Exome sequencing identifies novel genes associated with cerebellar volume and microstructure

Proteins encoded by exons are critical for cellular functions, and mutations in these genes often result in significant phenotypic effects. The cerebellum is linked to various heritable human disease phenotypes, yet genome-wide association studies have struggled to capture the effects of rare variants on cerebellar traits. This study conducts a large-scale exome association analysis using data from approximately 35,000 UK Biobank participants, examining seven cerebellar traits, including total cerebellar volume and white matter microstructure. We identify 90 genes associated with cerebellar traits, 60 of which were previously unreported in genome-wide association studies. Notable findings include the discovery of genes like PRKRA and TTK, as well as RASGRP3, linked to cerebellar volume and white matter microstructure. Gene enrichment analysis reveals associations with non-coding RNA processing, cognitive function, neurodegenerative diseases, and mental disorders, suggesting shared biological mechanisms between cerebellar phenotypes and neuropsychiatric diseases.

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Journal
Communications Biology
Published
2025-03-01
DOI
https://doi.org/10.1038/s42003-025-07797-3
Primary Topic
Genetic Syndromes and Imprinting
Type
article
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article

Exome sequencing identifies novel genes associated with cerebellar volume and microstructure

Chunyan Zuo, Changhe Shi, Ole A. Andreassen, Shasha Qi et al.
1 links
Communications Biology
Genetic Syndromes and Imprinting
article

Exome sequencing identifies novel genes associated with cerebellar volume and microstructure

Chunyan Zuo, Changhe Shi, Ole A. Andreassen, Shasha Qi, Yuming Xu, Yunpeng Wang, Mengjie Li, Zhiyun Wang, Yanmei Feng, Xiaoyan Hao, Yuanyuan Liang, Shuangjie Li, Shilei Sun, Chenwei Hao, Yuemeng Sun, Dongrui Ma
article en

Abstract

Proteins encoded by exons are critical for cellular functions, and mutations in these genes often result in significant phenotypic effects. The cerebellum is linked to various heritable human disease phenotypes, yet genome-wide association studies have struggled to capture the effects of rare variants on cerebellar traits. This study conducts a large-scale exome association analysis using data from approximately 35,000 UK Biobank participants, examining seven cerebellar traits, including total cerebellar volume and white matter microstructure. We identify 90 genes associated with cerebellar traits, 60 of which were previously unreported in genome-wide association studies. Notable findings include the discovery of genes like PRKRA and TTK, as well as RASGRP3, linked to cerebellar volume and white matter microstructure. Gene enrichment analysis reveals associations with non-coding RNA processing, cognitive function, neurodegenerative diseases, and mental disorders, suggesting shared biological mechanisms between cerebellar phenotypes and neuropsychiatric diseases.

Communications BiologyVol. 8(1)
University of Oslo (NO), Zhengzhou University (CN), First Affiliated Hospital of Zhengzhou University (CN)
Zero hunger
Openalex Percentile: Top 95%
Genetic Syndromes and Imprinting
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