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Dppa3 在胚胎干细胞多能性维持和早期胚胎发生中的作用。

Dppa3 in pluripotency maintenance of ES cells and early embryogenesis.

机构信息

School of Medicine, Nankai University, Tianjin, China.

Department of Genetics and Cell Biology, College of Life Sciences, Nankai University, Tianjin, China.

出版信息

J Cell Biochem. 2019 Apr;120(4):4794-4799. doi: 10.1002/jcb.28063. Epub 2018 Nov 11.

Abstract

Embryonic development is precisely regulated by a network of signal pathways and specific genes. Dppa3 (also known as Pgc7 or Stella) plays an important role in early embryonic development during the cleavage stage as a maternal effect gene. Dppa3 expresses in many species, and its homologous gene in human and rat genomes is located at the same chromosomal regions and have the same exon-intron structure. However, unlike mouse embryonic stem (ES) cells, in which the Dppa3 promoter maintains hypomethylation that allows a high transcription level, the DPPA3 promoter region in human ES cells is methylated, much like that of mouse epiblast stem cell. Dppa3 is essential for early embryogenesis and pluripotency maintenance; however, the precise mechanism and downstream passage remains unknown. In this review, we will summarize some important functions of Dppa3 in early embryogenesis and pluripotency maintenance of mouse ES cells.

摘要

胚胎发育是通过信号通路和特定基因的网络精确调控的。Dppa3(也称为 Pgc7 或 Stella)作为一种母源效应基因,在卵裂期的早期胚胎发育中发挥重要作用。Dppa3 在许多物种中表达,其在人类和大鼠基因组中的同源基因位于同一染色体区域,具有相同的外显子-内含子结构。然而,与在小鼠胚胎干细胞(ES 细胞)中不同,Dppa3 启动子保持低甲基化,允许高水平转录,而人类 ES 细胞中的 DPPA3 启动子区域被甲基化,与小鼠胚胎外胚层干细胞非常相似。Dppa3 对于早期胚胎发生和多能性维持是必需的;然而,其确切的机制和下游途径仍不清楚。在这篇综述中,我们将总结 Dppa3 在早期胚胎发生和小鼠 ES 细胞多能性维持中的一些重要功能。

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