妊娠早期子宫成纤维细胞依赖kdm6b的表观遗传编程调节小鼠分娩时间

IF 45.5 1区 生物学 Q1 BIOCHEMISTRY & MOLECULAR BIOLOGY Cell Pub Date : 2025-01-21 DOI:10.1016/j.cell.2024.12.019
Tara I. McIntyre, Omar Valdez, Nathan P. Kochhar, Brittany Davidson, Bushra Samad, Longhui Qiu, Kenneth Hu, Alexis J. Combes, Adrian Erlebacher
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引用次数: 0

摘要

目前对分娩时间机制的研究主要集中在妊娠后期分娩的近端触发因素上。通过研究子宫成纤维细胞组蛋白H3K27me3去甲基化酶KDM6B缺陷小鼠的延迟分娩表型,我们提供了分娩时间受妊娠早期发生的事件调节的证据。交配后,子宫成纤维细胞立即参与一个位点特异性的表观遗传程序,突然调整整个基因组中的H3K27me3水平。在缺乏KDM6B的情况下,许多调整后的基因座过度积累了H3K27me3。这种过度积累导致附近基因在妊娠中后期错误表达,这种延迟效应部分归因于植入后不久子宫成纤维细胞内启动的第二个基因座特异性但不依赖于kdm6b的过程。第二个过程采用H3K27me3的进行性丢失来暂时构建妊娠后基因诱导模式。进一步剖析子宫编程控制分娩时间的方式可能与人类妊娠并发症如早产有关。
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KDM6B-dependent epigenetic programming of uterine fibroblasts in early pregnancy regulates parturition timing in mice
Current efforts investigating parturition timing mechanisms have focused on the proximal triggers of labor onset generated in late pregnancy. By studying the delayed parturition phenotype of mice with uterine fibroblast deficiencies in the histone H3K27me3 demethylase KDM6B, we provide evidence that parturition timing is regulated by events that take place in early pregnancy. Immediately after copulation, uterine fibroblasts engage in a locus-specific epigenetic program that abruptly adjusts H3K27me3 levels across their genome. In the absence of KDM6B, many of the adjusted loci over-accumulate H3K27me3. This over-accumulation leads to nearby genes being misexpressed in mid-to-late gestation, a delayed effect partly attributable to a second locus-specific but KDM6B-independent process initiated within uterine fibroblasts soon after implantation. This second process employs progressive H3K27me3 loss to temporally structure post-midgestational patterns of gene induction. Further dissection of the ways uterine programming controls parturition timing may have relevance to human pregnancy complications such as preterm labor.
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来源期刊
Cell
Cell 生物-生化与分子生物学
CiteScore
110.00
自引率
0.80%
发文量
396
审稿时长
2 months
期刊介绍: Cells is an international, peer-reviewed, open access journal that focuses on cell biology, molecular biology, and biophysics. It is affiliated with several societies, including the Spanish Society for Biochemistry and Molecular Biology (SEBBM), Nordic Autophagy Society (NAS), Spanish Society of Hematology and Hemotherapy (SEHH), and Society for Regenerative Medicine (Russian Federation) (RPO). The journal publishes research findings of significant importance in various areas of experimental biology, such as cell biology, molecular biology, neuroscience, immunology, virology, microbiology, cancer, human genetics, systems biology, signaling, and disease mechanisms and therapeutics. The primary criterion for considering papers is whether the results contribute to significant conceptual advances or raise thought-provoking questions and hypotheses related to interesting and important biological inquiries. In addition to primary research articles presented in four formats, Cells also features review and opinion articles in its "leading edge" section, discussing recent research advancements and topics of interest to its wide readership.
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