Alternative RNA splicing: contribution to pain and potential therapeutic strategy

Since the sequencing of metazoan genomes began, it has become clear that the number of expressed proteins far exceeds the number of genes. It is now estimated that greater up to 98% of human genes give rise to multiple proteins through alternative pre-mRNA splicing. This review highlights the known...

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Main Authors: Donaldson, Lucy F., Beazley-Long, Nicholas
Format: Article
Published: Elsevier 2016
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Online Access:https://eprints.nottingham.ac.uk/34304/
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author Donaldson, Lucy F.
Beazley-Long, Nicholas
author_facet Donaldson, Lucy F.
Beazley-Long, Nicholas
author_sort Donaldson, Lucy F.
building Nottingham Research Data Repository
collection Online Access
description Since the sequencing of metazoan genomes began, it has become clear that the number of expressed proteins far exceeds the number of genes. It is now estimated that greater up to 98% of human genes give rise to multiple proteins through alternative pre-mRNA splicing. This review highlights the known alternative splice variants of many channels, receptors and growth factors important in nociception and pain. Recently, pharmacological control of alternative splicing has been proposed as potential therapy in cancer, wet age-related macular degeneration, retroviral infections and pain. In this review we consider the effects that known splice variants of molecules key to nociception/pain have on nociceptive processing and/or analgesic action, and the potential for control of alternative pre-mRNA splicing as a novel analgesic strategy.
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spelling nottingham-343042020-05-04T17:55:57Z https://eprints.nottingham.ac.uk/34304/ Alternative RNA splicing: contribution to pain and potential therapeutic strategy Donaldson, Lucy F. Beazley-Long, Nicholas Since the sequencing of metazoan genomes began, it has become clear that the number of expressed proteins far exceeds the number of genes. It is now estimated that greater up to 98% of human genes give rise to multiple proteins through alternative pre-mRNA splicing. This review highlights the known alternative splice variants of many channels, receptors and growth factors important in nociception and pain. Recently, pharmacological control of alternative splicing has been proposed as potential therapy in cancer, wet age-related macular degeneration, retroviral infections and pain. In this review we consider the effects that known splice variants of molecules key to nociception/pain have on nociceptive processing and/or analgesic action, and the potential for control of alternative pre-mRNA splicing as a novel analgesic strategy. Elsevier 2016-06-18 Article PeerReviewed Donaldson, Lucy F. and Beazley-Long, Nicholas (2016) Alternative RNA splicing: contribution to pain and potential therapeutic strategy. Drug Discovery Today . ISSN 1359-6446 Alternative pre-mRNA splicing; ion channel; G-protein coupled receptor; growth factor; nociception; pain https://doi.org/10.1016/j.drudis.2016.06.017 doi:10.1016/j.drudis.2016.06.017 doi:10.1016/j.drudis.2016.06.017
spellingShingle Alternative pre-mRNA splicing; ion channel; G-protein coupled receptor; growth factor; nociception; pain
Donaldson, Lucy F.
Beazley-Long, Nicholas
Alternative RNA splicing: contribution to pain and potential therapeutic strategy
title Alternative RNA splicing: contribution to pain and potential therapeutic strategy
title_full Alternative RNA splicing: contribution to pain and potential therapeutic strategy
title_fullStr Alternative RNA splicing: contribution to pain and potential therapeutic strategy
title_full_unstemmed Alternative RNA splicing: contribution to pain and potential therapeutic strategy
title_short Alternative RNA splicing: contribution to pain and potential therapeutic strategy
title_sort alternative rna splicing: contribution to pain and potential therapeutic strategy
topic Alternative pre-mRNA splicing; ion channel; G-protein coupled receptor; growth factor; nociception; pain
url https://eprints.nottingham.ac.uk/34304/
https://eprints.nottingham.ac.uk/34304/
https://eprints.nottingham.ac.uk/34304/