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MFAP5 基因调控区域的 cg06256735 和 cg15815843 位点在静脉曲张中出现低甲基化,显然是由于活性去甲基化所致。

Loci cg06256735 and cg15815843 in the MFAP5 gene regulatory regions are hypomethylated in varicose veins apparently due to active demethylation.

机构信息

Laboratory of Pharmacogenomics, Institute of Chemical Biology and Fundamental Medicine (ICBFM), Siberian Branch of the Russian Academy of Sciences (SB RAS), Novosibirsk 630090, Russia.

Department of Fundamental Medicine, V. Zelman Institute for Medicine and Psychology, Novosibirsk State University (NSU), Novosibirsk 630090, Russia.

出版信息

Biosci Rep. 2024 May 29;44(5). doi: 10.1042/BSR20231938.

DOI:10.1042/BSR20231938
PMID:38743016
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11139664/
Abstract

Varicose vein disease (VVD) is a common health problem worldwide. Microfibril-associated protein 5 (MFAP5) is one of the potential key players in its pathogenesis. Our previous microarray analysis revealed the cg06256735 and cg15815843 loci in the regulatory regions of the MFAP5 gene as hypomethylated in varicose veins which correlated with its up-regulation. The aim of this work was to validate preliminary microarray data, estimate the level of 5-hydroxymethylcytosine (5hmC) at these loci, and determine the methylation status of one of them in different layers of the venous wall. For this, methyl- and hydroxymethyl-sensitive restriction techniques were used followed by real-time PCR and droplet digital PCR, correspondingly, as well as bisulfite pyrosequencing of +/- oxidized DNA. Our microarray data on hypomethylation at the cg06256735 and cg15815843 loci in whole varicose vein segments were confirmed and it was also demonstrated that the level of 5hmC at these loci is increased in VVD. Specifically, among other layers of the venous wall, tunica (t.) intima is the main contributor to hypomethylation at the cg06256735 locus in varicose veins. Thus, it was shown that hypomethylation at the cg06256735 and cg15815843 loci takes place in VVD, with evidence to suggest that it happens through their active demethylation leading to up-regulation of the MFAP5 gene, and t. intima is most involved in this biochemical process.

摘要

静脉曲张疾病(VVD)是全球范围内常见的健康问题。微纤维相关蛋白 5(MFAP5)是其发病机制中的潜在关键因素之一。我们之前的微阵列分析显示,MFAP5 基因调控区域的 cg06256735 和 cg15815843 位点在静脉曲张中呈低甲基化状态,这与其上调相关。本研究旨在验证初步的微阵列数据,估计这些位点的 5-羟甲基胞嘧啶(5hmC)水平,并确定其中一个位点在静脉壁不同层中的甲基化状态。为此,我们使用了甲基化和羟甲基化敏感的限制技术,随后进行了实时 PCR 和液滴数字 PCR,以及 +/-氧化 DNA 的亚硫酸氢盐焦磷酸测序。我们关于整个静脉曲张段 cg06256735 和 cg15815843 位点低甲基化的微阵列数据得到了证实,并且还表明这些位点的 5hmC 水平在 VVD 中增加。具体而言,在静脉壁的其他层中,内膜(t.)是静脉曲张中 cg06256735 位点低甲基化的主要贡献者。因此,研究表明 VVD 中存在 cg06256735 和 cg15815843 位点的低甲基化,有证据表明这是通过其主动去甲基化导致 MFAP5 基因的上调,而 t.内膜最参与这一生化过程。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/192c/11139664/001c3a245b38/bsr-44-bsr20231938-g5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/192c/11139664/1692d7edf0e6/bsr-44-bsr20231938-g1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/192c/11139664/1a23a856b8a7/bsr-44-bsr20231938-g2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/192c/11139664/40a78162ddb9/bsr-44-bsr20231938-g3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/192c/11139664/d7d0e951da73/bsr-44-bsr20231938-g4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/192c/11139664/001c3a245b38/bsr-44-bsr20231938-g5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/192c/11139664/1692d7edf0e6/bsr-44-bsr20231938-g1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/192c/11139664/1a23a856b8a7/bsr-44-bsr20231938-g2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/192c/11139664/40a78162ddb9/bsr-44-bsr20231938-g3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/192c/11139664/d7d0e951da73/bsr-44-bsr20231938-g4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/192c/11139664/001c3a245b38/bsr-44-bsr20231938-g5.jpg

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本文引用的文献

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Microfibril-Associated Glycoprotein-2 Promoted Fracture Healing via Integrin αvβ3/PTK2/AKT Signaling.微纤维相关糖蛋白 2 通过整合素 αvβ3/PTK2/AKT 信号通路促进骨折愈合。
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正常人类细胞类型的 DNA 甲基化图谱。
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