Literature DB >> 11023972

Co-repressors 2000.

L J Burke1, A Baniahmad.   

Abstract

In the last 5 years, many co-repressors have been identified in eukaryotes that function in a wide range of species, from yeast to Drosophila and humans. Co-repressors are coregulators that are recruited by DNA-bound transcriptional silencers and play essential roles in many pathways including differentiation, proliferation, programmed cell death, and cell cycle. Accordingly, it has been shown that aberrant interactions of co-repressors with transcriptional silencers provide the molecular basis of a variety of human diseases. Co-repressors mediate transcriptional silencing by mechanisms that include direct inhibition of the basal transcription machinery and recruitment of chromatin-modifying enzymes. Chromatin modification includes histone deacetylation, which is thought to lead to a compact chromatin structure to which the accessibility of transcriptional activators is impaired. In a general mechanistic view, the overall picture suggests that transcriptional silencers and co-repressors act in analogy to transcriptional activators and coactivators, but with the opposite effect leading to gene silencing. We provide a comprehensive overview of the currently known higher eukaryotic co-repressors, their mechanism of action, and their involvement in biological and pathophysiological pathways. We also show the different pathways that lead to the regulation of co-repressor-silencer complex formation.

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Year:  2000        PMID: 11023972     DOI: 10.1096/fj.99-0943rev

Source DB:  PubMed          Journal:  FASEB J        ISSN: 0892-6638            Impact factor:   5.191


  70 in total

1.  Chromatin disruption and histone acetylation in regulation of the human immunodeficiency virus type 1 long terminal repeat by thyroid hormone receptor.

Authors:  Shao-Chung Victor Hsia; Yun-Bo Shi
Journal:  Mol Cell Biol       Date:  2002-06       Impact factor: 4.272

Review 2.  Multi-protein complexes in eukaryotic gene transcription.

Authors:  Ernest Martinez
Journal:  Plant Mol Biol       Date:  2002-12       Impact factor: 4.076

3.  The highly conserved region of the co-repressor Sin3A functionally interacts with the co-repressor Alien.

Authors:  Udo Moehren; Uwe Dressel; Christina A Reeb; Sami Väisänen; Thomas W Dunlop; Carsten Carlberg; Aria Baniahmad
Journal:  Nucleic Acids Res       Date:  2004-06-01       Impact factor: 16.971

4.  Dynamic nature of transcriptional regulation of nuclear receptor target genes in the context of chromatin organization.

Authors:  Sami Väisänen; Juha Matilainen; Carsten Carlberg
Journal:  Dermatoendocrinol       Date:  2011-07-01

5.  Liganded thyroid hormone receptor induces nucleosome removal and histone modifications to activate transcription during larval intestinal cell death and adult stem cell development.

Authors:  Kazuo Matsuura; Kenta Fujimoto; Liezhen Fu; Yun-Bo Shi
Journal:  Endocrinology       Date:  2011-12-06       Impact factor: 4.736

6.  Epigenetics in anoxia tolerance: a role for histone deacetylases.

Authors:  Anastasia Krivoruchko; Kenneth B Storey
Journal:  Mol Cell Biochem       Date:  2010-05-01       Impact factor: 3.396

7.  The hairless gene mutated in congenital hair loss disorders encodes a novel nuclear receptor corepressor.

Authors:  G B Potter; G M Beaudoin; C L DeRenzo; J M Zarach; S H Chen; C C Thompson
Journal:  Genes Dev       Date:  2001-10-15       Impact factor: 11.361

8.  Thyroid hormone activates protein arginine methyltransferase 1 expression by directly inducing c-Myc transcription during Xenopus intestinal stem cell development.

Authors:  Kenta Fujimoto; Kazuo Matsuura; Eileen Hu-Wang; Rosemary Lu; Yun-Bo Shi
Journal:  J Biol Chem       Date:  2012-02-07       Impact factor: 5.157

9.  Functional Studies of Transcriptional Cofactors via Microinjection-Mediated Gene Editing in Xenopus.

Authors:  Yuki Shibata; Lingyu Bao; Liezhen Fu; Bingyin Shi; Yun-Bo Shi
Journal:  Methods Mol Biol       Date:  2019

Review 10.  The Sox transcriptional factors: Functions during intestinal development in vertebrates.

Authors:  Liezhen Fu; Yun-Bo Shi
Journal:  Semin Cell Dev Biol       Date:  2016-08-25       Impact factor: 7.727

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