-
- Comment in:
-
Cell. 2004 Jan 23;116(2 Suppl):S53-6, 1 p following S59.
The C. elegans cell death gene ced-3 encodes a protein similar to mammalian interleukin-1 beta-converting enzyme.
Program of Neurosciences, Harvard Medical School, Boston, Massachusetts 02115.
We have cloned the C. elegans cell death gene ced-3. A ced-3 transcript is most abundant during embryogenesis, the stage during which most programmed cell deaths occur. The predicted CED-3 protein shows similarity to human and murine interleukin-1 beta-converting enzyme and to the product of the mouse nedd-2 gene, which is expressed in the embryonic brain. The sequences of 12 ced-3 mutations as well as the sequences of ced-3 genes from two related nematode species identify sites of potential functional importance. We propose that the CED-3 protein acts as a cysteine protease in the initiation of programmed cell death in C. elegans and that cysteine proteases also function in programmed cell death in mammals.
PMID: 8242740 [PubMed - indexed for MEDLINE]
-
Cited by over 100 PubMed Central articles
-
The function of a spindle checkpoint gene bub-1 in C. elegans development.
Wang X, Liu M, Li W, Suh CD, Zhu Z, Jin Y, Fan Q.
PLoS One. 2009 Jun 15; 4(6):e5912. Epub 2009 Jun 15.
[PLoS One. 2009]
-
Bicaudal is a conserved substrate for Drosophila and mammalian caspases and is essential for cell survival.
Creagh EM, Brumatti G, Sheridan C, Duriez PJ, Taylor RC, Cullen SP, Adrain C, Martin SJ.
PLoS One. 2009; 4(3):e5055. Epub 2009 Mar 30.
[PLoS One. 2009]
-
A caspase homolog keeps CED-3 in check.
Brady GF, Duckett CS.
Trends Biochem Sci. 2009 Mar; 34(3):104-7. Epub 2009 Jan 23.
[Trends Biochem Sci. 2009]
- » See all...