Suppr超能文献

保守的表观遗传调控逻辑推断出决定细胞身份的基因。

Conserved Epigenetic Regulatory Logic Infers Genes Governing Cell Identity.

作者信息

Shim Woo Jun, Sinniah Enakshi, Xu Jun, Vitrinel Burcu, Alexanian Michael, Andreoletti Gaia, Shen Sophie, Sun Yuliangzi, Balderson Brad, Boix Carles, Peng Guangdun, Jing Naihe, Wang Yuliang, Kellis Manolis, Tam Patrick P L, Smith Aaron, Piper Michael, Christiaen Lionel, Nguyen Quan, Bodén Mikael, Palpant Nathan J

机构信息

School of Chemistry and Molecular Biosciences, The University of Queensland, Brisbane, Australia.

Institute for Molecular Bioscience, The University of Queensland, Brisbane, Australia.

出版信息

Cell Syst. 2020 Dec 16;11(6):625-639.e13. doi: 10.1016/j.cels.2020.11.001. Epub 2020 Dec 4.

Abstract

Determining genes that orchestrate cell differentiation in development and disease remains a fundamental goal of cell biology. This study establishes a genome-wide metric based on the gene-repressive trimethylation of histone H3 at lysine 27 (H3K27me3) across hundreds of diverse cell types to identify genetic regulators of cell differentiation. We introduce a computational method, TRIAGE, which uses discordance between gene-repressive tendency and expression to identify genetic drivers of cell identity. We apply TRIAGE to millions of genome-wide single-cell transcriptomes, diverse omics platforms, and eukaryotic cells and tissue types. Using a wide range of data, we validate the performance of TRIAGE in identifying cell-type-specific regulatory factors across diverse species including human, mouse, boar, bird, fish, and tunicate. Using CRISPR gene editing, we use TRIAGE to experimentally validate RNF220 as a regulator of Ciona cardiopharyngeal development and SIX3 as required for differentiation of endoderm in human pluripotent stem cells. A record of this paper's transparent peer review process is included in the Supplemental Information.

摘要

确定在发育和疾病过程中协调细胞分化的基因仍然是细胞生物学的一个基本目标。本研究基于赖氨酸27处组蛋白H3的基因抑制性三甲基化(H3K27me3),在数百种不同细胞类型中建立了全基因组指标,以识别细胞分化的遗传调节因子。我们引入了一种计算方法TRIAGE,它利用基因抑制倾向和表达之间的不一致来识别细胞身份的遗传驱动因素。我们将TRIAGE应用于数百万个全基因组单细胞转录组、多种组学平台以及真核细胞和组织类型。利用广泛的数据,我们验证了TRIAGE在识别包括人类、小鼠、野猪、鸟类、鱼类和被囊动物在内的不同物种中细胞类型特异性调节因子方面的性能。通过CRISPR基因编辑,我们利用TRIAGE实验验证了RNF220是海鞘心脏咽发育的调节因子,以及SIX3是人类多能干细胞中内胚层分化所必需的。本文透明的同行评审过程记录包含在补充信息中。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/554b/7781436/33eec1cc4768/nihms-1653552-f0002.jpg

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验