Редактирование: GJB6 (раздел)

==Publications==

{{medline-entry
|title=The human deafness-associated connexin 30 T5M mutation causes mild hearing loss and reduces biochemical coupling among cochlear non-sensory cells in knock-in mice.
|pubmed-url=https://pubmed.ncbi.nlm.nih.gov/20858605
|abstract=Mutations in the [[GJB2]] and [[GJB6]] genes, respectively, coding for connexin26 (Cx26) and connexin30 (Cx30) proteins, are the most common cause for prelingual non-syndromic deafness in humans. In the inner ear, Cx26 and Cx30 are expressed in different non-sensory cell types, where they largely co-localize and may form heteromeric gap junction channels. Here, we describe the generation and characterization of a mouse model for human bilateral middle/high-frequency hearing loss based on the substitution of an evolutionarily conserved threonine by a methionine residue at position 5 near the N-terminus of Cx30 (Cx30T5M). The mutation was inserted in the mouse genome by homologous recombination in mouse embryonic stem cells. Expression of the mutated Cx30T5M protein in these transgenic mice is under the control of the endogenous Cx30 promoter and was analysed via activation of the lacZ reporter gene. When probed by auditory brainstem recordings, Cx30(T5M/T5M) mice exhibited a mild, but significant increase in their hearing thresholds of about 15 dB at all frequencies. Immunolabelling with antibodies to Cx26 or Cx30 suggested normal location of these proteins in the adult inner ear, but western blot analysis showed significantly down-regulated the expression levels of Cx26 and Cx30. In the developing cochlea, electrical coupling, probed by dual patch-clamp recordings, was normal. However, transfer of the fluorescent tracer calcein between cochlear non-sensory cells was reduced, as was intercellular Ca(2 ) signalling due to spontaneous ATP release from connexin hemichannels. Our findings link hearing loss to decreased biochemical coupling due to the point-mutated Cx30 in mice.
|mesh-terms=* Adenosine Triphosphate
* Aging
* Animals
* Calcium Signaling
* Cochlea
* Connexin 30
* Connexins
* Deafness
* Evoked Potentials, Auditory, Brain Stem
* Fluorescence Recovery After Photobleaching
* Gene Knock-In Techniques
* Hearing Loss, Bilateral
* Humans
* Immunoblotting
* Mice
* Mutation
* Organ of Corti
* Permeability
* Recombination, Genetic

|full-text-url=https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2989887
}}