Splicing factors facilitate RNAi-directed silencing in fission yeast

被引:103
作者
Bayne, Elizabeth H. [1 ,2 ]
Portoso, Manuela [1 ,2 ]
Kagansky, Alexander [1 ,2 ]
Kos-Braun, Isabelle C. [1 ,2 ]
Urano, Takeshi [3 ]
Ekwall, Karl [4 ]
Alves, Flavia [1 ,2 ]
Rappsilber, Juri [1 ,2 ]
Allshire, Robin C. [1 ,2 ]
机构
[1] Univ Edinburgh, Wellcome Trust Ctr Cell Biol, Sch Biol Sci, Edinburgh EH9 3JR, Midlothian, Scotland
[2] Univ Edinburgh, Inst Cell Biol, Sch Biol Sci, Edinburgh EH9 3JR, Midlothian, Scotland
[3] Shimane Univ, Fac Med, Dept Biochem, Izumo, Shimane 6938501, Japan
[4] Univ Coll Sodertorn, Karolinska Inst, Dept Biosci & Med Nutr, S-14157 Huddinge, Sweden
基金
英国医学研究理事会; 英国惠康基金;
关键词
D O I
10.1126/science.1164029
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
Heterochromatin formation at fission yeast centromeres is directed by RNA interference (RNAi). Noncoding transcripts derived from centromeric repeats are processed into small interfering RNAs (siRNAs) that direct the RNA-induced transcriptional silencing (RITS) effector complex to engage centromer transcripts, resulting in recruitment of the histone H3 lysine 9 methyltransferase Clr4, and hence silencing. We have found that defects in specific splicing factors, but not splicing itself, affect the generation of centromeric siRNAs and consequently centromeric heterochromatin integrity. Moreover, splicing factors physically associate with Cid12, a component of the RNAi machinery, and with centromeric chromatin, consistent with a direct role in RNAi. We propose that spliceosomal complexes provide a platform for siRNA generation and hence facilitate effective centromere repeat silencing.
引用
收藏
页码:602 / 606
页数:5
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