Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
10959579 | Seminars in Cell & Developmental Biology | 2005 | 9 Pages |
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 5â² untranslated region as a major site of translational regulation. Many growth-related mRNAs have atypical 5â² 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 5â² 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 5â² UTR can regulate translation and how mutations that perturb these secondary structural elements can have implications for disease and tumourigenesis.
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Authors
Becky M Pickering, Anne E Willis,