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使用单细胞表观基因组学进行顺式调控元件的特征分析。

Characterizing cis-regulatory elements using single-cell epigenomics.

机构信息

Center for Epigenomics, University of California San Diego, La Jolla, CA, USA.

Institute of Experimental and Clinical Pharmacology and Toxicology, Faculty of Medicine, University of Freiburg, Freiburg, Germany.

出版信息

Nat Rev Genet. 2023 Jan;24(1):21-43. doi: 10.1038/s41576-022-00509-1. Epub 2022 Jul 15.

Abstract

Cell type-specific gene expression patterns and dynamics during development or in disease are controlled by cis-regulatory elements (CREs), such as promoters and enhancers. Distinct classes of CREs can be characterized by their epigenomic features, including DNA methylation, chromatin accessibility, combinations of histone modifications and conformation of local chromatin. Tremendous progress has been made in cataloguing CREs in the human genome using bulk transcriptomic and epigenomic methods. However, single-cell epigenomic and multi-omic technologies have the potential to provide deeper insight into cell type-specific gene regulatory programmes as well as into how they change during development, in response to environmental cues and through disease pathogenesis. Here, we highlight recent advances in single-cell epigenomic methods and analytical tools and discuss their readiness for human tissue profiling.

摘要

在发育或疾病过程中,细胞类型特异性基因表达模式和动态由顺式调控元件(CREs)控制,如启动子和增强子。不同类别的 CREs 可以通过其表观基因组特征来表征,包括 DNA 甲基化、染色质可及性、组蛋白修饰的组合以及局部染色质构象。使用批量转录组学和表观基因组学方法,在人类基因组中对 CRE 进行编目方面已经取得了巨大进展。然而,单细胞表观基因组学和多组学技术有可能深入了解细胞类型特异性基因调控程序,以及它们在发育过程中、对环境线索的反应以及通过疾病发病机制如何变化。在这里,我们重点介绍单细胞表观基因组学方法和分析工具的最新进展,并讨论它们在人类组织分析方面的准备情况。

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