Liu Y, Lehmann M
Department of Biological Sciences, University of Arkansas, Fayetteville, AR 72701-1201, USA.
Insect Mol Biol. 2008 Apr;17(2):91-101. doi: 10.1111/j.1365-2583.2007.00785.x.
The larval salivary glands of Drosophila express the FOXA transcription factor Fork head (Fkh) before, but not after, puparium formation. Forced expression of Fkh in late prepupae prevents the programmed destruction of the tissue, which normally occurs in the early pupa. Using Affymetrix GeneChips, we analysed changes in gene expression brought about by Fkh when expressed shortly before the normal time of salivary gland death. Genes identified as responsive to Fkh include not only cell death genes, but also genes involved in autophagy, phospholipid metabolism and hormone-controlled signalling pathways. In addition, Fkh changed the expression of genes involved in glucose and fatty acid metabolism that are known to be target genes of the FOXAs in vertebrates. Premature loss of fkh induced by RNAi and gain of Fkh by ectopic expression at earlier times of development confirmed that genes identified in the microarray study are under normal developmental control by Fkh. These genes include Eip63F-1, which is expressed in both salivary glands and Malpighian tubules, suggesting that Fkh controls common aspects of the secretory function of the two organs. Eip63F-1 is one of many genes controlled by the steroid hormone 20-hydroxyecdysone that appear to be co-regulated by Fkh.
果蝇幼虫的唾液腺在化蛹前表达叉头框(FOX)转录因子叉头(Fkh),但在化蛹后则不表达。在蛹前期后期强制表达Fkh可防止组织的程序性破坏,而这种破坏通常发生在蛹早期。我们使用Affymetrix基因芯片分析了在唾液腺正常死亡时间前不久表达Fkh所引起的基因表达变化。被确定对Fkh有反应的基因不仅包括细胞死亡基因,还包括参与自噬、磷脂代谢和激素控制信号通路的基因。此外,Fkh改变了参与葡萄糖和脂肪酸代谢的基因的表达,而这些基因已知是脊椎动物中FOXA的靶基因。通过RNA干扰诱导fkh过早缺失以及在发育早期通过异位表达使Fkh增加,证实了在微阵列研究中鉴定出的基因在正常发育过程中受Fkh控制。这些基因包括Eip63F - 1,它在唾液腺和马氏管中均有表达,这表明Fkh控制着这两个器官分泌功能的共同方面。Eip63F - 1是受类固醇激素20 - 羟基蜕皮激素控制的众多基因之一,这些基因似乎受Fkh共同调控。