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Transcription factor YY1 functions as a PcG protein in vivo

2003; Springer Nature; Volume: 22; Issue: 6 Linguagem: Inglês

10.1093/emboj/cdg124

1460-2075

Lakshmi Atchison, A. Ghias, Frank Wilkinson, Nancy M. Bonini, Michael L. Atchison,

Genomics and Chromatin Dynamics

Article17 March 2003free access Transcription factor YY1 functions as a PcG protein in vivo Lakshmi Atchison Lakshmi Atchison Department of Biology, Chestnut Hill College, 9601 Germantown Avenue, Philadelphia, PA, 19118 USA Search for more papers by this author Ayesha Ghias Ayesha Ghias Department of Animal Biology, University of Pennsylvania, School of Veterinary Medicine, 3800 Spruce Street, Philadelphia, PA, 19104 USA Search for more papers by this author Frank Wilkinson Frank Wilkinson Department of Animal Biology, University of Pennsylvania, School of Veterinary Medicine, 3800 Spruce Street, Philadelphia, PA, 19104 USA Search for more papers by this author Nancy Bonini Nancy Bonini Department of Biology, Howard Hughes Medical Institute, University of Pennsylvania, Philadelphia, PA, 19104 USA Search for more papers by this author Michael L. Atchison Corresponding Author Michael L. Atchison Department of Animal Biology, University of Pennsylvania, School of Veterinary Medicine, 3800 Spruce Street, Philadelphia, PA, 19104 USA Search for more papers by this author Lakshmi Atchison Lakshmi Atchison Department of Biology, Chestnut Hill College, 9601 Germantown Avenue, Philadelphia, PA, 19118 USA Search for more papers by this author Ayesha Ghias Ayesha Ghias Department of Animal Biology, University of Pennsylvania, School of Veterinary Medicine, 3800 Spruce Street, Philadelphia, PA, 19104 USA Search for more papers by this author Frank Wilkinson Frank Wilkinson Department of Animal Biology, University of Pennsylvania, School of Veterinary Medicine, 3800 Spruce Street, Philadelphia, PA, 19104 USA Search for more papers by this author Nancy Bonini Nancy Bonini Department of Biology, Howard Hughes Medical Institute, University of Pennsylvania, Philadelphia, PA, 19104 USA Search for more papers by this author Michael L. Atchison Corresponding Author Michael L. Atchison Department of Animal Biology, University of Pennsylvania, School of Veterinary Medicine, 3800 Spruce Street, Philadelphia, PA, 19104 USA Search for more papers by this author Author Information Lakshmi Atchison1, Ayesha Ghias2, Frank Wilkinson2, Nancy Bonini3 and Michael L. Atchison 2 1Department of Biology, Chestnut Hill College, 9601 Germantown Avenue, Philadelphia, PA, 19118 USA 2Department of Animal Biology, University of Pennsylvania, School of Veterinary Medicine, 3800 Spruce Street, Philadelphia, PA, 19104 USA 3Department of Biology, Howard Hughes Medical Institute, University of Pennsylvania, Philadelphia, PA, 19104 USA *Corresponding author. E-mail: [email protected] The EMBO Journal (2003)22:1347-1358https://doi.org/10.1093/emboj/cdg124 PDFDownload PDF of article text and main figures. ToolsAdd to favoritesDownload CitationsTrack CitationsPermissions ShareFacebookTwitterLinked InMendeleyWechatReddit Figures & Info Polycomb group (PcG) proteins function as high molecular weight complexes that maintain transcriptional repression patterns during embryogenesis. The vertebrate DNA binding protein and transcriptional repressor, YY1, shows sequence homology with the Drosophila PcG protein, pleiohomeotic (PHO). YY1 might therefore be a vertebrate PcG protein. We used Drosophila embryo and larval/imaginal disc transcriptional repression systems to determine whether YY1 repressed transcription in a manner consistent with PcG function in vivo. YY1 repressed transcription in Drosophila, and this repression was stable on a PcG-responsive promoter, but not on a PcG-non-responsive promoter. PcG mutants ablated YY1 repression, and YY1 could substitute for PHO in repressing transcription in wing imaginal discs. YY1 functionally compensated for loss of PHO in pho mutant flies and partially corrected mutant phenotypes. Taken together, these results indicate that YY1 functions as a PcG protein. Finally, we found that YY1, as well as Polycomb, required the co-repressor protein CtBP for repression in vivo. These results provide a mechanism for recruitment of vertebrate PcG complexes to DNA and demonstrate new functions for YY1. Introduction Polycomb group (PcG) proteins were first identified in Drosophila as proteins required to maintain repression of homeotic genes necessary for anterior–posterior development (McKeon and Brock, 1991; Simon et al., 1992). Homeotic gene expression patterns are initiated early in development by the maternal and segmentation genes such as the gap and pair-rule genes (Beinz and Muller, 1995). The gap and pair-rule genes are expressed transiently, but homeotic gene expression must be continuous for proper development. Two additional families of regulatory proteins are necessary for the maintenance of homeotic gene expression. These are the trithorax group proteins, which maintain active homeotic gene expression where the genes were originally expressed (Kennison, 1993), and the PcG proteins, which maintain the repressed state where homeotic gene expression was originally inactive (Paro, 1993; Pirrotta, 1997a,b; Schumacher and Magnuson, 1997). In PcG loss-of-function mutants, homeotic gene expression is correctly initiated, but as expression of maternal and segmentation genes decays, the anterior boundaries of homeotic gene expression are not properly maintained but are shifted toward the anterior (Duncan and Lewis, 1982). This results in posterior homeotic transformation where ectopic expression of homeotic genes takes place. A number of vertebrate proteins homologous to Drosophila PcG proteins have been identified. These mammalian PcG proteins can regulate hox gene expression and are important for skeletal development and hematopoiesis (van der Lugt et al., 1994; Akasaka et al., 1997, 2001; Bel et al., 1998). Like their Drosophila counterparts, mammalian PcG gene mutants result in segmentation defects characterized by posterior transformations of various skeletal structures (van der Lugt et al., 1994; Alkema et al., 1995; Akasaka et al., 1996; Bel et al., 1998). A subset of mammalian and Drosophila PcG mutants result in lethality very early in embryogenesis, indicating important functions in both early and late developmental stages (van der Lugt et al., 1994; O'Carroll et al., 2001). Although mammalian and Drosophila PcG proteins are generally believed to mediate similar functions, only a single mammalian PcG protein has been shown to function in Drosophila to correct a PcG mutant phenotype (Muller et al., 1995). PcG proteins function as high molecular weight complexes that, in Drosophila, bind to regulatory elements termed Polycomb (Pc) response elements (PRE) (Pirrotta, 1997a,b, 1999; Satijn and Otte, 1999; Brock and van Lohuizen, 2001; Francis and Kingston, 2001). No mammalian PREs have been identified, partly because hardly any PcG proteins individually bind to DNA specifically. A single Drosophila PcG protein, pleiohomeotic (PHO), has been shown to bind to DNA specifically (Brown et al., 1998), and therefore may function to nucleate PcG complexes on DNA. PHO can bind to specific sites in many PRE sequences, and mutation of either PHO DNA binding site or the PHO protein itself can reduce PcG silencing (Girton and Jeon, 1994; Brown et al., 1998; Fritsch et al., 1999; Busturia et al., 2001; Mishra et al., 2001). PHO can physically interact with some PcG proteins and can generate ternary complexes on DNA with the Pc protein (Mohd-Sarip et al., 2002). Therefore, PHO appears to be an important component of at least some PcG repression systems. Interestingly, PHO has sequence homology to the well-characterized vertebrate transcription repressor, YY1. YY1 is a 414 amino acid, multifunctional transcription factor that can either activate or repress transcription, depending upon promoter contextual differences, or specific protein interactions (reviewed in Shrivastava and Calame, 1994; Shi et al., 1997; Thomas and Seto, 1999). Some of the domains responsible for YY1 function have been mapped, with most studies showing that sequences near the C-terminus (which overlap the YY1 zinc fingers) can repress transcription (Bushmeyer and Atchison, 1998; Thomas and Seto, 1999). However, some studies indicate that other sequences are also involved in transcriptional repression (Yang et al., 1996). YY1 sequences important for transcriptional activation reside near the N-terminus (Lee et al., 1994, 1995; Bushmeyer et al., 1995; Austen et al., 1997). The mechanism by which YY1 activates or represses transcription is presently unclear. A number of repression mechanisms have been proposed, but nearly all of the transcriptional properties of YY1 have been defined by transient expression assays. Although mouse knock-out studies show that YY1 homozygous mutants die peri-implantation (Donohoe et al., 1999), little is know about the function of YY1 in vivo. The homology between YY1 and Drosophila PHO resides in two YY1 domains: sequences 298–414 constituting the four zinc fingers (95% identical) and a short segment between residues 205–226 (82% identity) with no defined function. Although the remainder of YY1 shows no similarity to PHO, the above homologies suggest that YY1 might be a vertebrate counterpart of PHO and thus function as a PcG protein. If so, the finding would provide a mechanism for nucleating mammalian PcG complexes to DNA and assist in the identification of mammalian PREs, since the YY1 DNA binding site is well characterized (Hyde-DeRuyscher et al., 1995). Although YY1 has not been observed as a component of the known PcG complexes, it can physically interact with the vertebrate PcG protein, EED (Satijn et al., 2001). As described above, YY1 knock-out mutants are embryonic lethal (Donohoe et al., 1999), similar to some PcG genes (Schumacher et al., 1996; O'Carroll et al., 2001). However, YY1 has never been tested in an in vivo system that would reveal PcG function. We therefore set out to address the mechanism of YY1 transcriptional repression in vivo, using a system that would enable us to test its potential PcG function. We show here that YY1 can repress transcription in developing Drosophila embryos and in larval imaginal discs. Similar to known PcG proteins, stable repression by YY1 was observed with a promoter responsive to PcG function, but not with a PcG-non-responsive promoter. Using various PcG mutant backgrounds, we found that YY1 transcriptional repression was dependent on PcG function. We also found that human YY1 could functionally compensate for PHO to correct phenotypic defects in pho mutant flies. Taken together, our results demonstrate that YY1 functions like a PcG protein. Finally, we have identified the co-repressor protein, CtBP, as a possible link between YY1 and the PcG complex. Results YY1 can repress transcription in developing Drosophila embryos We wished to study YY1 function in a developing organism where its role in transcription and potential PcG function could be assessed in vivo. PcG function is well studied in Drosophila, and transgenic reporters are available that are repressed in a PcG-dependent fashion. Previously, it was shown that chimeric GAL-PcG proteins can nucleate PcG complexes to DNA and repress endogenous or ectopic reporter genes by a PcG-dependent mechanism (Muller, 1995). One known PcG-responsive construct consists of a LacZ gene under the control of the Ultrabithorax (Ubx) BXD enhancer and the Ubx promoter adjacent to GAL4 binding sites (BXDGALUbxLacZ; abbreviated to BGUZ; see Figure 1B) (Muller, 1995). This reporter gene is expressed ubiquitously during embryogenesis but is selectively repressed in a PcG-dependent fashion by the Pc protein linked to the GAL4 DNA binding domain (Muller, 1995). Therefore, we prepared transgenic Drosophila lines expressing a GALYY1 fusion construct driven by the hunchback promoter (hbGALYY1; Figure 1A). This construct delivers a pulse of GALYY1 in the anterior ends of developing Drosophila embryos. We crossed hbGALYY1 transgenic lines with the BGUZ reporter line and assayed the resulting embryos for LacZ expression. If GALYY1 can repress the BGUZ reporter transgene, one would expect LacZ expression only in the posterior ends where hbGALYY1 is not expressed (see Figure 1B for strategy). Indeed, two independent hbGALYY1 transgenic lines repressed LacZ expression in the embryonic anterior ends (Figure 1C), while no repression was observed with the GAL DNA binding domain alone (Figure 1D). The GALYY1 repression is similar to the repression previously observed with the hb driven GAL-Pc gene (Muller, 1995). Figure 1.(A) Transgenic constructs. The top construct shows the YY1 cDNA (Park and Atchison, 1991) (black rectangle) under control of the armadillo promoter at the 5′ side, with the hsp70 poly(A) site on the 3′ side (Muller et al., 1995). The same expression plasmid was also used for making the arm-pho transgene (Brown et al., 1998) (second construct). The third and fourth constructs show the YY1 cDNA (black rectangle) fused to the GAL4 DNA binding domain (sequences 1–147, cross hatched rectangle) (Bushmeyer et al., 1995) under control of either the hunchback promoter or the hsp70 promoter on the 5′ side and the hsp70 poly(A) site on the 3′ side (Muller, 1995). (B) Strategy for crosses to determine the repression activity of GALYY1 in transgenic flies. The reporter construct (Muller, 1995) in transgenic fly strain BGUZ is shown at top. The expression pattern of this gene in embryos (i.e. throughout the embryo) is shown at the right, with the ‘A’ denoting anterior, and the ‘P’ posterior ends of the embryo. The GALYY1 effector plasmid expression pattern in the anterior half of embryos is shown at the right by black shading. Anticipated pattern of expression of embros from a cross between the reporter and effector transgenic lines (should repression occur), is shown at the bottom. LacZ expression will only be observed in the posterior ends of the embryos. (C) YY1 represses transcription in Drosophila embryos. LacZ expression in embryos (blue color) is shown in the parental reporter line (BGUZ; left panel) and embryos derived from crosses with two independent hbGALYY1 transgenic lines (middle and right panels). In each cross, LacZ expression is observed to be repressed in the anterior half of the embryo in either 10 h (middle panel) or 6 h (right panel) embryos. (D) The GAL DNA binding domain alone does not repress the BGUZ reporter. LacZ expression is shown in embryos of a cross between transgene lines hbGAL and BGUZ. Download figure Download PowerPoint YY1 repression is stable in vivo One hallmark of PcG proteins is their ability to generate stable transcriptional repression. Our results shown in Figure 1C suggest that stable repression was observed because repression persisted at the 16 h time point, long after YY1 expression had ceased. To further define the stability of YY1 repression, we placed the GALYY1 sequence under control of the heat shock protein 70 (hsp70) promoter (Figure 1A). The hsp70GALYY1 transgene was crossed with the BGUZ reporter line and embryos were heat shocked at various times after laying. All embryos were then harvested at 16 h and processed for LacZ expression. Interestingly, if embryos were heat shocked at 2 h, transcriptional repression persisted for 16 h (Figure 2). Likewise, a single heat shock treatment at either 3 or 4 h resulted in stable repression out to 16 h. Low levels of LacZ expression were observed when embryos were heat shocked at either 5 or 6 h, while somewhat higher expression was observed with the 10 h sample (Figure 2). Since the BGUZ reporter first becomes active ∼4 h post-laying, these levels of expression may be indicative of the LacZ expressed prior to GALYY1 expression. Even the 10 h heat shock sample showed less LacZ expression than the untreated control, suggesting that subsequent LacZ expression was repressed after the appearance of GALYY1. In summary, the above results indicate that YY1 can stably repress transcription similar to a PcG protein, and that YY1 appears to repress previously active genes. This feature of YY1 will be elaborated on in the Discussion. Figure 2.Transcriptional repression by YY1 is stable. The BGUZ reporter line was crossed with the hsp70GALYY1 line. Embryos were either untreated, or heat shocked at 37°C for 45 min at various times, and embryos were processed for staining 16 h after laying. Download figure Download PowerPoint We next tested YY1 repression with a distinct LacZ reporter gene system that does not exhibit stable repression dependent upon PcG function. This LacZ transgene contains GAL4 binding sites adjacent to a synthetic NP6 enhancer and yields expression in late embryonic development (Muller, 1995). The GAL4-NP6 reporter does not respond to stable PcG-dependent repression, but can be repressed transiently by the GAL-Pc protein if expressed shortly before GAL4-NP6 expression (Muller, 1995). We first crossed the hbGALYY1 line with the GAL4-NP6 reporter transgene line. Transient GALYY1 expression from the hunchback promoter did not lead to stable repression (Figure 3A and B), similar to results with the GAL-Pc protein (Muller, 1995). To determine whether GALYY1 could repress GAL4-NP6 expression if GALYY1 was expressed later, we used the hsp70GALYY1 transgene. Embryos from GAL4-NP6 × hsp70GALYY1 crosses were heat shocked at various times after laying and embryos were harvested at 18 h. In this case, GALYY1 only repressed expression if heat shock occurred just prior to GAL4-NP6 expression (heat shock at 15 h post-laying; Figure 4). From these experiments we conclude that GALYY1 expressed prior to 15 h is not able to establish a stable repression mechanism on the GAL4-NP6 construct. Apparently, as GALYY1 levels decay after the heat shock, insufficient protein is available to mediate repression. However, if GALYY1 is expressed just prior to GAL4-NP6 expression, sufficient GALYY1 is present to repress the promoter. Therefore, YY1 repression showed specificity between the two reporter constructs (BGUZ and GAL4-NP6). This specificity is identical to that previously observed with GAL-Pc when it was assayed with the same reporter lines (Muller, 1995). Therefore, YY1 behaves in the same fashion as a known PcG protein with these reporter constructs. Figure 3.Early embryonic YY1 expression cannot repress the GAL4-NP6 gene. (A) Strategy for potential repression using the GAL4-NP6 reporter line. A synthetic NP6 enhancer and minimal heat shock promoter yields the expression pattern shown at the right. Anticipated potential repression with hbGALYY1 is shown at the bottom. (B) Transient YY1 expression from the hb promoter does not lead to repression of the GAL4-NP6 reporter. Similar staining patterns were observed either in the absence (left) or presence (right) of hbGALYY1. Download figure Download PowerPoint Figure 4.YY1 expressed late in embryonic development can repress GAL4-NP6 expression. Embryos from hsp70GALYY1 X GAL4-NP6 crosses were heat shocked at various times, harvested at 18 h after laying, then processed for LacZ staining. Only YY1 induced at 15 h was able to strongly repress GAL4-NP6 activity. Download figure Download PowerPoint YY1 repression requires PcG function The YY1 repression patterns observed above were the same as those obtained previously with a known PcG protein. Therefore, we asked whether YY1 repression required PcG function. To determine this, we prepared an hbGALYY1 BGUZ recombinant chromosome line and crossed this chromosome into various homozygous PcG mutant backgrounds. Since PcG proteins function as complexes, mutation of a single PcG gene often abrogates PcG-dependent repression (Jurgens, 1985; Muller, 1995). Strikingly, homozygous mutant Polycomb (Pc), Polycomb-like (Pcl) or Sex combs on midleg (Scm) backgrounds led to complete derepression of YY1 function (Figure 5D–F) compared with controls (Figure 5A–C). Even heterozygous Pc and Pcl mutants abolished YY1 repression (data not shown). Homozygous mutant Sex combs extra (Sce), Additional sex combs (Asx) or Suppressor of zeste [Su(Z)2] plus Posterior sex combs (Psc) backgrounds yielded partial derepression of YY1 activity, perhaps due to maternal effects (Figure 5G–I). Therefore, YY1 repression in vivo required PcG function. Figure 5.YY1 transcriptional repression requires PcG function and can occur at both embryonic and larval stages. Embryos were collected from the BGUZ parent (A), the BGUZ hbGALYY1 recombinant chromosome line (B and C), and the recombinant chromosome line in various PcG homozygous mutant backgrounds (D–J). Embryos were collected at 16 h [or 6 h; (C)] and processed for LacZ staining. Blue staining indicates LacZ expression and light colored areas indicate repression of LacZ expression by GALYY1. The source of each embryo is shown at the right. (K) GALYY1 can compensate for PHO in wing imaginal discs. A diagram of the recombinant chromosome containing the hsp70GALYY1 and PBX-PRE-IDE-LacZ transgenes is shown at the top. This recombinant chromosome was crossed into either a wild type or a pho−/− (pho1/pho1) mutant background and developing larvae were either untreated or heat shocked twice daily. In the pho−/− crosses 18% of larvae are expected to contain the recombinant chromosome and the pho1/pho1 alleles to yield derepression of the reporter gene and resultant LacZ expression. As expected, 13 out of 75 larvae (17%) yielded wing imaginal discs that expressed LacZ (a representative positive wing disc is shown in the middle panel). The half of the larvae from the same cross that were heat shocked to induce GALYY1 expression showed dramatically different results. Only a single larvae out of 83 (1%) yielded wing discs staining positive for LacZ (a representative of the 82 negative imaginal discs is shown). The single positive larvae likely represents an organism in which the two transgenes became unlinked during the second cross due to absence of the balancer chromosome. Download figure Download PowerPoint Two distinct PcG complexes have been identified. The first complex, termed the PRC1 complex, contains Pc, Scm, Polyhomeotic (Ph) and Psc proteins (Shao et al., 1999). This complex is clearly necessary for YY1 repression since Pc and Scm mutants abolished YY1 function (Figure 5D and F). The second complex contains Esc and E(z) (Jones et al., 1998; Tie et al., 1998, 2001; Ng et al., 2000). As mentioned above, YY1 physically interacts with EED, the vertebrate homolog of Drosophila Esc (Satijn et al., 2001). Therefore, we tested the necessity of Esc for YY1 repression in vivo. Homozygous mutation of the esc gene caused partial loss of YY1 repression (Figure 5J). Thus, both complexes are needed for maximal YY1 repression, although mutations of proteins in the PRC1 complex cause more dramatic loss of YY1 repression. YY1 can repress transcription in larval imaginal discs The above results demonstrated that GALYY1 can repress transcription in a PcG-dependent fashion in embryos through synthetic GAL4 DNA binding sites. We wanted to test YY1 function at a later developmental stage using a reporter with native regulatory elements. Therefore, we obtained the PBX-PRE-IDE-LacZ reporter developed by Fritsch et al. (1999), which contains the PBX and IDE enhancers flanking the Ubx PRED element (see Figure 5K). In the absence of the PRED sequence, the IDE enhancer drives LacZ expression in larval wing imaginal discs, while in the presence of the PRED sequence expression is repressed. However, in a pho1/pho1 mutant background, PHO no longer binds to the six PHO binding sites in the PRE and repression is lost, resulting in LacZ expression (Fritsch et al., 1999). Since YY1 can bind to PHO binding sites (Brown et al., 1998), we sought to determine whether YY1 could repress transcription in third instar larvae through a native PRE sequence. We prepared a fly line with a recombinant chromosome containing the PBX-PRE-IDE-LacZ reporter and our hsp70GALYY1 transgene. This recombinant chromosome was crossed into a pho1/pho1 mutant background and developing larvae were either untreated, or heat shocked twice daily. Third instar larval wing discs were then isolated and processed for LacZ expression. As expected, wing discs for wild-type larvae showed no LacZ expression (Figure 5K, bottom left panel). In a pho1/pho1 background PRE activity was lost, resulting in activation of the LacZ gene by the IDE enhancer (Figure 5K, middle panel). However, LacZ expression was repressed in wing discs isolated from larvae that were heat shocked to express GALYY1 (Figure 5K, bottom right panel). Therefore, GALYY1 can repress transcription through a native PRE sequence at late developmental stages. YY1 can correct phenotypic defects in pho mutant flies Our results suggest that YY1 is a vertebrate PcG protein. If true, YY1 might function in fly development to compensate for loss of PHO function in a pho mutant background. Drosophila mutants bearing the pho1/phocv alleles show a number of homeotic defects including partial transformation of antennal structures into legs, partial transformation of mesothoracic and methathoracic legs into prothoracic legs, and partial transformation of abdominal segments into more posterior abdominal segments (Girton and Jeon, 1994). We found that the Drosophila pho cDNA driven by the ubiquitously expressed armadillo promoter (arm-pho; Figure 1A) nearly completely corrected segmentation, and antennal and leg defects (Figure 6A–C; Table I). Only ectopic pigmentation on tergite 4 and occasional extra sex combs or antennal defects distinguished these flies from wild type. Figure 6.GALYY1 and PHO can partially correct phenotypic defects in pho1/phocv mutant flies. (A) PHO and YY1 partially correct segmentation defects. Wild-type, pho1/phocv mutant, arm-pho-bearing and hsp70GALYY1-bearing pho1/phocv flies are shown. Wild-type male flies are darkly pigmented on the tergites of the last two posterior segments (segments 5 and 6, left panel). Mutant flies show posterior transformation of the segmentation pattern that results in pigmentation on tergite 4 (and sometimes tergites 3 and 2; see arrows pointing to extra pigment). In addition, males lack segment A7 (the posterior-most segment) and transformation of A6 towards A7 can be detected as a smaller A6 which causes the male genitalia to protrude more than in wild-type flies (see mutant panel, smaller A6). In pho1/phocv flies bearing the arm-pho transgene, the posterior-most segment is wild type, although pigmentation is still abnormal on tergite number 4 (right panel). In pho1/phocv flies bearing the hsp70GALYY1 transgene, segmentation pattern is almost completely normal, although pigmentation is not complete. (B) The arm-pho and hsp70GALYY1 transgenes can rescue antenna development. Head mount photographs of wild-type, pho1/phocv mutant, arm-pho-corrected and hsp70GALYY1-corrected flies are shown. The arrows point to arista structures. The arista (an appendage of the antenna) is normally bushy and branch like. In pho1/phocv mutants the aristae are either absent, or are poorly developed and clumped (middle panel). In 85–90% of pho1/phocv mutant flies bearing the arm-pho transgene and 95% of flies bearing the hsp70GALYY1 transgene, the aristae were of normal appearance, indicating substantial correction of the mutant phenotype (right panel). (C) The arm-pho and hsp70GALYY1 transgenes can completely correct the sex comb and claw defects found in pho1/phocv mutant flies. Leg mounts are shown of wild-type, pho1/phocv mutant, arm-pho-corrected pho1/phocv mutant and hsp70GALYY1-corrected pho1/phocv mutant flies. Arrows point to sex comb and claw structures. (D) GALYY1 protein is expressed after heat shock of hspGALYY1 transgenic embryos. Embryos from hsp70GALYY1 flies were either untreated or heat shocked for 45 min at 37°C. Western blots of lysates were assayed with either GAL4 or YY1 specific antibodies. The arrow points to the induced GALYY1 band. Download figure Download PowerPoint Table 1. Correction of pho mutant flies by the arm-pho and hsp70GALYY1 transgenes Body structure Wild type pho1/phocv mutants arm-pho corrected hsp70GALYY1 corrected Arista and antenna (% bushy) 100 0a 85–90 95 Average no. sex combs per flyb 2 ± 0 5.1 ± 1.3 2.7 ± 1.4 (72% = 2.0) 2 ± 0 Leg claws per flyb 6 ± 0 0.07 ± 0.4 6 ± 0 4.4 ± 1.6 Data were obtained using arm-pho transgene line 27a (18 flies), hsp70GALYY1 line 44H (19 flies) and pho mutant alleles pho1/phocv (28 flies). a One hundred percent missing or clumped. b Numbers represent averages ± SD of the mean. We tested YY1 rescue of the pho mutant phenotype using the same arm promoter system (arm-YY1; Figure 1A), but initially found no correction. However, these transgenes failed to express detectable YY1 protein (data not shown). Therefore, we used the inducible hsp70 promoter to drive expression of a GALYY1 chimera (hsp70GALYY1; Figure 1). Transgenic embryos bearing the hsp70GALYY1 transgene produced GALYY1 protein after heat shock (Figure 6D). This transgenic construct was crossed into a pho1/phocv mutant background and developing flies were heat shocked twice daily. The results on phenotypic correction were dramatic. GALYY1 expression nearly completely corrected the antennal and sex comb defects in pho1/phocv mutant flies (Figures 6A and 3B; Table I). Segmentation was largely normal, although pigmentation on tergite 5 was not always complete. Correction of claw structures was variable ranging from complete to partial correction (Table I). Flies with partial correction (three to four claws rather than six) appeared normal, but were clu