Transcriptional repression by the SMRT-mSin3 corepressor: multiple interactions, multiple mechanisms, and a potential role for TFIIB. (Q33779119)

29 July 2017

title

Transcriptional repression by the SMRT-mSin3 corepressor: multiple interactions, multiple mechanisms, and a potential role for TFIIB. (English)

1 reference

29 July 2017

C W Wong

1

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29 July 2017

M L Privalsky

series ordinal

2

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29 July 2017

language of work or name

English

0 references

publication date

1 September 1998

1 reference

Molecular and Cellular Biology

29 July 2017

published in

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29 July 2017

volume

18

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29 July 2017

issue

9

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29 July 2017

page(s)

5500-5510

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The corepressor N-CoR and its variants RIP13a and RIP13Delta1 directly interact with the basal transcription factors TFIIB, TAFII32 and TAFII70.

29 July 2017

cites work

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4 July 2018

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Cloning and characterization of a corepressor and potential component of the nuclear hormone receptor repression complex

4 July 2018

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Corepressor SMRT binds the BTB/POZ repressing domain of the LAZ3/BCL6 oncoprotein

4 July 2018

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Differential recognition of liganded and unliganded thyroid hormone receptor by retinoid X receptor regulates transcriptional repression

4 July 2018

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SMRT corepressor interacts with PLZF and with the PML-retinoic acid receptor alpha (RARalpha) and PLZF-RARalpha oncoproteins associated with acute promyelocytic leukemia

4 July 2018

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4 July 2018

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The partial agonist activity of antagonist-occupied steroid receptors is controlled by a novel hinge domain-binding coactivator L7/SPA and the corepressors N-CoR or SMRT

4 July 2018

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Coactivator and corepressor regulation of the agonist/antagonist activity of the mixed antiestrogen, 4-hydroxytamoxifen.

4 July 2018

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4 July 2018

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Repression by Ume6 involves recruitment of a complex containing Sin3 corepressor and Rpd3 histone deacetylase to target promoters

4 July 2018

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Histone deacetylases and SAP18, a novel polypeptide, are components of a human Sin3 complex

4 July 2018

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Histone deacetylases associated with the mSin3 corepressor mediate mad transcriptional repression

4 July 2018

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Histone deacetylase activity is required for full transcriptional repression by mSin3A

4 July 2018

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4 July 2018

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4 July 2018

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4 July 2018

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A complex containing N-CoR, mSin3 and histone deacetylase mediates transcriptional repression

4 July 2018

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4 July 2018

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4 July 2018

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

4 July 2018

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4 July 2018

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4 July 2018

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4 July 2018

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

4 July 2018

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

4 July 2018

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4 July 2018

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SMRT isoforms mediate repression and anti-repression of nuclear receptor heterodimers

4 July 2018

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4 July 2018

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Suppressors of defective silencing in yeast: effects on transcriptional repression at the HMR locus, cell growth and telomere structure.

4 July 2018

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Unliganded thyroid hormone receptor alpha can target TATA-binding protein for transcriptional repression

4 July 2018

1 reference

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

4 July 2018

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Mxi1, a protein that specifically interacts with Max to bind Myc-Max recognition sites

4 July 2018

1 reference

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

4 July 2018

1 reference

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Interaction of human thyroid hormone receptor beta with transcription factor TFIIB may mediate target gene derepression and activation by thyroid hormone

4 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=109135

The centromere and promoter factor, 1, CPF1, of Saccharomyces cerevisiae modulates gene activity through a family of factors including SPT21, RPD1 (SIN3), RPD3 and CCR4.

4 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=109135

The erbA oncogene represses the actions of both retinoid X and retinoid A receptors but does so by distinct mechanisms

4 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=109135

Functional evidence for ligand-dependent dissociation of thyroid hormone and retinoic acid receptors from an inhibitory cellular factor

4 July 2018

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Epistasis analysis of suppressor mutations that allow HO expression in the absence of the yeast SW15 transcriptional activator

4 July 2018

1 reference

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

4 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=109135

The tau 4 activation domain of the thyroid hormone receptor is required for release of a putative corepressor(s) necessary for transcriptional silencing

4 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=109135

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4 July 2018

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4 July 2018

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Polarity-specific activities of retinoic acid receptors determined by a co-repressor.

4 July 2018

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4 July 2018

1 reference

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4 July 2018

1 reference

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1 reference

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4 July 2018

1 reference

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4 July 2018

1 reference

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Protein encoded by v-erbA functions as a thyroid-hormone receptor antagonist

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Activation of the yeast HO gene by release from multiple negative controls

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https://pubmed.ncbi.nlm.nih.gov/9710634

12 December 2020

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/9710634

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Repression of transcription mediated at a thyroid hormone response element by the v-erb-A oncogene product

1 reference

https://pubmed.ncbi.nlm.nih.gov/9710634

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Stoichiometric and steric principles governing repression by nuclear hormone receptors

1 reference

https://pubmed.ncbi.nlm.nih.gov/9710634

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Gene silencing by chicken ovalbumin upstream promoter-transcription factor I (COUP-TFI) is mediated by transcriptional corepressors, nuclear receptor-corepressor (N-CoR) and silencing mediator for retinoic acid receptor and thyroid hormone receptor

1 reference

https://pubmed.ncbi.nlm.nih.gov/9710634

12 December 2020

1 reference

https://pubmed.ncbi.nlm.nih.gov/9710634

12 December 2020

Identifiers

DOI

10.1128/MCB.18.9.5500

1 reference

29 July 2017

1 reference

29 July 2017

1 reference