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具有增强子和沉默子潜力的非编码基因组区域与健康衰老和超长生存期相关。

Non-coding genomic regions possessing enhancer and silencer potential are associated with healthy aging and exceptional survival.

作者信息

Kim Sangkyu, Welsh David A, Myers Leann, Cherry Katie E, Wyckoff Jennifer, Jazwinski S Michal

机构信息

Tulane Center for Aging and Department of Medicine, Tulane University Health Sciences Center, New Orleans, LA 70112, USA.

Department of Medicine, Louisiana State University Health Sciences Center, New Orleans, LA 70112, USA.

出版信息

Oncotarget. 2015 Feb 28;6(6):3600-12. doi: 10.18632/oncotarget.2877.

Abstract

We have completed a genome-wide linkage scan for healthy aging using data collected from a family study, followed by fine-mapping by association in a separate population, the first such attempt reported. The family cohort consisted of parents of age 90 or above and their children ranging in age from 50 to 80. As a quantitative measure of healthy aging, we used a frailty index, called FI34, based on 34 health and function variables. The linkage scan found a single significant linkage peak on chromosome 12. Using an independent cohort of unrelated nonagenarians, we carried out a fine-scale association mapping of the region suggestive of linkage and identified three sites associated with healthy aging. These healthy-aging sites (HASs) are located in intergenic regions at 12q13-14. HAS-1 has been previously associated with multiple diseases, and an enhancer was recently mapped and experimentally validated within the site. HAS-2 is a previously uncharacterized site possessing genomic features suggestive of enhancer activity. HAS-3 contains features associated with Polycomb repression. The HASs also contain variants associated with exceptional longevity, based on a separate analysis. Our results provide insight into functional genomic networks involving non-coding regulatory elements that are involved in healthy aging and longevity.

摘要

我们利用从一项家庭研究中收集的数据,完成了一次针对健康衰老的全基因组连锁扫描,随后在另一独立人群中进行了关联精细定位,这是首次报告的此类尝试。该家庭队列由90岁及以上的父母及其年龄在50至80岁之间的子女组成。作为健康衰老的定量指标,我们使用了一种基于34项健康和功能变量的衰弱指数,称为FI34。连锁扫描在12号染色体上发现了一个显著的连锁峰。我们利用一个由不相关的九旬老人组成的独立队列,对提示连锁的区域进行了精细尺度的关联图谱绘制,并确定了三个与健康衰老相关的位点。这些健康衰老位点(HASs)位于12q13 - 14的基因间区域。HAS - 1此前已与多种疾病相关,最近在该位点内绘制并通过实验验证了一个增强子。HAS - 2是一个此前未被表征的位点,具有提示增强子活性的基因组特征。HAS - 3包含与多梳抑制相关的特征。基于另一项分析,这些HASs还包含与特别长寿相关的变异。我们的结果为涉及非编码调控元件的功能基因组网络提供了见解,这些元件参与了健康衰老和长寿过程。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f740/4414140/9fb71024765f/oncotarget-06-3600-g001.jpg

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