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人类顺式调控元件和转录因子结合位点的哺乳动物进化。

Mammalian evolution of human cis-regulatory elements and transcription factor binding sites.

机构信息

Program in Bioinformatics and Integrative Biology, University of Massachusetts Chan Medical School, Worcester, MA, USA.

Broad Institute of MIT and Harvard, Cambridge, MA 02139, USA.

出版信息

Science. 2023 Apr 28;380(6643):eabn7930. doi: 10.1126/science.abn7930.

Abstract

Understanding the regulatory landscape of the human genome is a long-standing objective of modern biology. Using the reference-free alignment across 241 mammalian genomes produced by the Zoonomia Consortium, we charted evolutionary trajectories for 0.92 million human candidate cis-regulatory elements (cCREs) and 15.6 million human transcription factor binding sites (TFBSs). We identified 439,461 cCREs and 2,024,062 TFBSs under evolutionary constraint. Genes near constrained elements perform fundamental cellular processes, whereas genes near primate-specific elements are involved in environmental interaction, including odor perception and immune response. About 20% of TFBSs are transposable element-derived and exhibit intricate patterns of gains and losses during primate evolution whereas sequence variants associated with complex traits are enriched in constrained TFBSs. Our annotations illuminate the regulatory functions of the human genome.

摘要

了解人类基因组的调控格局是现代生物学的长期目标。利用 Zoonomia 联盟生成的 241 种哺乳动物基因组的无参考对齐,我们绘制了 92 万个人类候选顺式调控元件 (cCRE) 和 1560 万个人类转录因子结合位点 (TFBS) 的进化轨迹。我们鉴定出 439461 个 cCRE 和 2024062 个 TFBS 受到进化约束。受约束元件附近的基因执行基本的细胞过程,而灵长类动物特有的元件附近的基因则参与环境相互作用,包括嗅觉感知和免疫反应。大约 20%的 TFBS 来自转座元件,并在灵长类动物进化过程中表现出复杂的增益和损失模式,而与复杂特征相关的序列变体在受约束的 TFBS 中富集。我们的注释阐明了人类基因组的调控功能。

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