Alternative cleavage and polyadenylation: the long and short of it

被引:241
|
作者
Tian, Bin [1 ]
Manley, James L. [2 ]
机构
[1] Univ Med & Dent New Jersey, New Jersey Med Sch, Dept Biochem & Mol Biol, Newark, NJ 07103 USA
[2] Columbia Univ, Dept Biol Sci, New York, NY 10027 USA
基金
美国国家卫生研究院;
关键词
PRE-MESSENGER-RNA; 3' UNTRANSLATED REGIONS; GENOME-WIDE ANALYSIS; MOLECULAR-MECHANISMS; TRANSCRIPTION TERMINATION; PROCESSING FACTORS; UPSTREAM SEQUENCE; SITE SELECTION; NONCODING RNA; STEM-CELLS;
D O I
10.1016/j.tibs.2013.03.005
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
Cleavage and polyadenylation (C/P) of nascent transcripts is essential for maturation of the 3' ends of most eukaryotic mRNAs. Over the past three decades, biochemical studies have elucidated the machinery responsible for the seemingly simple C/P reaction. Recent genomic analyses have indicated that most eukaryotic genes have multiple cleavage and polyadenylation sites (pAs), leading to transcript isoforms with different coding potentials and/or variable 3' untranslated regions (UTRs). As such, alternative cleavage and polyadenylation (APA) is an important layer of gene regulation impacting mRNA metabolism. Here, we review our current understanding of APA and recent progress in this field.
引用
收藏
页码:312 / 320
页数:9
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