The precise determination of when and where cells undergo programmed cell death is critical for normal development and tissue homeostasis. Cao et al. (2007; see p. 843 of this issue) report that the Fork head (Fkh) transcription factor, which is essential for the early development and function of the larval salivary glands in Drosophila melanogaster, also contributes to its demise. These authors show that fkh expression in the salivary glands is normally lost at puparium formation, which is ∼12 h before they undergo massive cell death triggered by the steroid hormone ecdysone, making room for their developing adult counterparts. The loss of Fkh eliminates its role in blocking cell death, allowing for subsequent ecdysone-induced reaper and head involution defective death activator expression and tissue destruction. This study provides new insights into the transcriptional regulation of programmed cell death and the mechanisms that underlie the precise spatial and temporal control of hormone responses during development.
Article navigation
12 March 2007
Spotlight|
March 05 2007
To die or not to die—a role for Fork head
Carl S. Thummel
Carl S. Thummel
Department of Human Genetics, University of Utah School of Medicine, Salt Lake City, UT 84112
Search for other works by this author on:
Carl S. Thummel
Department of Human Genetics, University of Utah School of Medicine, Salt Lake City, UT 84112
Correspondence to Carl S. Thummel: [email protected]
Abbreviation used in this paper: hid, head involution defective.
Received:
February 12 2007
Accepted:
February 13 2007
Online ISSN: 1540-8140
Print ISSN: 0021-9525
The Rockefeller University Press
2007
J Cell Biol (2007) 176 (6): 737–739.
Article history
Received:
February 12 2007
Accepted:
February 13 2007
Citation
Carl S. Thummel; To die or not to die—a role for Fork head . J Cell Biol 12 March 2007; 176 (6): 737–739. doi: https://doi.org/10.1083/jcb.200702075
Download citation file:
Sign in
Don't already have an account? Register
Suggested Content
Email alerts
Advertisement
