Overlapping and Unique Roles for C-Terminal Binding Protein 1 (CtBP1) and CtBP2 during Mouse Development

REFERENCES

• Anson-Cartwright, L., K. Dawson, D. Holmyard, S. J. Fisher, R. A. Lazzarini, and J. C. Cross. 2000. The glial cells missing-1 protein is essential for branching morphogenesis in the chorioallantoic placenta. Nat. Genet. 25: 311–314.
   PubMed Web of Science ®Google Scholar
• Brannon, M., J. D. Brown, R. Bates, D. Kimelman, and R. T. Moon. 1999. XCtBP is a XTcf-3 co-repressor with roles throughout Xenopus development. Development 126: 3159–3170.
   PubMed Web of Science ®Google Scholar
• Brown, M., M. McCormack, K. G. Zinn, M. P. Farrell, I. Bikel, and D. M. Livingston. 1986. A recombinant murine retrovirus for simian virus 40 large T cDNA transforms mouse fibroblasts to anchorage-independent growth. J. Virol. 60: 290–293.
   PubMed Web of Science ®Google Scholar
• Criqui-Filipe, P., C. Ducret, S. M. Maira, and B. Wasylyk. 1999. Net, a negative Ras-switchable TCF, contains a second inhibition domain, the CID, that mediates repression through interactions with CtBP and de-acetylation. EMBO J. 18: 3392–3403.
   PubMedGoogle Scholar
• Deconinck, A. E., P. E. Mead, S. G. Tevosian, J. D. Crispino, S. G. Katz, L. I. Zon, and S. H. Orkin. 2000. FOG acts as a repressor of red blood cell development in Xenopus. Development 127: 2031–2040.
   PubMedGoogle Scholar
• Dressel, U., P. J. Bailey, S. C. Wang, M. Downes, R. M. Evans, and G. E. Muscat. 2001. A dynamic role for HDAC7 in MEF2-mediated muscle differentiation. J. Biol. Chem. 276: 17007–17013.
   PubMed Web of Science ®Google Scholar
• Friedrich, G., and P. Soriano. 1991. Promoter traps in embryonic stem cells: a genetic screen to identify and mutate developmental genes in mice. Genes Dev. 5: 1513–1523.
   PubMed Web of Science ®Google Scholar
• Frohman, M. A., M. K. Dush, and G. R. Martin. 1988. Rapid production of full-length cDNAs from rare transcripts: amplification using a single gene-specific oligonucleotide primer. Proc. Natl. Acad. Sci. USA 85: 8998–9002.
   PubMed Web of Science ®Google Scholar
• Furusawa, T., H. Moribe, H. Kondoh, and Y. Higashi. 1999. Identification of CtBP1 and CtBP2 as corepressors of zinc finger- homeodomain factor deltaEF1. Mol. Cell. Biol. 19: 8581–8590.
   PubMedGoogle Scholar
• Galceran, J., I. Farinas, M. J. Depew, H. Clevers, and R. Grosschedl. 1999. Wnt3a−/−-like phenotype and limb deficiency in Lef1−/−Tcf1−/− mice. Genes Dev. 13: 709–717.
   PubMed Web of Science ®Google Scholar
• Greco, T. L., S. Takada, M. M. Newhouse, J. A. McMahon, A. P. McMahon, and S. A. Camper. 1996. Analysis of the vestigial tail mutation demonstrates that Wnt-3a gene dosage regulates mouse axial development. Genes Dev. 10: 313–324.
   PubMedGoogle Scholar
• Gripp, K. W., D. Wotton, M. C. Edwards, E. Roessler, L. Ades, P. Meinecke, A. Richieri-Costa, E. H. Zackai, J. Massague, M. Muenke, and S. J. Elledge. 2000. Mutations in TGIF cause holoprosencephaly and link NODAL signalling to human neural axis determination. Nat. Genet. 25: 205–208.
   PubMedGoogle Scholar
• Grooteclaes, M. L., and S. M. Frisch. 2000. Evidence for a function of CtBP in epithelial gene regulation and anoikis. Oncogene 19: 3823–3828.
   PubMed Web of Science ®Google Scholar
• Hildebrand, J. D., M. D. Schaller, and J. T. Parsons. 1993. Identification of sequences required for the efficient localization of the focal adhesion kinase, pp125FAK, to cellular focal adhesions. J. Cell Biol. 123: 993–1005.
   PubMed Web of Science ®Google Scholar
• Hildebrand, J. D., and P. Soriano. 1999. Shroom, a PDZ domain-containing actin-binding protein, is required for neural tube morphogenesis in mice. Cell 99: 486–497.
   Google Scholar
• Hogan, B., R. Beddington, F. Constantini, and E. Lacy. 1994. Manipulating the mouse embryo: a laboratory manual. Cold Spring Harbor Laboratory, Cold Spring Harbor, N.Y.
   Google Scholar
• Izutsu, K., M. Kurokawa, Y. Imai, K. Maki, K. Mitani, and H. Hirai. 2001. The corepressor CtBP interacts with Evi-1 to repress transforming growth factor beta signaling. Blood 97: 2815–2822.
   PubMed Web of Science ®Google Scholar
• Koipally, J., and K. Georgopoulos. 2000. Ikaros interactions with CtBP reveal a repression mechanism that is independent of histone deacetylase activity. J. Biol. Chem. 275: 19594–19602.
   PubMedGoogle Scholar
• Komada, M., D. J. McLean, M. D. Griswold, L. D. Russell, and P. Soriano. 2000. E-MAP-115, encoding a microtubule-associated protein, is a retinoic acid-inducible gene required for spermatogenesis. Genes Dev. 14: 1332–1342.
   PubMed Web of Science ®Google Scholar
• Laherty, C. D., W. M. Yang, J. M. Sun, J. R. Davie, E. Seto, and R. N. Eisenman. 1997. Histone deacetylases associated with the mSin3 corepressor mediate mad transcriptional repression. Cell 89: 349–356.
   PubMed Web of Science ®Google Scholar
• Lin, Q., J. Lu, H. Yanagisawa, R. Webb, G. E. Lyons, J. A. Richardson, and E. N. Olson. 1998. Requirement of the MADS-box transcription factor MEF2C for vascular development. Development 125: 4565–4574.
   PubMedGoogle Scholar
• Lu, J., T. A. McKinsey, C. L. Zhang, and E. N. Olson. 2000. Regulation of skeletal myogenesis by association of the MEF2 transcription factor with class II histone deacetylases. Mol. Cell 6: 233–244.
   PubMed Web of Science ®Google Scholar
• MacArthur, H., and G. Walter. 1984. Monoclonal antibodies specific for the carboxy terminus of simian virus 40 large T antigen. J. Virol. 52: 483–491.
   PubMed Web of Science ®Google Scholar
• Melhuish, T. A., and D. Wotton. 2000. The interaction of the carboxyl terminus-binding protein with the Smad corepressor TGIF is disrupted by a holoprosencephaly mutation in TGIF. J. Biol. Chem. 275: 39762–39766.
   PubMed Web of Science ®Google Scholar
• Nibu, Y., and M. S. Levine. 2001. CtBP-dependent activities of the short-range Giant repressor in the Drosophila embryo. Proc. Natl. Acad. Sci. USA 98: 6204–6208.
   PubMedGoogle Scholar
• Nibu, Y., H. Zhang, and M. Levine. 1998. Interaction of short-range repressors with Drosophila CtBP in the embryo. Science 280: 101–104.
   PubMedGoogle Scholar
• Phippen, T. M., A. L. Sweigart, M. Moniwa, A. Krumm, J. R. Davie, and S. M. Parkhurst. 2000. Drosophila C-terminal binding protein functions as a context-dependent transcriptional co-factor and interferes with both Mad and Groucho transcriptional repression. J. Biol. Chem. 275: 37628–37637.
   PubMedGoogle Scholar
• Pinson, K. I., J. Brennan, S. Monkley, B. J. Avery, and W. C. Skarnes. 2000. An LDL-receptor-related protein mediates Wnt signalling in mice. Nature 407: 535–538.
   PubMed Web of Science ®Google Scholar
• Poortinga, G., M. Watanabe, and S. M. Parkhurst. 1998. Drosophila CtBP: a Hairy-interacting protein required for embryonic segmentation and Hairy-mediated transcriptional repression. EMBO J. 17: 2067–2078.
   PubMedGoogle Scholar
• Postigo, A. A., and D. C. Dean. 1999. ZEB represses transcription through interaction with the corepressor CtBP. Proc. Natl. Acad. Sci. USA 96: 6683–6688.
   PubMedGoogle Scholar
• Postigo, A. A., and D. C. Dean. 1997. ZEB, a vertebrate homolog of Drosophila Zfh-1, is a negative regulator of muscle differentiation. EMBO J. 16: 3935–3943.
   PubMedGoogle Scholar
• Rossant, J., and J. C. Cross. 2001. Placental development: lessons from mouse mutants. Nat. Rev. Genet. 2: 538–548.
   PubMed Web of Science ®Google Scholar
• Sakai, T., A. Toyoda, K. Hashimoto, and H. Maeda. 2000. Isolation and characterization of a novel zinc finger gene, ZNF219, and mapping to the human chromosome 14q11 region. DNA Res. 7: 137–141.
   PubMedGoogle Scholar
• Schaeper, U., J. M. Boyd, S. Verma, E. Uhlmann, T. Subramanian, and G. Chinnadurai. 1995. Molecular cloning and characterization of a cellular phosphoprotein that interacts with a conserved C-terminal domain of adenovirus E1A involved in negative modulation of oncogenic transformation. Proc. Natl. Acad. Sci. USA 92: 10467–10471.
   PubMed Web of Science ®Google Scholar
• Schaller, M. D., J. D. Hildebrand, J. D. Shannon, J. W. Fox, R. R. Vines, and J. T. Parsons. 1994. Autophosphorylation of the focal adhesion kinase, pp125FAK, directs SH2-dependent binding of pp60src. Mol. Cell. Biol. 14: 1680–1688.
   PubMed Web of Science ®Google Scholar
• Schmitz, F., A. Konigstorfer, and T. C. Sudhof. 2000. RIBEYE, a component of synaptic ribbons: a protein's journey through evolution provides insight into synaptic ribbon function. Neuron 28: 857–872.
   PubMedGoogle Scholar
• Schorpp-Kistner, M., Z. Q. Wang, P. Angel, and E. F. Wagner. 1999. JunB is essential for mammalian placentation. EMBO J. 18: 934–948.
   PubMed Web of Science ®Google Scholar
• Sewalt, R. G., M. J. Gunster, J. van der Vlag, D. P. Satijn, and A. P. Otte. 1999. C-terminal binding protein is a transcriptional repressor that interacts with a specific class of vertebrate Polycomb proteins. Mol. Cell. Biol. 19: 777–787.
   PubMed Web of Science ®Google Scholar
• Spano, S., M. G. Silletta, A. Colanzi, S. Alberti, G. Fiucci, C. Valente, A. Fusella, M. Salmona, A. Mironov, A. Luini, D. Corda, and S. Spanfo. 1999. Molecular cloning and functional characterization of brefeldin A-ADP-ribosylated substrate. A novel protein involved in the maintenance of the Golgi structure. J. Biol. Chem. 274: 17705–17710.
   PubMedGoogle Scholar
• Sundqvist, A., E. Bajak, S. D. Kurup, K. Sollerbrant, and C. Svensson. 2001. Functional knockout of the corepressor ctbp by the second exon of adenovirus e1a relieves repression of transcription. Exp. Cell Res. 268: 284–293.
   PubMedGoogle Scholar
• Sundqvist, A., K. Sollerbrant, and C. Svensson. 1998. The carboxy-terminal region of adenovirus E1A activates transcription through targeting of a C-terminal binding protein-histone deacetylase complex. FEBS Lett. 429: 183–188.
   PubMed Web of Science ®Google Scholar
• Takada, S., K. L. Stark, M. J. Shea, G. Vassileva, J. A. McMahon, and A. P. McMahon. 1994. Wnt-3a regulates somite and tailbud formation in the mouse embryo. Genes Dev. 8: 174–189.
   PubMed Web of Science ®Google Scholar
• Takagi, T., H. Moribe, H. Kondoh, and Y. Higashi. 1998. DeltaEF1, a zinc finger and homeodomain transcription factor, is required for skeleton patterning in multiple lineages. Development 125: 21–31.
   PubMed Web of Science ®Google Scholar
• Turner, J., and M. Crossley. 1998. Cloning and characterization of mCtBP2, a co-repressor that associates with basic Kruppel-like factor and other mammalian transcriptional regulators. EMBO J. 17: 5129–5140.
   PubMed Web of Science ®Google Scholar
• Turner, J., and M. Crossley. 2001. The CtBP family: enigmatic and enzymatic transcriptional co-repressors. Bioessays 23: 683–690.
   PubMedGoogle Scholar
• Vojtek, A. B., S. M. Hollenberg, and J. A. Cooper. 1993. Mammalian Ras interacts directly with the serine/threonine kinase Raf. Cell 74: 205–214.
   PubMed Web of Science ®Google Scholar
• Weigert, R., M. G. Silletta, S. Spano, G. Turacchio, C. Cericola, A. Colanzi, S. Senatore, R. Mancini, E. V. Polishchuk, M. Salmona, F. Facchiano, K. N. Burger, A. Mironov, A. Luini, and D. Corda. 1999. CtBP/BARS induces fission of Golgi membranes by acylating lysophosphatidic acid. Nature 402: 429–433.
   PubMed Web of Science ®Google Scholar
• Wen, Y., D. Nguyen, Y. Li, and Z. C. Lai. 2000. The N-terminal BTB/POZ domain and C-terminal sequences are essential for Tramtrack69 to specify cell fate in the developing Drosophila eye. Genetics 156: 195–203.
   PubMedGoogle Scholar
• Wotton, D., R. S. Lo, S. Lee, and J. Massague. 1999. A Smad transcriptional corepressor. Cell 97: 29–39.
   PubMed Web of Science ®Google Scholar
• Wotton, D., R. S. Lo, L. A. Swaby, and J. Massague. 1999. Multiple modes of repression by the Smad transcriptional corepressor TGIF. J. Biol. Chem. 274: 37105–37110.
   PubMedGoogle Scholar
• Yamaguchi, T. P., S. Takada, Y. Yoshikawa, N. Wu, and A. P. McMahon. 1999. T (Brachyury) is a direct target of Wnt3a during paraxial mesoderm specification. Genes Dev. 13: 3185–3190.
   PubMed Web of Science ®Google Scholar
• Zhang, C. L., T. A. McKinsey, J. R. Lu, and E. N. Olson. 2001. Association of COOH-terminal-binding protein (CtBP) and MEF2- interacting transcription repressor (MITR) contributes to transcriptional repression of the MEF2 transcription factor. J. Biol. Chem. 276: 35–39.
   PubMed Web of Science ®Google Scholar