NIR is a novel INHAT repressor that modulates the transcriptional activity of p53. (Q24297694)

5 July 2017

title

NIR is a novel INHAT repressor that modulates the transcriptional activity of p53. (English)

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NOC2 like nucleolar associated transcriptional repressor

5 July 2017

main subject

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tumor protein p53

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negative regulation of intrinsic apoptotic signaling pathway

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Nucleolar complex protein 2 homolog

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Histone H3 Dmel_CG31613

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Histone H4 replacement Dmel_CG3379

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author

Leo A van Grunsven

11

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Roland Schüle

16

object named as

Roland Schüle

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5 July 2017

Philip Hublitz

1

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5 July 2017

Natalia Kunowska

2

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5 July 2017

Ulrich P Mayer

3

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5 July 2017

Judith M Müller

4

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5 July 2017

Kristina Heyne

5

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5 July 2017

Na Yin

6

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5 July 2017

Claudia Fritzsche

7

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5 July 2017

Cecilia Poli

8

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5 July 2017

Laurent Miguet

9

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5 July 2017

Ingo W Schupp

10

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5 July 2017

Noëlle Potiers

12

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5 July 2017

Alain van Dorsselaer

13

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5 July 2017

Eric Metzger

14

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5 July 2017

Klaus Roemer

15

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5 July 2017

language of work or name

English

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publication date

1 December 2005

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5 July 2017

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5 July 2017

volume

19

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5 July 2017

issue

23

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5 July 2017

page(s)

2912-2924

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Characterization of four autonomous repression domains in the corepressor receptor interacting protein 140

5 July 2017

cites work

1 reference

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19 March 2017

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High-level and high-throughput recombinant protein production by transient transfection of suspension-growing human 293-EBNA1 cells

19 March 2017

1 reference

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The corepressor mSin3a interacts with the proline-rich domain of p53 and protects p53 from proteasome-mediated degradation

19 March 2017

1 reference

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19 March 2017

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mHDA1/HDAC5 histone deacetylase interacts with and represses MEF2A transcriptional activity

19 March 2017

1 reference

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Recruitment of SMRT/N-CoR-mSin3A-HDAC-repressing complexes is not a general mechanism for BTB/POZ transcriptional repressors: the case of HIC-1 and gammaFBP-B

19 March 2017

1 reference

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The TAF(II)250 subunit of TFIID has histone acetyltransferase activity

19 March 2017

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19 March 2017

Surfing the p53 network

1 reference

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The language of covalent histone modifications

7 April 2017

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7 April 2017

1 reference

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The transcriptional coactivators p300 and CBP are histone acetyltransferases

19 March 2017

1 reference

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The coregulator exchange in transcriptional functions of nuclear receptors

19 March 2017

1 reference

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The transcriptional corepressor, PELP1, recruits HDAC2 and masks histones using two separate domains

19 March 2017

1 reference

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Hdm2 recruits a hypoxia-sensitive corepressor to negatively regulate p53-dependent transcription

19 March 2017

1 reference

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Ataxin-3 is a histone-binding protein with two independent transcriptional corepressor activities

19 March 2017

1 reference

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Ikaros-CtIP interactions do not require C-terminal binding protein and participate in a deacetylase-independent mode of repression

19 March 2017

1 reference

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Regulation of histone acetylation and transcription by INHAT, a human cellular complex containing the set oncoprotein

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1315397

p53 Functions through Stress- and Promoter-Specific Recruitment of Transcription Initiation Components before and after DNA Damage

19 March 2017

1 reference

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Biological roles and mechanistic actions of co-repressor complexes

19 March 2017

1 reference

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

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1315397

The p53 pathway: positive and negative feedback loops

19 March 2017

1 reference

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Remodelling chromatin on a global scale: a novel protective function of p53.

7 April 2017

1 reference

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A signaling role of histone-binding proteins and INHAT subunits pp32 and Set/TAF-Ibeta in integrating chromatin hypoacetylation and transcriptional repression.

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1315397

Direct binding of INHAT to H3 tails disrupted by modifications

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1315397

The activation domains, the proline-rich domain, and the C-terminal basic domain in p53 are necessary for acetylation of histones on the proximal p21 promoter and interaction with p300/CREB-binding protein.

27 September 2017

1 reference

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Formation of the androgen receptor transcription complex

27 September 2017

1 reference

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The transcriptional coactivator FHL2 transmits Rho signals from the cell membrane into the nucleus

27 September 2017

1 reference

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Chromatin immunoprecipitation analysis fails to support the latency model for regulation of p53 DNA binding activity in vivo

27 September 2017

1 reference

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p21 Waf1/Cip1 can protect human colon carcinoma cells against p53-dependent and p53-independent apoptosis induced by natural chemopreventive and therapeutic agents

27 September 2017

1 reference

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Stra13 expression is associated with growth arrest and represses transcription through histone deacetylase (HDAC)-dependent and HDAC-independent mechanisms

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1315397

Transcriptional repression by wild-type p53 utilizes histone deacetylases, mediated by interaction with mSin3a.

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1315397

Characterization of structural p53 mutants which show selective defects in apoptosis but not cell cycle arrest

27 September 2017

1 reference

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Direct p53 transcriptional repression: in vivo analysis of CCAAT-containing G2/M promoters.

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1315397

Regulation of histone acetylation and transcription by nuclear protein pp32, a subunit of the INHAT complex.

30 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1315397

Interaction and functional collaboration of p300/CBP and bHLH proteins in muscle and B-cell differentiation

30 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1315397

Nucleosome arrays inhibit both initiation and elongation of transcripts by bacteriophage T7 RNA polymerase

30 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1315397

Transcriptional regulation by p53 through intrinsic DNA/chromatin binding and site-directed cofactor recruitment.

30 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1315397

p53 amino acids 339-346 represent the minimal p53 repression domain

29 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1315397

29 November 2018

Identifiers

DOI

10.1101/GAD.351205

1 reference

5 July 2017

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5 July 2017

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