[Frontiers in Bioscience E3, 115-124, January 1, 2011]

Overexpression of p204 leads to abnormal embryos and osteogenesis in zebrafish

Hai-Bin Zhao, Wen-Wen Wang, Zai-Li Luo, Hui-Ren Cao, Yong-Xiang Shi

School of Life Science, Shandong University, Jinan 250100, China

TABLE OF CONTENTS

1. Abstract
2. Introduction
3. Materials and methods
3.1. Larval rearing and maintenance
3.2. Construction of expression plasmids
3.3. Microinjection of Embryos with DNA and observation of GFP expression
3.4. Quantitative real-time PCR
3.5. In situ Hybridization
4. Results
4.1. GFP expression patterns of zebrafish embryos after CMV-post-p204 injection
4.2. Abnormal embryos induced by p204 injection and statistical analysis
4.3. p204 regulates the expression of runx2b, vent, and osn
4.4. p204 injection increases the expression of zebrafish runx2b, assayed by whole-mount in situ hybridization
5. Discussion
5.1. The expression pattern of p204-GFP in zebrafish embryos
5.2. Malformed zebrafish embryos were induced after p204 injection
6. Acknowledgements
6. References

1. ABSTRACT

p204, an inteferon-inducible protein, is known to play an important role in modulating cell proliferation, cell cycling, and the differentiation of various tissues, including osteoblasts. In order to determine the role of p204 during development in vivo, the teleost zebrafish (Danio rerio), an established vertebrate model for developmental studies, was employed. p204 cDNA was introduced into zebrafish by microinjection, and p204 was ectopically expressed throughout the whole embryo during the early stages of zebrafish embryogenesis, then its expression gradually decreased, mainly in ventrally located cells and retina capsules. Importantly, overexpression of p204 in zebrafish resulted in striking malformations such as bent spine and expanded belly. Furthermore, the expressions of some genes (vent, runx2b, osn) involved in dorsoventral patterning and osteogenesis were significantly upregulated after p204 injection. This study provides not only the in vivo evidences demonstrating the role of p204 during embryonic development, but also new insights into the molecular mechanism by which p204 mediate osteogenesis.