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ZFIN ID: ZDB-PUB-060906-26
The physiological role of CTGF/CCN2 in zebrafish notochond development and biological analysis of the proximal promoter region
Chiou, M.J., Chao, T.T., Wu, J.L., Kuo, C.M., and Chen, J.Y.
Date: 2006
Source: Biochemical and Biophysical Research Communications 349(2): 750-758 (Journal)
Registered Authors: Chen, Jyh-Yih, Wu, Jen-Leih
Keywords: Connective tissue growth factor gene, Promoter analysis, Zebrafish, Morpholino
MeSH Terms:
  • Animals
  • Connective Tissue Growth Factor
  • DNA, Complementary/metabolism
  • Exons
  • Gene Expression Regulation, Developmental*
  • Green Fluorescent Proteins/metabolism
  • HeLa Cells
  • Humans
  • Immediate-Early Proteins/biosynthesis
  • Immediate-Early Proteins/physiology*
  • Intercellular Signaling Peptides and Proteins/biosynthesis
  • Intercellular Signaling Peptides and Proteins/physiology*
  • Mice
  • Notochord/metabolism*
  • Promoter Regions, Genetic*
  • Transcription Factors/metabolism
  • Transgenes
  • Zebrafish
PubMed: 16950203 Full text @ Biochem. Biophys. Res. Commun.
FIGURES
ABSTRACT
During mouse embryogenesis, CTGF/CCN2 is expressed in zones containing hypertrophic chondroctyes and calcifying cartilage such as long bones, ribs, vertebral column, and phalanges. But in fish, its expression is yet unclear. Development of the vertebrae is morphologically similar among vertebrates, indicating that the underlying mechanism regulating the process is highly conserved during evolution. Analysis of 3.2kb of the CTGF/CCN2 proximal promoter sequence revealed a consensus TATAA box, putative AP1, Brn-2, CdxA, C/EBP alpha, C/EBP beta, C-Ets-, delta E, HFH-2, and HSF2 binding sites. Transient expression experiments with a 5'-deletion revealed at least 4 regulatory regions in the zebrafish CTGF/CCN2 gene, 2 with a stimulatory effect on transcription and 2 with an apparent inhibitory effect after IGF-I treatment in the ZFL cell line. To study the promoter-specific expression, we constructed a series of CTGF/CCN2 (3.0-, 2.5-, 2.0-, 1.5-, 1.0-, and 0.4-kb) promoter-driven green fluorescent protein (GFP) fragments encoding the GFP cDNA transgene which was microinjected into zebrafish embryos. Morphological studies of transgenic zebrafish indicated that the CTGF/CCN2 promoter-driven GFP transcripts appeared in the notochord. Targeted knockdown of the CTGF/CCN2 gene by two antisense morpholino oligonucleotides resulted in disruptions to notochord development. From a comparative point of view, this study of the CTGF/CCN2 gene in zebrafish may correlate well with those previously published on the mouse. These molecular results suggest that CTGF/CCN2 plays an important role in notochord development and is required for general embryonic development.
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