New VMD2 gene mutations identified in patients affected by Best vitelliform macular dystrophy

Détails

ID Serval
serval:BIB_FB63E6A54C7B
Type
Article: article d'un périodique ou d'un magazine.
Collection
Publications
Titre
New VMD2 gene mutations identified in patients affected by Best vitelliform macular dystrophy
Périodique
Journal of Medical Genetics
Auteur(s)
Marchant  D., Yu  K., Bigot  K., Roche  O., Germain  A., Bonneau  D., Drouin-Garraud  V., Schorderet  D. F., Munier  F., Schmidt  D., Le Neindre  P., Marsac  C., Menasche  M., Dufier  J. L., Fischmeister  R., Hartzell  C., Abitbol  M.
ISSN
1468-6244 (Electronic)
Statut éditorial
Publié
Date de publication
03/2007
Volume
44
Numéro
3
Pages
e70
Notes
Journal Article
Research Support, N.I.H., Extramural
Research Support, Non-U.S. Gov't --- Old month value: Mar
Résumé
PURPOSE: The mutations responsible for Best vitelliform macular dystrophy (BVMD) are found in a gene called VMD2. The VMD2 gene encodes a transmembrane protein named bestrophin-1 (hBest1) which is a Ca(2+)-sensitive chloride channel. This study was performed to identify disease-specific mutations in 27 patients with BVMD. Because this disease is characterised by an alteration in Cl(-) channel function, patch clamp analysis was used to test the hypothesis that one of the VMD2 mutated variants causes the disease. METHODS: Direct sequencing analysis of the 11 VMD2 exons was performed to detect new abnormal sequences. The mutant of hBest1 was expressed in HEK-293 cells and the associated Cl(-) current was examined using whole-cell patch clamp analysis. RESULTS: Six new VMD2 mutations were identified, located exclusively in exons four, six and eight. One of these mutations (Q293H) was particularly severe. Patch clamp analysis of human embryonic kidney cells expressing the Q293H mutant showed that this mutant channel is non-functional. Furthermore, the Q293H mutant inhibited the function of wild-type bestrophin-1 channels in a dominant negative manner. CONCLUSIONS: This study provides further support for the idea that mutations in VMD2 are a necessary factor for Best disease. However, because variable expressivity of VMD2 was observed in a family with the Q293H mutation, it is also clear that a disease-linked mutation in VMD2 is not sufficient to produce BVMD. The finding that the Q293H mutant does not form functional channels in the membrane could be explained either by disruption of channel conductance or gating mechanisms or by improper trafficking of the protein to the plasma membrane.
Mots-clé
Age of Onset Amino Acid Substitution Cell Line Child Child, Preschool Chlorides/metabolism DNA Mutational Analysis Exons/genetics Eye Proteins/*genetics Female Genes, Dominant Humans Ion Transport/genetics Kidney Macular Degeneration/diagnosis/*genetics Male Mutagenesis, Site-Directed Mutant Proteins/*genetics Mutation, Missense Patch-Clamp Techniques Pedigree Point Mutation Protein Structure, Tertiary Recombinant Fusion Proteins/physiology Sequence Analysis, DNA Structure-Activity Relationship Transfection
Pubmed
Web of science
Open Access
Oui
Création de la notice
28/01/2008 12:58
Dernière modification de la notice
20/08/2019 16:26
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