High-resolution mapping of the protein interaction network for the human transcription machinery and affinity purification of RNA polymerase II-associated complexes

被引:73
作者
Cloutier, Philippe
Al-Khoury, Racha
Lavallee-Adam, Mathieu [2 ]
Faubert, Denis
Jiang, Heng
Poitras, Christian
Bouchard, Annie
Forget, Diane
Blanchette, Mathieu [2 ]
Coulombe, Benoit [1 ,3 ]
机构
[1] Inst Rech Clin Montreal, Lab Gene Transcript & Prote, Prote Discovery Platform, Montreal, PQ H2W 1R7, Canada
[2] McGill Univ, McGill Ctr Bioinformat, Montreal, PQ, Canada
[3] Univ Montreal, Dept Biochim, Montreal, PQ H3C 3J7, Canada
基金
加拿大健康研究院;
关键词
Protein affinity purification; RNA polymerase II; Protein interaction networks; Protein complexes; Proteomics; Bioinformatics; PROTEOMICS; CHAPERONE;
D O I
10.1016/j.ymeth.2009.05.005
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Thirty years of research on gene transcription has uncovered a myriad of factors that regulate, directly or indirectly, the activity of RNA polymerase II (RNAPII) during mRNA synthesis. Yet many regulatory factors remain to be discovered. Using protein affinity purification coupled to mass spectrometry (AP-MS), we recently unraveled a high-density interaction network formed by RNAPII and its accessory factors from the soluble fraction of human cell extracts. Validation of the dataset using a machine learning approach trained to minimize the rate of false positives and false negatives yielded a high-confidence dataset and uncovered novel interactors that regulate the RNAPII transcription machinery, including a new protein assembly we named the RNAPII-Associated Protein 3 (RPAP3) complex. (C) 2009 Elsevier Inc. All rights reserved.
引用
收藏
页码:381 / 386
页数:6
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