*** TEST ***
Helmholtz Gemeinschaft

Search
Browse
Statistics
Feeds

Post-transcriptional regulation by 3' UTRs can be masked by regulatory elements in 5' UTRs

[thumbnail of Article]
Preview
PDF (Article) - Requires a PDF viewer such as GSview, Xpdf or Adobe Acrobat Reader
3MB
[thumbnail of Supplemental Information]
Preview
PDF (Supplemental Information) - Requires a PDF viewer such as GSview, Xpdf or Adobe Acrobat Reader
1MB

Item Type:Article
Title:Post-transcriptional regulation by 3' UTRs can be masked by regulatory elements in 5' UTRs
Creators Name:Theil, K., Herzog, M. and Rajewsky, N.
Abstract:In mRNA sequences, 3' UTRs are thought to contain most elements that specifically regulate localization, turnover, and translation. Although high-throughput experiments indicate that many RNA-binding proteins (RBPs) also bind 5' UTRs, much less is known about specific post-transcriptional control exerted by 5' UTRs. GLD-1 is a conserved RBP and a translational repressor with essential roles in Caenorhabditis elegans germ cell development. Previously, we showed that GLD-1 binds highly conserved sites in both 3' and 5' UTRs. Here, by targeted single-copy insertion of transgenes, we systematically tested in vivo functionality of 5' and 3' UTR binding sites individually and in combination. Our data show that sites in 5' UTRs mediate specific and strong translational repression, independent of exact position. Intriguingly, we found that the functionality of 3' UTR sites can be masked by 5' UTR sites and vice versa. We conclude that it is important to study both UTRs simultaneously.
Keywords:Gene Regulation, Ost-Transcriptional Regulation, 5' UTR, Translational Repression, GLD-1, Animals, Caenorhabditis elegans
Source:Cell Reports
ISSN:2211-1247
Publisher:Cell Press / Elsevier
Volume:22
Number:12
Page Range:3217-3226
Date:20 March 2018
Official Publication:https://doi.org/10.1016/j.celrep.2018.02.094
PubMed:View item in PubMed

Repository Staff Only: item control page

Downloads

Downloads per month over past year

Open Access
MDC Library