Splicing Factors Facilitate RNAi-Directed Silencing in Fission Yeast

Author:

Bayne Elizabeth H.123,Portoso Manuela123,Kagansky Alexander123,Kos-Braun Isabelle C.123,Urano Takeshi123,Ekwall Karl123,Alves Flavia123,Rappsilber Juri123,Allshire Robin C.123

Affiliation:

1. Wellcome Trust Centre for Cell Biology and Institute of Cell Biology, School of Biological Sciences, University of Edinburgh, 6.34 Swann Building, Edinburgh EH9 3JR, UK.

2. Department of Biochemistry, Shimane University Faculty of Medicine, 89-1 Enya-cho, Izumo 693-8501, Japan.

3. Karolinska Institute, Department of Biosciences and Medical Nutrition, University College Sodertorn, Novum 141, 57 Huddinge, Sweden.

Abstract

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 centromere 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.

Publisher

American Association for the Advancement of Science (AAAS)

Subject

Multidisciplinary

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