人类DNA损伤修复基因中的致病变体大多出现在最近的人类历史中
Bojin Zhao1, Jiaheng Li1, Siddharth Sinha1
1Cancer Centre and Institute of Translational Medicine, Faculty of Health Sciences, University of Macau, Taipa, 999078, Macau SAR, China.
BMC cancer
|April 4, 2024
概括
人类DNA损伤修复 (DDR) 病原变异 (PVs) 在很大程度上起源于最近的人类历史,而不是来自跨物种的保护. 这些与癌症风险相关的变异可能是人类进化的副产品.
科学领域:
- 基因组学就是基因组学.
- 进化生物学 进化生物学
- 人类遗传学 人类遗传学
背景情况:
- 基因组的稳定性依赖于DNA损伤修复 (DDR) 系统.
- 在DDR基因的致病变异 (PVs) 增加疾病和癌症的风险.
- 了解DDR PVs的进化起源对于疾病病因学至关重要.
研究的目的:
- 研究人类DNA损伤修复 (DDR) 基因中病原变异 (PVs) 的进化起源.
- 为了确定人类的DDR PV是否起源于跨物种的保护或最近的人类进化.
主要方法:
- 从ClinVar.发现了169个DDR基因和人类PVs.
- 使用PHAST对100种脊椎动物进行了植物遗传分析.
- 进行了分子考古学分析,比较古代和现代人类的DDR PVs,包括古代人类DDR PVs的数据库.
主要成果:
- 遗传学分析排除了跨物种的保护作为人类DDR PVs的起源.
- 分子考古学揭示了古代和现代人类之间共享的大量DDR PV,主要来自过去5000年.
- 确定了与尼安德特人共享的特定DDR PVs (ATM,BRCA2,CHEK2).
结论:
- 人类的DDR PV主要出现在最近的人类历史中.
- 与DDR PVs相关的高癌症风险可能是一个进化副产品.
- 这一发现为人类疾病的病因和进化提供了洞察力.
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