Myocyte-specific enhancer factor 2A is essential for zebrafish posterior somite development
- Wang, Y., Qian, L., Dong, Y., Jiang, Q., Gui, Y., Zhong, T.P., and Song, H.
- Mechanisms of Development 123(10): 783-791 (Journal)
- Registered Authors
- Dong, Yongxin, Jiang, Qiu, Qian, Linxi, Song, Houyan, Wang, Yuexiang, Zhong, Tao P.
- MEF2A, Somite, Development, Morpholino, Morphant, Microarray, Danio rerio
- MeSH Terms
- Body Patterning
- Gene Expression Profiling
- Hedgehog Proteins/genetics
- Hedgehog Proteins/metabolism
- MEF2 Transcription Factors
- Myogenic Regulatory Factors/genetics
- Myogenic Regulatory Factors/metabolism*
- Oligonucleotide Array Sequence Analysis
- Oligonucleotides, Antisense/genetics
- Oligonucleotides, Antisense/metabolism
- Signal Transduction/physiology
- Zebrafish*/anatomy & histology
- 16942865 Full text @ Mech. Dev.
Wang, Y., Qian, L., Dong, Y., Jiang, Q., Gui, Y., Zhong, T.P., and Song, H. (2006) Myocyte-specific enhancer factor 2A is essential for zebrafish posterior somite development. Mechanisms of Development. 123(10):783-791.
Somite development is governed tightly by genetic factors. In the large-scale mutagenesis screens of zebrafish, no mutations were linked to myocyte enhancer factor 2A (MEF2A) locus. In this study, we find that MEF2A knock-down embryos display a downward tail curvature and have U-shaped posterior somites. Furthermore, we demonstrate that MEF2A is required for Hedgehog signaling. MEF2A inhibition results in induction of apoptosis in the posterior somites. We further find that Hedgehog signaling can negatively regulate MEF2A expression in the somites. Microarray studies reveal a number of genes that are differentially expressed in the MEF2A morphants. Our studies suggest that MEF2A is essential for zebrafish posterior somite development.
Genes / Markers
Mutations / Transgenics
Human Disease / Model
Sequence Targeting Reagents
Engineered Foreign Genes