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通过单细胞转录组和甲基化组分析探索自噬在人类早期胚胎发育中的作用。

Exploring the role of autophagy during early human embryonic development through single-cell transcriptome and methylome analyses.

机构信息

Center for Reproductive Medicine, Department of Obstetrics and Gynecology, Peking University Third Hospital, Beijing, 100191, China.

National Clinical Research Center for Obstetrics and Gynecology (Peking University Third Hospital), Beijing, 100191, China.

出版信息

Sci China Life Sci. 2022 May;65(5):940-952. doi: 10.1007/s11427-021-1948-1. Epub 2021 Jul 22.

Abstract

Early human embryogenesis is a very sophisticated process due to its unique gene regulatory network. Autophagy has been suggested to play an important role in mediating the development of early embryonic cells in mammals. However, evidence showing how autophagy regulates early human embryogenesis remains to be further explored. In this study, we systematically investigated the human transcriptome and methylome patterns of autophagy-related (ATG) genes in early embryonic cells at single-cell resolution. We analyzed the transcriptomic data of 365 cells and methylome data of 265 cells. The results showed that most ATG genes remained epigenetically active and were expressed stably throughout early embryogenesis, whereas the dynamics varied among different developmental stages. This evidence indicated that the autophagy pathway was constitutively activated and exerted a fundamental role in early human embryo development. Our work, for the first time, comprehensively reveals the features of autophagy during early human embryo development.

摘要

早期人类胚胎发生是一个非常复杂的过程,这是由于其独特的基因调控网络。自噬被认为在调节哺乳动物早期胚胎细胞的发育中发挥重要作用。然而,自噬如何调节早期人类胚胎发生的证据仍有待进一步探索。在这项研究中,我们系统地研究了早期胚胎细胞中与自噬相关(ATG)基因的人类转录组和甲基组模式,在单细胞分辨率下进行分析。我们分析了 365 个细胞的转录组数据和 265 个细胞的甲基组数据。结果表明,大多数 ATG 基因在整个早期胚胎发生过程中保持表观遗传活性和稳定表达,而不同发育阶段的动态变化。这一证据表明,自噬途径持续激活,并在早期人类胚胎发育中发挥基本作用。我们的工作首次全面揭示了自噬在早期人类胚胎发育过程中的特征。

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