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Series GSE116982 Query DataSets for GSE116982
Status Public on Jul 13, 2018
Title Cancer associated mutants of eIF1A impair Rps3/Rps10 binding and enhance scanning of cell cycle genes [Mars-seq]
Organism Mus musculus
Experiment type Expression profiling by high throughput sequencing
Summary The Ribo-seq analysis demonstrated that eIF1A is predominantly essential for translation of genes with long 5'UTR genes including cell proliferation and cell cycle progression genes. eIF1A depletion causes broad stimulation of initiation in 5’UTRs at near-cognate AUG codons that diminshes the translation initiation fidelity
 
Overall design Mars-seq analysis was performed either in contol or eIF1A knockdown MEFs
 
Contributor(s) Sehrawat U, Ashkanazi S, Koning F, Stelzer G, Leshkowitz D, Dikstein R
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Submission date Jul 12, 2018
Last update date Mar 25, 2019
Contact name Dena Leshkowitz
E-mail(s) dena.leshkowitz@weizmann.ac.il
Organization name Weizmann Institute of Science
Department Bioinformatics Unit, Life Sciences Core Facilities
Street address P.O.B. 26
City Rehovot
ZIP/Postal code 76100
Country Israel
 
Platforms (1)
GPL19057 Illumina NextSeq 500 (Mus musculus)
Samples (4)
GSM3266822 Control 1 [Mars-seq]
GSM3266823 Control 2 [Mars-seq]
GSM3266824 eIF1A KD1 [Mars-seq]
This SubSeries is part of SuperSeries:
GSE116983 Cancer associated mutants of eIF1A impair Rps3/Rps10 binding and enhance scanning of cell cycle genes
Relations
BioProject PRJNA480788
SRA SRP153151

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
GSE116982_Mars-seq_norm_counts.txt.gz 95.6 Kb (ftp)(http) TXT
SRA Run SelectorHelp
Raw data are available in SRA
Processed data are available on Series record

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