Role for N-CoR and histone deacetylase in Sin3-mediated transcriptional repression (Q28513708)

25 January 2017

title

Role for N-CoR and histone deacetylase in Sin3-mediated transcriptional repression (English)

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Nuclear receptor corepressor 1

25 January 2017

main subject

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GOA release 2020-03-11

Histone deacetylase 1

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GOA release 2020-03-11

author name string

L. Alland

1

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25 January 2017

R. Muhle

2

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25 January 2017

H. Hou

3

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25 January 2017

J. Potes

4

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25 January 2017

L. Chin

5

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25 January 2017

N. Schreiber-Agus

6

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25 January 2017

R. A. DePinho

7

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25 January 2017

publication date

1 May 1997

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25 January 2017

language of work or name

0 references

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25 January 2017

volume

387

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25 January 2017

issue

6628

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25 January 2017

page(s)

49–55

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Mad-Max transcriptional repression is mediated by ternary complex formation with mammalian homologs of yeast repressor Sin3

25 January 2017

cites work

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7 January 2021

An amino-terminal domain of Mxi1 mediates anti-Myc oncogenic activity and interacts with a homolog of the yeast transcriptional repressor SIN3

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Sin3 corepressor function in Myc-induced transcription and transformation

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Mad proteins contain a dominant transcription repression domain.

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The Saccharomyces cerevisiae SIN3 gene, a negative regulator of HO, contains four paired amphipathic helix motifs

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Transcriptional repression in Saccharomyces cerevisiae by a SIN3-LexA fusion protein

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RPD1 (SIN3/UME4) is required for maximal activation and repression of diverse yeast genes

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Yeast SNF/SWI transcriptional activators and the SPT/SIN chromatin connection

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Both positive and negative regulators of HO transcription are required for mother-cell-specific mating-type switching in yeast

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RPD3 encodes a second factor required to achieve maximum positive and negative transcriptional states in Saccharomyces cerevisiae

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A mammalian histone deacetylase related to the yeast transcriptional regulator Rpd3p

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7 January 2021

Transcriptional repression by YY1 is mediated by interaction with a mammalian homolog of the yeast global regulator RPD3

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7 January 2021

Histone deacetylase: a regulator of transcription

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Ligand-independent repression by the thyroid hormone receptor mediated by a nuclear receptor co-repressor

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A nuclear hormone receptor corepressor mediates transcriptional silencing by receptors with distinct repression domains.

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Mammalian Ras interacts directly with the serine/threonine kinase Raf

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Chromatin structure of the yeast SUC2 promoter in regulatory mutants

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The global transcriptional regulators, SSN6 and TUP1, play distinct roles in the establishment of a repressive chromatin structure

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Functional dissection of the yeast Cyc8–Tupl transcriptional co-repressor complex

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BRG1 contains a conserved domain of the SWI2/SNF2 family necessary for normal mitotic growth and transcription

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A human homologue of Saccharomyces cerevisiae SNF2/SWI2 and Drosophila brm genes potentiates transcriptional activation by the glucocorticoid receptor

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Two human homologues of Saccharomyces cerevisiae SWI2/SNF2 and Drosophila brahma are transcriptional coactivators cooperating with the estrogen receptor and the retinoic acid receptor

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The retinoblastoma protein and BRG1 form a complex and cooperate to induce cell cycle arrest

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c-Myc represses transcription in vivo by a novel mechanism dependent on the initiator element and Myc box II

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A link between c-Myc-mediated transcriptional repression and neoplastic transformation

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Targeting chromatin disruption: Transcription regulators that acetylate histones

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7 January 2021

Special HATs for special occasions: linking histone acetylation to chromatin assembly and gene activation

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HDA1 and RPD3 are members of distinct yeast histone deacetylase complexes that regulate silencing and transcription

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The histone deacetylase RPD3 counteracts genomic silencing in Drosophila and yeast

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myc family oncogenes in the development of normal and neoplastic cells.

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Mad: a heterodimeric partner for Max that antagonizes Myc transcriptional activity

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Adenovirus E1B oncoprotein tethers a transcriptional repression domain to p53.

1 reference

7 January 2021