NCBI Logo
GEO Logo
   NCBI > GEO > Accession DisplayHelp Not logged in | LoginHelp
GEO help: Mouse over screen elements for information.
          Go
Series GSE73110 Query DataSets for GSE73110
Status Public on Nov 12, 2015
Title Genome-wide profiling of total RNA from mutants that affect chromatin dynamics: RTT109, SWR1, and the nuclear RNA exosome RRP6
Organism Saccharomyces cerevisiae
Experiment type Expression profiling by genome tiling array
Third-party reanalysis
Summary The histone variant H2A.Z is a hallmark of nucleosomes flanking the promoters of protein coding genes, and is often found in nucleosomes that also carry lysine 56- acetylated histone H3 (H3-K56Ac), a mark which promotes rapid replication- independent turnover of nucleosomes. Although H2A.Z and H3-K56Ac have been generally implicated in transcriptional activation, their exact contributions have remained elusive. Here we find that H3-K56Ac promotes RNA polymerase II occupancy at a large number of protein coding and noncoding loci, yet neither H3- K56Ac nor H2A.Z has a significant impact on steady state mRNA levels in yeast. Instead, broad effects of H3-K56Ac or H2A.Z on levels of both coding and noncoding RNAs (ncRNAs) are only revealed in the absence of the nuclear RNA exosome. H2A.Z is also necessary for expression of divergent, promoter-proximal ncRNAs in mouse embryonic stem cells, suggesting a conserved role for H2A.Z across eukaryotes. Finally, we show that H2A.Z functions with H3-K56Ac in chromosome folding, facilitating formation of chromosome interaction domains (CIDs). Our study suggests that H2A.Z and H3-K56Ac work in concert with the RNA exosome to control mRNA and ncRNA expression, perhaps in part by regulating higher order chromatin structures.
 
Overall design Total RNA isolated from 27 samples with replicates of each strain ranging from 2 to 5. 12 samples from the Proudfoot lab [deposited in ArrayExpress, accession number E-TABM-936] were downloaded as .CEL files and analyzed alongside samples generated in this study. The identical processing for used for both sets of samples. For details refer to supplementary methods in the paper.
Web link http://www.sciencedirect.com/science/article/pii/S2211124715012000
 
Contributor(s) Steinmetz LM, Peterson CL
Citation(s) 26586442
Submission date Sep 16, 2015
Last update date Dec 20, 2018
Contact name Craig L Peterson
E-mail(s) craig.peterson@umassmed.edu
Phone 508-856-5858
Organization name University of Massachusetts Medical School
Department Program in Molecular Medicine
Street address 373 Plantation Street
City Worcester
State/province MASSACHUSETTS
ZIP/Postal code 01605
Country USA
 
Platforms (1)
GPL19774 [Scerevisiae_tlg] Affymetrix Saccharomyces cerevisiae tiling array
Samples (27)
GSM1886863 35_wt
GSM1886864 36_wt
GSM1886865 37_wt
This SubSeries is part of SuperSeries:
GSE73145 Chromatin dynamics and the RNA exosome function in concert to regulate transcriptional homeostasis
Relations
BioProject PRJNA296115

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
GSE73110_RAW.tar 685.7 Mb (http)(custom) TAR (of CEL)
GSE73110_normProbeIntensity.txt.gz 795.8 Mb (ftp)(http) TXT
GSE73110_sup3_MR.txt.gz 1.9 Mb (ftp)(http) TXT
Processed data are available on Series record

| NLM | NIH | GEO Help | Disclaimer | Accessibility |
NCBI Home NCBI Search NCBI SiteMap