Butterfield Sarah, Herbst Susanne, Lewis Patrick Alfryn
Department of Comparative Biomedical Sciences, Royal Veterinary College, Camden Town, UK.
Department of Neurodegenerative disease, UCL Queen Square Institute of Neurology, London, UK.
Protein Sci. 2025 Jul;34(7):e70190. doi: 10.1002/pro.70190.
The LRRK2 gene is a key contributor to the genetic risk of Parkinson's disease, and a priority drug target for the disorder. Leucine Rich Repeat Kinase 2, the protein product of LRRK2, is a multidomain enzyme implicated in a range of cellular processes-including endolysosomal trafficking and damage response. Based on the report that truncation and structural variants resulting in loss of LRRK2 protein are observed in human populations, genomic sequence repositories were queried for coding variants affecting key catalytic residues in LRRK2-resulting in the identification of three variants (K1347E, K1347R, and T1348P) predicted to ablate the capacity of LRRK2 to bind GTP. Biochemical and cellular characterization of these variants confirmed loss of GTP binding, as well as reduced or loss of kinase activity. These data demonstrate the presence of rare coding enzymatic loss-of-function variants in humans, with implications for our understanding of LRRK2 as a driver of disease and as a drug target.
LRRK2基因是帕金森病遗传风险的关键因素,也是该疾病的首要药物靶点。LRRK2的蛋白质产物富含亮氨酸重复激酶2是一种多结构域酶,参与一系列细胞过程,包括内溶酶体运输和损伤反应。基于在人群中观察到导致LRRK2蛋白缺失的截短和结构变异的报告,研究人员查询了基因组序列数据库,以寻找影响LRRK2中关键催化残基的编码变异,结果鉴定出三个变异(K1347E、K1347R和T1348P),预计这些变异会消除LRRK2结合GTP的能力。对这些变异的生化和细胞特性分析证实了GTP结合的丧失以及激酶活性的降低或丧失。这些数据表明人类中存在罕见的编码酶功能丧失变异,这对我们理解LRRK2作为疾病驱动因素和药物靶点具有重要意义。