Cytoplasmic intron retention, function, splicing, and the sentinel RNA hypothesis

被引:49
作者
Buckley, Peter T. [1 ,2 ]
Khaladkar, Mugdha [2 ,3 ]
Kim, Junhyong [2 ,3 ,4 ]
Eberwine, James [1 ,2 ,4 ]
机构
[1] Univ Penn, Dept Pharmacol, Perelman Sch Med, Philadelphia, PA 19104 USA
[2] Univ Penn, Sch Arts & Sci, Philadelphia, PA 19104 USA
[3] Univ Penn, Dept Biol, Perelman Sch Med, Philadelphia, PA 19104 USA
[4] Univ Penn, PENN Genome Frontiers Inst, Perelman Sch Med, Philadelphia, PA 19104 USA
关键词
UNFOLDED PROTEIN RESPONSE; ENDOPLASMIC-RETICULUM STRESS; MESSENGER-RNA; MINOR SPLICEOSOME; NUCLEUS; GENE; NEURONS; CELLS; DECAY; SIRNA;
D O I
10.1002/wrna.1203
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Cytoplasmic splicing represents a newly emerging level of transcriptional regulation adding to the molecular diversity of mammalian cells. As examples of this noncanonical form of transcript processing are discovered, the evidence of its importance to normal cellular function grows. Work from a number of groups using a variety of cell types is steadily identifying a large number of transcripts (and soon to be even larger as genome-wide analyses of retained introns across a number of cellular phenotypes are currently underway) that undergo some level of regulated endogenous extranuclear splicing as part of their normal biosynthetic pathway. Here, we review the existing data covering cytoplasmic retained intron sequences and suggest that such sequences may be a component of 'sentinel RNA' that serves to generate transcript variants within the cytoplasm as well as a source for RNA-based secondary messages. (C) 2013 John Wiley & Sons, Ltd.
引用
收藏
页码:223 / 230
页数:8
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