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Transcriptome analysis of alternative splicing events regulated by SRSF10 reveals position-dependent splicing modulation

Splicing factor SRSF10 is known to function as a sequence-specific splicing activator. Here, we used RNA-seq coupled with bioinformatics analysis to identify the extensive splicing network regulated by SRSF10 in chicken cells. We found that SRSF10 promoted both exon inclusion and exclusion. Motif an...

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Autores principales: Zhou, Xuexia, Wu, Wenwu, Li, Huang, Cheng, Yuanming, Wei, Ning, Zong, Jie, Feng, Xiaoyan, Xie, Zhiqin, Chen, Dai, Manley, James L., Wang, Hui, Feng, Ying
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2014
Materias:
RNA
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3973337/
https://www.ncbi.nlm.nih.gov/pubmed/24442672
http://dx.doi.org/10.1093/nar/gkt1387
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author Zhou, Xuexia
Wu, Wenwu
Li, Huang
Cheng, Yuanming
Wei, Ning
Zong, Jie
Feng, Xiaoyan
Xie, Zhiqin
Chen, Dai
Manley, James L.
Wang, Hui
Feng, Ying
author_facet Zhou, Xuexia
Wu, Wenwu
Li, Huang
Cheng, Yuanming
Wei, Ning
Zong, Jie
Feng, Xiaoyan
Xie, Zhiqin
Chen, Dai
Manley, James L.
Wang, Hui
Feng, Ying
author_sort Zhou, Xuexia
collection PubMed
description Splicing factor SRSF10 is known to function as a sequence-specific splicing activator. Here, we used RNA-seq coupled with bioinformatics analysis to identify the extensive splicing network regulated by SRSF10 in chicken cells. We found that SRSF10 promoted both exon inclusion and exclusion. Motif analysis revealed that SRSF10 binding to cassette exons was associated with exon inclusion, whereas the binding of SRSF10 within downstream constitutive exons was associated with exon exclusion. This positional effect was further demonstrated by the mutagenesis of potential SRSF10 binding motifs in two minigene constructs. Functionally, many of SRSF10-verified alternative exons are linked to pathways of stress and apoptosis. Consistent with this observation, cells depleted of SRSF10 expression were far more susceptible to endoplasmic reticulum stress-induced apoptosis than control cells. Importantly, reconstituted SRSF10 in knockout cells recovered wild-type splicing patterns and considerably rescued the stress-related defects. Together, our results provide mechanistic insight into SRSF10-regulated alternative splicing events in vivo and demonstrate that SRSF10 plays a crucial role in cell survival under stress conditions.
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spelling pubmed-39733372014-04-04 Transcriptome analysis of alternative splicing events regulated by SRSF10 reveals position-dependent splicing modulation Zhou, Xuexia Wu, Wenwu Li, Huang Cheng, Yuanming Wei, Ning Zong, Jie Feng, Xiaoyan Xie, Zhiqin Chen, Dai Manley, James L. Wang, Hui Feng, Ying Nucleic Acids Res RNA Splicing factor SRSF10 is known to function as a sequence-specific splicing activator. Here, we used RNA-seq coupled with bioinformatics analysis to identify the extensive splicing network regulated by SRSF10 in chicken cells. We found that SRSF10 promoted both exon inclusion and exclusion. Motif analysis revealed that SRSF10 binding to cassette exons was associated with exon inclusion, whereas the binding of SRSF10 within downstream constitutive exons was associated with exon exclusion. This positional effect was further demonstrated by the mutagenesis of potential SRSF10 binding motifs in two minigene constructs. Functionally, many of SRSF10-verified alternative exons are linked to pathways of stress and apoptosis. Consistent with this observation, cells depleted of SRSF10 expression were far more susceptible to endoplasmic reticulum stress-induced apoptosis than control cells. Importantly, reconstituted SRSF10 in knockout cells recovered wild-type splicing patterns and considerably rescued the stress-related defects. Together, our results provide mechanistic insight into SRSF10-regulated alternative splicing events in vivo and demonstrate that SRSF10 plays a crucial role in cell survival under stress conditions. Oxford University Press 2014-04 2014-01-17 /pmc/articles/PMC3973337/ /pubmed/24442672 http://dx.doi.org/10.1093/nar/gkt1387 Text en © The Author(s) 2014. Published by Oxford University Press. http://creativecommons.org/licenses/by-nc/3.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com
spellingShingle RNA
Zhou, Xuexia
Wu, Wenwu
Li, Huang
Cheng, Yuanming
Wei, Ning
Zong, Jie
Feng, Xiaoyan
Xie, Zhiqin
Chen, Dai
Manley, James L.
Wang, Hui
Feng, Ying
Transcriptome analysis of alternative splicing events regulated by SRSF10 reveals position-dependent splicing modulation
title Transcriptome analysis of alternative splicing events regulated by SRSF10 reveals position-dependent splicing modulation
title_full Transcriptome analysis of alternative splicing events regulated by SRSF10 reveals position-dependent splicing modulation
title_fullStr Transcriptome analysis of alternative splicing events regulated by SRSF10 reveals position-dependent splicing modulation
title_full_unstemmed Transcriptome analysis of alternative splicing events regulated by SRSF10 reveals position-dependent splicing modulation
title_short Transcriptome analysis of alternative splicing events regulated by SRSF10 reveals position-dependent splicing modulation
title_sort transcriptome analysis of alternative splicing events regulated by srsf10 reveals position-dependent splicing modulation
topic RNA
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3973337/
https://www.ncbi.nlm.nih.gov/pubmed/24442672
http://dx.doi.org/10.1093/nar/gkt1387
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