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SR proteins regulate V(6) exon splicing of CD44 pre-mRNA
CD44 pre-mRNA includes 20 exons, of which exons 1–5 (C(1)–C(5)) and exons 16–20 (C(6)–C(10)) are constant exons, whereas exons 6–15 (V(1)–V(10)) are variant exons. V(6)-exon-containing isoforms have been known to be implicated in tumor cell invasion and metastasis. In the present study, we performed...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Korean Society for Biochemistry and Molecular Biology
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5346321/ https://www.ncbi.nlm.nih.gov/pubmed/27530682 http://dx.doi.org/10.5483/BMBRep.2016.49.11.118 |
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author | Loh, Tiing Jen Moon, Heegyum Jang, Ha Na Liu, Yongchao Choi, Namjeong Shen, Shengfu Williams, Darren Reece Jung, Da-Woon Zheng, Xuexiu Shen, Haihong |
author_facet | Loh, Tiing Jen Moon, Heegyum Jang, Ha Na Liu, Yongchao Choi, Namjeong Shen, Shengfu Williams, Darren Reece Jung, Da-Woon Zheng, Xuexiu Shen, Haihong |
author_sort | Loh, Tiing Jen |
collection | PubMed |
description | CD44 pre-mRNA includes 20 exons, of which exons 1–5 (C(1)–C(5)) and exons 16–20 (C(6)–C(10)) are constant exons, whereas exons 6–15 (V(1)–V(10)) are variant exons. V(6)-exon-containing isoforms have been known to be implicated in tumor cell invasion and metastasis. In the present study, we performed a SR protein screen for CD44 V(6) splicing using overexpression and lentivirus-mediated shRNA treatment. Using a CD44 V(6) minigene, we demonstrate that increased SRSF3 and SRSF4 expression do not affect V(6) splicing, but increased expression of SRSF1, SRSF6 and SRSF9 significantly inhibit V(6) splicing. In addition, using a constitutive exon-specific primer set, we could not detect alterations of CD44 splicing after SR protein-targeting shRNA treatment. However, using a V(6) specific primer, we identified that reduced SRSF2 expression significantly reduced the V(6) isoform, but increased V(6–10) and V(6,8–10) isoforms. Our results indicate that SR proteins are important regulatory proteins for CD44 V(6) splicing. |
format | Online Article Text |
id | pubmed-5346321 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Korean Society for Biochemistry and Molecular Biology |
record_format | MEDLINE/PubMed |
spelling | pubmed-53463212017-04-06 SR proteins regulate V(6) exon splicing of CD44 pre-mRNA Loh, Tiing Jen Moon, Heegyum Jang, Ha Na Liu, Yongchao Choi, Namjeong Shen, Shengfu Williams, Darren Reece Jung, Da-Woon Zheng, Xuexiu Shen, Haihong BMB Rep Articles CD44 pre-mRNA includes 20 exons, of which exons 1–5 (C(1)–C(5)) and exons 16–20 (C(6)–C(10)) are constant exons, whereas exons 6–15 (V(1)–V(10)) are variant exons. V(6)-exon-containing isoforms have been known to be implicated in tumor cell invasion and metastasis. In the present study, we performed a SR protein screen for CD44 V(6) splicing using overexpression and lentivirus-mediated shRNA treatment. Using a CD44 V(6) minigene, we demonstrate that increased SRSF3 and SRSF4 expression do not affect V(6) splicing, but increased expression of SRSF1, SRSF6 and SRSF9 significantly inhibit V(6) splicing. In addition, using a constitutive exon-specific primer set, we could not detect alterations of CD44 splicing after SR protein-targeting shRNA treatment. However, using a V(6) specific primer, we identified that reduced SRSF2 expression significantly reduced the V(6) isoform, but increased V(6–10) and V(6,8–10) isoforms. Our results indicate that SR proteins are important regulatory proteins for CD44 V(6) splicing. Korean Society for Biochemistry and Molecular Biology 2016 2016-11-30 /pmc/articles/PMC5346321/ /pubmed/27530682 http://dx.doi.org/10.5483/BMBRep.2016.49.11.118 Text en Copyright © 2016 by the The Korean Society for Biochemistry and Molecular Biology http://creativecommons.org/licenses/by-nc/4.0 This is an open-access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Articles Loh, Tiing Jen Moon, Heegyum Jang, Ha Na Liu, Yongchao Choi, Namjeong Shen, Shengfu Williams, Darren Reece Jung, Da-Woon Zheng, Xuexiu Shen, Haihong SR proteins regulate V(6) exon splicing of CD44 pre-mRNA |
title | SR proteins regulate V(6) exon splicing of CD44 pre-mRNA |
title_full | SR proteins regulate V(6) exon splicing of CD44 pre-mRNA |
title_fullStr | SR proteins regulate V(6) exon splicing of CD44 pre-mRNA |
title_full_unstemmed | SR proteins regulate V(6) exon splicing of CD44 pre-mRNA |
title_short | SR proteins regulate V(6) exon splicing of CD44 pre-mRNA |
title_sort | sr proteins regulate v(6) exon splicing of cd44 pre-mrna |
topic | Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5346321/ https://www.ncbi.nlm.nih.gov/pubmed/27530682 http://dx.doi.org/10.5483/BMBRep.2016.49.11.118 |
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