Long-range chromatin interactions in pathogenic gene expression control.

IF 3.6 Q2 BIOCHEMISTRY & MOLECULAR BIOLOGY
Transcription-Austin Pub Date : 2020-10-01 Epub Date: 2020-11-05 DOI:10.1080/21541264.2020.1843958
Nahyun Kong, Inkyung Jung
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引用次数: 4

Abstract

A large number of distal cis-regulatory elements (cREs) have been annotated in the human genome, which plays a central role in orchestrating spatiotemporal gene expression. Since many cREs regulate non-adjacent genes, long-range cRE-promoter interactions are an important factor in the functional characterization of the engaged cREs. In this regard, recent studies have demonstrated that identification of long-range target genes can decipher the effect of genetic mutations residing within cREs on abnormal gene expression. In addition, investigation of altered long-range cREs-promoter interactions induced by chromosomal rearrangements has revealed their critical roles in pathogenic gene expression. In this review, we briefly discuss how the analysis of 3D chromatin structure can help us understand the functional impact of cREs harboring disease-associated genetic variants and how chromosomal rearrangements disrupting topologically associating domains can lead to pathogenic gene expression.

致病性基因表达控制中的远程染色质相互作用。
大量的远端顺式调控元件(cREs)在人类基因组中被标注,它们在调控基因时空表达中起着核心作用。由于许多cre调控非相邻基因,远程cre -启动子相互作用是参与cre功能表征的重要因素。在这方面,最近的研究表明,鉴定远程靶基因可以破译位于cre内的基因突变对异常基因表达的影响。此外,对染色体重排诱导的远程cre -启动子相互作用改变的研究揭示了它们在致病基因表达中的关键作用。在这篇综述中,我们简要地讨论了三维染色质结构分析如何帮助我们了解含有疾病相关遗传变异的cre的功能影响,以及染色体重排破坏拓扑相关结构域如何导致致病基因表达。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Transcription-Austin
Transcription-Austin BIOCHEMISTRY & MOLECULAR BIOLOGY-
CiteScore
6.50
自引率
5.60%
发文量
9
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