Molecular Genetics Group, Institute of Biology, Humboldt University of Berlin, Berlin, Germany.
Laboratory of Aging Physiology and Molecular Evolution, Biology Department, Ghent University, Ghent, Belgium.
Biogerontology. 2022 Aug;23(4):431-452. doi: 10.1007/s10522-022-09969-8. Epub 2022 Jun 24.
To find drivers of healthy ageing, a genome-wide association study (GWAS) was performed in healthy and unhealthy older individuals. Healthy individuals were defined as free from cardiovascular disease, stroke, heart failure, major adverse cardiovascular event, diabetes, dementia, cancer, chronic obstructive pulmonary disease (COPD), asthma, rheumatism, Crohn's disease, malabsorption or kidney disease. Six single nucleotide polymorphisms (SNPs) with unknown function associated with ten human genes were identified as candidate healthspan markers. Thirteen homologous or closely related genes were selected in the model organism C. elegans for evaluating healthspan after targeted RNAi-mediated knockdown using pathogen resistance, muscle integrity, chemotaxis index and the activity of known longevity and stress response pathways as healthspan reporters. In addition, lifespan was monitored in the RNAi-treated nematodes. RNAi knockdown of yap-1, wwp-1, paxt-1 and several acdh genes resulted in heterogeneous phenotypes regarding muscle integrity, pathogen resistance, chemotactic behaviour, and lifespan. Based on these observations, we hypothesize that their human homologues WWC2, CDKN2AIP and ACADS may play a role in health maintenance in the elderly.
为了寻找健康衰老的驱动因素,对健康和不健康的老年人进行了全基因组关联研究(GWAS)。健康个体被定义为没有心血管疾病、中风、心力衰竭、主要不良心血管事件、糖尿病、痴呆、癌症、慢性阻塞性肺疾病(COPD)、哮喘、风湿病、克罗恩病、吸收不良或肾脏疾病。确定了与十个人类基因相关的六个具有未知功能的单核苷酸多态性(SNP)作为候选健康寿命标记物。在模式生物秀丽隐杆线虫中选择了 13 个同源或密切相关的基因,用于评估靶向 RNAi 介导的敲低后,使用病原体抗性、肌肉完整性、趋化指数和已知长寿和应激反应途径的活性作为健康寿命报告者。此外,还监测了 RNAi 处理线虫的寿命。yap-1、wwp-1、paxt-1 和几个 acdh 基因的 RNAi 敲低导致肌肉完整性、病原体抗性、趋化行为和寿命的表型不均匀。基于这些观察结果,我们假设它们的人类同源物 WWC2、CDKN2AIP 和 ACADS 可能在老年人的健康维持中发挥作用。