MPZL2, encoding the epithelial junctional protein myelin protein zero-like 2, is essential for hearing in man and mouse.
Am. J. Hum. Genet. 103, 74-88 (2018)
In a Dutch consanguineous family with recessively inherited nonsyndromic hearing impairment (HI), homozygosity mapping combined with whole-exome sequencing revealed a MPZL2 homozygous truncating variant, c.72del(p.Ile24Metfs*22). By screening a cohort of phenotype-matched subjects and a cohort of HI subjects in whom WES had been performed previously, we identified two additional families with biallelic truncating variants of MPZL2. Affected individuals demonstrated symmetric, progressive, mild to moderate sensorineural HI. Onset of HI was in the first decade, and high-frequency hearing was more severely affected. There was no vestibular involvement. MPZL2 encodes myelin protein zero-like 2, an adhesion molecule that mediates epithelial cell-cell interactions in several (developing) tissues. Involvement of MPZL2 in hearing was confirmed by audiometric evaluation of Mpzl2-mutant mice. These displayed early-onset progressive sensorineural HI that was more pronounced in the high frequencies. Histological analysis of adult mutant mice demonstrated an altered organization of outer hair cells and supporting cells and degeneration of the organ of Corti. In addition, we observed mild degeneration of spiral ganglion neurons, and this degeneration was most pronounced at the cochlear base. Although MPZL2 is known to function in cell adhesion in several tissues, no phenotypes other than HI were found to be associated with MPZL2 defects. This indicates that MPZL2 has a unique function in the inner ear. The present study suggests that deleterious variants of Mplz2/MPZL2 affect adhesion of the inner-ear epithelium and result in loss of structural integrity of the organ of Corti and progressive degeneration of hair cells, supporting cells, and spiral ganglion neurons.
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Publikationstyp Artikel: Journalartikel
Dokumenttyp Wissenschaftlicher Artikel
Schlagwörter Deiters Cells ; Mpzl2 ; Cochlea ; Deafness ; Hair Cells ; Hearing Impairment ; Human ; Mouse; Recessive Deafness Dfnb29; Outer Hair Cell; Sensory Neuropathy; Gene-expression; Immunoglobulin Superfamily; Adhesion Molecule; Hereditary Motor; Dejerine-sottas; Antigen Eva; E-cadherin
ISSN (print) / ISBN 0002-9297
Zeitschrift American Journal of Human Genetics, The
Quellenangaben Band: 103, Heft: 1, Seiten: 74-88
Verlag Elsevier ; Cell Press
Verlagsort New York, NY
Institut(e) Institute of Human Genetics (IHG)