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神经疾病中的氨酰-tRNA合成酶缺陷

Aminoacyl-tRNA synthetase defects in neurological diseases.

作者信息

Zhang Hong, Ling Jiqiang

机构信息

Department of Cell Biology and Molecular Genetics, The University of Maryland, College Park, Maryland, USA.

出版信息

IUBMB Life. 2025 Jan;77(1):e2924. doi: 10.1002/iub.2924. Epub 2024 Nov 2.

DOI:10.1002/iub.2924
PMID:39487674
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11611227/
Abstract

Aminoacyl-tRNA synthetases (aaRSs) are essential enzymes to support protein synthesis in all organisms. Recent studies, empowered by advancements in genome sequencing, have uncovered an increasing number of disease-causing mutations in aaRSs. Monoallelic aaRS mutations typically lead to dominant peripheral neuropathies such as Charcot-Marie-Tooth (CMT) disease, whereas biallelic aaRS mutations often impair the central nervous system (CNS) and cause neurodevelopmental disorders. Here, we review recent progress in the disease onsets, molecular basis, and potential therapies for diseases caused by aaRS mutations, with a focus on biallelic mutations in cytoplasmic aaRSs.

摘要

氨酰-tRNA合成酶(aaRSs)是支持所有生物体蛋白质合成的必需酶。最近,受基因组测序技术进步的推动,研究发现aaRSs中越来越多的致病突变。单等位基因aaRS突变通常导致诸如夏科-马里-图思(CMT)病等显性周围神经病,而双等位基因aaRS突变往往损害中枢神经系统(CNS)并导致神经发育障碍。在此,我们综述了由aaRS突变引起的疾病在发病机制、分子基础和潜在治疗方法方面的最新进展,重点关注细胞质aaRSs中的双等位基因突变。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d845/11611227/72b4e0df7076/IUB-77-0-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d845/11611227/2af12b9b4b83/IUB-77-0-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d845/11611227/72b4e0df7076/IUB-77-0-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d845/11611227/2af12b9b4b83/IUB-77-0-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d845/11611227/72b4e0df7076/IUB-77-0-g002.jpg

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tRNA Dysregulation in Neurodevelopmental and Neurodegenerative Diseases.神经发育和神经退行性疾病中的转运RNA失调
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Recessive aminoacyl-tRNA synthetase disorders: lessons learned from disease models.隐性氨酰-tRNA合成酶疾病:从疾病模型中获得的经验教训。
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