| Literature DB >> 10882128 |
Abstract
Loss-of-function mutations in the gene ced-8 lead to the late appearance of cell corpses during embryonic development in C. elegans. ced-8 functions downstream of or in parallel to-the regulatory cell death gene ced-9 and may function as a cell death effector downstream of the caspase encoded by the programmed cell death killer gene ced-3. In ced-8 mutants, embryonic programmed cell death probably initiates normally but proceeds slowly. ced-8 encodes a transmembrane protein that appears to be localized to the plasma membrane. The CED-8 protein is similar to human XK, a putative membrane transport protein implicated in McLeod Syndrome, a form of hereditary neuroacanthocytosis.Entities:
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Year: 2000 PMID: 10882128 DOI: 10.1016/s1097-2765(00)80437-2
Source DB: PubMed Journal: Mol Cell ISSN: 1097-2765 Impact factor: 17.970