Heterogeneity in mammalian RNA 3′ end formation

被引:32
作者
Neilson, Joel R. [1 ,2 ]
Sandberg, Rickard [3 ]
机构
[1] Baylor Coll Med, Dept Physiol & Mol Biophys, Houston, TX 77030 USA
[2] Baylor Coll Med, Dan L Duncan Canc Ctr, Houston, TX 77030 USA
[3] Karolinska Inst, Dept Cell & Mol Biol, S-17177 Stockholm, Sweden
基金
瑞典研究理事会;
关键词
RNA Processing; Post-transcriptional; Untranslated Regions; Genomics; Bioinformatics; PRE-MESSENGER-RNA; POLYADENYLATION SPECIFICITY FACTOR; DISEASE-ASSOCIATED VARIANTS; POLY(A) SITE SELECTION; LARGE-SCALE ANALYSIS; SNRNP-A PROTEIN; ALTERNATIVE POLYADENYLATION; UNTRANSLATED REGIONS; CLEAVAGE FACTOR; POLYMERASE-II;
D O I
10.1016/j.yexcr.2010.02.040
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Precisely directed cleavage and polyadenylation of mRNA is a fundamental part of eukaryotic gene expression. Yet, 3' end heterogeneity has been documented for thousands of mammalian genes, and usage of one cleavage and polyadenylation signal over another has been shown to impact gene expression in many cases. Building upon the rich biochemical and genetic understanding of the 3' end formation, recent genomic studies have begun to suggest that widespread changes in mRNA cleavage and polyadenylation may be a part of large, dynamic gene regulatory programs. In this review, we begin with a modest overview of the studies that defined the mechanisms of mammalian 3' end formation, and then discuss how recent genomic studies intersect with these more traditional approaches, showing that both will be crucial for expanding our understanding of this facet of gene regulation. (C) 2010 Elsevier Inc. All rights reserved.
引用
收藏
页码:1357 / 1364
页数:8
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