Ceap/BLOS2 interacts with BRD7 and selectively inhibits its transcription-suppressing effect on cellular proliferation-associated genes (Q24308923)

1

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Jing Nie

2

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Bingtao Hao

3

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Lu Li

4

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Guichun Xing

5

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Zhaoqing Wang

6

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Ying Zhou

7

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Qihong Sun

8

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Guiyuan Li

9

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Lingqiang Zhang

10

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Fuchu He

Molecular characterization of celtix-1, a bromodomain protein interacting with the transcription factor interferon regulatory factor 2

11

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language of work or name

English

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publication date

June 2008

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published in

Cellular Signalling

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volume

20

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issue

6

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page(s)

1151-8

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cites work

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Lysine acetylation and the bromodomain: a new partnership for signaling

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The transcriptional regulation role of BRD7 by binding to acetylated histone through bromodomain

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Identification of nuclear localization signal that governs nuclear import of BRD7 and its essential roles in inhibiting cell cycle progression

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BRD7, a novel bromodomain gene, inhibits G1-S progression by transcriptionally regulating some important molecules involved in ras/MEK/ERK and Rb/E2F pathways

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BRD2 is one of BRD7-interacting proteins and its over-expression could initiate apoptosis

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BRD7 suppresses the growth of Nasopharyngeal Carcinoma cells (HNE1) through negatively regulating beta-catenin and ERK pathways

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Solution structure of BRD7 bromodomain and its interaction with acetylated peptides from histone H3 and H4

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Direct association of hepatopoietin with thioredoxin constitutes a redox signal transduction in activation of AP-1/NF-kappaB.

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CKIP-1 recruits nuclear ATM partially to the plasma membrane through interaction with ATM.

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NuSAP is degraded by APC/C-Cdh1 and its overexpression results in mitotic arrest dependent of its microtubules' affinity

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E2F3-a novel repressor of the ARF/p53 pathway

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Characterization of Ceap-11 and Ceap-16, two novel splicing-variant-proteins, associated with centrosome, microtubule aggregation and cell proliferation

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Selective recognition of acetylated histones by bromodomain proteins visualized in living cells

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Emerging roles for E2F: Beyond the G1/S transition and DNA replication

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The language of covalent histone modifications

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A dual-kinase mechanism for Wnt co-receptor phosphorylation and activation

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Double chromodomains cooperate to recognize the methylated histone H3 tail

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Role for the pleckstrin homology domain-containing protein CKIP-1 in AP-1 regulation and apoptosis

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The retinoblastoma gene family in differentiation and development.

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Regulation of transcription by the heterogeneous nuclear ribonucleoprotein E1B-AP5 is mediated by complex formation with the novel bromodomain-containing protein BRD7

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Identification of snapin and three novel proteins (BLOS1, BLOS2, and BLOS3/reduced pigmentation) as subunits of biogenesis of lysosome-related organelles complex-1 (BLOC-1)

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Differential expression of novel naturally occurring splice variants of PTEN and their functional consequences in Cowden syndrome and sporadic breast cancer

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The bromodomain: a conserved sequence found in human, Drosophila and yeast proteins

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E2F3 activity is regulated during the cell cycle and is required for the induction of S phase.

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Translating the Histone Code

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Combined Action of PHD and Chromo Domains Directs the Rpd3S HDAC to Transcribed Chromatin

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The histone H3 acetylase dGcn5 is a key player in Drosophila melanogaster metamorphosis

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Expression of tumor related genes NGX6, NAG-7, BRD7 in gastric and colorectal cancer

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Effector proteins for methylated histones: an expanding family

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Identifiers

DOI

1 reference

Consolidated OpenCitations Corpus – April 2017

1 reference

Consolidated OpenCitations Corpus – April 2017

PubMed publication ID

18329849

1 reference

Consolidated OpenCitations Corpus – April 2017