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早发性阿尔茨海默病中的TYROBP基因变异

TYROBP genetic variants in early-onset Alzheimer's disease.

作者信息

Pottier Cyril, Ravenscroft Thomas A, Brown Patricia H, Finch NiCole A, Baker Matt, Parsons Meeia, Asmann Yan W, Ren Yingxue, Christopher Elizabeth, Levitch Denise, van Blitterswijk Marka, Cruchaga Carlos, Campion Dominique, Nicolas Gaël, Richard Anne-Claire, Guerreiro Rita, Bras Jose T, Zuchner Stephan, Gonzalez Michael A, Bu Guojun, Younkin Steven, Knopman David S, Josephs Keith A, Parisi Joseph E, Petersen Ronald C, Ertekin-Taner Nilüfer, Graff-Radford Neill R, Boeve Bradley F, Dickson Dennis W, Rademakers Rosa

机构信息

Department of Neuroscience, Mayo Clinic, Jacksonville, FL, USA.

Division of Biomedical Statistics and Informatics, Mayo Clinic, Jacksonville, FL, USA.

出版信息

Neurobiol Aging. 2016 Dec;48:222.e9-222.e15. doi: 10.1016/j.neurobiolaging.2016.07.028. Epub 2016 Aug 8.

Abstract

We aimed to identify new candidate genes potentially involved in early-onset Alzheimer's disease (EOAD). Exome sequencing was conducted on 45 EOAD patients with either a family history of Alzheimer's disease (AD, <65 years) or an extremely early age at the onset (≤55 years) followed by multiple variant filtering according to different modes of inheritance. We identified 29 candidate genes potentially involved in EOAD, of which the gene TYROBP, previously implicated in AD, was selected for genetic and functional follow-up. Using 3 patient cohorts, we observed rare coding TYROBP variants in 9 out of 1110 EOAD patients, whereas no such variants were detected in 1826 controls (p = 0.0001), suggesting that at least some rare TYROBP variants might contribute to EOAD risk. Overexpression of the p.D50_L51ins14 TYROBP mutant led to a profound reduction of TREM2 expression, a well-established risk factor for AD. This is the first study supporting a role for genetic variation in TYROBP in EOAD, with in vitro support for a functional effect of the p.D50_L51ins14 TYROBP mutation on TREM2 expression.

摘要

我们旨在鉴定可能与早发性阿尔茨海默病(EOAD)相关的新候选基因。对45例有阿尔茨海默病(AD,<65岁)家族史或发病年龄极早(≤55岁)的EOAD患者进行了外显子组测序,随后根据不同的遗传模式进行了多重变异筛选。我们鉴定出29个可能与EOAD相关的候选基因,其中先前已被证明与AD有关的TYROBP基因被选作遗传和功能后续研究对象。利用3个患者队列,我们在1110例EOAD患者中的9例中观察到罕见的TYROBP编码变异,而在1826例对照中未检测到此类变异(p = 0.0001),这表明至少某些罕见的TYROBP变异可能会增加EOAD风险。p.D50_L51ins14 TYROBP突变体的过表达导致TREM2表达显著降低,TREM2是一种公认的AD风险因素。这是第一项支持TYROBP基因变异在EOAD中起作用的研究,并在体外证实了p.D50_L51ins14 TYROBP突变对TREM2表达的功能影响。

相似文献

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TYROBP genetic variants in early-onset Alzheimer's disease.早发性阿尔茨海默病中的TYROBP基因变异
Neurobiol Aging. 2016 Dec;48:222.e9-222.e15. doi: 10.1016/j.neurobiolaging.2016.07.028. Epub 2016 Aug 8.

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