נגישות
menu      
חיפוש מתקדם
תחביר
חפש...
הספר "אוצר וולקני"
אודות
תנאי שימוש
ניהול
קהילה:
אסיף מאגר המחקר החקלאי
פותח על ידי קלירמאש פתרונות בע"מ -
Microcephaly-dystonia due to mutated PLEKHG2 with impaired actin polymerization
Year:
2016
Source of publication :
Neurogenetics
Authors :
צינמון, יובל
;
.
Volume :
17
Co-Authors:
Edvardson, S., Monique and Jacques Roboh Department of Genetic Research, Hadassah-Hebrew University Medical Center, Jerusalem, Israel, Pediatric Neurology Unit, Hadassah-Hebrew University Medical Center, Jerusalem, Israel
Wang, H., Department of Pharmacology, Roy J. and Lucille A. Carver College of Medicine, University of Iowa, Iowa City, IA, United States, Department of Internal Medicine, Roy J. and Lucille A. Carver College of Medicine, University of Iowa, Iowa City, IA, United States
Dor, T., Pediatric Neurology Unit, Hadassah-Hebrew University Medical Center, Jerusalem, Israel
Atawneh, O., Department of Pediatrics, Palestinian Red Cross Society Hospital, Hebron, Palestine
Yaacov, B., Monique and Jacques Roboh Department of Genetic Research, Hadassah-Hebrew University Medical Center, Jerusalem, Israel
Gartner, J., Department of Pediatrics and Adolescent Medicine, Division of Pediatric Neurology, University Medical Center, Göttingen, Germany
Cinnamon, Y., Monique and Jacques Roboh Department of Genetic Research, Hadassah-Hebrew University Medical Center, Jerusalem, Israel
Chen, S., Department of Pharmacology, Roy J. and Lucille A. Carver College of Medicine, University of Iowa, Iowa City, IA, United States, Department of Internal Medicine, Roy J. and Lucille A. Carver College of Medicine, University of Iowa, Iowa City, IA, United States
Elpeleg, O., Monique and Jacques Roboh Department of Genetic Research, Hadassah-Hebrew University Medical Center, Jerusalem, Israel
Facilitators :
From page:
25
To page:
30
(
Total pages:
6
)
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. © 2015, Springer-Verlag Berlin Heidelberg.
Note:
Related Files :
Actin
Dystonia
Microcephaly
PLEKHG2
עוד תגיות
תוכן קשור
More details
DOI :
10.1007/s10048-015-0464-y
Article number:
Affiliations:
Database:
סקופוס
Publication Type:
מאמר
;
.
Language:
אנגלית
Editors' remarks:
ID:
21350
Last updated date:
02/03/2022 17:27
Creation date:
16/04/2018 23:43
Scientific Publication
Microcephaly-dystonia due to mutated PLEKHG2 with impaired actin polymerization
17
Edvardson, S., Monique and Jacques Roboh Department of Genetic Research, Hadassah-Hebrew University Medical Center, Jerusalem, Israel, Pediatric Neurology Unit, Hadassah-Hebrew University Medical Center, Jerusalem, Israel
Wang, H., Department of Pharmacology, Roy J. and Lucille A. Carver College of Medicine, University of Iowa, Iowa City, IA, United States, Department of Internal Medicine, Roy J. and Lucille A. Carver College of Medicine, University of Iowa, Iowa City, IA, United States
Dor, T., Pediatric Neurology Unit, Hadassah-Hebrew University Medical Center, Jerusalem, Israel
Atawneh, O., Department of Pediatrics, Palestinian Red Cross Society Hospital, Hebron, Palestine
Yaacov, B., Monique and Jacques Roboh Department of Genetic Research, Hadassah-Hebrew University Medical Center, Jerusalem, Israel
Gartner, J., Department of Pediatrics and Adolescent Medicine, Division of Pediatric Neurology, University Medical Center, Göttingen, Germany
Cinnamon, Y., Monique and Jacques Roboh Department of Genetic Research, Hadassah-Hebrew University Medical Center, Jerusalem, Israel
Chen, S., Department of Pharmacology, Roy J. and Lucille A. Carver College of Medicine, University of Iowa, Iowa City, IA, United States, Department of Internal Medicine, Roy J. and Lucille A. Carver College of Medicine, University of Iowa, Iowa City, IA, United States
Elpeleg, O., Monique and Jacques Roboh Department of Genetic Research, Hadassah-Hebrew University Medical Center, Jerusalem, Israel
Microcephaly-dystonia due to mutated PLEKHG2 with impaired actin polymerization
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. © 2015, Springer-Verlag Berlin Heidelberg.
Scientific Publication
You may also be interested in