PUBLICATION

The physiological characterization of Connexin41.8 and Connexin39.4, which are involved in the stripe pattern formation of zebrafish

Authors
Watanabe, M., Sawada, R., Aramaki, T., Skerrett, I.M., Kondo, S.
ID
ZDB-PUB-151125-6
Date
2016
Source
The Journal of biological chemistry   291(3): 1053-63 (Journal)
Registered Authors
Kondo, Shigeru, Watanabe, Masakatsu
Keywords
connexin, connexon (hemichannel), electrophysiology, gap junction, skin pattern, stripe, transgenic, zebrafish
MeSH Terms
  • Amino Acid Sequence
  • Amino Acid Substitution
  • Animals
  • Animals, Genetically Modified
  • Connexins/chemistry
  • Connexins/genetics
  • Connexins/metabolism*
  • Electrophysiological Phenomena
  • Female
  • Gap Junctions/physiology*
  • Gene Deletion
  • Gene Transfer Techniques
  • In Vitro Oocyte Maturation Techniques/veterinary
  • Male
  • Molecular Sequence Data
  • Mutation
  • Oocytes/cytology
  • Oocytes/metabolism
  • Patch-Clamp Techniques
  • Phylogeny
  • Recombinant Proteins/metabolism
  • Sequence Alignment
  • Skin Pigmentation*
  • Zebrafish/genetics
  • Zebrafish/physiology*
  • Zebrafish Proteins/chemistry
  • Zebrafish Proteins/genetics
  • Zebrafish Proteins/metabolism*
PubMed
26598520 Full text @ J. Biol. Chem.
Abstract
The zebrafish has a stripe skin pattern on its body, and Connexin41.8 (Cx41.8) and Cx39.4 are involved in stripe pattern formation. Mutations in these connexins change the stripe pattern to a spot or labyrinth pattern. In this study, we characterized Cx41.8 and Cx39.4 after expression in Xenopus oocytes. In addition, we analyzed Cx41.8 mutants Cx41.8I203F and Cx41.8M7, which caused spot or labyrinth skin patterns respectively in transgenic zebrafish. In the electrophysiological analysis, the gap junctions formed by Cx41.8 and Cx39.4 showed distinct sensitivity to transjunctional voltage. Analysis of non-junctional (hemichannel) currents revealed a large voltage-dependent current in Cx39.4-expressing oocytes that was absent in cells expressing Cx41.8. Junctional currents induced by both Cx41.8 and Cx39.4 were reduced by co-expression of Cx41.8I203F and abolished by co-expression of Cx41.8M7. In the transgenic experiment, Cx41.8I203F partially rescued the Cx41.8 null mutant phenotype, whereas Cx41.8M7 failed to rescue the null mutant, and it elicited a more severe phenotype than the Cx41.8 null mutant, as evidenced by a smaller spot pattern. Our results provide evidence that gap junctions formed by Cx41.8 play an important role in stripe/spot patterning and suggest that mutations in Cx41.8 can effect patterning by way of reduced function (I203F) and dominant negative effects (M7). Our results suggest that functional differences in Cx41.8 and Cx39.4 relate to spot or labyrinth mutant phenotypes and also provide evidence for these two connexins interact in vivo and in vitro.
Genes / Markers
Figures
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Expression
Phenotype
Mutations / Transgenics
Human Disease / Model
Sequence Targeting Reagents
Fish
Antibodies
Orthology
Engineered Foreign Genes
Mapping