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巴松管蛋白(BSN)中预测的功能丧失等位基因与肥胖有关。

Predicted loss of function alleles in Bassoon (BSN) are associated with obesity.

作者信息

Zhu Na, LeDuc Charles A, Fennoy Ilene, Laferr Re Blandine, Doege Claudia A, Shen Yufeng, Chung Wendy K, Leibel Rudolph L

出版信息

medRxiv. 2023 Feb 23:2023.02.19.23285978. doi: 10.1101/2023.02.19.23285978.

Abstract

Bassoon ( ) is a component of a hetero-dimeric presynaptic cytomatrix protein that orchestrates neurotransmitter release with Piccolo ( ) from glutamatergic neurons throughout the brain. Heterozygous missense variants in have previously been associated with neurodegenerative disorders in humans. We performed an exome-wide association analysis of ultra-rare variants in about 140,000 unrelated individuals from the UK Biobank to search for new genes associated with obesity. We found that rare heterozygous predicted loss of function (pLoF) variants in are associated with higher BMI with log10-p value of 11.78 in the UK biobank cohort. The association was replicated in the All of Us whole genome sequencing data. Additionally, we have identified two individuals (one of whom has a variant) with a heterozygous pLoF variant in a cohort of early onset or extreme obesity at Columbia University. Like the individuals identified in the UKBB and All of us Cohorts, these individuals have no history of neurobehavioral or cognitive disability. Heterozygosity for pLoF variants constitutes a new etiology for obesity.

摘要

巴松管蛋白( )是一种异二聚体突触前细胞基质蛋白的组成部分,它与 piccolo 蛋白( )共同协调全脑谷氨酸能神经元的神经递质释放。此前, 基因中的杂合错义变异与人类神经退行性疾病有关。我们对来自英国生物银行的约 14 万名无亲缘关系个体的超罕见变异进行了全外显子组关联分析,以寻找与肥胖相关的新基因。我们发现,在英国生物银行队列中, 基因中罕见的杂合预测功能丧失(pLoF)变异与较高的体重指数相关,对数 10 - p 值为 11.78。该关联在“我们所有人”全基因组测序数据中得到了重复验证。此外,在哥伦比亚大学的一个早发或极度肥胖队列中,我们鉴定出两名个体(其中一人携带 变异)携带杂合 pLoF 变异。与在英国生物银行和“我们所有人”队列中鉴定出的个体一样,这些个体没有神经行为或认知障碍史。pLoF 变异的杂合性构成了肥胖的一种新病因。

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