusters of intercellular channels allowing direct passage of small molecules (<1000-2500 daltons) between coupled cells. They are widespread in multicellular organisms, although different gene families encode the protein subunits in invertebrates (innexins) and vertebrates (primarily connexins) (Skerrett and Williams, 2017). While the capability of small molecules to pass through gap junctions can be shown readily in cultured cells, identification of essential molecules that must pass through channels in vivo is challenging. Additionally, disruption of gap junction coupling can affect cell adhesion (Meyer et al., 1992), and resultant defects in intercellular communication may not necessarily relate to the passage of molecules through junctional channels.
In Caenorhabditis elegans, germ cells are coupled throughout their development to the somatic gonad by gap junctions (Starich et al., 2014). Germ cells progress in assembly-line fashion through the early stages of meiosis ( Figure 1A). Gonadal gap junctions have been implicated in germ cell proliferation, oocyte growth, regulation of oocyte meiotic maturation, early embryogenesis and sperm guidance (Govindan et al., 2006;Whitten and Miller, 2007;Nadarajan et al., 2009;Edmonds et al., 2011;Starich et al., 2014). Octameric gap junction hemichannels (half-channels) in the somatic gonad are comprised of the recently duplicated innexins INX-8 and INX-9; apposing germ cell hemichannels are heteromeric and consist of INX-14 in conjunction with either INX-21 or INX-22 (Figure 1-figure supplement 1). Germ cells fail to proliferate in inx-8(0) inx-9(0) mutants, at a point upstream of, or parallel to, GLP-1/Notch activation of germ cells by Delta class ligands LAG-2 and APX-1. These ligands are produced in the distal tip cell (DTC) that provides the proliferative stem cell niche (Austin and Kimble, 1987;Austin and Kimble, 1989;Henderson et al., 1994;Nadarajan et al., 2009). Posterior arm shows the positions of the somatic distal tip cell (DTC) and five pairs of sheath cells (nuclei are numbered). Anterior arm shows the underlying germline, approximate regions of germ cell proliferation (Prolif.), meiotic pachytene stage (Pach.), and developing oocytes. Embryos typically undergo some cell division in the uterus before being laid. Sp, spermatheca; vul, vulva. (B) Compared to the wild type (N2), ovulation in inx-8(tn1513 tn1555rf) inx-9(ok1502null) mutants (a.k.a. inx-8 [rf]) is delayed~18 hr. Bars representing 1-3 hr windows indicate approximate time of the fourth larval stage (L4 to adult) molt, followed by time of appearance of the first fertilized embryo ovulated into the uterus. (C-E) Onset of gfp::lin-41 expression as a marker of oocyte development is delayed when sheath-germline gap junction coupling is perturbed. Panels show DIC and fluorescent images from Figure 1 continued on next page Germ cell proliferation can be rescued in inx-8(0) inx-9(0) mutants to half the level of wild type by driving inx-8 expression in the DTC with the lag-2 promoter (Starich et al., 2014). In these animals, gap junctions between soma and germline are established in the distal gonad arm, but ostensibly not in the proximal arm. Many resultant embryos arrest prior to morphogenesis and exhibit defects in cytokinesis, polar body extrusion, and eggshell development, including loss of the permeability barrier. These phenotypes resemble the Pod (Polarity and Osmotic sensitivity Defect) class of mutant embryos (Tagawa et al., 2001).
Disruption of genes required for fatty acid synthesis (FAS) can give rise to Pod embryos (Rappleye et al., 1999;Rappleye et al., 2003). In C. elegans, the pod-2 gene encodes acetyl-CoA carboxylase (ACC) Type 1, which produces the malonyl-CoA subunits used for fatty acid chain elongation. emb-8 encodes an NADPH-cytochrome P450 oxidoreductase that potentially modifies fatty acids. Wild-type one-cell embryos redistribute proteins to establish polarity with a resultant asymmetric first cell division. Conditional mutant alleles and RNAi silencing of both pod-2 and emb-8 were shown to produce high percentages of embryos that fail to properly establish polarity and divide symmetrically at the first division (Rappleye et al., 2003). fasn-1 (fatty acid synthase) uses malonyl-CoA to synthesize C-16 palmitate, which can be further modified to supply a wide array of fatty acids. RNAi silencing of fasn-1 similarly disrupted polarity establishment of one-cell embryos. In addition to loss of polarity, the osmotic barrier associated with eggshell synthesis is defective in all these embryos (Rappleye et al., 2003). RNAi silencing of a pair of highly similar cytochrome P450s (pod-7 and pod-8) also gives rise to Pod embryos (Benenati et al., 2009). These P450s are implicated in hydoxylation of fatty acids. A lipid extract from pod-7/8(+) embryos, but not emb-8 mutant embryos, can rescue the Pod phenotype resulting from pod-7/8(RNAi), suggesting pod-7/8 and emb-8 may operate in the same pathway (Benenati et al., 2009). pod-2/ACC requires post-translational covalent attachment of biotin for enzymatic activity, and bpl-1 (biotin protein ligase-1) is the C. elegans ortholog of the necessary holocarboxylase synthetase (Watts et al., 2018). Fatty acid precursors obtained from the bacterial diet enable bpl-1 homozygous mutants from +/bpl-1 mothers to develop to adulthood. However, resultant homozygous bpl-1 embryos exhibit a Pod phenotype, and it was shown this is due to an early embryonic requirement for de novo fatty acid synthesis, especially for polyunsaturated fatty acids (PUFAs) (Watts et al., 2018).
Together these results firmly establish a requirement for fatty acid synthesis in determining polarity, implementing proper cytokinesis, and synthesizing an eggshell with an intact permeability barrier. However, mutations in non-FAS genetic pathways can also result in Pod embryos, including those affecting the APC/separase pathway (Rappleye et al., 2002) and genes more specifically involved in eggshell synthesis (Zhang et al., 2005;Johnston et al., 2006;Olson et al., 2006).
Molecules moving through soma-germ cell gap junctions necessary for proliferation and early embryogenesis are unknown. Because the disruption of gap junction coupling in the gonad can produce Pod-like embryos, we explored a potential relationship between FAS genes and gap junctions. We use genetic methods to show that malonyl-CoA (mal-CoA) is produced by POD-2/ACC in the soma. The integrity of INX-8-containing channels impacts the transfer of mal-CoA to the germline for use by FASN-1 even under conditions in which gap junction formation and cell adhesion appear normal. Rescue of the Pod phenotype in pod-2 genetic mosaics indicates a somatic sheath focus of   ]-shows a similar delayed onset of gfp::lin-41 expression as inx-8(rf). spe, sperm. Bar, 20 mm. The online version of this article includes the following source data and figure supplement(s) for figure 1: Source data 1. inx-8(rf) exhibits reduced brood size and interacts with FA synthesis pathway genes. Source data 2. Brood counts for Figure 1. Source data 3. Reduced soma-germline gap junction coupling delays gametogenesis. Figure supplement 1. Predicted topological sites of amino acids mutated in inx-8(tn1513 tn1555) inx-9(0). action. Our results support a model in which mal-CoA transits from soma to germline through gap junction channels to facilitate embryogenesis.

Results
Gametogenesis is delayed by the inx-8(tn1513 tn1555) reduction-offunction (rf) mutation We previously isolated (in an inx-9 null background) a strong loss-of-function inx-8 allele (tn1513) with sufficient residual function to contribute to channel formation and cell adhesion but not support germ cell proliferation (Starich et al., 2014). tn1513 encodes a T239I change in the second extracellular loop of the innexin monomer, predicted to be involved in docking with hemichannels on apposing cells (Figure 1-figure supplement 1; Oshima et al., 2016). Using this allele in a genetic screen for restoration of germ cell proliferation, six inx-8 intragenic suppressor mutations were isolated (to be described elsewhere). One of these, tn1555, encodes a D24N change in the amino terminus (Figure 1-figure supplement 1), near a site that may associate with a cytoplasmic dome structure surrounding the hemichannel outer pore (Oshima et al., 2016). Hermaphrodites of genotype inx-8 (tn1513 tn1555rf) inx-9(ok1502null)-for brevity to be referred to as inx-8(rf)-are predicted to produce homozygous hemichannels in the soma consisting of INX-8(T239I D24N) subunits. inx-8(rf) animals show partially restored germ cell numbers and fertility approximating one-third the level of wild type (Figure 1-source data 1; Figure 1-source data 2). inx-8(rf) is rescued by an inx-8(+) extrachromosomal array, and rescue of inx-8(0) inx-9(0) with an inx-8(rf)::gfp array mimics the phenotype of the suppressor mutant; therefore observed phenotypes can be attributed to inx-8(rf) and not to other possible background mutations.
There is an~18 hr delay to the onset of fertilization in inx-8(rf) compared to the wild type, as determined by relating the timing of first ovulation to the L4 molt (L4-to-adult transition) ( Figure 1B). This delay correlates with late expression of gfp::lin41 in relation to L4 sub-stages of vulval development (Mok et al., 2015); LIN-41 is the earliest known marker of oogenesis (Spike et al., 2014). In the wild type at 20˚C, gfp::lin41 appears by sub-stage L4.7 ( Figure 1C); in inx-8(rf), gfp:: lin41 is expressed after completion of vulval morphogenesis but prior to the L4 molt ( Figure 1D; Figure 1-source data 3). Spermatogenesis is also delayed-wild-type sperm appear as early as the L4.7 stage, but inx-8(rf) sperm first appear after completion of vulval morphogenesis (Figure 1source data 3). Once started, egg-laying in inx-8(rf) continues apace such that~99% of progeny are laid within a 96 hr window (3144/3179 larvae; n = 25), similar to the wild type (5847/5929 larvae; n = 21).
We conclude that delayed gametogenesis in inx-8(rf) mutants arises from compromised somagermline gap junction communication, due to altered channel properties that influence the formation and localization of gap junctions, especially in the loop and proximal arm.
Germline fasn-1 requires somatic pod-2 Genetic interactions between inx-8 and FAS genes could represent activity in the same or parallel pathways. We reasoned that if gap junctions are positioned in the FAS pathway, it might be possible to find a step within this pathway where gene function shifts from a somatic to a germline focus. C. elegans is particularly amenable to such an investigation because simple (highly repetitive) extrachromosomal arrays used to rescue gene function tend to express well in the soma, whereas arrays with more sequence complexity are generally required to prevent silencing of multi-copy gene expression in the germline (Kelly et al., 1997). Previous characterization of pod-2 implied rescue by a simple array (Rappleye et al., 2003); we likewise found that pod-2(ye60cs) is rescued by simple extrachromosomal arrays at 15˚C (see Materials and methods). In contrast, two fosmids encoding emb-8, used individually to generate simple arrays, yielded 65 transformed lines, only one of which rescued emb-8(hc69ts) at 25˚C; the array in this line was eventually silenced. For fasn-1, two fosmids used to generate 93 simple array lines and 20 complex array lines failed to rescue fasn-1(g43ts). These results were consistent with a model in which FAS affecting embryonic development requires pod-2 in the soma to support a germline requirement for fasn-1 and emb-8.
The special nature of a conditional allele could lead to a misinterpretation of rescue results. Because null alleles of these FAS genes had not been isolated, we generated knockouts of pod-2 (tn1691) and fasn-1(tn1762)-simplified to (0)-using CRISPR-Cas9 methodology ( Figure 3B and C). pod-2(0) embryos from pod-2(0)/+ parents arrest late in embryogenesis (pretzel stage; Figure 3D). Most fasn-1(0) embryos from fasn-1(0)/+ parents exhibit signs of differentiation, and many arrest late in embryogenesis; occasional hatchlings emerge with probable hypodermal defects ( Figure 3E-G). The terminal stages of developmental progression in both pod-2(0) and fasn-1(0) embryos derived from heterozygous parents are more advanced than classic Pod embryos, which arrest prior to signs of morphogenesis. This indicates a maternal rescue by pod-2 and fasn-1 of the early embryonic Pod defects.
pod-2(0) was rescued by simple extrachromosomal arrays, supporting probable somatic function. Using a PCR-amplified genomic fragment, we were able to rescue somatic but not germline function of fasn-1(0) with a simple or complex array (see Materials and methods). A genetically balanced line with a complex array, fasn-1(0)/hT2; Ex[fasn-1(+); sur-5::gfp(+)], segregates healthy homozygous fasn-1(0); Ex[fasn-1(+); sur-5::gfp(+)] adults that lay almost exclusively dead embryos ( Table 1). [sur-5::gfp is a co-injection marker expressed in somatic cell nuclei (Yochem et al., 1998); corresponding extrachromosomal arrays can be lost mitotically to generate mosaics-see below)]. Gonad arms appear normal, and animals lay wild-type numbers of typical Pod embryos ( Table 1); many of these display polarity defects (4/14 symmetric first divisions) and exhibit extra nuclei in early embryos. Embryos generally arrest prior to morphogenesis (see below). We conclude this fasn-1(+) PCR fragment rescues somatic fasn-1 function and is either silenced in the germline or lacks an element necessary for sufficient germline expression; in either case, a germline requirement is indicated. In sum, rescue results are consistent with a fertility requirement for pod-2 in the somatic gonad and fasn-1 in the germline. This conclusion is supported by genetic mosaic analysis and gene expression data described below. If inx-8 gap junctions act in this pathway, it would position these junctions as possible mediators of mal-CoA transfer from POD-2 in the soma to FASN-1 in the germline.
GFP::POD-2 and GFP::FASN-1 are tissue restricted We generated endogenous, homozygous-viable, and fertile GFP-labeled alleles of pod-2 and fasn-1 to determine whether their patterns of localization are consistent with their predicted foci of action. The GFP moiety in gfp::pod-2(tn1765) is expected to label all three predicted isoforms ( Figure 3B) (WormBase, 2020). GFP::POD-2 expression is strongest in the intestine, and prominent in the hypodermis, gonad sheath (especially proximal sheath), CAN neuron, and excretory duct ( Figure 4A-C).
No germline expression of any of these GFP-tagged genes was detected, including by anti-GFP staining of dissected gonads ( Figure 4C; Figure 5C,F). This was most clearly observed by examination of the distal gonad ( Figure 4C; Figure 5F); however, abundant GFP::POD-2 or FASN-1::GFP expression in the proximal sheath cells made it more difficult to evaluate expression in the proximal germline. GFP::POD-2 expression in embryos first appears with development of hypodermal and intestinal cells ( Figure 4D,E). In adults, GFP::POD-2 intestinal expression was found to decrease in response to starvation ( Figure 4F). The earliest detectable GFP-tagged FASN-1 in embryos appears in developing hypodermis ( Figure 5D). Expression of both genes is consistent with primarily somatic functions, while germline fasn-1 activity may derive from low levels of maternal expression.
inx-8(+) hemichannels can have both a positive (emb-8) and a negative (fasn-1) genetic effect on FAS mutations which function downstream of overexpressed pod-2(+). This finding is a strong indication that inx-8 acts in the same pathway as pod-2, rather than a parallel pathway. These results are consistent with gap junctions acting as conveyors of mal-CoA from soma to germline, and they fit a model in which INX-8 gap junctions are positioned between pod-2 and fasn-1 ( Figure 6C), but not downstream of fasn-1 ( Figure 6D).
Within the first class of mosaics, five animals lost the array in all sheath cells in both gonad arms. Three other animals exhibited a difference in phenotypic severity between gonad arms-embryos derived from one arm developed to later multicellular stages in utero ( Figure 7B-D). Differences were coincident with loss of the array from all sheath cells in the more severely affected arm, versus retention of the array in a single sheath cell of the better arm. In subsequent screening, five more mosaics were identified that displayed phenotypic disparity between the two gonad arms; in one example, one arm produced defective embryos while the better arm gave rise to wild-type embryos  (producing !40 viable progeny). These results indicate that the focus of pod-2(0) rescue is autonomous to each gonad arm, consistent with the interpretation that pod-2 expression in the somatic sheath is essential to embryonic viability.
In subsequent screening for germline (P 4 -) mosaics, four animals were identified that maintained the array in the soma but lost the array in all embryos ( Figure 7A). The terminal stages of embryonic development resembled those of pod-2(0) embryos derived from +/pod-2(0) parents, that is embryos developed to threefold or pretzel stages but failed to hatch ( Figure 7E-G). These stages are more advanced than terminal stages of many dead embryos derived from parents with somatic (but not germline) loss of the rescuing array; such embryos fail to differentiate ( Figure 7H). This early developmental arrest resembles terminal-stage Pod embryos from fasn-1(0); Ex[fasn-1(+)] (compare panels H and I in Figure 7). We conclude that somatic pod-2(+) supplies sufficient levels of mal-CoA to the germline not only to establish a wild-type one-cell embryo, but also to support continued development, presumably until zygotic pod-2 expression becomes adequate for completion of embryogenesis. These studies establish that metabolites essential for embryonic development can be produced in the somatic gonad and provided to the oocyte through gap junctions.
Intestinal loss of pod-2, but not fasn-1, results in a germline starvationlike phenotype The other class of pod-2(0) genetic mosaics producing dead embryos in our original screen lost Ex [pod-2(+); sur-5::gfp] from the intestine (E-) ( Figure 7A). E(-) mosaic animals were smaller than wild type, and gonad arms were severely reduced in size ( Figure 8A). Only the most proximal oocytes showed appreciable growth. E(-) mosaic gonad arms resemble those seen in gonads undergoing the oocyte starvation response, or adult reproductive diapause (ARD), a process induced by starvation during the L4 larval stage proposed to maintain germline stem cells for repopulation of the gonad upon the resumption of feeding (Angelo and Van Gilst, 2009;Seidel and Kimble, 2011). During ARD, germline stem cells cease dividing, the gonad shrinks due to extensive apoptosis of differentiated germ cells, and growth is largely restricted to the most proximal oocyte.
The C. elegans intestine is enriched with lipid droplets, produces yolk lipoproteins (Kimble and Sharrock, 1983) and is regarded as a major site of FAS (Watts and Ristow, 2017). A genetic pathway in C. elegans required for intestinal apical polarity establishment leading to proper lumen formation has been described; genes in this pathway, including pod-2, encode enzymes required for glycosphingolipid synthesis . Lipid biosynthesis is required throughout larval growth, coincident with membrane expansion. Our isolation of adult mosaics lacking pod-2(+) in the intestine was therefore surprising. We subsequently identified two presumptive P 1 (-) pod-2 mosaics, predicted to have lost pod-2(+) function in the intestine, somatic gonad, germline, and many muscle and hypodermal cells, among others ( Figure 7A). The most striking phenotype distinguishing these animals from E(-) mosaics was an extremely constipated intestine ( Figure 8B). Therefore the absence of this constipation in E(-) mosaic animals implies that loss of pod-2(+) from the intestine does not prevent the processing of bacteria through the intestinal lumen. (Both P 1 mosaics showed tissue extruded from the rectum, which may be the cause of constipation.) Although gfp::fasn-1(tn1782) is not detected in the intestine, we asked if there is a functional role for fasn-1 similar to pod-2. As described above, homozygous fasn-1(0); Ex[fasn-1(+); sur-5::gfp] progeny from heterozygous parents produce Pod embryos but exhibit no other phenotype; within this class of progeny we screened for E(-) mosaics. Ten (of 800) such animals were identified ( Figure 7A); in stark contrast to pod-2, their gonad arms appeared normal. These animals displayed no overt defects outside of Pod embryo production ( Figure 8C). Because maternal FASN-1 rescues fasn-1(0) homozygotes to later embryonic stages, an early intestinal function for fasn-1 equivalent to pod-2 could be rescued maternally. However, the surprising conclusion from this mosaic analysis is that there is no significant intestinal requirement for zygotic fasn-1 in larval and adult stages. The

Is malonyl-CoA required in other germline processes?
inx-8(rf) and inx-8/9(0); Ex ] mutants share delayed oogenesis and a reduction in gap junction coupling, germ cell proliferation, and brood size ( Table 1). inx-21(0) mutants are sterile, and inx-22(0) mutants are fertile (Starich et al., 2014); therefore, mal-CoA required for embryonic development must minimally transit through gap junction channels composed of INX-14/INX-21 germline hemichannels. These channels are strongly expressed throughout the distal arm, but expression wanes in the proximal arm ( Figure 2B), a pattern somewhat incongruous with mal-CoA being required only for embryo integrity. Because inx-8/9(0); Ex ] mutants appear to have no sheath-germline gap junction coupling, their associated phenotypes should represent the most severe defects possible if all gap-junctional mal-CoA transfer from sheath to germline is eliminated, that is, reduction of germ cell numbers by half, delayed gametogenesis, or very low embryo output (Table 1). We asked if mal-CoA levels might indeed influence phenotypes preceding embryogenesis.
Effects of global mal-CoA levels were indirectly examined by comparing higher or lower pod-2(+) copy number rescue of pod-2(0); numbers of dead eggs and larvae were summed to reflect total embryo output ( Table 1). Lower copy number rescue coincided with reduced embryo output (84% of wild-type) and lower proportion of viable larvae within a brood (~37% of total embryos) ( Table 1). Embryo output may therefore be impacted by pod-2 expression; however, somatic cells outside the gonad could be responsible for mediating this effect.

Discussion
The genetic analysis of mutant inx-8 soma-germline gap junction channels has led us to three conclusions that have significance beyond the C. elegans model system. First, mal-CoA produced in the somatic sheath is delivered through gap junctions to the germline ( Figure 9); somatically derived mal-CoA is necessary to establish a proper one-cell embryo and to support continued embryogenesis. This conclusion is supported by genetic mosaic analysis of pod-2, transformation rescue of pod-2, fasn-1 and emb-8 mutants, as well as genetic interactions between inx-8(rf) and FAS mutants. The contrasting responses of fasn-1(g43ts) and emb-8(hc69ts) to over-expression of pod-2(+) in the context of mutant INX-8 hemichannels, strongly support a model positioning gap junctions between pod-2 and fasn-1 (Figure 9). Furthermore, the nature of the products of these enzymes is consistent with such an interpretation. Mal-CoA produced by POD-2 is a hydrophilic, membrane impermeable molecule of a size (854 daltons) which is well within the range known to traverse the aqueous pore size of innexin gap junctions (~20-30 Å or up to~2500 daltons; Skerrett and Williams, 2017). In contrast, palmitate and downstream fatty acids can cross cell membranes (Schwenk et al., 2010). Indeed, palmitate added to the media was shown to rescue one-cell polarity, but not osmotic integrity, in pod-2(ye60cs) embryos (Rappleye et al., 2003), suggesting that dietary palmitate can traffic from the intestine to the gonad; this result also supports a special germline role for fasn-1 that is not complemented by dietary palmitate.
Second, pod-2 expression (and presumably mal-CoA production) is exceptionally robust in the intestine and essential for normal germline development. In the absence of intestinal POD-2, the germline exhibits phenotypic hallmarks of the germline ARD response despite the presence of a replete food source. By contrast, intestinal fasn-1 expression is not similarly required. (A possible caveat is that maternal fasn-1 in the intestine may be sufficient to reach adulthood, which would be surprising.) In light of the abundant expression level of gfp::pod-2 in the intestine and our finding that mal-CoA can be directionally transferred intercellularly, the question arises as to whether the intestine provides mal-CoA to other cells. At least one additional route may deliver mal-CoA to the germline early in its development-the primordial germ cells Z2 and Z3 associate with a pair of intestinal cells during embryogenesis, but these contacts are lost before hatching (Sulston et al., 1983;Abdu et al., 2016). Therefore, an early germline requirement for mal-CoA could be fulfilled directly from the intestine; loss of such a function would be encompassed within the ARD-like phenotype seen in pod-2 E(-) mosaics. Potentially, mal-CoA produced in the intestine may augment levels in the somatic gonad as well as other tissues, perhaps via specific transporters or vesicles, a possibility we have not explored but which might be investigated using genetic mosaics or an auxin-inducible degron engineered into pod-2 (Zhang et al., 2015). Reduced mal-CoA production in the intestine might be interpreted globally in the worm and contribute to a systemic starvation response. Recent results show that the HLH-30/TEFB transcription factor functions as a master regulator of the ARD state (Gerisch et al., 2020). hlh-30 mutants fail to effect the system-wide changes promoting longterm survival and recovery associated with ARD. ARD longevity does not appear to rely on fatty acid metabolism. However, entry of hlh-30 mutants into the ARD state appears normal. If decreased mal- CoA expression in the intestine is part of the worm's initial response to starvation, such a response would lie upstream of hlh-30 activity.
Third, a pronounced delay in gametogenesis along with reduction in brood size results from reduced soma-germline gap junction communication; it is unknown if this delay derives from generally slower mitotic or meiotic progression, or from a developmental block at a particular meiotic stage. The nature of potential molecules passing through gap junctions that are responsible for timely meiotic progression is unknown, but our evidence thus far has not specifically implicated mal-CoA.
Our results indicating that somatic mal-CoA transits from somatic sheath to the germline via gap junctions are consistent with other findings in C. elegans related to fatty acid metabolism in oocytes, particularly a strict requirement for PUFA synthesis (Watts et al., 2018). PUFA-dependent prostaglandin signaling from developing oocytes influences sperm guidance, and reduction of inx-14 function disrupts this signaling (Kubagawa et al., 2006;Edmonds et al., 2011). We suggest that lower levels of mal-CoA delivered to the oogenic germline through mutant INX-14-containing gap junctions reduce prostaglandin synthesis and its signaling function for sperm migration.
To our knowledge, this segregation of the cellular source of mal-CoA from the eventual cell type in which it is used as substrate is novel. As the rate-limiting step in FAS, mal-CoA production is an attractive control point to tie aspects of germ cell developmental progression to somatic control. However, although genetic evidence indicates a germline role for fasn-1, the inability to visualize GFP-tagged FASN-1 suggests maternal fasn-1 is expressed at very low levels. We therefore consider whether mal-CoA could function in the germline outside the standard FAS pathway, a possibility we attempted to examine using embryo output as a parameter.
Cytoplasmic FAS is carried out by a multifunctional megasynthase like that encoded by fasn-1 (type-I system). Mitochondria carry out FAS independently using monofunctional enzymes resembling the bacterial FAS type-II system (recently reviewed by Kastaniotis et al., 2017). Mitochondrial FAS utilizes an acyl-carrier protein rather than CoA to shuttle the substrate between enzymes. An ACC enzyme has been found in the mitochondria of S. cerevisiae but not mammals. In mammals, the ACSF3 enzyme uses malonate as a substrate to synthesize mal-CoA and could contribute to mitochondrial FAS. However, malonate is a toxic metabolite that inhibits succinate dehydrogenase, and knockout of ACSF3 in cultured cells suggests this enzyme is more critical for eliminating toxic malonate from mitochondria rather than serving an essential function for mitochondrial FAS (Bowman et al., 2017). The sources of malonate and mal-CoA in mitochondria are still unclear, although it has been suggested that hydrolysis of cytosolic mal-CoA may produce malonate that is taken up by mitochondria (Bowman et al., 2017). If this is the case, reduced levels of cytoplasmic mal-CoA could negatively impact mitochondrial FAS.
In addition to its metabolic function in FAS, mal-CoA has established roles as a regulatory molecule. It inhibits uptake and therefore oxidation of fatty acyl-CoAs by carnitine palmitoyltransferase I (CPT-1). Beta-oxidation of fatty acids in mitochondria provides energy through oxidative phosphorylation. The inhibitory mal-CoA in some tissues that exhibit low levels of FAS (heart and skeletal) derives from a second acetyl-CoA carboxylase (ACC2), which associates with the mitochondrial Figure 9. Model for malonyl-CoA transfer from soma to germline. Enzymes (blue) implicated in germline FAS. Malonyl-CoA transits from somatic sheath to germline through gap junction channels comprised of INX-8/9 (soma) and INX-14/INX-21 (germline) hemichannels. Germline FASN-1 uses malonyl-CoA to synthesize palmitate, which may be further extended and modified to produce other long-chain fatty acids. EMB-8 (NADPH-dependent CYP450 reductase) and POD-7/8 (CYP450s) are necessary to synthesize the lipid-rich (inner) layer of the eggshell and support polarity establishment (Rappleye et al., 2003;Benenati et al., 2009); the composition of lipid layer fatty acids is unknown. de novo PUFA synthesis is required in the germline for embryonic viability and is implicated in sperm guidance (Kubagawa et al., 2006;Watts et al., 2018). The identities of other long-chain fatty acids that may be synthesized in the germline are unknown. PUFAs, polyunsaturated fatty acids; LFAs, long-chain fatty acids; MUFA, monounsaturated fatty acids; pm, plasma membrane. membrane to produce mal-CoA regulating CPT-1. Manipulation of mal-CoA levels in the mouse hypothalamus regulates food intake (Wolfgang and Lane, 2006). Regulation is effected through the brain-specific CPT1-c, via a mechanism distinct from the enzymatic activity of other CPT1 enzymes (Sierra et al., 2008;Reilly and Mak, 2012). Little information regarding the C. elegans ACC2 is available. Therefore, pod-2/ACC type I-derived mal-CoA delivered from the somatic sheath could in effect be relaying the state of nutrition to the germline and modulating regulation of fatty acid betaoxidation in mitochondria accordingly.
Malonylation as a post-translational lysine modification has recently been described (Peng et al., 2011). Malonylation may inhibit target proteins, such as the glycolytic enzymes glyceraldehyde 3phosphate dehydrogenase and pyruvate kinase (Kulkarni et al., 2017), and ACSF3 was shown to be essential for malonylation of mitochondrial protein targets (Bowman et al., 2017). Malonylation of mTOR reduces mTORC1 complex activity, decreasing endothelial cell proliferation and reducing angiogenesis in a human umbilical model (Bruning et al., 2018). Together these studies and others suggest a possibly pervasive role for mal-CoA in sensing and responding to nutritional status. Levels of mal-CoA provided to the C. elegans germline from the soma could potentially regulate a number of metabolic processes in both mitochondria and the cytoplasm.
Finally, we note that one trait associated with rapid tumor growth is an increase in FAS, and FASN has been explored as a cancer therapy target (Menendez and Lupu, 2007). Possibly, the ability of mal-CoA to transit through gap junctions might sustain FAS during tumor progression. The discovery that mal-CoA transits through gap junctions from soma to germline may be indicative of other unappreciated intercellular roles for this important molecule.
To generate fasn-1::gfp, the fasn-1 specific 20-nucleotide sequence for crRNA was selected with help of a guide RNA design checker from Integrated DNA Technologies (IDT) (https://www.idtdna. com) and was synthesized as a 20 nmol product from Dharmacon (https://dharmacon.horizondiscovery.com), along with tracrRNA. The repair template was amplified from plasmid pDD282 (https:// www.addgene.org/66823/) and designed to include a flexible linker (GASGASGAS) and GFP at the C-terminus of the fasn-1 endogenous locus. These were designed using a standard protocol (Paix et al., 2015). Approximately 30 young gravid animals were injected with the CRISPR/Cas9 injection mix as described in the standard protocol. Homozygous genome-edited animals were screened by PCR and confirmed by Sanger sequencing (Eurofins). mex-5p::gfp::pod-2::tbb-2-3'UTR was constructed by Gibson assembly of component PCR products representing the mex-5 promoter, the 'a' isoform of gfp::pod-2, and the tbb-2-3'UTR to prevent germline RNA degradation.
For fasn-1(av138[fasn-1::gfp]) imaging data, animals were immobilized on 7% agarose pads with 0.05 mm polystyrene beads and imaged using a spinning disk confocal system with a Nikon 60 Â 1.2 NA water objective, a Photometrics Prime 95B EMCCD camera, and a Yokogawa CSU-X1 confocal scanner unit. Images were acquired and analyzed by Nikon's NIS imaging software and ImageJ/FIJI Bio-formats plugin (National Institutes of Health) (Linkert et al., 2010;Schindelin et al., 2012). The acquisition of GFP and DIC images was performed with 1 mm z-step size and 15-20 z planes.

Genetic mosaic analysis
To associate the somatic focus of action of pod-2 with germline phenotypes, array losses were characterized in animals of genotype pod-2(tn1691null); tnEx212[W09B6-pod-2(+)-20 ng/l-hi copy; sur-5::gfp] that were isolated on the basis of sterility. Subsequently, potential candidate mosaics of interest were prescreened directly at the dissecting microscope level for asymmetry in the phenotypic severity seen between anterior and posterior gonad arms, and then examined at the compound microscope level for loss of sur-5::gfp expression. Potential pod-2(tn1691null); tnEx219 [W09B6-pod-2(+)-4 ng/l-lo copy; sur-5::gfp] genetic mosaics were also prescreened in this manner. Intestinal (E-) mosaics were prescreened using a low-power fluorescence SMZ18 Nikon (Melville, NY) microscope with a Lumencor (Beaverton, OR) SOLA Light Engine, but for pod-2 many of these candidate mosaics were seen to express sur-5::gfp at very low levels, or in just a few intestinal cells, when examined at high power. This was not an issue when isolating fasn-1(tn1762null); tnEx218[fasn-1(+); sur-5::gfp] E(-) mosaics.