Hyun Joogyung, Jasper Heinrich, Bohmann Dirk
Department of Biomedical Genetics, The Aab Institute of Biomedical Sciences, University of Rochester Medical Center, 601 Elmwood Avenue, Box 633, Rochester, NY 14642, USA.
Mol Cell Biol. 2005 Jul;25(13):5590-8. doi: 10.1128/MCB.25.13.5590-5598.2005.
Based on overexpression studies and target gene analyses, the transcription factor DNA replication-related element factor (DREF) has been proposed to regulate growth and replication in Drosophila melanogaster. Here we present loss-of-function experiments to analyze the contribution of DREF to these processes. RNA interference-mediated extinction of DREF function in vivo demonstrates a requirement for the protein for normal progression through the cell cycle and consequently for growth of imaginal discs and the derived adult organs. We show that DREF regulates the expression of genes that are required for the transition of imaginal disc cells through S phase. In conditions of suppressed apoptosis, DREF activation can cause overgrowth of developing organs. These data establish DREF as a global regulator of transcriptional programs that mediate cell proliferation and organ growth during animal development.
基于过表达研究和靶基因分析,有人提出转录因子DNA复制相关元件因子(DREF)可调节黑腹果蝇的生长和复制。在此,我们进行功能缺失实验,以分析DREF在这些过程中的作用。RNA干扰介导的体内DREF功能缺失表明,该蛋白是细胞周期正常进展所必需的,因此也是成虫盘及其衍生的成虫器官生长所必需的。我们发现,DREF调节成虫盘细胞通过S期转变所需基因的表达。在凋亡受到抑制的情况下,DREF激活可导致发育中器官过度生长。这些数据表明,DREF是转录程序的全局调节因子,在动物发育过程中介导细胞增殖和器官生长。