The implications of structured 5' untranslated regions on translation and disease
The implications of structured 5' untranslated regions on translation and disease
Translational control is a key step in eukaryotic gene expression. The majority of translational control occurs at the level of initiation, thus implicating the 5? untranslated region as a major site of translational regulation. Many growth-related mRNAs have atypical 5? UTRs, which are often long and GC-rich. Such features promote formation of stable secondary structure, and many mRNAs encoding proteins involved in cell growth, proliferation and apoptosis have structured 5? UTRs, which in many cases harbour internal ribosome entry sites (IRESs) and upstream open-reading frames (uORFs). In this review we discuss how secondary structural elements in the 5? UTR can regulate translation and how mutations that perturb these secondary structural elements can have implications for disease and tumourigenesis.
internal ribosome entry, 5? untranslated region, IRES, translation
39-47
Pickering, Becky M.
94be5c5d-f45f-4baf-a5e9-6b7bfc16be25
Willis, Anne E.
70657c98-607d-4626-8bdf-1468e8653f98
2005
Pickering, Becky M.
94be5c5d-f45f-4baf-a5e9-6b7bfc16be25
Willis, Anne E.
70657c98-607d-4626-8bdf-1468e8653f98
Pickering, Becky M. and Willis, Anne E.
(2005)
The implications of structured 5' untranslated regions on translation and disease.
Seminars in Cell and Developmental Biology, 16 (1), .
(doi:10.1016/j.semcdb.2004.11.006).
Abstract
Translational control is a key step in eukaryotic gene expression. The majority of translational control occurs at the level of initiation, thus implicating the 5? untranslated region as a major site of translational regulation. Many growth-related mRNAs have atypical 5? UTRs, which are often long and GC-rich. Such features promote formation of stable secondary structure, and many mRNAs encoding proteins involved in cell growth, proliferation and apoptosis have structured 5? UTRs, which in many cases harbour internal ribosome entry sites (IRESs) and upstream open-reading frames (uORFs). In this review we discuss how secondary structural elements in the 5? UTR can regulate translation and how mutations that perturb these secondary structural elements can have implications for disease and tumourigenesis.
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Published date: 2005
Keywords:
internal ribosome entry, 5? untranslated region, IRES, translation
Identifiers
Local EPrints ID: 26528
URI: http://eprints.soton.ac.uk/id/eprint/26528
ISSN: 1084-9521
PURE UUID: e2dbb996-7e29-4c14-ad8b-b98e498be56b
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Date deposited: 10 Apr 2006
Last modified: 15 Mar 2024 07:11
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Author:
Becky M. Pickering
Author:
Anne E. Willis
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