TY - JOUR
T1 - Noncanonical cell death programs in the nematode Caenorhabditis elegans
AU - Blum, E. S.
AU - Driscoll, M.
AU - Shaham, S.
N1 - Funding Information:
Acknowledgements. We thank Michael Chiorazzi for comments on the manuscript. ESB is supported in part by The Rockefeller University’s Women & Science Fellowship Program and by a grant from the NIH. MD is supported by NIH grant R01NS034435 and by the NJ Commission on Spinal Cord Research. SS is a Klingenstein fellow in the neurosciences and a Monique Weill-Caulier Scholar. This work was supported in part by a grant from the NIH to SS. We take this opportunity to offer our best wishes to Richard Lockshin, a key figure in developing the concept of programmed cell death, on the occasion of his 70th birthday.
PY - 2008/7
Y1 - 2008/7
N2 - Genetic studies of the nematode Caenorhabditis elegans have uncovered four genes, egl-1 (BH3 only), ced-9 (Bcl-2 related), ced-4 (apoptosis protease activating factor-1), and ced-3 (caspase), which function in a linear pathway to promote developmental cell death in this organism. While this core pathway functions in many cells, recent studies suggest that additional regulators, acting on or in lieu of these core genes, can promote or inhibit the onset of cell death. Here, we discuss the evidence for these noncanonical mechanisms of C. elegans cell death control. We consider novel modes for regulating the core apoptosis genes, and describe a newly identified cell death pathway independent of all known C. elegans cell death genes. The existence of these noncanonical cell death programs suggests that organisms have evolved multiple ways to ensure appropriate cellular demise during development.
AB - Genetic studies of the nematode Caenorhabditis elegans have uncovered four genes, egl-1 (BH3 only), ced-9 (Bcl-2 related), ced-4 (apoptosis protease activating factor-1), and ced-3 (caspase), which function in a linear pathway to promote developmental cell death in this organism. While this core pathway functions in many cells, recent studies suggest that additional regulators, acting on or in lieu of these core genes, can promote or inhibit the onset of cell death. Here, we discuss the evidence for these noncanonical mechanisms of C. elegans cell death control. We consider novel modes for regulating the core apoptosis genes, and describe a newly identified cell death pathway independent of all known C. elegans cell death genes. The existence of these noncanonical cell death programs suggests that organisms have evolved multiple ways to ensure appropriate cellular demise during development.
UR - http://www.scopus.com/inward/record.url?scp=45449095005&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=45449095005&partnerID=8YFLogxK
U2 - 10.1038/cdd.2008.56
DO - 10.1038/cdd.2008.56
M3 - Review article
C2 - 18437162
AN - SCOPUS:45449095005
SN - 1350-9047
VL - 15
SP - 1124
EP - 1131
JO - Cell Death and Differentiation
JF - Cell Death and Differentiation
IS - 7
ER -