A subset of p53-deficient embryos exhibit exencephaly
- 1 June 1995
- journal article
- Published by Springer Nature in Nature Genetics
- Vol. 10 (2) , 175-180
- https://doi.org/10.1038/ng0695-175
Abstract
Defects in neural tube formation are among the most common malformations leading to infant mortality. Although numerous genetic loci appear to contribute to the defects observed in humans and in animal model systems, few of the genes involved have been characterized at the molecular level. Mice lacking the p53 tumour suppressor gene are predisposed to tumours, but the viability of these animals indicates that p53 function is not essential for embryonic development. Here, we demonstrate that a fraction of p53-deficient embryos in fact do not develop normally. These animals display defects in neural tube closure resulting in an overgrowth of neural tissue in the region of the mid-brain, a condition known as exencephaly.Keywords
This publication has 35 references indexed in Scilit:
- p53-Dependent apoptosis suppresses tumor growth and progression in vivoCell, 1994
- Abrogation of oncogene-associated apoptosis allows transformation of p53-deficient cells.Proceedings of the National Academy of Sciences, 1994
- Clinical Implications of the p53 Tumor-Suppressor GeneNew England Journal of Medicine, 1993
- p53-dependent apoptosis modulates the cytotoxicity of anticancer agentsCell, 1993
- Thymocyte apoptosis induced by p53-dependent and independent pathwaysNature, 1993
- Wild-type p53 mediates apoptosis by E1A, which is inhibited by E1B.Genes & Development, 1993
- p53 is required for radiation-induced apoptosis in mouse thymocytesNature, 1993
- A mammalian cell cycle checkpoint pathway utilizing p53 and GADD45 is defective in ataxia-telangiectasiaCell, 1992
- Induction of apoptosis by wild-type p53 in a human colon tumor-derived cell line.Proceedings of the National Academy of Sciences, 1992
- Wild-type p53 induces apoptosis of myeloid leukaemic cells that is inhibited by interleukin-6Nature, 1991