PUBLICATION
The Functional Role of CONNEXIN 26 Mutation in Nonsyndromic Hearing Loss, Demonstrated by Zebrafish Connexin 30.3 Homologue Model
- Authors
- Su, H.A., Lai, T.W., Li, S.Y., Su, T.R., Yang, J.J., Su, C.C.
- ID
- ZDB-PUB-200528-5
- Date
- 2020
- Source
- Cells 9(5): (Journal)
- Registered Authors
- Keywords
- CONNEXIN 26, Connexin 30.3, GJB2, behavioral assay, non-syndromic hearing loss, zebrafish
- MeSH Terms
-
- Animals
- Animals, Genetically Modified
- Behavior, Animal
- Biological Assay
- Connexin 26/genetics*
- Connexins/chemistry
- Connexins/genetics*
- Deafness/genetics*
- Disease Models, Animal
- Ear, Inner/metabolism
- Ear, Inner/pathology
- Green Fluorescent Proteins/metabolism
- HeLa Cells
- Humans
- Mutant Proteins/chemistry
- Mutation/genetics*
- Zebrafish/genetics*
- PubMed
- 32455934 Full text @ Cells
Citation
Su, H.A., Lai, T.W., Li, S.Y., Su, T.R., Yang, J.J., Su, C.C. (2020) The Functional Role of CONNEXIN 26 Mutation in Nonsyndromic Hearing Loss, Demonstrated by Zebrafish Connexin 30.3 Homologue Model. Cells. 9(5):.
Abstract
Nonsyndromic hearing loss (NSHL) is of great clinical importance, and mutations in the GJB2 gene and the encoded human CONNEXIN 26 (CX26) protein play important roles in the genetic pathogenesis. The CX26 p.R184Q mutation was shown to be a dominant-negative effect in our previous study. Previously, we also demonstrated that zebrafish Cx30.3 is orthologous to human CX26. In the present study, we established transgenic zebrafish models with mutated Cx30.3 specifically expressed in the supporting cells of zebrafish inner ears driven by the agr2 promoter, to demonstrate and understand the mechanism by which the human CX26 R.184 mutation causes NSHL. Our results indicated that significant structural changes in the inner ears of transgenic lines with mutations were measured and compared to wild-type zebrafish. Simultaneously, significant alterations of transgenic lines with mutations in swimming behavior were analyzed with the zebrafish behavioral assay. This is the first study to investigate the functional results of the CX26 p.R184Q mutation with in vivo disease models. Our work supports and confirms the pathogenic role of the CX26 p.R184Q mutation in NSHL, with a hypothesized mechanism of altered interaction among amino acids in the connexins.
Genes / Markers
Expression
Phenotype
Mutations / Transgenics
Human Disease / Model
Sequence Targeting Reagents
Fish
Orthology
Engineered Foreign Genes
Mapping