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小鼠卵母细胞在构型转变过程中的染色质可及性图谱。

The chromatin accessibility landscape of mouse oocytes during configuration transition.

作者信息

Zhu Shuai, Li Jiashuo, Wang Xiuwan, Jin Yifei, Wang Hengjie, An Huiqing, Sun Hongzheng, Han Longsen, Shen Bin, Wang Qiang

机构信息

State Key Laboratory of Reproductive Medicine and Offspring Health, Changzhou Maternity and Child Health Care Hospital, Changzhou Medical Center, Nanjing Medical University, Nanjing, China.

Center for Global Health, School of Public Health, Nanjing Medical University, Nanjing, China.

出版信息

Cell Prolif. 2025 Jan;58(1):e13733. doi: 10.1111/cpr.13733. Epub 2024 Sep 8.

Abstract

The transition of chromatin configuration in mammalian oocytes from a non-surrounded nucleolus (NSN) to a surrounded nucleolus (SN) is critical for acquiring the developmental competence. However, the genomic and epigenomic features underlying this process remain poorly understood. In the present study, we first establish the chromatin accessibility landscape of mouse oocytes from NSN to SN stage. Through the integrative analysis of multi-omics, we find that the establishment of DNA methylation in oocytes is independent of the dynamics of chromatin accessibility. In contrast, histone H3K4me3 status is closely associated with the dynamics of accessible regions during configuration transition. Furthermore, by focusing on the actively transcribed genes in NSN and SN oocytes, we discover that chromatin accessibility coupled with histone methylation (H3K4me3 and H3K27me3) participates in the transcriptional control during phase transition. In sum, our data provide a comprehensive resource for probing configuration transition in oocytes, and offer insights into the mechanisms determining chromatin dynamics and oocyte quality.

摘要

哺乳动物卵母细胞中染色质构型从非环绕核仁(NSN)向环绕核仁(SN)的转变对于获得发育能力至关重要。然而,这一过程背后的基因组和表观基因组特征仍知之甚少。在本研究中,我们首先建立了从小鼠卵母细胞NSN期到SN期的染色质可及性图谱。通过多组学的综合分析,我们发现卵母细胞中DNA甲基化的建立独立于染色质可及性的动态变化。相反,组蛋白H3K4me3状态与构型转变过程中可及区域的动态变化密切相关。此外,通过聚焦于NSN和SN卵母细胞中活跃转录的基因,我们发现染色质可及性与组蛋白甲基化(H3K4me3和H3K27me3)共同参与了相变过程中的转录调控。总之,我们的数据为探究卵母细胞中的构型转变提供了全面的资源,并为确定染色质动态变化和卵母细胞质量的机制提供了见解。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/171b/11693577/4c126de7f380/CPR-58-e13733-g006.jpg

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