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Series GSE68484 Query DataSets for GSE68484
Status Public on May 01, 2016
Title Native elongating transcript sequencing (NET-seq), nascnet RNA-seq, and total RNA-seq of wild type and RNA polymerase II C-terminal domain mutants and ChIP-nexus of RNA polymerase II C-terminal domains phosphoisoforms and splicing factors in S. cerevisiae
Organism Saccharomyces cerevisiae BY4741
Experiment type Expression profiling by high throughput sequencing
Other
Summary Transcription controls splicing and other gene regulatory processes, yet mechanisms remain obscure due to our fragmented knowledge of the molecular connections between the dynamically phosphorylated RNA polymerase II (Pol II) C-terminal domain (CTD) and regulatory factors. By systematically isolating phosphorylation states of the CTD heptapeptide repeat (Y1S2P3T4S5P6S7), we identify hundreds of protein factors that are differentially enriched, revealing unappreciated connections between the Pol II CTD and co-transcriptional processes. These data uncover a novel role for threonine-4 in 3’ end processing through controlling the transition between cleavage and termination. Furthermore, serine-5 phosphorylation seeds spliceosomal assembly immediately downstream of 3’ splice sites through a direct interaction with spliceosomal subcomplex, U1. Strikingly, threonine-4 phosphorylation also impacts splicing through serving as a mark of spliceosomal release and ensuring efficient post-transcriptional splicing genome-wide. Thus, comprehensive Pol II interactomes identify the complex and functional connections between transcription machinery and other gene regulatory complexes.
 
Overall design NET-seq of WT, rai1, rtt103 and Pol II CTD threonine-4 mutants. Nascent RNA-seq of WT and Pol II CTD threonine-4 mutant. RNA-seq of WT and Pol II CTD threonine-4 mutants. ChIP-nexus analysis of phospho-Ser5 and phospho-Thr4 of the Pol II CTD and ChIP-nexus of splicing factors.
 
Contributor(s) Harlen KM, Churchman LS
Citation(s) 27239037
Submission date May 03, 2015
Last update date May 15, 2019
Contact name Stirling Churchman
E-mail(s) churchman@genetics.med.harvard.edu
Organization name Harvard Medical School
Department Genetics
Lab Churchman Lab
Street address NRB Rm 356, 77 Ave Loius Pasteur
City Boston
State/province MA
ZIP/Postal code 02115
Country USA
 
Platforms (2)
GPL20138 Illumina NextSeq 500 (Saccharomyces cerevisiae BY4741)
GPL21372 Illumina MiSeq (Saccharomyces cerevisiae BY4741)
Samples (25)
GSM1673641 wild type NET-seq
GSM1673642 wild type NET-seq replicate 2
GSM1673643 T4V NET-seq
Relations
BioProject PRJNA282886
SRA SRP057947

Download family Format
SOFT formatted family file(s) SOFTHelp
MINiML formatted family file(s) MINiMLHelp
Series Matrix File(s) TXTHelp

Supplementary file Size Download File type/resource
GSE68484_RAW.tar 621.8 Mb (http)(custom) TAR (of BEDGRAPH)
SRA Run SelectorHelp
Raw data are available in SRA
Processed data provided as supplementary file

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