Quantitative Proteomics of the CDK9 Interactome Reveals a Function of the HSP90-CDC37-P-TEFb Complex for BETi-Induced HIV-1 Latency Reactivation-Reference-Cited by-同舟云学术

Quantitative Proteomics of the CDK9 Interactome Reveals a Function of the HSP90-CDC37-P-TEFb Complex for BETi-Induced HIV-1 Latency Reactivation

Published:2023-08-04 Issue:9 Volume:22 Page:2880-2889
ISSN:1535-3893
Container-title:Journal of Proteome Research
language:en
Short-container-title:J. Proteome Res.

Author:

Wang Cong¹²,Chen Chunjing¹,Pan Zhenrui¹,He Yaohui¹,Zhang Zhanming¹,Liu Rongdiao¹³,Xue Yuhua¹,Zhou Qiang³⁴,Gao Xiang¹^ORCID

Affiliation:

1. State Key Laboratory of Cellular Stress Biology and Fujian Provincial Key Laboratory of Innovative Drug Target Research, School of Pharmaceutical Sciences, Xiamen University, Xiamen, Fujian 361102, China

2. Medical Center of Hematology, The Second Affiliated Hospital, Army Medical University, Chongqing 400000, China

3. Department of Molecular and Cell Biology, University of California, Berkeley, California 94720, United States

4. School of Biological Sciences, Faculty of Science, The University of Hong Kong, Hong Kong 999077, China

Funder

National Key Research and Development Program of China

China Postdoctoral Science Foundation

Xiamen Southern Oceanographic Center

National Natural Science Foundation of China

National Institutes of Health

Publisher

American Chemical Society (ACS)

Subject

General Chemistry,Biochemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/acs.jproteome.3c00162

Reference49 articles.

1. Structure and ligand of a histone acetyltransferase bromodomain

2. BRD4 is a histone acetyltransferase that evicts nucleosomes from chromatin

3. HDAC inhibition results in widespread alteration of the histone acetylation landscape and BRD4 targeting to gene bodies

4. Recruitment of P-TEFb for Stimulation of Transcriptional Elongation by the Bromodomain Protein Brd4

5. The Bromodomain Protein Brd4 Is a Positive Regulatory Component of P-TEFb and Stimulates RNA Polymerase II-Dependent Transcription

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