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Emerging roles of histone modifications and HDACs in RNA splicing

机译:在RNA剪接中的组蛋白修饰和HDAC的新兴作用

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摘要

Histone modifications and RNA splicing, two seemingly unrelated gene regulatory processes, greatly increase proteome diversity and profoundly influence normal as well as pathological eukaryotic cellular functions. Like many histone modifying enzymes, histone deacetylases (HDACs) play critical roles in governing cellular behaviors and are indispensable in numerous biological processes. While the association between RNA splicing and histone modifications is beginning to be recognized, a lack of knowledge exists regarding the role of HDACs in splicing. Recent studies however, reveal that HDACs interact with spliceosomal and ribonucleoprotein complexes, actively control the acetylation states of splicing-associated histone marks and splicing factors, and thereby unexpectedly could modulate splicing. Here, we review the role of histone/protein modifications and HDACs in RNA splicing and discuss the convergence of two parallel fields, which supports the argument that HDACs, and perhaps most histone modifying enzymes, are much more versatile and far more complicated than their initially proposed functions. Analogously, an HDAC-RNA splicing connection suggests that splicing is regulated by additional upstream factors and pathways yet to be defined or not fully characterized. Some human diseases share common underlying causes of aberrant HDACs and dysregulated RNA splicing and, thus, further support the potential link between HDACs and RNA splicing.
机译:组蛋白修饰和RNA剪接,两个看似无关基因的调节过程,大大增加蛋白质组多样性和深刻以及病理真核细胞功能的影响正常。像许多组蛋白修饰酶,组蛋白脱乙酰化酶(HDAC)执政细胞行为中发挥关键作用,并在许多生物过程是必不可少的。虽然RNA剪接和组蛋白修饰之间的关系开始被认可,缺乏知识就存在HDAC的拼接过程中的作用。然而,最近的研究表明,HDAC的与剪接体和核糖核蛋白复合物相互作用,积极控制拼接相关的组蛋白标记和剪接因子的乙酰化状态,从而出人意料地可以调节拼接。在这里,我们审查的组蛋白/蛋白修饰和HDAC的在RNA剪接中的作用,并讨论两个平行领域的融合,它支持的论点,即HDAC的,也许是最组蛋白修饰酶,是更灵活,远远超过其最初复杂建议的职能。类似地,一个HDAC-RNA剪接连接表明拼接由附加的上游因素和途径调节待定义或不完全表征。一些人类疾病共享异常HDAC的共同的潜在原因和失调的RNA剪接,因此,进一步的支持类HDAC和RNA剪接之间的潜在联系。

著录项

  • 来源
    《Nucleic Acids Research》 |2019年第10期|共16页
  • 作者

    Rahhal Raneen; Seto Edward;

  • 作者单位

    George Washington Univ Sch Med &

    Hlth Sci George Washington Canc Ctr Dept Biochem &

    Mol Med Washington DC 20037 USA;

    George Washington Univ Sch Med &

    Hlth Sci George Washington Canc Ctr Dept Biochem &

    Mol Med Washington DC 20037 USA;

  • 收录信息
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类 生物化学;
  • 关键词

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