PUBLICATION

Mvda is required for zebrafish early development

Authors
Wong, W., Huang, Y., Wu, Z., Kong, Y., Luan, J., Zhang, Q., Pan, J., Yan, K., Zhang, Z.
ID
ZDB-PUB-210601-2
Date
2021
Source
Biological research   54: 17 (Journal)
Registered Authors
Keywords
Angiogenesis, Epidermis, Mevalonate pathway, Mvda, Zebrafish
MeSH Terms
  • Animals
  • Animals, Genetically Modified
  • Cell Differentiation
  • Humans
  • Morphogenesis/genetics
  • Phenotype
  • Zebrafish*/genetics
PubMed
34051853 Full text @ Biol. Res.
Abstract
The MVD gene mutations are identified in porokeratosis, which is considered a skin-specific autoinflammatory keratinization disease. However, the biological function of MVD gene remains largely unknown. Therefore, we analyzed the function of mvda gene, orthologous to the human MVD gene, in developing zebrafish.
Morpholino antisense oligonucleotide technique was used to generate mvda loss-of-function phenotypes. Knockdown of mvda was confirmed by RT-PCR and Sanger sequencing. Scanning and transmission electron microscopy were performed to analyze the morphology of the epidermis. Angiogenesis study was presented using the Tg(fli1a:EGFP)y1 transgenic strain. In addition, acridine orange staining was used to examine the apoptotic cells in vivo.
As expected, the mvda morphants showed abnormal morphology of the epidermis. Moreover, we observed ectopic sprouts in trunk angiogenesis and impaired formation of the caudal vein plexus in the mvda-deficient zebrafish. Besides, increased apoptosis was found throughout the tail, heart, and eyes in mvda zebrafish morphants.
These findings indicated the essential role of mvda in the early development of zebrafish. This was the first in vivo knockdown study of the zebrafish mvda gene, which might offer insight into the biological function of the human MVD gene.
Genes / Markers
Figures
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Expression
Phenotype
Mutations / Transgenics
Human Disease / Model
Sequence Targeting Reagents
Fish
Antibodies
Orthology
Engineered Foreign Genes
Mapping