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Regulatory roles and mechanisms of alternative RNA splicing in adipogenesis and human metabolic health

Alternative splicing (AS) regulates gene expression patterns at the post-transcriptional level and generates a striking expansion of coding capacities of genomes and cellular protein diversity. RNA splicing could undergo modulation and close interaction with genetic and epigenetic machinery. Notably...

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Autores principales: Chao, Yunqi, Jiang, Yonghui, Zhong, Mianling, Wei, Kaiyan, Hu, Chenxi, Qin, Yifang, Zuo, Yiming, Yang, Lili, Shen, Zheng, Zou, Chaochun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8017860/
https://www.ncbi.nlm.nih.gov/pubmed/33795017
http://dx.doi.org/10.1186/s13578-021-00581-w
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author Chao, Yunqi
Jiang, Yonghui
Zhong, Mianling
Wei, Kaiyan
Hu, Chenxi
Qin, Yifang
Zuo, Yiming
Yang, Lili
Shen, Zheng
Zou, Chaochun
author_facet Chao, Yunqi
Jiang, Yonghui
Zhong, Mianling
Wei, Kaiyan
Hu, Chenxi
Qin, Yifang
Zuo, Yiming
Yang, Lili
Shen, Zheng
Zou, Chaochun
author_sort Chao, Yunqi
collection PubMed
description Alternative splicing (AS) regulates gene expression patterns at the post-transcriptional level and generates a striking expansion of coding capacities of genomes and cellular protein diversity. RNA splicing could undergo modulation and close interaction with genetic and epigenetic machinery. Notably, during the adipogenesis processes of white, brown and beige adipocytes, AS tightly interplays with the differentiation gene program networks. Here, we integrate the available findings on specific splicing events and distinct functions of different splicing regulators as examples to highlight the directive biological contribution of AS mechanism in adipogenesis and adipocyte biology. Furthermore, accumulating evidence has suggested that mutations and/or altered expression in splicing regulators and aberrant splicing alterations in the obesity-associated genes are often linked to humans’ diet-induced obesity and metabolic dysregulation phenotypes. Therefore, significant attempts have been finally made to overview novel detailed discussion on the prospects of splicing machinery with obesity and metabolic disorders to supply featured potential management mechanisms in clinical applicability for obesity treatment strategies.
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spelling pubmed-80178602021-04-05 Regulatory roles and mechanisms of alternative RNA splicing in adipogenesis and human metabolic health Chao, Yunqi Jiang, Yonghui Zhong, Mianling Wei, Kaiyan Hu, Chenxi Qin, Yifang Zuo, Yiming Yang, Lili Shen, Zheng Zou, Chaochun Cell Biosci Review Alternative splicing (AS) regulates gene expression patterns at the post-transcriptional level and generates a striking expansion of coding capacities of genomes and cellular protein diversity. RNA splicing could undergo modulation and close interaction with genetic and epigenetic machinery. Notably, during the adipogenesis processes of white, brown and beige adipocytes, AS tightly interplays with the differentiation gene program networks. Here, we integrate the available findings on specific splicing events and distinct functions of different splicing regulators as examples to highlight the directive biological contribution of AS mechanism in adipogenesis and adipocyte biology. Furthermore, accumulating evidence has suggested that mutations and/or altered expression in splicing regulators and aberrant splicing alterations in the obesity-associated genes are often linked to humans’ diet-induced obesity and metabolic dysregulation phenotypes. Therefore, significant attempts have been finally made to overview novel detailed discussion on the prospects of splicing machinery with obesity and metabolic disorders to supply featured potential management mechanisms in clinical applicability for obesity treatment strategies. BioMed Central 2021-04-01 /pmc/articles/PMC8017860/ /pubmed/33795017 http://dx.doi.org/10.1186/s13578-021-00581-w Text en © The Author(s) 2021 Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Review
Chao, Yunqi
Jiang, Yonghui
Zhong, Mianling
Wei, Kaiyan
Hu, Chenxi
Qin, Yifang
Zuo, Yiming
Yang, Lili
Shen, Zheng
Zou, Chaochun
Regulatory roles and mechanisms of alternative RNA splicing in adipogenesis and human metabolic health
title Regulatory roles and mechanisms of alternative RNA splicing in adipogenesis and human metabolic health
title_full Regulatory roles and mechanisms of alternative RNA splicing in adipogenesis and human metabolic health
title_fullStr Regulatory roles and mechanisms of alternative RNA splicing in adipogenesis and human metabolic health
title_full_unstemmed Regulatory roles and mechanisms of alternative RNA splicing in adipogenesis and human metabolic health
title_short Regulatory roles and mechanisms of alternative RNA splicing in adipogenesis and human metabolic health
title_sort regulatory roles and mechanisms of alternative rna splicing in adipogenesis and human metabolic health
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8017860/
https://www.ncbi.nlm.nih.gov/pubmed/33795017
http://dx.doi.org/10.1186/s13578-021-00581-w
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