Impaired Function is a Common Feature of Neuropathy‐Associated Glycyl‐tRNA Synthetase Mutations. Issue 11 (November 2014)

• Record Type: Journal Article
• Authors: Griffin, Laurie B.; Sakaguchi, Reiko; McGuigan, David; Gonzalez, Michael A.; Searby, Charles; Züchner, Stephan; Hou, Ya‐Ming; Antonellis, Anthony
• Is Part Of: Human mutation. Volume 35:Issue 11(2014:Nov.)
• Page Start: 1363
• Page End: 1371
• Publication Date: 2014-11
• Subjects: Human chromosome abnormalities -- Periodicals; Mutation (Biology) -- Periodicals; 616.04205
• DOI: 10.1002/humu.22681
• Languages: English
• ISSNs: 1059-7794

Abstract

<abstract abstract-type="main"> <title>ABSTRACT</title> <p>Charcot–Marie–Tooth disease type 2D (CMT2D) is an autosomal‐dominant axonal peripheral neuropathy characterized by impaired motor and sensory function in the distal extremities. Mutations in the glycyl‐tRNA synthetase (<italic>GARS</italic>) gene cause CMT2D. GARS is a member of the ubiquitously expressed aminoacyl‐tRNA synthetase (ARS) family and is responsible for charging tRNA with glycine. To date, 13 <italic>GARS</italic> mutations have been identified in patients with CMT disease. While functional studies have revealed loss‐of‐function characteristics, only four <italic>GARS</italic> mutations have been rigorously studied. Here, we report the functional evaluation of nine CMT‐associated <italic>GARS</italic> mutations in tRNA charging, yeast complementation, and subcellular localization assays. Our results demonstrate that impaired function is a common characteristic of CMT‐associated <italic>GARS</italic> mutations. Additionally, one mutation previously associated with CMT disease (p.Ser581Leu) does not demonstrate impaired function, was identified in the general population, and failed to segregate with disease in two newly identified families with CMT disease. Thus, we propose that this variant is not a disease‐causing mutation. Together, our data indicate that impaired function is a key component of <italic>GARS</italic>‐mediated CMT disease and emphasize the need for careful genetic and functional evaluation before implicating a variant in disease onset.</p> </abstract>