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Emerging roles of histone modifications and HDACs in RNA splicing

机译:组蛋白修饰和HDAC在RNA剪接中的新兴作用

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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剪接这两个看似无关的基因调节过程,极大地增加了蛋白质组多样性,并深刻影响了正常的和病理的真核细胞功能。像许多组蛋白修饰酶一样,组蛋白脱乙酰基酶(HDAC)在控制细胞行为中起关键作用,并且在许多生物学过程中都是必不可少的。虽然RNA剪接和组蛋白修饰之间的联系已开始被认识,但有关HDAC在剪接中的作用的知识仍然不足。但是,最近的研究表明,HDAC与剪接体和核糖核蛋白复合物相互作用,可以主动控制与剪接相关的组蛋白标记和剪接因子的乙酰化状态,从而出乎意料地可以调节剪接。在这里,我们回顾了组蛋白/蛋白质修饰和HDAC在RNA剪接中的作用,并讨论了两个平行场的融合,这支持了这样一个论点,即HDAC和大多数的组蛋白修饰酶比起初它们具有更多的通用性和复杂性建议的功能。类似地,HDAC-RNA剪接连接表明剪接受尚待定义或尚未充分表征的其他上游因子和途径调控。一些人类疾病具有导致HDAC异常和RNA剪接失调的常见根本原因,因此,进一步支持了HDAC和RNA剪接之间的潜在联系。

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