The Conserved RNA Binding Cyclophilin, Rct1, Regulates Small RNA Biogenesis and Splicing Independent of Heterochromatin Assembly

被引:8
作者
Chang, An-Yun [1 ,2 ]
Castel, Stephane E. [1 ,3 ]
Ernst, Evan [1 ]
Kim, Hyun Soo [1 ]
Martienssen, Robert A. [1 ,2 ,3 ,4 ]
机构
[1] Cold Spring Harbor Lab, POB 100, Cold Spring Harbor, NY 11724 USA
[2] SUNY Stony Brook, Mol & Cellular Biol Program, Stony Brook, NY 11794 USA
[3] Cold Spring Harbor Lab, Watson Sch Biol Sci, POB 100, Cold Spring Harbor, NY 11724 USA
[4] Cold Spring Harbor Lab, Howard Hughes Med Inst, Cold Spring Harbor, NY 11724 USA
基金
加拿大自然科学与工程研究理事会; 美国国家卫生研究院;
关键词
H3; LYSINE-9; METHYLATION; HISTONE H3; UBIQUITIN LIGASE; POLYMERASE-II; FISSION YEAST; MULTIDOMAIN CYCLOPHILIN; SILENCING FACTORS; SIRNA GENERATION; QUALITY-CONTROL; COMPLEX;
D O I
10.1016/j.celrep.2017.05.086
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
RNAi factors and their catalytic activities are essential for heterochromatin assembly in S. pombe. This has led to the idea that siRNAs can promote H3K9 methylation by recruiting the cryptic loci regulator complex (CLRC), also known as recombination in K complex (RIKC), to the nucleation site. The conserved RNA-binding protein Rct1 (AtCyp59/SIG-7) interacts with splicing factors and RNA polymerase II. Here we show that Rct1 promotes processing of pericentromeric transcripts into siRNAs via the RNA recognition motif. Surprisingly, loss of siRNA in rct1 mutants has no effect on H3K9 di- or tri-methylation, resembling other splicing mutants, suggesting that post-transcriptional gene silencing per se is not required to maintain heterochromatin. Splicing of the Argonaute gene is also defective in rct1 mutants and contributes to loss of silencing but not to loss of siRNA. Our results suggest that Rct1 guides transcripts to the RNAi machinery by promoting splicing of elongating non-coding transcripts.
引用
收藏
页码:2477 / 2489
页数:13
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