NCBI Logo
GEO Logo
   NCBI > GEO > Accession DisplayHelp Not logged in | LoginHelp
GEO help: Mouse over screen elements for information.
          Go
Series GSE75897 Query DataSets for GSE75897
Status Public on Feb 10, 2016
Title Improved ribosome-footprint and mRNA measurements provide insights into dynamics and regulation of yeast translation
Organism Saccharomyces cerevisiae
Experiment type Expression profiling by high throughput sequencing
Third-party reanalysis
Summary Ribosome-footprint profiling provides genome-wide snapshots of translation, but technical challenges can confound its analysis. Here, we use improved methods to obtain ribosome-footprint profiles and mRNA abundances that more faithfully reflect gene expression in Saccharomyces cerevisiae. Our results support proposals that both the beginning of coding regions and codons matching rare tRNAs are more slowly translated. They also indicate that emergent polypeptides with as few as three basic residues within a 10-residue window tend to slow translation. With the improved mRNA measurements, the variation attributable to translational control in exponentially growing yeast was less than previously reported, and most of this variation could be predicted with a simple model that considered mRNA abundance, upstream open reading frames, cap-proximal structure and nucleotide composition, and lengths of the coding and 5'-untranslated regions. Collectively, our results provide a framework for executing and interpreting ribosome-profiling studies and reveal key features of translational control in yeast.
 
Overall design Ribosome-footprint profiling and RNA-seq (total RNA, poly(A) selected, RiboMinus treated, or Ribo-Zero treated) from log-phase S. cerevisiae. The study includes a reanalysis of the two Samples from GSE53313. The reanalyzed data is linked to the Series record.
 
Contributor(s) Weinberg DE, Shah P, Eichhorn SW, Hussmann JA, Plotkin JB, Bartel DP
Citation(s) 26876183, 27692069
NIH grant(s)
Grant ID Grant title Affiliation Name
DP5 OD017895 Formation and regulation of the translating mRNP University of California San Francisco Weinberg
Submission date Dec 10, 2015
Last update date Jul 16, 2019
Contact name David Eric Weinberg
E-mail(s) [email protected]
Phone 415-514-9723
Organization name University of California, San Francisco
Lab Weinberg
Street address 600 16th Street, GH S572F
City San Francisco
State/province CA
ZIP/Postal code 94158
Country USA
 
Platforms (1)
GPL13821 Illumina HiSeq 2000 (Saccharomyces cerevisiae)
Samples (3)
GSM1969533 RNA-seq, unselected (total) RNA
GSM1969534 RNA-seq, poly(A) selected using Dynabeads oligo(dT)
GSM1969535 RNA-seq, rRNA depleted using RiboMinus
Relations
Reanalysis of GSM1289256
Reanalysis of GSM1289257
BioProject PRJNA305643
SRA SRP067237

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
GSE75897_RAW.tar 90.0 Kb (http)(custom) TAR (of TXT)
GSE75897_RPF_RPKMs.txt.gz 27.8 Kb (ftp)(http) TXT
GSE75897_RiboZero_RPKMs.txt.gz 28.1 Kb (ftp)(http) TXT
SRA Run SelectorHelp
Raw data are available in SRA
Processed data provided as supplementary file
Processed data are available on Series record

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