학술논문
Alterations in the ankyrin domain of TRPV4 cause congenital distal SMA, scapuloperoneal SMA and HMSN2C.
Document Type
Article
Author
Auer-Grumbach, Michaela; Olschewski, Andrea; Papić, Lea; Kremer, Hannie; McEntagart, Meriel E.; Uhrig, Sabine; Fischer, Carina; Fröhlich, Eleonore; Bálint, Zoltán; Bi Tang; Strohmaier, Heimo; Lochmüller, Hanns; Schlotter-Weigel, Beate; Senderek, Jan; Krebs, Angelika; Dick, Katherine J.; Petty, Richard; Longman, Cheryl; Anderson, Neil E.; Padberg, George W.
Source
Subject
*SPINAL muscular atrophy
*PERIPHERAL neuropathy
*GENETIC disorders
*NEURODEGENERATION
*MUSCLE cells
*PHENOTYPES
*CHROMOSOMES
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Language
ISSN
1061-4036
Abstract
Spinal muscular atrophies (SMA, also known as hereditary motor neuropathies) and hereditary motor and sensory neuropathies (HMSN) are clinically and genetically heterogeneous disorders of the peripheral nervous system. Here we report that mutations in the TRPV4 gene cause congenital distal SMA, scapuloperoneal SMA, HMSN 2C. We identified three missense substitutions (R269H, R315W and R316C) affecting the intracellular N-terminal ankyrin domain of the TRPV4 ion channel in five families. Expression of mutant TRPV4 constructs in cells from the HeLa line revealed diminished surface localization of mutant proteins. In addition, TRPV4-regulated Ca2+ influx was substantially reduced even after stimulation with 4αPDD, a TRPV4 channel-specific agonist, and with hypo-osmotic solution. In summary, we describe a new hereditary channelopathy caused by mutations in TRPV4 and present evidence that the resulting substitutions in the N-terminal ankyrin domain affect channel maturation, leading to reduced surface expression of functional TRPV4 channels. [ABSTRACT FROM AUTHOR]