Suppr超能文献

DNA N6-甲基腺苷修饰对东亚人群转录遗传变异的选择性影响。

Selective Effect of DNA N6-Methyladenosine Modification on Transcriptional Genetic Variations in East Asian Samples.

机构信息

School of Basic Medicine, Harbin Medical University, Harbin 150081, China.

Guangzhou Women and Children's Medical Center, Guangzhou Medical University, Guangzhou 511436, China.

出版信息

Int J Mol Sci. 2024 Sep 27;25(19):10400. doi: 10.3390/ijms251910400.

Abstract

Genetic variations and DNA modification are two common dominant factors ubiquitous across the entire human genome and induce human disease, especially through static genetic variations in DNA or RNA that cause human genetic diseases. DNA N6-methyladenosine (6mA) methylation, as a new epigenetic modification mark, has been widely studied for regulatory biological processes in humans. However, the effect of DNA modification on dynamic transcriptional genetic variations from DNA to RNA has rarely been reported. Here, we identified DNA, RNA and transcriptional genetic variations from Illumina short-read sequencing data in East Asian samples (HX1 and AK1) and detected global DNA 6mA modification using single-molecule, real-time sequencing (SMRT) data. We decoded the effects of DNA 6mA modification on transcriptional genetic variations in East Asian samples and the results were extensively verified in the HeLa cell line. DNA 6mA modification had a stabilized distribution in the East Asian samples and the methylated genes were less likely to mutate than the non-methylated genes. For methylated genes, the 6mA density was positively correlated with the number of variations. DNA 6mA modification had a selective effect on transcriptional genetic variations from DNA to RNA, in which the dynamic transcriptional variations of heterozygous (0/1 to 0/1) and homozygous (1/1 to 1/1) were significantly affected by 6mA modification. The effect of DNA methylation on transcriptional genetic variations provides new insights into the influencing factors of DNA to RNA transcriptional regulation in the central doctrine of molecular biology.

摘要

遗传变异和 DNA 修饰是普遍存在于整个人类基因组中的两个常见的主要因素,它们会导致人类疾病,尤其是通过 DNA 或 RNA 中的静态遗传变异导致人类遗传疾病。DNA N6-甲基腺嘌呤(6mA)甲基化作为一种新的表观遗传修饰标记,已广泛研究其在人类调节生物过程中的作用。然而,DNA 修饰对从 DNA 到 RNA 的动态转录遗传变异的影响很少有报道。在这里,我们从东亚样本(HX1 和 AK1)的 Illumina 短读测序数据中鉴定了 DNA、RNA 和转录遗传变异,并使用单分子实时测序(SMRT)数据检测了全局 DNA 6mA 修饰。我们解码了东亚样本中 DNA 6mA 修饰对转录遗传变异的影响,并且在 HeLa 细胞系中进行了广泛的验证。DNA 6mA 修饰在东亚样本中具有稳定的分布,并且甲基化基因比非甲基化基因更不容易突变。对于甲基化基因,6mA 密度与变异数量呈正相关。DNA 6mA 修饰对从 DNA 到 RNA 的转录遗传变异具有选择性影响,其中杂合子(0/1 到 0/1)和纯合子(1/1 到 1/1)的动态转录变异受 6mA 修饰的显著影响。DNA 甲基化对转录遗传变异的影响为分子生物学中心法则中 DNA 到 RNA 转录调控的影响因素提供了新的见解。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3cfc/11477068/89e9c3f098d1/ijms-25-10400-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