| Literature DB >> 26573021 |
Simon Edvardson1,2, Haibo Wang3,4, Talya Dor2, Osamah Atawneh5, Barak Yaacov1, Jutta Gartner6, Yuval Cinnamon1, Songhai Chen7,8, Orly Elpeleg9.
Abstract
Rearrangement of the actin cytoskeleton is controlled by RhoGTPases which are activated by RhoGEFs. We identified homozygosity for Arg204Trp mutation in the Rho guanidine exchange factor (RhoGEF) PLEKHG2 gene in five patients with profound mental retardation, dystonia, postnatal microcephaly, and distinct neuroimaging pattern. The activity of the mutant PLEKHG2 was significantly decreased, both in basal state and when Gβγ- or lysophosphatidic acid (LPA)-stimulated. SDF1a-stimulated actin polymerization was significantly impaired in patient cells, and this abnormality was duplicated in control cells when PLEKHG2 expression was downregulated. These results underscore the role of PLEKHG2 in actin polymerization and delineate the clinical and radiological findings in PLEKHG2 deficiency.Entities:
Keywords: Actin; Dystonia; Microcephaly; PLEKHG2
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Year: 2015 PMID: 26573021 DOI: 10.1007/s10048-015-0464-y
Source DB: PubMed Journal: Neurogenetics ISSN: 1364-6745 Impact factor: 2.660