Literature DB >> 8625838

A role for mel-18, a Polycomb group-related vertebrate gene, during theanteroposterior specification of the axial skeleton.

T Akasaka1, M Kanno, R Balling, M A Mieza, M Taniguchi, H Koseki.   

Abstract

Segment identity in both invertebrates and vertebrates is conferred by spatially restricted distribution of homeotic gene products. In Drosophila, the expression of Homeobox genes during embryogenesis is initially induced by segmentation gene products and then maintained by Polycomb group and Trithorax group gene products. Polycomb group gene homologs are conserved in vertebrates. Murine mel-18 and closely related bmi-1 are homologous to posterior sex combs and suppressor two of zeste. Mel-18 protein mediates a transcriptional repression via direct binding to specific DNA sequences. To gain further insight into the function of Mel-18, we have inactivated the mel-18 locus by homologous recombination. Mice lacking mel-18 survive to birth and die around 4 weeks after birth after exhibiting strong growth retardation. Similar to the Drosophila posterior sex combs mutant, posterior transformations of the axial skeleton were reproducibly observed in mel-18 mutants. The homeotic transformations were correlated with ectopic expression of Homeobox cluster genes along the anteroposterior axis in the developing paraxial mesoderm. Surprisingly, mel-18-deficient phenotypes are reminiscent of bmi-1 mutants. These results indicate that the vertebrate Polycomb group genes mel-18 and bmi-1, like Drosophila Polycomb group gene products, might play a crucial role in maintaining the silent state of Homeobox gene expression during paraxial mesoderm development.

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Year:  1996        PMID: 8625838     DOI: 10.1242/dev.122.5.1513

Source DB:  PubMed          Journal:  Development        ISSN: 0950-1991            Impact factor:   6.868


  79 in total

1.  Randomly inserted and targeted Hox/reporter fusions transcriptionally silenced in Polycomb mutants.

Authors:  Wim d Graaff; Daihachiro Tomotsune; Tony Oosterveen; Yoshihiro Takihara; Haruhiko Koseki; Jacqueline Deschamps
Journal:  Proc Natl Acad Sci U S A       Date:  2003-10-31       Impact factor: 11.205

Review 2.  Extra sex combs, chromatin, and cancer: exploring epigenetic regulation and tumorigenesis in Drosophila.

Authors:  Can Zhang; Bo Liu; Guangyao Li; Lei Zhou
Journal:  J Genet Genomics       Date:  2011-09-24       Impact factor: 4.275

3.  Skeletal development in sloths and the evolution of mammalian vertebral patterning.

Authors:  Lionel Hautier; Vera Weisbecker; Marcelo R Sánchez-Villagra; Anjali Goswami; Robert J Asher
Journal:  Proc Natl Acad Sci U S A       Date:  2010-10-18       Impact factor: 11.205

4.  Evolutionary conservation and predicted structure of the Drosophila extra sex combs repressor protein.

Authors:  J Ng; R Li; K Morgan; J Simon
Journal:  Mol Cell Biol       Date:  1997-11       Impact factor: 4.272

5.  YY1 DNA binding and PcG recruitment requires CtBP.

Authors:  Lakshmi Srinivasan; Michael L Atchison
Journal:  Genes Dev       Date:  2004-11-01       Impact factor: 11.361

6.  Mammalian polycomb-mediated repression of Hox genes requires the essential spliceosomal protein Sf3b1.

Authors:  Kyoichi Isono; Yoko Mizutani-Koseki; Toshihisa Komori; Marion S Schmidt-Zachmann; Haruhiko Koseki
Journal:  Genes Dev       Date:  2005-03-01       Impact factor: 11.361

7.  Interaction proteomics analysis of polycomb proteins defines distinct PRC1 complexes in mammalian cells.

Authors:  Julien Vandamme; Pamela Völkel; Claire Rosnoblet; Perrine Le Faou; Pierre-Olivier Angrand
Journal:  Mol Cell Proteomics       Date:  2011-01-31       Impact factor: 5.911

8.  Ring1A is a transcriptional repressor that interacts with the Polycomb-M33 protein and is expressed at rhombomere boundaries in the mouse hindbrain.

Authors:  J Schoorlemmer; C Marcos-Gutiérrez; F Were; R Martínez; E García; D P Satijn; A P Otte; M Vidal
Journal:  EMBO J       Date:  1997-10-01       Impact factor: 11.598

9.  The core of the polycomb repressive complex is compositionally and functionally conserved in flies and humans.

Authors:  Stuart S Levine; Alona Weiss; Hediye Erdjument-Bromage; Zhaohui Shao; Paul Tempst; Robert E Kingston
Journal:  Mol Cell Biol       Date:  2002-09       Impact factor: 4.272

10.  The Polycomb-group gene Rae28 sustains Nkx2.5/Csx expression and is essential for cardiac morphogenesis.

Authors:  Manabu Shirai; Tomoaki Osugi; Hideyuki Koga; Yoshikazu Kaji; Eiki Takimoto; Issei Komuro; Junichi Hara; Takeshi Miwa; Keiko Yamauchi-Takihara; Yoshihiro Takihara
Journal:  J Clin Invest       Date:  2002-07       Impact factor: 14.808

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