Thummel Carl S
Department of Human Genetics, University of Utah School of Medicine, Salt Lake City, UT 84112, USA.
J Cell Biol. 2007 Mar 12;176(6):737-9. doi: 10.1083/jcb.200702075. Epub 2007 Mar 5.
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 approximately 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.
精确确定细胞何时何地经历程序性细胞死亡对于正常发育和组织稳态至关重要。曹等人(2007年;见本期第843页)报告称,叉头(Fkh)转录因子对黑腹果蝇幼虫唾液腺的早期发育和功能至关重要,它也会导致唾液腺的消亡。这些作者表明,唾液腺中的fkh表达通常在化蛹时消失,此时距离它们受到类固醇激素蜕皮激素触发而发生大规模细胞死亡约12小时,为发育中的成虫唾液腺腾出空间。Fkh的缺失消除了其在阻止细胞死亡中的作用,使得随后蜕皮激素诱导的收割者和头部内卷缺陷死亡激活因子得以表达并导致组织破坏。这项研究为程序性细胞死亡的转录调控以及发育过程中激素反应精确的时空控制机制提供了新的见解。