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Low‐density lipoprotein receptor‐related protein 6 regulates alternative pre‐mRNA splicing

Low‐density lipoprotein receptor‐related protein 6 (LRP6) serves as a Wnt coreceptor. Although Wnt/LRP6 signalling is best known for the β‐catenin‐dependent regulation of target genes in tissue development and homeostasis, emerging evidence demonstrates the biological aspects of LRP6 beyond a Wnt co...

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Autores principales: Yuan, Tianyou, Wang, Shiyi, Hu, Chaoyue, Wu, Yufei, Liang, Dandan, Li, Li, Liu, Yi, Li, Jun, Chen, Yi‐Han
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6156287/
https://www.ncbi.nlm.nih.gov/pubmed/30070011
http://dx.doi.org/10.1111/jcmm.13682
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author Yuan, Tianyou
Wang, Shiyi
Hu, Chaoyue
Wu, Yufei
Liang, Dandan
Li, Li
Liu, Yi
Li, Jun
Chen, Yi‐Han
author_facet Yuan, Tianyou
Wang, Shiyi
Hu, Chaoyue
Wu, Yufei
Liang, Dandan
Li, Li
Liu, Yi
Li, Jun
Chen, Yi‐Han
author_sort Yuan, Tianyou
collection PubMed
description Low‐density lipoprotein receptor‐related protein 6 (LRP6) serves as a Wnt coreceptor. Although Wnt/LRP6 signalling is best known for the β‐catenin‐dependent regulation of target genes in tissue development and homeostasis, emerging evidence demonstrates the biological aspects of LRP6 beyond a Wnt coreceptor. Whether LRP6 modulates tissue development in a Wnt/β‐catenin signalling‐independent manner remains unknown. Using a model of striated muscle development, we observed that LRP6 was almost undetectable in proliferating myoblasts, whereas its expression gradually increased in the nucleus of myodifferentiating cells. During myodifferentiation, LRP6 modulated the muscle‐specific splicing of integrin‐β1D and consequent myotube maturation independently of the β‐catenin‐dependent Wnt signalling. Furthermore, we identified that the carboxy‐terminal serine‐rich region in LRP6 bond to the adenine‐rich sequence within alternative exon D (AED) of integrin‐β1 pre‐mRNA, and therefore, elicited AED inclusion when the spliceosome was recruited to the splice site. The interaction of LRP6 with the adenine‐rich sequence was sufficient to overcome AED exclusion by a splicing repressor, polypyrimidine tract binding protein‐1. Besides the integrin‐β1, deep RNA sequencing in different types of cells revealed that the LRP6‐mediated splicing regulation was widespread. Thus, our findings implicate LRP6 as a potential regulator for alternative pre‐mRNA splicing.
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spelling pubmed-61562872018-10-01 Low‐density lipoprotein receptor‐related protein 6 regulates alternative pre‐mRNA splicing Yuan, Tianyou Wang, Shiyi Hu, Chaoyue Wu, Yufei Liang, Dandan Li, Li Liu, Yi Li, Jun Chen, Yi‐Han J Cell Mol Med Original Articles Low‐density lipoprotein receptor‐related protein 6 (LRP6) serves as a Wnt coreceptor. Although Wnt/LRP6 signalling is best known for the β‐catenin‐dependent regulation of target genes in tissue development and homeostasis, emerging evidence demonstrates the biological aspects of LRP6 beyond a Wnt coreceptor. Whether LRP6 modulates tissue development in a Wnt/β‐catenin signalling‐independent manner remains unknown. Using a model of striated muscle development, we observed that LRP6 was almost undetectable in proliferating myoblasts, whereas its expression gradually increased in the nucleus of myodifferentiating cells. During myodifferentiation, LRP6 modulated the muscle‐specific splicing of integrin‐β1D and consequent myotube maturation independently of the β‐catenin‐dependent Wnt signalling. Furthermore, we identified that the carboxy‐terminal serine‐rich region in LRP6 bond to the adenine‐rich sequence within alternative exon D (AED) of integrin‐β1 pre‐mRNA, and therefore, elicited AED inclusion when the spliceosome was recruited to the splice site. The interaction of LRP6 with the adenine‐rich sequence was sufficient to overcome AED exclusion by a splicing repressor, polypyrimidine tract binding protein‐1. Besides the integrin‐β1, deep RNA sequencing in different types of cells revealed that the LRP6‐mediated splicing regulation was widespread. Thus, our findings implicate LRP6 as a potential regulator for alternative pre‐mRNA splicing. John Wiley and Sons Inc. 2018-08-01 2018-10 /pmc/articles/PMC6156287/ /pubmed/30070011 http://dx.doi.org/10.1111/jcmm.13682 Text en © 2018 The Authors. Journal of Cellular and Molecular Medicine published by John Wiley & Sons Ltd and Foundation for Cellular and Molecular Medicine. This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Articles
Yuan, Tianyou
Wang, Shiyi
Hu, Chaoyue
Wu, Yufei
Liang, Dandan
Li, Li
Liu, Yi
Li, Jun
Chen, Yi‐Han
Low‐density lipoprotein receptor‐related protein 6 regulates alternative pre‐mRNA splicing
title Low‐density lipoprotein receptor‐related protein 6 regulates alternative pre‐mRNA splicing
title_full Low‐density lipoprotein receptor‐related protein 6 regulates alternative pre‐mRNA splicing
title_fullStr Low‐density lipoprotein receptor‐related protein 6 regulates alternative pre‐mRNA splicing
title_full_unstemmed Low‐density lipoprotein receptor‐related protein 6 regulates alternative pre‐mRNA splicing
title_short Low‐density lipoprotein receptor‐related protein 6 regulates alternative pre‐mRNA splicing
title_sort low‐density lipoprotein receptor‐related protein 6 regulates alternative pre‐mrna splicing
topic Original Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6156287/
https://www.ncbi.nlm.nih.gov/pubmed/30070011
http://dx.doi.org/10.1111/jcmm.13682
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