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RNA Binding Protein/RNA Element Interactions and the Control of Translation

期刊

CURRENT PROTEIN & PEPTIDE SCIENCE
卷 13, 期 4, 页码 294-304

出版社

BENTHAM SCIENCE PUBL LTD
DOI: 10.2174/138920312801619475

关键词

Translation; 5 ' untranslated region; IRES; uORF; TOP; polyA tail

资金

  1. Wellcome Trust
  2. BBSRC
  3. CRUK
  4. MRC
  5. Biotechnology and Biological Sciences Research Council [BB/H024980/1, BB/F02326X/2, BB/F000065/2, BB/F000065/1, BB/F014279/2, BB/F018738/2] Funding Source: researchfish
  6. Medical Research Council [MC_UP_A600_1023] Funding Source: researchfish
  7. BBSRC [BB/F02326X/2, BB/F018738/2, BB/H024980/1, BB/F014279/2, BB/F000065/2, BB/F000065/1] Funding Source: UKRI
  8. MRC [MC_UP_A600_1023] Funding Source: UKRI

向作者/读者索取更多资源

A growing body of work demonstrates the importance of post-transcriptional control, in particular translation initiation, in the overall regulation of gene expression. Here we focus on the contribution of regulatory elements within the 5' and 3' untranslated regions of mRNA to gene expression in eukaryotic cells including terminal oligopyrimidine tracts, internal ribosome entry segments, upstream open reading frames and cytoplasmic polyadenylation elements. These mRNA regulatory elements may adopt complex secondary structures and/or contain sequence motifs that allow their interaction with a variety of regulatory proteins, RNAs and RNA binding proteins, particularly hnRNPs. The resulting interactions are context-sensitive, and provide cells with a sensitive and fast response to cellular signals such as hormone exposure or cytotoxic stress. Importantly, an increasing number of diseases have been identified, particularly cancers and those associated with neurodegeneration, which originate either from mutation of these regulatory motifs, or from deregulation of their cognate binding partners.

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