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Series GSE90647 Query DataSets for GSE90647
Status Public on Mar 20, 2017
Title Transcriptome-wide analysis of alternative routes for RNA substrates into the exosome complex
Organism Saccharomyces cerevisiae
Experiment type Other
Summary The RNA exosome complex functions in both the accurate processing and rapid degradation of many different classes of RNA. Functional and structural analyses indicate that RNA can either be threaded through the central channel of the exosome or more directly access the active sites of the ribonucleases Rrp44 and Rrp6, but it was unclear how many substrates follow each pathway in vivo. To address this we used UV crosslinking in growing cells to identify transcriptome-wide interactions of RNAs with the major nuclear exosome-cofactor Mtr4 and with individual exosome subunits (Rrp6, Csl4, Rrp41 and Rrp44) along the threaded RNA path. We performed comparative analyses on exosome complexes lacking the exonucleolytic activity of Rrp44, either carrying a mutation in the Rrp44 S1 RNA-binding domain, predicted to disfavor direct access to the Rrp44 exonuclease active site, or with multiple mutations in Rrp41, reported to block RNA passage through the central channel. Our analysis identified targets using preferentially channel-threading pathway such as mRNAs, 5S rRNA or scR1. Our results suggest as well that aborted tRNAs transcripts, released during transcription, would be rapidly degraded using this route. Alternatively, pre-tRNAs appears to access Rrp44 directly. Both routes seems to be involved for degradation or maturation of RNAPI transcripts. The Rrp41 mutations were found to block substrate passage to Rrp44 only for cytoplasmic mRNAs, apparently confirming the prediction of widening of the lumen in the nuclear, Rrp6-associated complex.
 
Overall design 13 samples were analysed from strains carrying HTP tagged protein. Duplicate CRAC experiments were carried out for each protein
 
Contributor(s) Delan-Forino C, Schneider C, Tollervey D
Citation(s) 28355211
Submission date Nov 29, 2016
Last update date Jul 02, 2019
Contact name Clementine Delan-Forino
E-mail(s) clementine.delanforino@gmail.com
Phone 01316507093
Organization name University of Edinburgh - WTCCB
Lab Tollervey lab
Street address Michael Swann Building 5.1, King's Buildings, Mayfield Road
City Edinburgh
ZIP/Postal code EH9 3JR
Country United Kingdom
 
Platforms (2)
GPL13821 Illumina HiSeq 2000 (Saccharomyces cerevisiae)
GPL22715 Illumina MiniSeq (Saccharomyces cerevisiae)
Samples (13)
GSM2409856 Rrp44-exo-S1-HTP_1
GSM2409857 Rrp44-exo-S1-HTP_2
GSM2409858 Mtr4-HTP_Rrp44-exo_1
Relations
BioProject PRJNA355277
SRA SRP094053

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Supplementary file Size Download File type/resource
GSE90647_RAW.tar 31.6 Mb (http)(custom) TAR (of GTF)
SRA Run SelectorHelp
Raw data are available in SRA
Processed data provided as supplementary file

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