Reference : Seizures, sensorineural deafness, ataxia, mental retardation, and electrolyte imbalance ...
Scientific journals : Article
Human health sciences : Neurology
http://hdl.handle.net/2268/110939
Seizures, sensorineural deafness, ataxia, mental retardation, and electrolyte imbalance (SeSAME syndrome) caused by mutations in KCNJ10.
English
Scholl, Ute I [> > > >]
Choi, Murim [> > > >]
Liu, Tiewen [> > > >]
RAMAEKERS, Vincent mailto [Centre Hospitalier Universitaire de Liège - CHU > > Pédiatrie]
Hausler, Martin G [> > > >]
Grimmer, Joanne [> > > >]
Tobe, Sheldon W [> > > >]
Farhi, Anita [> > > >]
Nelson-Williams, Carol [> > > >]
Lifton, Richard P [> > > >]
2009
Proceedings of the National Academy of Sciences of the United States of America
National Academy of Sciences
106
14
5842-7
Yes (verified by ORBi)
International
0027-8424
1091-6490
Washington
DC
[en] Abnormalities, Multiple/etiology/genetics ; Animals ; Ataxia ; Chromosomes, Human, Pair 1 ; Hearing Loss, Sensorineural/genetics ; Humans ; Intellectual Disability/genetics ; Mice ; Mice, Knockout ; Mutation ; Potassium Channels, Inwardly Rectifying/deficiency/genetics/physiology ; Seizures/genetics ; Syndrome ; Tissue Distribution ; Water-Electrolyte Balance/genetics
[en] We describe members of 4 kindreds with a previously unrecognized syndrome characterized by seizures, sensorineural deafness, ataxia, mental retardation, and electrolyte imbalance (hypokalemia, metabolic alkalosis, and hypomagnesemia). By analysis of linkage we localize the putative causative gene to a 2.5-Mb segment of chromosome 1q23.2-23.3. Direct DNA sequencing of KCNJ10, which encodes an inwardly rectifying K(+) channel, identifies previously unidentified missense or nonsense mutations on both alleles in all affected subjects. These mutations alter highly conserved amino acids and are absent among control chromosomes. Many of these mutations have been shown to cause loss of function in related K(+) channels. These findings demonstrate that loss-of-function mutations in KCNJ10 cause this syndrome, which we name SeSAME. KCNJ10 is expressed in glia in the brain and spinal cord, where it is believed to take up K(+) released by neuronal repolarization, in cochlea, where it is involved in the generation of endolymph, and on the basolateral membrane in the distal nephron. We propose that KCNJ10 is required in the kidney for normal salt reabsorption in the distal convoluted tubule because of the need for K(+) recycling across the basolateral membrane to enable normal activity of the Na(+)-K(+)-ATPase; loss of this function accounts for the observed electrolyte defects. Mice deficient for KCNJ10 show a related phenotype with seizures, ataxia, and hearing loss, further supporting KCNJ10's role in this syndrome. These findings define a unique human syndrome, and establish the essential role of basolateral K(+) channels in renal electrolyte homeostasis.
Leducq transatlantic network in hypertension and the Yale O'Brien center
http://hdl.handle.net/2268/110939
10.1073/pnas.0901749106

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