SR Proteins in Vertical Integration of Gene Expression from Transcription to RNA Processing to Translation

被引:249
作者
Zhong, Xiang-Yang [1 ]
Wang, Pingping [1 ]
Han, Joonhee [1 ]
Rosenfeld, Michael G. [2 ]
Fu, Xiang-Dong [1 ]
机构
[1] Univ Calif San Diego, Dept Cellular & Mol Med, La Jolla, CA 92093 USA
[2] Univ Calif San Diego, Howard Hughes Med Inst, La Jolla, CA 92093 USA
关键词
SPLICING FACTOR ASF/SF2; MESSENGER-RNA; IN-VIVO; MAMMALIAN-CELLS; NUCLEAR-ORGANIZATION; TOPOISOMERASE-I; FACTOR SF2/ASF; FACTOR SC35; PHOSPHORYLATION; ELONGATION;
D O I
10.1016/j.molcel.2009.06.016
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
SR proteins have been studied extensively as a family of RNA-binding proteins that participate in both constitutive and regulated pre-mRNA splicing in mammalian cells. However, SR proteins were first discovered as factors that interact with transcriptionally active chromatin. Recent studies have now uncovered properties that connect these once apparently disparate functions, showing that a subset of SR proteins seem to bind directly to the histone 3 tail, play an active role in transcriptional elongation, and colocalize with genes that are engaged in specific intra- and interchromosome interactions for coordinated regulation of gene expression in the nucleus. These transcription-related activities are also coupled with a further expansion of putative functions of specific SR protein family members in RNA metabolism downstream of mRNA splicing, from RNA export to stability control to translation. These findings, therefore, highlight the broader roles of SR proteins in vertical integration of gene expression and provide mechanistic insights into their contributions to genome stability and proper cell-cycle progression in higher eukaryotic cells.
引用
收藏
页码:1 / 10
页数:10
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