Pseudogene-derived small interfering RNAs regulate gene expression in mouse oocytes

被引:782
作者
Tam, Oliver H. [1 ,2 ]
Aravin, Alexei A. [1 ,2 ]
Stein, Paula [3 ]
Girard, Angelique [1 ,2 ]
Murchison, Elizabeth P. [1 ,2 ]
Cheloufi, Sihem [1 ,2 ]
Hodges, Emily [1 ,2 ]
Anger, Martin [3 ]
Sachidanandam, Ravi [1 ,2 ]
Schultz, Richard M. [3 ]
Hannon, Gregory J. [1 ,2 ]
机构
[1] Cold Spring Harbor Lab, Watson Sch Biol Sci, Cold Spring Harbor, NY 11724 USA
[2] Cold Spring Harbor Lab, Howard Hughes Med Inst, Cold Spring Harbor, NY 11724 USA
[3] Univ Penn, Dept Biol, Lynch Labs 205, Philadelphia, PA 19104 USA
关键词
D O I
10.1038/nature06904
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Pseudogenes populate the mammalian genome as remnants of artefactual incorporation of coding messenger RNAs into transposon pathways(1). Here we show that a subset of pseudogenes generates endogenous small interfering RNAs (endo-siRNAs) in mouse oocytes. These endo-siRNAs are often processed from double-stranded RNAs formed by hybridization of spliced transcripts from protein-coding genes to antisense transcripts from homologous pseudogenes. An inverted repeat pseudogene can also generate abundant small RNAs directly. A second class of endosiRNAs may enforce repression of mobile genetic elements, acting together with Piwi-interacting RNAs. Loss of Dicer, a protein integral to small RNA production, increases expression of endosiRNA targets, demonstrating their regulatory activity. Our findings indicate a function for pseudogenes in regulating gene expression by means of the RNA interference pathway and may, in part, explain the evolutionary pressure to conserve argonautemediated catalysis in mammals.
引用
收藏
页码:534 / U8
页数:6
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