PUBLICATION

Microarray analysis of zebrafish cloche mutant using amplified cDNA and identification of potential downstream target genes

Authors
Qian, F., Zhen, F., Ong, C., Jin, S.W., Meng Soo, H., Stainier, D.Y., Lin, S., Peng, J., and Wen, Z.
ID
ZDB-PUB-050607-23
Date
2005
Source
Developmental Dynamics : an official publication of the American Association of Anatomists   233(3): 1163-1172 (Journal)
Registered Authors
Jin, Suk-Won, Lin, Shuo, Peng, Jinrong, Stainier, Didier, Wen, Zilong
Keywords
zebrafish; microarray; hematopoiesis; cloche
MeSH Terms
  • Animals
  • DNA, Complementary/genetics*
  • Down-Regulation
  • Embryo, Nonmammalian/embryology
  • Embryo, Nonmammalian/metabolism
  • Gene Expression Profiling
  • Gene Expression Regulation, Developmental
  • Genotype
  • Homozygote
  • Mutation/genetics*
  • Nucleic Acid Amplification Techniques*
  • Oligonucleotide Array Sequence Analysis*
  • RNA, Messenger/genetics
  • RNA, Messenger/metabolism
  • Somites/metabolism
  • Zebrafish/embryology
  • Zebrafish/genetics*
  • Zebrafish/metabolism
  • Zebrafish Proteins/genetics*
  • Zebrafish Proteins/metabolism*
PubMed
15937927 Full text @ Dev. Dyn.
Abstract
Zebrafish is an excellent model organism for studying vertebrate development and human disease. With the availability of increased numbers of zebrafish mutants and microarray chips, gene expression profiling has become a powerful tool for identification of downstream target genes perturbed by a specific mutation. One of the obstacles often encountered, however, is to isolate large numbers of zebrafish mutant embryos that are indistinguishable in morphology from the wild-type siblings for microarray analysis. Here, we report a method using amplified cDNA derived from five embryos for gene expression profiling of the 18-somite zebrafish cloche (clo) mutant, in which development of hematopoietic and endothelial lineages is severely impaired. In total, 31 differentially expressed target genes are identified, of which 13 have not been reported previously. We further determine that of these 13 new targets, 8 genes, including coproporphyrinogen oxidase (cpo), carbonic anhydrase (cahz), claudin g (cldn g), zinc-finger-like gene 2 (znfl2), neutrophil cytosol factor 1 (ncf1), matrix metalloproteinase 13 (mmp13), dual specificity phosphatase 5 (dusp5), and a novel gene referred as zebrafish vessel-specific gene 1 (zvsg1) are predominantly expressed in hematopoietic and endothelial cells. Comparative analysis demonstrates that this method is comparable and complementary to that of the conventional approach using unamplified sample. Our study provides valuable information for studying hematopoiesis and vessel formation. The method described here offers a powerful tool for gene expression profiling of zebrafish mutants in general. Developmental Dynamics 233:1163-1172, 2005. (c) 2005 Wiley-Liss, Inc.
Genes / Markers
Figures
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Expression
Phenotype
Mutations / Transgenics
Human Disease / Model
Sequence Targeting Reagents
Fish
Antibodies
Orthology
Engineered Foreign Genes
Mapping