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CpG 位点甲基化调控小鼠 Rec8 基因启动子活性。

CpG site methylation regulates mouse Rec8 gene promoter activity.

作者信息

Rong Mei, Feng Na, Li Jinghuan, Dalai Wuyun

机构信息

College of Life Science and Technology, Inner Mongolia Normal University, Hohhot 010022, Inner Mongolia, China.

Key Laboratory of Biodiversity conservation and Sustainable utilization in Mongolian Plateau for College and University of Inner Mongolia Autonomous Region, Hohhot 010022, China.

出版信息

J Reprod Dev. 2025 Jun 6;71(3):145-153. doi: 10.1262/jrd.2024-077. Epub 2025 Apr 4.

Abstract

The Rec8 gene is specifically expressed in fetal and adult gonads. Although the importance of REC8 in gametogenesis is widely acknowledged, the mechanisms underlying its germ cell-specific expression remain unclear. In this study, we utilized the mouse Rec8 gene sequence to construct a 2577 bp sequence, which included intron 1 (180 bp), exon 1 (118 bp), and an upstream 2279 bp region. The dual-luciferase assay results showed significant differences in promoter activity between -650 bp and -385 bp and between -89 bp and -35 bp. This indicated that the core promoter region of the Rec8 gene may exist within these regions. Bisulfite sequencing PCR results showed that CpGs 10-19 were largely unmethylated in the testes but hypermethylated in other tissues. Interestingly, correlation analysis between CpG methylation status and Rec8 mRNA expression levels showed that methylation of CpGs 10 to 19 was negatively correlated with Rec8 mRNA expression levels (Pearson's r = -0.991, P = 0.009). Furthermore, RNA-Seq data and bioinformatic analyses suggested that the specific expression of Rec8 may be linked to the presence of TATA-like sequences within its core promoter region. Overall, these findings indicate that Rec8 expression is regulated by the low methylation of CpG sites and the presence of TATA-like sequences in its core promoter.

摘要

Rec8基因在胎儿和成年性腺中特异性表达。尽管REC8在配子发生中的重要性已得到广泛认可,但其在生殖细胞中特异性表达的机制仍不清楚。在本研究中,我们利用小鼠Rec8基因序列构建了一个2577 bp的序列,其中包括内含子1(180 bp)、外显子1(118 bp)和上游2279 bp区域。双荧光素酶报告基因检测结果显示,-650 bp与-385 bp之间以及-89 bp与-35 bp之间的启动子活性存在显著差异。这表明Rec8基因的核心启动子区域可能存在于这些区域内。亚硫酸氢盐测序PCR结果显示,睾丸中第10至19位的CpG大多未甲基化,而在其他组织中则高度甲基化。有趣的是,CpG甲基化状态与Rec8 mRNA表达水平的相关性分析表明,第10至19位的CpG甲基化与Rec8 mRNA表达水平呈负相关(Pearson相关系数r = -0.991,P = 0.009)。此外,RNA测序数据和生物信息学分析表明,Rec8的特异性表达可能与其核心启动子区域内存在类似TATA的序列有关。总体而言,这些发现表明,Rec8的表达受CpG位点低甲基化及其核心启动子中类似TATA序列的调控。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bb30/12151637/413f860cf724/jrd-71-145-g001.jpg

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