Suppr超能文献

孤雌生殖的植入前小鼠胚胎发育过程中的表观遗传损伤。

Epigenetic impairments in development of parthenogenetic preimplantation mouse embryos.

作者信息

Ho Ngan Thi Kim, Nguyen Thuy Van Thi, Nguyen Thuan Van, Bui Hong-Thuy

机构信息

Cellular Reprogramming Laboratory, School of Biotechnology, International University, Vietnam National University, Ho Chi Minh City 700000, Vietnam.

出版信息

J Reprod Dev. 2019 Feb 8;65(1):83-90. doi: 10.1262/jrd.2018-028. Epub 2018 Dec 29.

Abstract

Parthenogenesis is an activation process of oocytes that occur without the participation of sperm. Evidence suggests that normal development of embryos requires proper expression of several imprinted genes inherited from both the paternal and maternal genomes. Compared to gene expression, histone modifications and chromatin remodeling are not well-documented. In this research, by using immunofluorescence staining for several developmental-associated histone modifications, we investigated whether epigenetic impairments in parthenogenetic embryos act as constraints for proper development. At early stages, fertilized embryos exhibited high methylation of histone H3 at lysine 9 (Me-H3-K9) and Heterochromatin Protein 1 (HP1) present in the maternal chromatin, while paternal chromatin showed weaker HP1 signals. We found that at the two-cell stage in fertilized embryos, HP1, initially detected around the nucleolus, colocalized with chromocenters at one pole of the blastomere, while parthenotes showed a diffused distribution pattern of HP1 throughout the entire nucleoplasm. At the four-cell stage, methylation of histone H3 at arginine 26 (Me-H3-R26) increased at nascent RNA repression sites in fertilized embryos, while parthenotes recorded weaker signals throughout the nucleoplasm, suggesting differences in pluripotency of the ICM cells between the two types of embryos. Moreover, at the blastocyst stage, we observed that the acetylation level of histone H4 at lysine 12 (Ac-H4-K12) was significantly decreased in parthenogenetic ICM compared to that in its fertilized counterpart. To summarize, differences in epigenetic modifications correlating with paternal chromatin's capacity to regulate nascent RNA repression may contribute to aberrant development and lineage allocation in mouse parthenogenetic embryos.

摘要

孤雌生殖是卵母细胞在没有精子参与的情况下发生的激活过程。有证据表明,胚胎的正常发育需要从父本和母本基因组遗传的几个印记基因的正确表达。与基因表达相比,组蛋白修饰和染色质重塑的记录并不充分。在本研究中,我们通过对几种与发育相关的组蛋白修饰进行免疫荧光染色,研究了孤雌生殖胚胎中的表观遗传损伤是否对正常发育起到限制作用。在早期阶段,受精胚胎在赖氨酸9处的组蛋白H3(Me-H3-K9)高度甲基化,并且母本染色质中存在异染色质蛋白1(HP1),而父本染色质显示较弱的HP1信号。我们发现,在受精胚胎的二细胞阶段,最初在核仁周围检测到的HP1与卵裂球一极的染色中心共定位,而孤雌生殖胚胎中的HP1在整个核质中呈弥散分布模式。在四细胞阶段,受精胚胎中新生RNA抑制位点处的精氨酸26处的组蛋白H3甲基化(Me-H3-R26)增加,而孤雌生殖胚胎在整个核质中记录到较弱的信号,表明两种胚胎之间内细胞团(ICM)细胞的多能性存在差异。此外,在囊胚阶段,我们观察到,与受精胚胎的内细胞团相比,孤雌生殖的内细胞团中赖氨酸12处的组蛋白H4乙酰化水平(Ac-H4-K12)显著降低。总之,与父本染色质调节新生RNA抑制能力相关的表观遗传修饰差异可能导致小鼠孤雌生殖胚胎的异常发育和谱系分配。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/723c/6379762/7c84b0e577c9/jrd-65-083-g001.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