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Status |
Public on May 15, 2014 |
Title |
CFIm25 links alternative polyadenylation to glioblastoma tumour suppression |
Organism |
Homo sapiens |
Experiment type |
Expression profiling by high throughput sequencing
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Summary |
Purpose: To identify all of the APA targets of CFIm25 on a global scale and develop an algorithm that can idenitify APA events from standard RNA-seq data
Methods: RNA from HeLa cells treated with control siRNA and CFIm25 siRNA were subject to RNA-Seq. Using a custom-designed algorithm to mine RNA-seq data for novel APA events regulated by CFIm25.
Results: We identified over 1,400 genes with shortened 3’UTRs after CFIm25 knockdown. Importantly, we show that as a consequence of APA, many of these mRNAs have greatly enhanced protein expression due to the loss of destabilizing features within the 3’UTR.
Conclusions: Our study underscored the critical function of the CFIm complex members in governing APA and establish a previously unknown link between APA and metabolic pathways important for tumor progression.
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Overall design |
Hela cell line mRNA profiles of control treated and CFIm25 Knockdown were generated by RNA-Seq using Illumina GAIIx.
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Contributor(s) |
Masamha CP, Xia Z, Albrecht TR, Li W, Shyu A, Wagner EJ |
Citation(s) |
24814343 |
Submission date |
Nov 20, 2012 |
Last update date |
May 15, 2019 |
Contact name |
Zheng Xia |
E-mail(s) |
xiaz@ohsu.edu
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Organization name |
Oregon Health & Science University
|
Department |
Department of Biomedical Engineering
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Lab |
Xia Lab
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Street address |
3181 SW Sam Jackson Park Rd
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City |
Portland |
State/province |
Oregon |
ZIP/Postal code |
97239 |
Country |
USA |
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Platforms (1) |
GPL11154 |
Illumina HiSeq 2000 (Homo sapiens) |
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Samples (4)
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Relations |
BioProject |
PRJNA182153 |
SRA |
SRP017305 |