Histone acetyltransferase activity of CBP is controlled by cycle-dependent kinases and oncoprotein E1A. (Q42824374)

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6 December 2019

title

Histone acetyltransferase activity of CBP is controlled by cycle-dependent kinases and oncoprotein E1A (English)

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6 December 2019

6

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6 December 2019

Didier Trouche

11

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6 December 2019

Bernard Ducommun

10

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6 December 2019

Annick Harel-Bellan

12

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6 December 2019

author name string

S Ait-Si-Ali

1

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6 December 2019

S Ramirez

2

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6 December 2019

F X Barre

3

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6 December 2019

F Dkhissi

4

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6 December 2019

L Magnaghi-Jaulin

5

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P Robin

7

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6 December 2019

M Knibiehler

8

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L L Pritchard

9

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6 December 2019

publication date

1 November 1998

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6 December 2019

language of work or name

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6 December 2019

volume

396

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6 December 2019

issue

6707

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6 December 2019

page(s)

184-186

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Transcriptional control by the retinoblastoma protein

6 December 2019

cites work

1 reference

Retinoblastoma protein switches the E2F site from positive to negative element

21 January 2018

1 reference

Phosphorylated CREB binds specifically to the nuclear protein CBP

21 January 2018

1 reference

Nuclear protein CBP is a coactivator for the transcription factor CREB

21 January 2018

1 reference

Retinoblastoma protein represses transcription by recruiting a histone deacetylase

21 January 2018

1 reference

Retinoblastoma protein recruits histone deacetylase to repress transcription

21 January 2018

1 reference

Rb Interacts with Histone Deacetylase to Repress Transcription

21 January 2018

1 reference

The CBP co-activator is a histone acetyltransferase

21 January 2018

1 reference

The transcriptional coactivators p300 and CBP are histone acetyltransferases

21 January 2018

1 reference

Analysis with specific polyclonal antiserum indicates that the E1A-associated 300-kDa product is a stable nuclear phosphoprotein that undergoes cell cycle phase-specific modification

21 January 2018

1 reference

Regulation of NF-kappaB by cyclin-dependent kinases associated with the p300 coactivator

21 January 2018

1 reference

The translocation t(8;16)(p11;p13) of acute myeloid leukaemia fuses a putative acetyltransferase to the CREB-binding protein

21 January 2018

1 reference

E2F1 and E1A(12S) have a homologous activation domain regulated by RB and CBP.

21 January 2018

1 reference

Functional analysis of E2F transcription factor

21 January 2018

1 reference

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

21 January 2018

1 reference

Differential roles of p300 and PCAF acetyltransferases in muscle differentiation

21 January 2018

1 reference

Transcription Factor-Specific Requirements for Coactivators and Their Acetyltransferase Functions

21 January 2018

1 reference

The CREB-binding protein (CBP) cooperates with the serum response factor for transactivation of the c-fos serum response element

21 January 2018

1 reference

The acetyltransferase activity of CBP stimulates transcription

21 January 2018

1 reference

Physical interaction between the mitogen-responsive serum response factor and myogenic basic-helix-loop-helix proteins

21 January 2018

1 reference

A rapid and sensitive assay for histone acetyl-transferase activity

21 January 2018

1 reference

Adenoviral ElA-associated protein p300 as a functional homologue of the transcriptional co-activator CBP

21 January 2018

1 reference

A family of transcriptional adaptor proteins targeted by the E1A oncoprotein

21 January 2018

1 reference

Identification of specific adenovirus E1A N-terminal residues critical to the binding of cellular proteins and to the control of cell growth

21 January 2018

1 reference

inferred from DOI database lookup

7 January 2021

based on heuristic

Phosphorylation of the adenovirus E1A-associated 300 kDa protein in response to retinoic acid and E1A during the differentiation of F9 cells

1 reference

inferred from DOI database lookup

7 January 2021

based on heuristic

CREB-binding protein activates transcription through multiple domains

1 reference

inferred from DOI database lookup

7 January 2021

based on heuristic

Identifiers

DOI

10.1038/24190

1 reference

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Dimensions Publication ID

6 December 2019

1012984838

0 references

1 reference