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p53 in worms

Jonathan B Weitzman

Author Affiliations

Genome Biology 2001, 2:spotlight-20010914-01  doi:10.1186/gb-spotlight-20010914-01

The electronic version of this article is the complete one and can be found online at:


Published:14 September 2001

© 2001 BioMed Central Ltd

Research news

Early analysis of the Caenorhabditis elegans genome failed to detect a gene resembling the important mammalian tumour suppressor gene p53. In the September 13 ScienceXpress, Brent Derry and colleagues at the University of California, Santa Barbara report that there is a nematode p53 orthologue that is involved in apoptosis and the stress response (zdoi;10.1126/science.1065486). They named the gene cep-1 (C. elegans p53-like 1). Disrupting cep-1 expression (by mutation or RNAi experiments) had no affect on developmental cell death, but rendered germline cells resistant to apoptosis induced by ionizing radiation. Like the Drosophila homologue, C. elegans p53 seems not to be involved in cell-cycle arrest. Overexpression of CEP-1 caused caspase (ced3)-independent cell death and lethality. These results offer a system to screen for genetic modifiers of the p53 pathway.

References

  1. Comparative genomics of the eukaryotes

    PubMed Abstract | Publisher Full Text OpenURL

  2. [http://www.sciencexpress.org] webcite

    ScienceXpress

  3. [http://www.ucsb.edu] webcite

    University of California, Santa Barbara

  4. Drosophila p53 is a structural and functional homolog of the tumor suppressor p53.

    PubMed Abstract | Publisher Full Text OpenURL