The role of the 3' untranslated region in post-transcriptional regulation of protein expression in mammalian cells
Language English Country United States Media print-electronic
Document type Journal Article, Research Support, Non-U.S. Gov't, Review
PubMed
22614827
DOI
10.4161/rna.20231
PII: 20231
Knihovny.cz E-resources
- MeSH
- 3' Untranslated Regions * MeSH
- Humans MeSH
- RNA, Messenger genetics metabolism MeSH
- MicroRNAs genetics physiology MeSH
- Polyadenylation MeSH
- RNA Processing, Post-Transcriptional MeSH
- Promoter Regions, Genetic MeSH
- RNA-Binding Proteins physiology MeSH
- RNA Interference * MeSH
- Base Sequence MeSH
- Animals MeSH
- Check Tag
- Humans MeSH
- Animals MeSH
- Publication type
- Journal Article MeSH
- Research Support, Non-U.S. Gov't MeSH
- Review MeSH
- Names of Substances
- 3' Untranslated Regions * MeSH
- RNA, Messenger MeSH
- MicroRNAs MeSH
- RNA-Binding Proteins MeSH
The untranslated regions (UTRs) at the 3'end of mRNA transcripts contain important sequences that influence the fate of mRNA and thus proteosynthesis. In this review, we summarize the information known to date about 3'end processing, sequence characteristics including related binding proteins and the role of 3'UTRs in several selected signaling pathways to delineate their importance in the regulatory processes in mammalian cells. In addition to reviewing recent advances in the more well known aspects, such as cleavage and polyadenylation processes that influence mRNA stability and location, we concentrate on some newly emerging concepts of the role of the 3'UTR, including alternative polyadenylation sites in relation to proliferation and differentiation and the recognition of the multi-functional properties of non-coding RNAs, including miRNAs that commonly target the 3'UTR. The emerging picture is of a highly complex set of regulatory systems that include autoregulation, cooperativity and competition to fine tune proteosynthesis in context-dependent manners.
References provided by Crossref.org
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