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The neurofibromatosis type I pre-mRNA is a novel target of CELF protein-mediated splicing regulation
The CUG-BP and ETR-3 like factors (CELF) are a family of six highly conserved RNA-binding proteins that preferentially bind to UG-rich sequences. One of the key functions of these proteins is to mediate alternative splicing in a number of tissues, including brain, heart and muscle. To fully understa...
Autores principales: | , , , , |
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Formato: | Texto |
Lenguaje: | English |
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Oxford University Press
2010
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2800208/ https://www.ncbi.nlm.nih.gov/pubmed/19854948 http://dx.doi.org/10.1093/nar/gkp766 |
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author | Barron, Victoria A. Zhu, Hui Hinman, Melissa N. Ladd, Andrea N. Lou, Hua |
author_facet | Barron, Victoria A. Zhu, Hui Hinman, Melissa N. Ladd, Andrea N. Lou, Hua |
author_sort | Barron, Victoria A. |
collection | PubMed |
description | The CUG-BP and ETR-3 like factors (CELF) are a family of six highly conserved RNA-binding proteins that preferentially bind to UG-rich sequences. One of the key functions of these proteins is to mediate alternative splicing in a number of tissues, including brain, heart and muscle. To fully understand the function of CELF proteins, it is important to identify downstream targets of CELF proteins. In this communication, we report that neurofibromatosis type I (NF1) exon 23a is a novel target of CELF protein-mediated splicing regulation in neuron-like cells. NF1 regulates Ras signaling, and the isoform that excludes exon 23a shows 10 times greater ability to down-regulate Ras signaling than the isoform that includes exon 23a. Five of the six CELF proteins strongly suppress the inclusion of NF1 exon 23a. Over-expression or siRNA knockdown of these proteins in cell transfection experiments altered the levels of NF1 exon 23a inclusion. In vitro binding and splicing analyses demonstrate that CELF proteins block splicing through interfering with binding of U2AF(65). These studies, combined with our previous investigations demonstrating a role for Hu proteins and TIA-1/TIAR in controlling NF1 exon 23a inclusion, highlight the complex nature of regulation of this important alternative splicing event. |
format | Text |
id | pubmed-2800208 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2010 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-28002082009-12-31 The neurofibromatosis type I pre-mRNA is a novel target of CELF protein-mediated splicing regulation Barron, Victoria A. Zhu, Hui Hinman, Melissa N. Ladd, Andrea N. Lou, Hua Nucleic Acids Res RNA The CUG-BP and ETR-3 like factors (CELF) are a family of six highly conserved RNA-binding proteins that preferentially bind to UG-rich sequences. One of the key functions of these proteins is to mediate alternative splicing in a number of tissues, including brain, heart and muscle. To fully understand the function of CELF proteins, it is important to identify downstream targets of CELF proteins. In this communication, we report that neurofibromatosis type I (NF1) exon 23a is a novel target of CELF protein-mediated splicing regulation in neuron-like cells. NF1 regulates Ras signaling, and the isoform that excludes exon 23a shows 10 times greater ability to down-regulate Ras signaling than the isoform that includes exon 23a. Five of the six CELF proteins strongly suppress the inclusion of NF1 exon 23a. Over-expression or siRNA knockdown of these proteins in cell transfection experiments altered the levels of NF1 exon 23a inclusion. In vitro binding and splicing analyses demonstrate that CELF proteins block splicing through interfering with binding of U2AF(65). These studies, combined with our previous investigations demonstrating a role for Hu proteins and TIA-1/TIAR in controlling NF1 exon 23a inclusion, highlight the complex nature of regulation of this important alternative splicing event. Oxford University Press 2010-01 2009-10-23 /pmc/articles/PMC2800208/ /pubmed/19854948 http://dx.doi.org/10.1093/nar/gkp766 Text en © The Author(s) 2009. Published by Oxford University Press. http://creativecommons.org/licenses/by-nc/2.5/uk/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/2.5/uk/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | RNA Barron, Victoria A. Zhu, Hui Hinman, Melissa N. Ladd, Andrea N. Lou, Hua The neurofibromatosis type I pre-mRNA is a novel target of CELF protein-mediated splicing regulation |
title | The neurofibromatosis type I pre-mRNA is a novel target of CELF protein-mediated splicing regulation |
title_full | The neurofibromatosis type I pre-mRNA is a novel target of CELF protein-mediated splicing regulation |
title_fullStr | The neurofibromatosis type I pre-mRNA is a novel target of CELF protein-mediated splicing regulation |
title_full_unstemmed | The neurofibromatosis type I pre-mRNA is a novel target of CELF protein-mediated splicing regulation |
title_short | The neurofibromatosis type I pre-mRNA is a novel target of CELF protein-mediated splicing regulation |
title_sort | neurofibromatosis type i pre-mrna is a novel target of celf protein-mediated splicing regulation |
topic | RNA |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2800208/ https://www.ncbi.nlm.nih.gov/pubmed/19854948 http://dx.doi.org/10.1093/nar/gkp766 |
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