Visualization of specific repetitive genomic sequences with fluorescent TALEs in Arabidopsis thaliana

Highlight Transcription activator-like effectors fused to fluorescent proteins can visualize repetitive genomic sequences including centromere, telomere, and rDNA sequences for analysing chromatin dynamics in living plant cells.


Introduction
Genome organization is a dynamic process that influences gene expression, genome maintenance, and responses to environmental stimuli in many organisms (Kurz et al., 1996;Franklin and Cande, 1999;Cobbe and Heck, 2000;Misteli, 2007). Fluorescent in situ hybridization (FISH) is a powerful tool for determining the spatial organization of specific DNA sequences on chromosomes or in nuclei (Hans de Jong et al., 1999). Although FISH is, in principle, capable of detecting any specific sequence, it cannot provide information about chromatin dynamics, because FISH requires the fixation of cells and a high-temperature treatment for hybridization. To visualize chromatin organization without fixation and hybridization, several in vivo imaging techniques have been developed. The first report describing in vivo imaging of chromatin used DNA-binding domains of bacterial transcription factors, such as the lac repressor (LacI) or tetracycline repressor (TetR) systems (Robinett et al., 1996;Kato and Lam, 2001;Matzke et al., 2005). After repeats of the cognate DNA sequences recognized by these transcription factors are introduced into specific genomic regions, the nuclear localization of these regions can be observed by expressing GFP-tagged transcription factors. Using this system, the relationship between chromatin conformation, gene expression (Rosin et al., 2008) and DNA damage (Hirakawa et al., 2015) have been examined in plants.
However, as the preceding method requires the random insertion of exogenous DNA into the genome, it is not amenable to in vivo imaging of specific genomic loci. In order to solve this problem, an in vivo imaging strategy that made use of zincfinger domain containing proteins was developed (Lindhout et al., 2007). These domains contain a DNA-binding motif whose specificity can be engineered and that have previously been used for genome editing. Engineered zinc-finger domains have been used to detect endogenous centromere sequences (Lindhout et al., 2007). However, because each modular zinc-finger protein recognizes a DNA triplet with contextdependent interactions between neighbouring zinc-fingers, engineering proteins to recognize specific sequences can be challenging (Gaj et al., 2013). By contrast, TALEs contain a DNA binding domain comprising repeats of an approximately 34 amino acid-long DNA recognition module. Each module robustly recognizes a single nucleotide (Boch et al., 2009;Moscou and Bogdanove, 2009). In human and mouse cultured cells, TALE-FPs (also known as TGV, TALEColor, and dTALE) have been successfully used for the visualization of chromatin (Ma et al., 2013;Miyanari et al., 2013;Thanisch et al., 2014). Furthermore, transiently expressed TALE-FPs (TALE-light) have previously been used to analyse chromatin dynamics in Drosophila melanogaster (Yuan et al., 2014). Here we present stable transgenic lines expressing TALE-FPs for centromeric, telomeric, and rDNA sequences and analyse the dynamics of these sequences in the nuclei of plant organs.

Plasmid construction
TALEs were assembled in pZHY500 by Golden Gate assembly using the TAL effector toolbox (Cermak et al., 2011) obtained from Addgene. The target sequences are provided in Supplementary Table  S1 at JXB online. pCE1.2iFok was used for the construction of TALEfluorescent protein (FP) fusion expression cassettes. pCE1.2iFok was obtained by cloning the expression cassette, the 2xCaMV35S promoter with the omega enhancer-the FokI nuclease domain-and the Arabidopsis HSP18.2 gene terminator into the pCR8/GW/TOPO TA Cloning vector (ThermoFisher Scientific). The assembled TALEs were cloned into pCE-N-GFP, pCE-N-Venus, pCE-N-tdTomato, or pCE-N-3xGFP. pCE-N-FPs were constructed by modifying pCE1.2iFok, including replacement of the promoter region with a nuclear localization signal sequence by AscI and NcoI digestion and replacement of the FokI domain with sGFP, Venus (Nagai et al., 2002), tdTomato (Shaner et al., 2004) or 3xGFP (Ma et al., 2015) with an In-Fusion HD Cloning kit (Takara Bio Inc.). The sequence of pCE-N-GFP is provided in see Supplementary Fig. S1 at JXB online. The destination vector pGWB-RPS5a was obtained by modification of pGWB501 (Nakagawa et al., 2007). The 1.7-kb SbfI and XbaI fragment containing the RPS5a promoter (Weijers et al., 2001) was inserted into the SbfI-XbaI site of pGWB501 to yield pGWB-RPS5a. The TALE-FPs were transferred either to pGWB-RPS5a for microscopic observation or to pMDC32 (Curtis and Grossniklaus, 2003) for immunoprecipitation with LR clonase (Invitrogen). Details of vector construction are shown in Supplementary Fig. S2.

Plant materials and transformation
The plasmids encoding engineered TALE-FP fusions were introduced into Agrobacterium tumefaciens GV3101. Transformation of either A. thaliana accession Col-0 or the KU70 mutant (SALK_123114) (Gámez-Arjona et al., 2010) was performed by the floral dip method (Clough and Bent, 1998). The transformants were selected on solidified 1/2 MS medium containing claforan and hygromycin.
FISH was performed essentially as described previously by Shibata and Murata (2004) following immunofluorescence staining. Briefly, probes recognizing 180 bp centromeric repeats or telomeres were synthesized by nick translation using a DIG nick translation mix (Roche Diagnostics). The DIG-labelled probes were visualized using anti-digoxigenin-rhodamine Fab fragments (Roche).

Microscopy
For immunostaining and FISH, we used an upright microscope (BX53, Olympus, Tokyo, Japan) with a ×100 objective (UPLSAPO 100×, Olympus, Tokyo, Japan) and a CCD camera (DOC CAM U3-50S5M-C, Molecular Devices) controlled with MetaVue (Molecular Devices). For live imaging, we used an inverted microscope (IX81, Olympus, Tokyo, Japan) equipped with a spinning-disk confocal system (CSU-X disk, Yokogawa Electric, Tokyo, Japan) with ×40, ×60 or ×100 objectives (UPLFLN 40XO, PLAPO 60XO2PH, PLAPO 100XO) and a CMOS camera (Neo 5.5 sCMOS, ANDOR) controlled with MetaMorph (Molecular Devices). GFP and tdTomato were excited with 488 nm and 561 nm lasers, respectively. T 2 populations were sown on 1/2 MS medium in Petri dishes and grown for 5 d prior to analysis, with the exception of floral organ samples. Flower buds were used for floral organ samples. Whole plants or floral organs were placed between cover slips mounted with water. For time-lapse observation, T 2 populations were sown on solidified 1/2 MS medium in glass-bottomed dishes and grown for 7-14 d prior to imaging with confocal microscopy. Images were acquired every 2-5 min using multiple z-planes (0.6-1.0-μm intervals) and 10-20 planes per sample were collected. For higher-resolution imaging, we used a confocal microscope (FV1200, Olympus, Tokyo, Japan) with a ×60 or a ×100 objective (UPLSAPO 60XW, UPLSAPO 100XO) and GaAsP detectors controlled with FluoView (Olympus, Tokyo, Japan). GFP, Venus, and 3xGFP were excited with a 473 nm laser and tdTomato was excited with a 559 nm laser. Images were processed by Fiji to generate maximum intensity projection images, adjust the contrast, reduce the background, and to add colour.

Tracking analysis
TALE_telo-FP signals were plotted and the centres of the nuclear masses were calculated from the projection images of the time points (30 min). The mean-squared displacement (MSD) was calculated from the average change in distance between each TALE-FP signal and the nuclear centre of mass over the possible combinations of lag time (Δt). MSD values of the signals were averaged and the standard deviations were presented.

Co-immunoprecipitation and MS analysis
Seedlings of A. thaliana expressing TALE_180-GFP or TALE_ telo C-GFP were used for co-immunoprecipitation. Two grams of 3-week-old seedlings were fixed with 1% formaldehyde for 30 min, ground with a mortar and pestle, and lysed in immunoprecipitation buffer containing 50 mM HEPES-KOH (pH 7.5), 140 mM NaCl, 1 mM EDTA, 1% Triton X-100, 0.1% sodium deoxycholate, 1 mM PMSF, and Complete Protease Inhibitor Cocktail (Roche) (Mérai et al., 2014). The homogenates were filtered through two layers of Miracloth to remove cell debris. The flow-through fraction was sonicated with Bioruptor UCD-250 for 15 min at the middle intensity (200 W, 15/30 s ON/ OFF cycle) to shear chromatin and debris was then removed by centrifugation at 15 000×g for 30 min. The supernatant was used for immunoprecipitation with GFP trap magnetic beads. Washes were performed with immunoprecipitation buffer. SDS-PAGE was carried out according to the method described by Laemmli (1970). Co-immunoprecipitated samples were dissolved in sample buffer and resolved (~2 cm) using a slab gel. Each lane was divided into six pieces. In-gel digestion was performed according to the method described by Rosenfeld et al.(1992).
Samples were analysed by nano-flow reverse phase liquid chromatography followed by tandem MS, using a Triple TOF 5600+ (AB SCIEX, Concord, Canada). A capillary reverse phase HPLC-MS/ MS system composed of an Eksigent Ekspert nano-LC 400 HPLC system (AB SCIEX) connected directly to an AB SCIEX quadrupole time-of-flight (QqTOF) TripleTOF 5600+ mass spectrometer (AB SCIEX) in the trap and elute mode was used to identify the ensemble of proteins present in each sample. In the trap and elute mode, the samples were automatically injected using the Ekspert 400 system into a peptide trap column (ChromeXP, C18-CL, 200 µm I.D. ×0.5 mm, 3 µm particle size, 120 Å pore size, AB SCIEX) attached to a cHiPLC system (AB SCIEX) for desalting and the concentration of peptides. After washing the trap with MS-grade water containing 0.1% trifluoroacetic acid and 2% acetonitrile (solvent C), the peptides were loaded into a separation capillary reverse phase column (ChromeXP, C18-CL, 75 µm I.D. ×150 mm, 3 µm particle size, 120 Å pore size, AB SCIEX) by switching the valve. The eluents used were: (A) 100% water containing 0.1% formic acid and (B) 100% acetonitrile containing 0.1% formic acid. The column was developed at a flow rate of 0.5 μl min -1 with the following concentration gradient of acetonitrile: from 2% B to 32% B in 100 min, 32% B to 80% B in 1 min, sustaining 80% B for 10 min, from 80% B to 2% B in 1 min, and finally reequilibrating with 2% B for 15 min. Mass spectra and tandem mass spectra were recorded in positive-ion and 'high-sensitivity' mode with a resolution of ~35 000 full-width half-maximum. The nanospray needle voltage was typically 2 300 V in HPLC-MS mode. After the acquisition of approximately six samples, TOF MS spectra and TOF MS/ MS spectra were automatically calibrated during dynamic LC-MS and MS/MS autocalibration acquisitions by injecting 50 fmol BSA. The Analyst TF1.6 system (AB SCIEX) was used to record peptide spectra over the mass range of m/z 400-1250, and MS/MS spectra in information-dependent data acquisition over the mass range of m/z 100-1600. For CID-MS/MS, the mass window for precursor ion selection of the quadrupole mass analyser was set to 0.7 ± 0.1 Da. The precursor ions were fragmented in a collision cell using nitrogen as the collision gas. Advanced information-dependent acquisition (IDA) was used for MS/MS collection on the TripleTOF 5600+ to obtain MS/MS spectra for the 20 most abundant parent ions following each survey MS1 scan (250 ms acquisition time per MS1 scan, and typically 100 ms acquisition time per MS/MS). Dynamic exclusion features were based on m/z value and were set to an exclusion mass width of 50 mDa and an exclusion duration of 12 s. Searches were performed by using the Mascot server version 2.4.0 (Matrix Science, MA, USA) against the latest Swissprot database for protein identification. Search parameters were set as follows: the enzyme selected was used with three maximum missing cleavage sites, species limited to Arabidopsis thaliana (thale cress), a mass tolerance of 45 ppm for peptide tolerance, 0.1 Da for MS/MS tolerance, fixed modification of carbamidomethyl (C), and variable modification of oxidation (M). The maximum expectation value for accepting individual peptide ion scores [−10*Log(P)] was set to ≤0.05, where P is the probability that the observed match is a random event. Protein identification and modification information returned from Mascot were manually inspected and filtered to obtain confirmed protein identification and modification lists of CID MS/MS.

Visualization of endogenous genomic sequences of A. thaliana with fluorescent TALEs
To image endogenous genomic sequences in plant nuclei, we designed a TALE protein fused with a FP (TALE-FP) (Fig. 1A). We first investigated the localization of centromeres by targeting the 180 bp centromeric repeats known as pAL1 (Fig. 1B). This sequence belongs to the major centromeric satellite, forms tandem arrays approximately 2 Mbp in length, and occupies the centromeric regions of all chromosomes in A. thaliana (Copenhaver et al., 1999;Haupt et al., 2001). Such repetitive sequences permit the recruitment of multiple molecules of TALE-FP to the same locus. To construct TALEs that recognize 17 nt of the 180 bp centromeric repeat sequence (TALE_180) (Supplementary Table S1), we cloned DNA encoding these TALEs into a vector with an in-frame fusion to a FP under the RPS5a promoter. A. thaliana was transformed with these constructs using the floral dip method. Figure 1C (top) shows the root of a transformant stably expressing TALE_180-GFP. Ten discrete signals were usually detected in each nucleus of meristematic root cells, each presumably corresponding to one of the 10 centromeres of A. thaliana chromosomes (Fig. 1C).
To address whether the TALE-FP system can be used to visualize other repetitive genomic sequences, we next designed TALEs targeting the C-strand or G-strand of the telomeres, the 18S rDNA, or the 5S rDNA repeats (Fig. 1D-F; Supplementary Table S1) and fused them to FPs (TALE_ telo C-tdTomato, TALE_telo G-GFP, TALE_18S-Venus, and TALE_5S-GFP, respectively). We detected small, dotlike signals presumably corresponding to telomeres in cells expressing either of the TALE_telo-FP fusions (Fig. 1D).
In addition to small dot-like signals, two strong signals were observed in cells expressing TALE_telo G-GFP. We constructed a transgenic line expressing TALE_telo C-GFP, where we detected only weak signals of TALE_telo C-GFP. Thus, we constructed TALE_telo C-tdTomato, which is a red fluorescent protein that forms tandem dimers, and could detect TALE_telo C-tdTomato signals (Fig. 1D). However, the signal intensity of TALE_telo C-tdTomato was less than that observed in lines expressing TALE_telo G-GFP, despite repeated rounds of selection to isolate transgenic lines with strong expression of the TALE_telo C-tdTomato.
Therefore, to enhance the signal, we constructed a 3×GFP fusion for TALE_telo C visualization. TALE_telo C-3×GFP exhibited signal intensities comparable with TALE_telo G-GFP (Fig. 1D). This improvement demonstrated that the use of tandemly repeated FPs, at least up to trimers, is useful to enhance TALE-FP signals. All TALE_ telo-FPs showed signal numbers lower than the expected maximum number (20 signals) per nucleus. Because FISH, using probes directed against telomeric repeats, also shows a similar distribution of signals (Schubert et al., 2012), it is possible that close physical association of telomeres in A. thaliana (Feng et al., 2014) reduces the number of discrete signals that were observed, rather than a shortcoming in our method.
We also used fluorescent TALE fusions to observe rDNA repeats. When we visualized the 18S rDNA with TALE_18S-Venus, one to four bright signals were observed around the nucleoli (Fig. 1E). In the case of TALE_5S-GFP-mediated visualization, we observed three to six weak signals in the nuclei (Fig. 1F). This distribution of signal intensity of TALE-FP fusions specific for rDNA is consistent with the fact that 18S rDNA genes are located on chromosomes 2 and 4 (Murata et al., 1997;Fransz et al., 2002) while 5S rDNA genes are near the centromeres of chromosomes 3, 4, and 5 (Murata et al., 1997;Cloix et al., 2000).
Some of our transgenic lines exhibited background fluorescence in the nucleoli or throughout the cytoplasm which may have been derived from unbound or off-target TALE-FPs. To combat this, we performed repeated selection to recover lines with an improved signal-to-noise ratio. Transgenic lines with highly expressed and specifically localized TALE_180-GFP were readily recovered but lines expressing TALE_rDNAs with low background were more difficult to acquire.

Confirmation of plant TALE-FP localization by immunofluorescence and FISH
To verify the specific recognition of centromeres and telomeres by TALE-FP, we performed immunofluorescence and FISH to detect the repeat sequences. We analysed the centromere distribution by immunofluorescence using an anti-CENH3 antibody ( Fig. 2A) or FISH using a 180 bp repeat sequence as a probe (Fig. 2B). The centromere signals were widely dispersed and peripherally located in nuclei as reported by FISH (Armstrong et al., 2001). The signals were co-localized with the signals of TALE_180-GFP. The distribution of telomeres was analysed by FISH using the telomere repeat sequence as a probe. FISH experiments previously reported that telomere signals of A. thaliana were mainly clustered around the nucleolus (Armstrong et al., 2001). TALE_telo G and TALE_telo C signals were also distributed around the nucleolus and merged images showed that TALE_telo-FPs co-localized with the telomeres (Fig. 2C). Taken together, these results suggest that TALE-FPs are capable of performing reliable imaging of endogenous repetitive sequences in plants.
TALE-FPs also permit multiple colour imaging of genomic sequences. For imaging of centromeric DNA and a centromeric protein at the same time, we observed A. thaliana roots simultaneously expressing CENH3-tdTomato and TALE_180-GFP. In A. thaliana, CENH3 is a centromerespecific histone H3 variant that co-localizes with the 180 bp repetitive sequences of all centromeres (Talbert et al., 2002). Even though TALE_180-GFP co-localizes with CENH3, the signal intensity of TALE_180-GFP is not always consistent with that of CENH3 (Fig. 2D). This difference is presumably because TALE_180-GFP binds to both the core centromeric region as well as the pericentromeric region. Most CENH3 is thought to bind to 180 bp repeats (Nagaki et al., 2003); however, some clusters of 180 bp repeats, particularly those that are long, are not fully occupied by CENH3 (Shibata and Murata, 2004). Previously, the lengths of the 180 bp tandem repeats on each chromosome were estimated to be 2.26 Mbp (chromosome 1) to 1.4 Mbp (chromosome 3) from FISH experiments (Haupt et al., 2001).
Next, we observed cells simultaneously expressing TALE_180-tdTomato and TALE_telo G-GFP. The strong signals associated with TALE_telo G-GFP were partially colocalized with TALE_180-tdTomato (Fig. 2E). The intensity of signals of TALE_180-tdTomato was compared among the nuclei of root meristematic cells. The 180 bp signal intensity observed in centromeres associated with TALE_telo G is relatively high compared with those in other centromeres (Fig. 2F, G). Centromeric regions often contain long interstitial telomere sequences (ITSs) which consist of imperfect telomerelike repeats. A. thaliana has 349 kb ITSs within the centromere of chromosome 1 (Richards et al., 1991;Armstrong et al., 2001;Vannier et al., 2009). Telomere-associated proteins are specific for telomeres versus ITSs, suggesting that ITSs have no functional similarity with telomeres (Song et al., 2008;Surovtseva et al., 2009). The TALE_telo localizes not only to telomeres but also ITSs as TALE_telo associates with 2.6 telomeric repeats (Supplementary Table S1). Thus, we conclude that the bright spots observed in cells expressing TALE_telo G are the ITSs on chromosome 1. Moreover, the signals associated with the180 bp repeats of chromosome 1 are larger in area than those for other chromosomes which is consistent with previous studies of the 180 bp centromeric repeats by FISH (Haupt et al., 2001). TALE_telo C and TALE_telo G are targeted to CCCTAAA and TTTAGGG repeats, respectively. Not only CG but also CHG and CHH are methylated in plant genomes. Furthermore, plant heterochromatin is enriched in methylated cytosines, in particular, methylated CHH (Vaquero-Sedas and Vega-Palas, 2014; Widman et al., 2009). RVD HD shows a preference for cytosines, but not for methylated cytosines (Valton et al., 2012). Therefore, targeting to the interstitial telomere sequences of TALE_telo C seems to be diminished compared with that of TALE_telo G. As a result of the application of different TALE repeats, the pattern of fluorescent signals was different between TALE_telo C and TALE_telo G.

Identification of TALE-GFP binding histones by IP-MS
Recently, engineered DNA-binding molecule-mediated chromatin immunoprecipitation (enChIP) was developed for the purification of specific genomic regions using TALE (Fujita et al., 2013). To confirm that our TALE-GFP fusions specifically interact with centromeres or telomeres, a GFP-trap was used to immunoprecipitate TALE-GFP interacting histones from whole extracts prepared from seedlings. As TALE_telo G exhibited association with ITSs, we used only TALE_telo C for the identification of telomere-associated histones. Mass spectrometry confirmed the presence of various histones (Table 1). Compared with the population of histones associated with TALE_telo C, TALE_180-associated histones were enriched for CENH3. Furthermore, histone H1 enrichment is less for TALE_telo C than for TALE_180. These data suggest that TALE_180 localizes to centromeres. Consistent with this, previous studies demonstrate that histone H1 binds to the compacted nucleosomal arrays of telomeres but with reduced stoichiometry relative to other genomic regions in A. thaliana (Ascenzi and Gantt, 1999).

Live observation of centromere and telomere dynamics in vivo
One of the advantages of plant TALE-FP is that it permits the analysis of chromatin organization in nuclei without disrupting the cell wall or permeabilizing the cell membrane during fixation like FISH. To ascertain whether plant TALE-FP is effective in various organs, we observed the signals of TALE_180-GFP in nuclei of cells in various organs. Clear and distinct fluorescent signals derived from TALE_180-GFP were observed in the nuclei of various organs including roots, hypocotyls, leaves, and floral organs (Fig. 3A).  The fluorescence intensity of TALE-FP varies across plant organs unlike that observed in animal cultured cells because the nuclear size and morphology can be dynamically changed by endoreduplication and vacuole expansion (Matsunaga et al., 2013). In addition, the intensity of TALE-FP signals is influenced by light scattering and absorption dependent on the imaging depth, unlike the flat cultured cells that adhere to dishes. Plant TALE-FP also allows tracking of native chromatin mobility in living cells without inserting artificial reporter DNA sequences in the genome. We next analysed the chromatin dynamics throughout the cell cycle by time-lapse imaging of cells expressing TALE_180-GFP. TALE_180-GFP accumulates at centromeric regions throughout mitosis, albeit at diminished levels from prometaphase to telophase ( Fig. 3B;see Supplementary Movie S1 at JXB online). The diminishment on mitotic chromosomes suggests that chromatin compaction may prevent the binding of TALE-GFP to its target sequences. As mentioned above, telomeric repeats could be detected using TALE-FP fusions that specifically recognize telomeres but the signal intensity was insufficient for time-lapse imaging. Ku70 mutants of A. thaliana deregulate the control of telomere length resulting in elongation of telomeres to 20 kbp (Bundock et al., 2002;Riha et al., 2002). When TALE_telo FPs were expressed in ku70 plants, the signals were stronger than in wild-type plants ( Fig. 3C; Supplementary Fig. S3). The signals were observed as distinct puncta around the nucleolar periphery with low observable background signals in the nucleoplasm ( Fig. 3C; Supplementary Fig. S3). This suggests that the elongation of telomeres increases the binding of TALE_telo FPs with telomeres which increases the signal-to-noise ratio. Using the ku70 background, the mean-squared displacement (MSD) of telomeres was determined in meristematic cells and cells of the elongation zone of roots. Time-lapse observation of TALE_ telo G-GFP in root cells shows that the movement of telomere signals differed slightly between nuclei. The movement of telomere signals was dependent on association with the nucleolus ( Fig. 3C; Supplementary Fig. S3; Supplementary Movie S2). Observation of TALE_telo C-tdTomato in a nucleus of a root hair cell demonstrates that the mobility of each telomere was different. In addition, a few telomeres temporarily formed a cluster ( Fig. 3D; Supplementary Movie S3), demonstrating the telomere association described in Fig. 1D. To our knowledge, this is the first report of telomere dynamics in living plants.
Here, we report for the first time the successful construction of stable transgenic lines to visualize endogenous genomic loci in a living multicellular organism using TALE-FPs. These stable lines do not need the injection of TALE-FPs and retain the signal intensity even after long time-lapse observation following repeated cell divisions during organ development and differentiation. This method overcomes the limitations of previous chromatin analyses by FISH, such as the fixation of nuclei, hybridization with DNA probes, and permeabilization of cell walls. The observation of plant TALE-FPs without the isolation or squashing of nuclei enables us to analyse chromatin dynamics in three-or four-dimensions in several organs while retaining plant morphology. The convenient distribution of seeds of stably transgenic lines will contribute to progress in the analyses of chromatin dynamics in the nuclei of multicellular organs and tissues. Therefore, plant transgenic lines expressing TALE-FPs will be a powerful tool to investigate spatiotemporal chromatin organization during various events including development, fertilization, environmental responses, and microbe interaction. Further refinement of genome visualization with genome editing techniques in plants will permit the monitoring of single loci, mutation sites, and nucleotide polymorphisms which is essential for epigenetic analyses and molecular breeding.

Supplementary data
Supplementary data can be found at JXB online. Figure S1. Nucleotide sequence of pCE-N-GFP. Figure S2. Construction of TALE-FP expression vector. Figure S3. Maximum intensity projections of TALE_telo G-GFP. Table S1. Target sequences of TALE-FP. Movie S1. Time-lapse observation of 180 bp repeats through mitosis every 5 min in root meristematic cells.
Movie S2. Time-lapse observation of telomere repeats in a root elongation zone cell.
Movie S3. Time-lapse observation of telomere repeats in a root hair cell.