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Alternative splicing of Bcl-2-related genes: functional consequences and potential therapeutic applications
Authors:Email author" target="_blank">C?AkgulEmail author  D?A?Moulding  S?W?Edwards
Institution:(1) Faculty of Arts and Sciences, Department of Chemistry, Biochemistry Research Group, Canakkale Onsekiz Mart University, Terzioglu Campus, 17100 Canakkale, Turkey;(2) Molecular Haematology and Cancer Biology Unit, Camelia Botnar Laboratories, Institute of Child Health, University College London, 30 Guilford Street, WC1N 1EH London, United Kingdom;(3) School of Biological Sciences, Biosciences Building (BSB G09), University of Liverpool, Crown Street, L69 7ZB Liverpool, United Kingdom
Abstract:Apoptosis is a morphologically distinct form of cell death. It is executed and regulated by several groups of proteins. Bcl-2 family proteins are the main regulators of the apoptotic process acting either to inhibit or promote it. More than 20 members of the family have been identified so far and most have two or more isoforms. Alternative splicing is one of the major mechanisms providing proteomic complexity and functional diversification of the Bcl-2 family proteins. Pro- and anti-apoptotic Bcl-2 family members should function in harmony for the regulation of the apoptosis machinery, and their relative levels are critical for cell fate. Any mechanism breaking down this harmony by changing the relative levels of these antagonistic proteins could contribute to many diseases, including cancer and neurodegenerative disorders. Recent studies have shown that manipulation of the alternative splicing mechanisms could provide an opportunity to restore the proper balance of these regulator proteins. This review summarises current knowledge on the alternative splicing products of Bcl-2-related genes and modulation of splicing mechanisms as a potential therapeutic approach.Received 5 January 2004; received after revision 31 March 2004; accepted 6 April 2004
Keywords:Apoptosis  Bcl-2 family  alternative splicing  antisense
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