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When epigenetics meets alternative splicing: The roles of DNA methylation and GC architecture

机译:当表观遗传学遇到其他剪接时:DNA甲基化和GC结构的作用

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摘要

The process of pre-mRNA splicing has been studied for more than 30 years, yet it is far from being fully understood. Accumulating evidence suggests that many splicing events occur cotranscriptionally and that the mRNA precursor remains associated with the chromatin until all of the introns have been removed. Cotrans-criptional splicing adds many more factors that might take part in the complex and highly regulated process of exon recognition. If cis-acting regulatory factors, such as splice-site sequences and splicing factors binding domains, did not provide enough complexity, splicing researchers are now realizing that the chromatin structure itself might also affect the exon selection process [1].
机译:mRNA前剪接的过程已经研究了30多年,但是还没有被完全理解。越来越多的证据表明,许多剪接事件是共转录发生的,并且mRNA前体一直与染色质相关,直到所有内含子都被去除。共转录剪接增加了更多因素,这些因素可能参与外显子识别的复杂且受严格监管的过程。如果顺式作用调节因子(例如剪接位点序列和剪接因子结合域)没有提供足够的复杂性,则剪接研究人员现在意识到染色质结构本身也可能影响外显子选择过程[1]。

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