The Mdm2 protein is most probably the main negative cellular regulator of the p53 turner-suppressor protein. It was found to be overexpressed in a great number of human tumors and is considered as a potential target for anti-tumor therapies. Mdm2 is an essential gene in mice, yet its role in normal development and tissue differentiation is unknown. In order to study the role of this important protein in an evolutionary perspective, we cloned atl Mdm2 cDNA from the fish Danio rerio and analyzed its expression pattern as well as the phenotypic consequences of its overexpression. The main functional domains as well as the interaction between Mdm2 and p53 are conserved in zebrafish. Moreover, we show here that the gene is expressed specifically during early development in neural and muscular tissues. Surprisingly, microinjection of Mdm2 mRNA in two-cell-stage embryos led to inhibition of cellular convergence during gastrulation. The clones derived from Mdma microinjected blastomeres were significantly smaller than those derived from control microinjections, and, in contrast to what was observed in Xenopus, did not develop tumors. Our results suggest that Mdm2 expression may be important during the differentiation of neural and muscular tissues of zebrafish. They also point to important differences between phyla in the susceptibility to tumor formation.
The Mdm2 gene of zebrafish (Danio rerio): preferential expression duping development of neural and muscular tissues, and absence of tumor formation after overexpression of its cDNA during early embryogenesis
Thisse, C.; Neel, H.; Thisse, B.; Daujat, S.; Piette, J.
2000-10 / vol 66 / pages 61-70
activation; mdm2; p53; differentiation; development; amplification; cell-death; embryonic lethality; mdm2-deficient mice; no tail; oncogenesis; oncoprotein; p53 protein; wild-type; zebrafish