Data Entry: Please note that the research database will be replaced by UNIverse by the end of October 2023. Please enter your data into the system https://universe-intern.unibas.ch. Thanks

Login for users with Unibas email account...

Login for registered users without Unibas email account...

 
RNAi-dependent and -independent RNA turnover mechanisms contribute to heterochromatic gene silencing
JournalArticle (Originalarbeit in einer wissenschaftlichen Zeitschrift)
 
ID 85961
Author(s) Bühler, Marc; Haas, Wilhelm; Gygi, Steven P; Moazed, Danesh
Author(s) at UniBasel Bühler, Marc
Year 2007
Title RNAi-dependent and -independent RNA turnover mechanisms contribute to heterochromatic gene silencing
Journal Cell
Volume 129
Number 4
Pages / Article-Number 707-21
Abstract In fission yeast, the RNAi pathway is required for heterochromatin-dependent silencing of transgene insertions at centromeric repeats and acts together with other pathways to silence transgenes at the silent mating-type locus. Here, we show that transgene transcripts at centromeric repeats are processed into siRNAs and are therefore direct targets of RNAi. Furthermore, we show that Cid14, a member of the Trf4/5 family of poly(A) polymerases, has poly(A) polymerase activity that is required for heterochromatic gene silencing. Surprisingly, while siRNA levels in cid14Delta cells are dramatically reduced, the structural integrity of heterochromatin appears to be preserved. Cid14 resides in a complex similar to the TRAMP complex found in budding yeast, which is part of a nuclear surveillance mechanism that degrades aberrant transcripts. Our findings indicate that polyadenylation by a TRAMP-like complex contributes to robust silencing of heterochromatic genes in fission yeast via the recruitment of the exosome and/or the RNAi machinery.
Publisher Cell Press
ISSN/ISBN 0092-8674
edoc-URL http://edoc.unibas.ch/dok/A5251089
Full Text on edoc No
Digital Object Identifier DOI 10.1016/j.cell.2007.03.038
PubMed ID http://www.ncbi.nlm.nih.gov/pubmed/17512405
ISI-Number WOS:000246788300016
Document type (ISI) Journal Article
 
   

MCSS v5.8 PRO. 0.393 sec, queries - 0.000 sec ©Universität Basel  |  Impressum   |    
03/05/2024