a Key Laboratory of Stem Cell Engineering and Regenerative Medicine , Fujian Province University.
b Department of Human Anatomy, Histology and Embryology , Fujian Medical University , Fuzhou , P. R. China.
Cell Cycle. 2019 Feb;18(4):437-451. doi: 10.1080/15384101.2019.1577650. Epub 2019 Feb 12.
Zygotic genome activation (ZGA) is one of the most critical events at the beginning of mammalian preimplantation embryo development (PED). The mechanisms underlying mouse ZGA remain unclear although it has been widely studied. In the present study, we identified that tricho-rhino-phalangeal syndrome 1 (TRPS1), an atypical GATA family member, is an important factor for ZGA in mouse PED. We found that the Trps1 mRNA level peaked at the one-cell stage while TRPS1 protein did so at the two/four-cell stage. Knockdown of Trps1 by the microinjection of Trps1 siRNA reduced the developmental rate of mouse preimplantation embryos by approximately 30%, and increased the expression of ZGA marker genes MuERV-L and Zscan4d via suppressing the expression of major histone markers H3K4me3 and H3K27me3. Furthermore, Trps1 knockdown decreased the expression of Sox2 but increased Oct4 expression. We conclude that TRPS1 may be indispensable for zygotic genome activation during mouse PED.
合子基因组激活(ZGA)是哺乳动物胚胎植入前发育(PED)早期最关键的事件之一。尽管已经进行了广泛的研究,但小鼠 ZGA 的机制仍不清楚。在本研究中,我们鉴定出三指-鼻-唇综合征 1(TRPS1),一种非典型的 GATA 家族成员,是小鼠 PED 中 ZGA 的重要因素。我们发现 Trps1 mRNA 水平在单细胞期达到峰值,而 TRPS1 蛋白在二/四细胞期达到峰值。通过注射 Trps1 siRNA 对 Trps1 进行敲低,大约降低了 30%的小鼠胚胎植入前发育的速度,并通过抑制主要组蛋白标记物 H3K4me3 和 H3K27me3 的表达,增加了 ZGA 标记基因 MuERV-L 和 Zscan4d 的表达。此外,Trps1 敲低降低了 Sox2 的表达,但增加了 Oct4 的表达。我们的结论是,TRPS1 可能是小鼠 PED 中合子基因组激活所必需的。