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

机译:伴随症状和人类代谢健康中替代RNA剪接的调节作用及机制

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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.
机译:替代剪接(AS)调节在转录后水平的基因表达模式,产生基因组和细胞蛋白质多样性的编码能力的突出扩张。 RNA剪接可以接受与遗传和表观遗传机械的调制和密切相互作用。值得注意的是,在白色,棕色和米色脂肪细胞的脂肪发生过程中,与分化基因计划网络紧密相互作用。在这里,我们将可用的结果与不同的剪接调节器的特定拼接事件和不同功能集成为突出脂肪发生和脂肪细胞生物学的机制的指导生物学贡献。此外,积累的证据表明,剪​​接调节剂和肥胖相关基因中的异常剪接改变的突变和/或改变的表达通常与人类的饮食诱导的肥胖和代谢失调表型相关联。因此,终于对夏季性和代谢障碍拼接机械的前景进行了重大探讨,以供给肥胖治疗策略的临床适用性的特色潜在管理机制。

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