PUBLICATION

Molecular cloning and expression of a smooth muscle-specific gene SM22alpha in zebrafish

Authors
Yang, X.Y., Yao, J.H., Cheng, L., Wei, D.W., Xue, J.L., and Lu, D.R.
ID
ZDB-PUB-040113-7
Date
2003
Source
Biochemical and Biophysical Research Communications   312(3): 741-746 (Journal)
Registered Authors
Yang, Xueyan, Yao, Jihua
Keywords
none
MeSH Terms
  • Amino Acid Sequence
  • Animals
  • Cattle
  • Chickens
  • Cloning, Molecular
  • Gene Expression Profiling
  • Gene Expression Regulation, Developmental/physiology*
  • Humans
  • In Situ Hybridization
  • Mice
  • Microfilament Proteins/chemistry
  • Microfilament Proteins/genetics*
  • Microfilament Proteins/metabolism*
  • Molecular Sequence Data
  • Muscle Proteins/chemistry
  • Muscle Proteins/genetics*
  • Muscle Proteins/metabolism*
  • Muscle, Smooth/embryology
  • Muscle, Smooth/metabolism
  • Oligonucleotides, Antisense/genetics
  • Organ Specificity
  • Rats
  • Sequence Homology, Amino Acid
  • Species Specificity
  • Zebrafish/embryology*
  • Zebrafish/metabolism*
PubMed
14680827 Full text @ Biochem. Biophys. Res. Commun.
Abstract
SM22alpha is a kind of 22-kDa protein which is exclusively expressed in smooth muscle containing tissues of the vertebrates. Here we report molecular cloning of a novel zebrafish SM22alpha gene. The full length of zebrafish SM22alpha cDNA is 1296bp and it encodes a polypeptide of 201 amino acids which shares 69.2%, 69.7%, 69.2%, 67.2%, and 61.2% overall identity with human, mouse, rat, chicken, and bovine SM22alpha, respectively. Characterization of zebrafish SM22alpha genomic sequence reveals that it spans 7.7kb and contains five exons and four introns. The expression pattern of SM22alpha in zebrafish embryonic development is studied by whole-mount in situ hybridization. Strong expression is observed in vascular, gut, swim bladder, branchial arches, and fin epidermis. Furthermore, we carry out gene knock-down by antisense morpholino oligonucleotide, which results in disappearance of yolk extension, caudal fin aberrance, and deficiency of circulation system in zebrafish embryo. Cross-section of SM22alpha-deficient embryo suggests that SM22alpha may play roles in smooth muscle cell morphology transform.
Genes / Markers
Figures
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Expression
Phenotype
Mutations / Transgenics
Human Disease / Model
Sequence Targeting Reagents
Fish
Antibodies
Orthology
Engineered Foreign Genes
Mapping