Title: The Drosophila insulator proteins CTCF and CP190 link enhancer blocking to body patterning
Abstract: Article6 September 2007free access The Drosophila insulator proteins CTCF and CP190 link enhancer blocking to body patterning Man Mohan Man Mohan Institute for Genetics, Justus-Liebig-University Giessen, Heinrich-Buff-Ring, Giessen, Germany Search for more papers by this author Marek Bartkuhn Marek Bartkuhn Institute for Genetics, Justus-Liebig-University Giessen, Heinrich-Buff-Ring, Giessen, Germany Search for more papers by this author Martin Herold Martin Herold Institute for Genetics, Justus-Liebig-University Giessen, Heinrich-Buff-Ring, Giessen, Germany Search for more papers by this author Angela Philippen Angela Philippen Institute for Genetics, Justus-Liebig-University Giessen, Heinrich-Buff-Ring, Giessen, Germany Search for more papers by this author Nina Heinl Nina Heinl Institute for Genetics, Justus-Liebig-University Giessen, Heinrich-Buff-Ring, Giessen, Germany Search for more papers by this author Imke Bardenhagen Imke Bardenhagen Institute for Genetics, Justus-Liebig-University Giessen, Heinrich-Buff-Ring, Giessen, Germany Search for more papers by this author Joerg Leers Joerg Leers Institute for Genetics, Justus-Liebig-University Giessen, Heinrich-Buff-Ring, Giessen, Germany Search for more papers by this author Robert AH White Robert AH White Department of Physiology, Development and Neuroscience, University of Cambridge, Cambridge, UK Search for more papers by this author Renate Renkawitz-Pohl Renate Renkawitz-Pohl Philipps-Universität Marburg, Fachbereich Biologie, Entwicklungsbiologie, Marburg, Germany Search for more papers by this author Harald Saumweber Harald Saumweber Cytogenetics Division, Institute of Biology, Humboldt University, Berlin, Germany Search for more papers by this author Rainer Renkawitz Corresponding Author Rainer Renkawitz Institute for Genetics, Justus-Liebig-University Giessen, Heinrich-Buff-Ring, Giessen, Germany Search for more papers by this author Man Mohan Man Mohan Institute for Genetics, Justus-Liebig-University Giessen, Heinrich-Buff-Ring, Giessen, Germany Search for more papers by this author Marek Bartkuhn Marek Bartkuhn Institute for Genetics, Justus-Liebig-University Giessen, Heinrich-Buff-Ring, Giessen, Germany Search for more papers by this author Martin Herold Martin Herold Institute for Genetics, Justus-Liebig-University Giessen, Heinrich-Buff-Ring, Giessen, Germany Search for more papers by this author Angela Philippen Angela Philippen Institute for Genetics, Justus-Liebig-University Giessen, Heinrich-Buff-Ring, Giessen, Germany Search for more papers by this author Nina Heinl Nina Heinl Institute for Genetics, Justus-Liebig-University Giessen, Heinrich-Buff-Ring, Giessen, Germany Search for more papers by this author Imke Bardenhagen Imke Bardenhagen Institute for Genetics, Justus-Liebig-University Giessen, Heinrich-Buff-Ring, Giessen, Germany Search for more papers by this author Joerg Leers Joerg Leers Institute for Genetics, Justus-Liebig-University Giessen, Heinrich-Buff-Ring, Giessen, Germany Search for more papers by this author Robert AH White Robert AH White Department of Physiology, Development and Neuroscience, University of Cambridge, Cambridge, UK Search for more papers by this author Renate Renkawitz-Pohl Renate Renkawitz-Pohl Philipps-Universität Marburg, Fachbereich Biologie, Entwicklungsbiologie, Marburg, Germany Search for more papers by this author Harald Saumweber Harald Saumweber Cytogenetics Division, Institute of Biology, Humboldt University, Berlin, Germany Search for more papers by this author Rainer Renkawitz Corresponding Author Rainer Renkawitz Institute for Genetics, Justus-Liebig-University Giessen, Heinrich-Buff-Ring, Giessen, Germany Search for more papers by this author Author Information Man Mohan1, Marek Bartkuhn1, Martin Herold1, Angela Philippen1, Nina Heinl1, Imke Bardenhagen1, Joerg Leers1, Robert AH White2, Renate Renkawitz-Pohl3, Harald Saumweber4 and Rainer Renkawitz 1 1Institute for Genetics, Justus-Liebig-University Giessen, Heinrich-Buff-Ring, Giessen, Germany 2Department of Physiology, Development and Neuroscience, University of Cambridge, Cambridge, UK 3Philipps-Universität Marburg, Fachbereich Biologie, Entwicklungsbiologie, Marburg, Germany 4Cytogenetics Division, Institute of Biology, Humboldt University, Berlin, Germany *Corresponding author. Institute for Genetics, Justus-Liebig-University Giessen, Heinrich-Buff-Ring 58-62, Giessen 35392, Germany. Tel.: +49 641 99 35460; Fax: +49 641 99 35469; E-mail: [email protected] The EMBO Journal (2007)26:4203-4214https://doi.org/10.1038/sj.emboj.7601851 PDFDownload PDF of article text and main figures. ToolsAdd to favoritesDownload CitationsTrack CitationsPermissions ShareFacebookTwitterLinked InMendeleyWechatReddit Figures & Info Insulator sequences guide the function of distantly located enhancer elements to the appropriate target genes by blocking inappropriate interactions. In Drosophila, five different insulator binding proteins have been identified, Zw5, BEAF-32, GAGA factor, Su(Hw) and dCTCF. Only dCTCF has a known conserved counterpart in vertebrates. Here we find that the structurally related factors dCTCF and Su(Hw) have distinct binding targets. In contrast, the Su(Hw) interacting factor CP190 largely overlapped with dCTCF binding sites and interacts with dCTCF. Binding of dCTCF to targets requires CP190 in many cases, whereas others are independent of CP190. Analysis of the bithorax complex revealed that six of the borders between the parasegment specific regulatory domains are bound by dCTCF and by CP190 in vivo. dCTCF null mutations affect expression of Abdominal-B, cause pharate lethality and a homeotic phenotype. A short pulse of dCTCF expression during larval development rescues the dCTCF loss of function phenotype. Overall, we demonstrate the importance of dCTCF in fly development and in the regulation of abdominal segmentation. Introduction Eukaryotic genomes are highly organized into functional units containing individual genes or gene groups together with the corresponding regulatory elements. Regulatory elements may be separated from the transcriptional start sites by several thousands of base pairs. These functional units need to be insulated from each other in order to prevent illegitimate interactions of enhancers with other transcriptional units. Furthermore, a single regulatory element may control several genes, or several distinct regulatory elements may control the activity of a single gene in time and space. Again, a functional constraint for the appropriate regulator/gene interaction needs to be achieved. Insulator elements with enhancer blocking activity fulfill this function, such that only appropriate promoters and genes are activated (Holdridge and Dorsett, 1991; Geyer and Corces, 1992; Chung et al, 1993; Gaszner and Felsenfeld, 2006). In vertebrates, there is only one factor currently known that binds to enhancer-blocking elements and prevents the inappropriate activation by adjacent enhancers: CTC binding factor (CTCF) (Ohlsson et al, 2001). Binding sites for CTCF have been shown to be involved in gene repression (Baniahmad et al, 1990; Lobanenkov et al, 1990), in gene activation (Vostrov and Quitschke, 1997) and in enhancer blocking (Bell et al, 1999; Hark et al, 2000; Kanduri et al, 2000; Szabo et al, 2000; Lutz et al, 2003; Burke et al, 2005). Furthermore, vertebrate- and mammalian-specific functions, such as X-chromosome inactivation and control of the epigenetic DNA methylation state, seem to involve CTCF (for reviews see Lee, 2003; Lewis and Reik, 2006). In sharp contrast to vertebrates, the genome of Drosophila is much more compacted, primarily due to shorter distances between genes. Therefore, the need for insulators to separate genes is likely greater than in vertebrates. Indeed, five different insulator binding proteins have been identified in Drosophila. These are Zw5, BEAF-32 (Zhao et al, 1995; Gaszner et al, 1999), GAGA factor (Ohtsuki and Levine, 1998; Belozerov et al, 2003), Su(Hw) (Gerasimova et al, 1995) and a Drosophila orthologue of CTCF that we have identified (Moon et al, 2005). The function of enhancer blocking has evolved such that Drosophila utilizes several proteins and probably multiple mechanisms for enhancer blocking and insulation (Kuhn et al, 2003). However, with the exception of dCTCF, none of the other known Drosophila insulator proteins have a counterpart found to be conserved in vertebrates. Su(Hw), a 12-zinc-finger factor, resembles the 11-zinc-finger protein dCTCF with respect to the overall domain structure. Detailed study of Su(Hw) has revealed that a 350-bp DNA sequence of the gypsy insulator binds a protein complex consisting of at least three components, Su(Hw), Mod(mdg4)67.2 and CP190. Su(Hw) and CP190 can bind DNA directly via their zinc-finger domains, whereas Mod(mdg4)67.2 does not bind DNA directly, but is recruited to the gypsy insulator sequence through physical interactions with Su(Hw) and CP190 (Pai et al, 2004). Several hundred endogenous binding sites for Su(Hw) are found throughout the Drosophila genome (Gerasimova and Corces, 1998; Parnell et al, 2006; Ramos et al, 2006). Another perspective on the requirement for insulators comes from the fact that many genes are controlled by several regulatory elements needed for tissue- and cell-specific expression. For example, the three Drosophila homeotic genes of the bithorax complex (BX-C), Ultrabithorax (Ubx), abdominal A (abd-A) and Abdominal-B (Abd-B), are regulated by a cis-regulatory region comprising more than 300 kb. This region is subdivided into nine distinct regulatory domains controlling the three homeotic genes individually and specifically with respect to particular parasegments (Lewis, 1978; Sanchez-Herrero et al, 1985; Maeda and Karch, 2006). A striking feature of this complex regulatory region is the colinearity of regulatory domains controlling gene expression from the thoracic segment T3 through the abdominal segments A1–A9 (parasegments PS5–PS14). Of the eight boundaries between the nine regulatory domains, three have been functionally identified as chromatin insulators with enhancer blocking activity. These are Miscadastral pigmentation (Mcp), Frontabdominal-7 (Fab-7) and Frontabdominal-8 (Fab-8) (Maeda and Karch, 2006). The GAGA factor was shown to be required for the enhancer blocking function of Fab-7 (Schweinsberg et al, 2004). Previously we demonstrated that dCTCF binding sites are required for the function of Fab-8 (Moon et al, 2005), and that dCTCF is associated with all but one of the known or predicted insulators of BX-C (Holohan et al, 2007). Here we addressed whether dCTCF and Su(Hw) mediate similar molecular functions and biological effects, and whether dCTCF plays a functional role in the BX-C, which is finely subdivided by regulatory domain borders. We demonstrate that the overall binding pattern of Su(Hw) is distinct from dCTCF and that, in contrast to Su(Hw), a dCTCF-null mutation causes pharate lethality and hypomorphic mutations result in a homeotic phenotype. Despite these differences, both factors interact with CP190. Results dCTCF binds to many interbands without overlap with Su(Hw) binding sites dCTCF and Su(Hw) are similar factors in that both are multi zinc-finger proteins and both mediate enhancer blocking. To test whether both factors target to identical genomic sites, or whether separate sets of target sites are accessed, we analyzed the pattern of dCTCF bound to polytene chromosomes of third instar larvae. We used two different antibodies directed against the N-terminal or the C-terminal domain of dCTCF (Moon et al, 2005). Both antibodies resulted in the same pattern, when carefully compared in independent staining experiments with each other and with GFP signals from a CTCF-eGFP line (not shown). Analysis of the overall distribution of dCTCF showed that approximately 300 to 400 dCTCF target sites (CTS) are bound (Figure 1). The heterochromatic chromocenter region is essentially free of dCTCF binding. Close inspection at higher magnification revealed that all bound CTSs are located in interband regions. In many cases, when the chromosomal quality allowed high-resolution analysis, a location of the CTS at the interband/band border or at a puff border is evident (Figure 1B and C). Next we analyzed the distribution of binding sites for Su(Hw) relative to dCTCF. The Su(Hw) antibody stains several hundreds of sites located in interbands as well. At low magnification, only few sites seem to colocalize, which may be caused by both factors bound to the same target or by low resolution of separate targets. Upon magnification and inspection of high-quality regions, no colocalization could be detected (Figure 1G–I). Therefore, we conclude that at least for the polytene chromosomes, almost all dCTCF targets are different from those of Su(Hw). Figure 1.dCTCF binds to several hundred loci on polytene chromosomes, different from those bound by Su(Hw), but overlapping with CP190 signals. Immunostaining of salivary gland polytene chromosomes with α-dCTCF, α-Su(Hw) and α-CP190. (A–C) dCTCF (green) detected on interband or at band/interband transitions, flanked by bands stained with Hoechst 33342 (blue). Examples are pointed out (arrows) at higher magnification for chromosomes 3L (B) and X (C). Chromocenter ('C') of two nuclei, and the 2B puff (dashed circle) are negative for dCTCF. (D–I) α-dCTCF (green) and α-Su(Hw) (red) generate non-overlapping staining (F, I, merged). Higher magnification of the tip of 3L (G–I). (J–O) α-dCTCF (green) and α-CP190 (red) show overlapping localization. Merged picture of the whole chromosome set (L) indicates colocalization (orange signals). The enlarged view of the tip of the 3L chromosome (M–O) identifies colocalization in the split view (O, arrows). Download figure Download PowerPoint CP190 and dCTCF binding sites overlap and both factors interact in vivo We wondered whether dCTCF and Su(Hw) might share cofactors despite the differences in target site specificity. The protein Mod(mdg4) has been shown to be required for Su(Hw) function (Ghosh et al, 2001) and an analysis of Mod(mdg4) distribution over the polytene chromosomes revealed only a partial colocalization with dCTCF (not shown). In contrast, when we tested the binding pattern of CP190, another cofactor required for the function of Su(Hw) (Pai et al, 2004), we found that many of the CP190 sites are CTSs as well (Figure 1J–O). Indeed, analysis at high resolution revealed that the majority of CTSs are bound by CP190 (Figure 1O). The CP190 protein contains three classical C2H2 zinc-finger motifs and an N-terminal BTB/POZ domain. Both domains could potentially be involved in chromatin binding. On the other hand, chromatin binding might be achieved by interaction with other factors, such as dCTCF. We therefore tested for a possible interaction of dCTCF with CP190 using co-immunoprecipitation. Precipitation of CP190 from Schneider cell extracts resulted in the detection of dCTCF (Figure 2A). To confirm the interaction we expressed a FLAG-dCTCF fusion protein in Schneider cells and precipitated with either an antibody against CP190 or an antibody against FLAG (Figure 2B and C). The CP190 precipitate contained endogenous dCTCF as well as FLAG-dCTCF in the same ratio as the input, suggesting that both dCTCF proteins are similarly associated with CP190. Furthermore, the reverse experiment using FLAG precipitation demonstrated that dCTCF and CP190 interact in vivo. Figure 2.Co-immunoprecipitation of dCTCF and CP190. (A, B) Whole-cell extracts from S2 cells were precipitated with α-CP190 antibody and the precipitates were analyzed by SDS–PAGE and subsequent Western blotting with α-CP190 or α-dCTCF. CP190 coprecipitates dCTCF (A) and FLAG-dCTCF, as well as endogenous dCTCF (B). (C) α-FLAG antibody was used in the IP, and α-CP190 or α-FLAG for detection in Western blot. Control: precipitation with mouse IgG; input: 10% in panel A, 4% of extract in panels B and C. Download figure Download PowerPoint dCTCF mutants show a homeotic phenotype and pharate lethality We first tested the effect of dCTCF depletion from Schneider S2 cells by RNAi knockdown (Supplementary Figure). However, we could not detect any change in cell number or cell size after dCTCF depletion. Therefore, we wondered whether dCTCF may play a role in Drosophila development. The available deficiency Df(3L)pbl-X1 does not take out dCTCF (data not shown). Therefore, we generated a 16-kb deletion (Df(3L)0463) by recombination between FRT containing P-elements (Parks et al, 2004; Thibault et al, 2004) within the quemao gene at 65F5-F6 and within the bhringi gene at 65F7 (PBac{WH}qmf01604 and P{XP}bhrd01563). The deletion is recessive lethal and takes out dCTCF, pastrel, CG8583, Sh3beta and the 5′ region of bhringi (Figure 3A). In addition, we checked three different transposon elements residing within the dCTCF locus (Figure 3B). GE22007 and CTCFEY15833, each with a P-EP or a P-element positioned 15 or 35 bp downstream of the transcription start site of dCTCF show a 50–70% reduced amount of CTCF as determined in third instar larvae and in adults (Table I; Figure 3C). The reduction in protein amount is also seen in salivary gland polytene chromosomes, where the number of CTCF-bound sites is reduced to about 50%. Trans-heterozygotes GE22007/Df(3L)0463 and CTCFEY15833/Df(3L)0463 are without phenotype (Table I). Finally, GE24185 has a P-EP element located at the nucleotide triplet coding for amino acid 158. Few F1 homozygotes showed spreading of wings by 30–45° (Table I). The GE24185/Df(3L)0463 trans-heterozygotes showed a highly penetrant mild (60°) held out wing phenotype, various homeotic transformations (see below) and sterility in both males and females. Protein extracts prepared from 10 salivary glands showed a weak band, running at ∼90kDa when tested with the C-terminal antibody, but no specific band is detectable with the N-terminal antibody (Supplementary Figure 1C). Salivary gland polytene chromosome staining showed detectable dCTCF, although at a dramatically reduced number of sites (25% of wild type) using the antibody against the C-terminus of the dCTCF protein (Table I), whereas the antibody against the N-terminus of dCTCF did not show any signal. Similarly, RNA analysis by RT–PCR showed the presence of a transcript in reduced amount (Supplementary Figure 1B). Taken together, these data suggest that insertion of the P-element results in the reduced expression of a truncated dCTCF protein that is recognized by the C-terminal-specific antibody in a Western blot, and on polytene chromosomes. This small amount appears to be highly concentrated on a subset of binding sites (see also below). Figure 3.dCTCF mutations cause homeotic phenotypes. (A) View of the gbrowse genome browser (FlyBase) showing CTCF and its neighboring genes, and the two FRT elements PBac{WH}qmf01604 and P{XP}bhrd01563 used to generate Df(3L)0463 (long horizontal arrow). (B) Schematic representation of the dCTCF gene; locations of exons I–IV (thick horizontal arrows), of the transposons GE22007, GE24185 and EY15833, and of the deleted fragment in CTCFp30.6 are shown. (C) Western analysis of wild type (+/+), P-element and jump-out mutants. Single fly extracts from third instar larvae and young adults were loaded on each lane and probed with N- and C-terminal-specific dCTCF antibodies. Tubulin antibody was used as control. (D) Morphological defects of the indicated dCTCF mutants. Appearance of patchy pigmentation in A4 indicates a partial transformation to A5 (white arrow). Twisting of the male genital region (black arrows). (E) Cuticle preparations of the abdomen of the indicated male mutants show a patchy appearance of pigmentation in A4 tergite (arrowhead), and small white patches in A5 tergite toward the anterior side of the segment. Loss of pigmentation in A5 indicates transformation into A4. The more compact A5 sternite in wild type has elongated into a banana shape in the mutants. This indicates transformation of A5 to A6 segment. Up to eight bristles were seen in the sixth sternite (thin arrow), and a small seventh segment (thick arrow) is present. Females show transformation of A7, with an increased number of bristles of the seventh sternite, showing a different orientation. Download figure Download PowerPoint Table 1. dCTCF mutants Genotype dCTCF expressiona Phenotypeb P-strains GE22007/GE22007 W (50–70%) wt; F2 embryos die at various stages from secondary mutations (∼5/200 survivors) GE22007/Df(3L)0463 Not determined wt EY15833/EY15833 W (50–60%); P (50%) wt EY15833/Df(3L)0463 Not determined wt GE24185/GE24185 W (0%); P (25%) with C-terminal antibody Reduced viability (66%); embryos from F2 homozygotes do not eclose; held out wings (30% of survivors); male genitalia rotated up to 30° (10%); males: A4 patchy pigment, partial loss of pigment in A5, eight bristles on sixth sternite, small seventh tergite (10–20%) GE24185/Df(3L)0463 W (0%); P with C-terminal antibody (25%) Held out wings (100%); male and female sterile; male genitalia rotated by 40°–120° (100%); males: A4 patchy pigment, partial loss of pigment in A5 tergite, eight bristles on sixth sternite, small seventh tergite (100%); females: bristles on A7 sternite have lost orientation (100%) Jump-out strains P30.6/P30.6c W (0%); P (0%) Pharate lethal (100%); male genitalia rotated by 40°–90° (100%); males: A4 tergite with patchy pigmentation, A5 tergite shows a few white spots, A5 sternite is elongated into a banana shape, eight bristles on sixth sternite, small seventh tergite (100%); females: A7 sternite with up to 11 bristles pointing vertically downwards (100%) P30.6/Df(3L)0463 W (0%); P (0%) as P30.6/P30.6 P35.2/P35.2c W (0%) as P30.6/P30.6 E5.5/E5.5d W (0%) as P30.6/P30.6 R10.3/R10.3e W (0%) as P30.6/P30.6 R15.4/R15.4e W (0%) as P30.6/P30.6 wt, wild type. a (W) single fly western with the percentage of expression relative to wild type; (P) polytene chromosome staining with the percentage of the number of sites relative to wild type. b Phenotype with percentage of penetrance within the surviving group. c Jump-out from GE22007. d Jump-out from EY15833. e Jump-out from GE24185. To create amorphic alleles by imprecise excision, we performed jump-outs from all three insertions. When homozygous, all of these mutants died at the pharate stage, with about 50% being very short lived (up to 12–24 h) but able to eclose (Table I). Immunoblot analysis of single larval protein extracts showed no dCTCF protein and polytene chromosome squashes were completely negative (not shown). Similarly, absence of dCTCF was observed when these lines were crossed to Df(3L)0463 (Figure 3C). Thus, these mutations were considered to be amorphic dCTCF alleles. For further analysis we concentrated on jump-out strain CTCFp30.6, which we molecularly characterized to carry a deletion from nucleotide −537 upstream of the transcriptional start site to position +15 (Figure 3B). Careful inspection of the adults revealed a number of homeotic transformations in the GE24185 homozgygotes, in GE24185/Df(3L)0463 and even more severe in the amorphic mutants (Figure 3D). Some of the GE24185 homozygous males showed mild and patchy pigmentation of the abdominal segment A4, and formation of a small A7 tergite. They also showed various degrees (0–30°) of genital region rotation. This later phenotype is similar to a known homeotic mutation in the bithorax locus (Estrada et al, 2002). All GE24185/Df(3L)0463 males showed larger patches of pigmentation in A4 and formation of a small A7 tergite (Figure 3D and E). Cuticle preparations also showed a number of additional phenotypes. The dCTCFp30.6/Df(3L)0463 males have lost pigmentation in small patches toward the anterior of the A5 tergite, indicating that A5 is nominally transformed into A4 (Figure 3E). Interestingly, A5 sternite is banana shaped, which is a feature of the A6 sternite (Figure 3E). Hence, A5 shows anterior to posterior transformation, as well as posterior to anterior transformation. We also found up to eight bristles in the A6 sternite in the cuticle preparations, which are not seen in wild type. The genital region was extended out of the abdomen and rotation was more severe, from 60° to 120° (Figure 3D). Furthermore, GE24185/Df(3L)0463, as well as dCTCFp30.6/Df(3L)0463 females exhibit an A7 transformation. In the former case the bristles have lost their orientation, which in wild type is toward the mid axis. In the latter case the transformation is more apparent, as indicated by more bristles on the A7 sternite (up to 11 compared with eight in wild type), and by their vertical downward orientation (Figure 3E). The dCTCFp30.6 phenotype can be rescued by brief dCTCF expression at the larval stage In order to demonstrate that the phenotype seen in the various dCTCF mutants is caused by the loss of dCTCF, we generated rescue strains. First we produced genomic dCTCF transgenic flies by cloning the 5084-bp sequence spanning the dCTCF gene from a site within the quemao gene and extending to within the pastrel gene. We reasoned that the regulatory sequences for dCTCF expression in this gene dense region would most likely be framed by the two flanking genes (Figure 3A). A single integration of genomic dCTCF on the second chromosome (gCTCF) was able to rescue CTCFp30.6/Df(3L)0463, CTCFp30.6/CTCFp30.6, GE24185/Df(3L)0463 and GE24185/GE24185. We found a majority of the flies fully rescued, with a few showing various degrees of held out wings and that were unable to walk properly. The rescued flies were fertile and we could establish a breeding stock of gCTCF/gCTCF;GE24185/GE24185. Furthermore, we tested whether a pulse of dCTCF expression during larval development would be sufficient for the rescue or whether the flies might need a continuous supply of dCTCF. We generated UASdCTCF-EGFP transgenic flies by P-element transgenesis, and established lines with insertions on the X, second and third chromosomes. On driving UASdCTCF-EGFP in wild-type background with ubiquitous drivers such as tubulin-gal4 or actin-gal4, we found early embryonic lethality (data not shown). In order to express a moderate and controlled amount of dCTCF, we used a hsp70Gal4 driver line, and gave a single heat shock (37°C) for 20 min at various stages of development. We found that a single heat shock at 24, 48 or 72 of development was sufficient to phenotypically rescue the majority of flies with a dCTCFp30.6/Df(3L)0463 or a GE24185/Df(3L)0463 genetic background. Fertility tests of the rescued flies revealed that both males and females were fertile. A few flies still showed a very mild held out wing phenotype and some had a disorganized bristle pattern on the dorsal abdomen. Heat shock at the pupal stage could not rescue all the mutant phenotypes (not shown). Thus, a short pulse of dCTCF expression is sufficient to generate phenotypes close to wild type. Many, but not all dCTCF binding sites depend on CP190 Because we found that CP190 and dCTCF colocalize on polytene chromosomes and interact in vivo, we asked whether the overall amount of dCTCF protein might be changed in CP190-deficient third instar larvae. A Western blot analysis of both Cp1901 homozygotes (deficient in CP190) and wild-type larval extracts showed that the amount of dCTCF is reduced in Cp1901 homozygotes (Figure 4A). Figure 4.Many, but not all dCTCF binding sites depend on CP190. (A) Western analysis of dCTCF and tubulin in Cp1901 larval extracts. (B–F) Wild-type polytene chromosome 3L from third instar larval salivary glands stained for DNA (B), CTCF (D), CP190 (E) and the indicated merges are shown. Arrows point to all 12 CTSs as identified in panel D, counted from the tip of chromosome 3L and numbered. (G–I) Polytene 3L chromosomes from homozygote genotypes EY15833, GE24185 and CP1901, stained with DAPI and for dCTCF. Numbered arrows point to the corresponding locations as in wild type. (J) Analysis of the first 12 CTS at the 3L chromosome tip as numbered in panel D. Occupancy (+) for dCTCF and for CP190 in different genotypes. The total number of CTSs on chromosome 3 is given±the number of weak signals, which cannot be interpreted. Download figure Download PowerPoint Next we wanted to know whether the reduced amount of dCTCF caused by the loss of CP190 affects dCTCF binding on the polytene chromosomes. We found that the total number of dCTCF labeled sites is reduced in the Cp1901 mutant, whereas the number of CP190 sites was not affected by dCTCF mutants (not shown and below). As mentioned above, the analysis of dCTCF binding in the two hypomorphic mutants CTCFEY15833/CTCFEY15833 and GE24185/GE24185 revealed that that the number of bound sites is reduced to about 50 and 25%, respectively (Table I). By close inspection of the chromosomes we found that the set of dCTCF sites missing in the CP190 or in the dCTCF mutants overlap but are not identical. This is exemplified with the first 12 CTS at the tip of chromosome 3L (Figure 4B–I). We find four types of sites: (a) those binding dCTCF only, affected by both hypomorphic dCTCF mutations, but not by CP1901 (site 6 in Figure 4G–J), (b) sites binding dCTCF only, and neither affected by hypomorphic dCTCF mutations nor by CP1901 (site 1), (c) sites binding both proteins, and dCTCF binding affected by CP1901 a