Kalb John M, Beaster-Jones Laura, Fernandez Anthony P, Okkema Peter G, Goszczynski Barbara, McGhee James D
Department of Biochemistry and Molecular Biology, Genes and Development Research Group, Faculty of Medicine, Health Sciences Centre, University of Calgary, 3330 Hospital Drive NW, Calgary, Alberta, Canada T2N 4N1.
J Mol Biol. 2002 Jul 19;320(4):697-704. doi: 10.1016/s0022-2836(02)00555-7.
PHA-4 is a forkhead/winged helix transcription factor that acts as an organ identity factor in the development of the Caenorhabditis elegans pharynx. PEB-1 is a novel DNA-binding protein also involved in pharyngeal morphogenesis. PHA-4 and PEB-1 bind at overlapping sites on the C183 sequence element that controls pharynx-specific expression of the C. elegans myo-2 gene. It has been suggested that PHA-4 and PEB-1 act cooperatively on the C183 sequence. In this study, we test this model and assess the C183-dependent transcriptional activity of PHA-4 and PEB-1, both individually and in combination. We show that PHA-4 and PEB-1 are both modest transcriptional activators in yeast but that co-expression of the two factors does not result in significantly increased expression of a C183-regulated reporter gene. Electrophoretic mobility-shift assays provide no evidence for the formation of a PHA-4/PEB-1 complex in vitro but rather show that PHA-4 and PEB-1 cannot bind C183 simultaneously. As we have reported previously, ectopic expression of PHA-4 in C. elegans causes ectopic expression of a C183-regulated reporter gene. We show that ectopic expression of PEB-1 cannot cause ectopic expression of the same reporter but rather ectopic PEB-1 inhibits reporter gene activation by PHA-4. Overall, our results do not support a model in which PHA-4 and PEB-1 synergize in vivo but rather support a model in which PEB-1 may negatively modulate PHA-4's ability to activate transcription through C183 during formation of the C. elegans pharynx.
PHA-4是一种叉头/翼状螺旋转录因子,在秀丽隐杆线虫咽的发育过程中作为器官身份因子发挥作用。PEB-1是一种新型的DNA结合蛋白,也参与咽的形态发生。PHA-4和PEB-1在控制秀丽隐杆线虫肌动蛋白-2基因咽特异性表达的C183序列元件的重叠位点结合。有人提出PHA-4和PEB-1在C183序列上协同作用。在本研究中,我们测试了该模型,并分别和联合评估了PHA-4和PEB-1依赖C183的转录活性。我们发现PHA-4和PEB-1在酵母中都是适度的转录激活因子,但这两种因子的共表达并不会导致C183调控的报告基因表达显著增加。电泳迁移率变动分析没有提供体外形成PHA-4/PEB-1复合物的证据,而是表明PHA-4和PEB-1不能同时结合C183。正如我们之前报道的,PHA-4在秀丽隐杆线虫中的异位表达会导致C183调控的报告基因异位表达。我们发现PEB-1的异位表达不会导致同一报告基因的异位表达,而是异位的PEB-1会抑制PHA-4对报告基因的激活。总体而言,我们的结果不支持PHA-4和PEB-1在体内协同作用的模型,而是支持一种模型,即PEB-1可能在秀丽隐杆线虫咽形成过程中通过C183负向调节PHA-4激活转录的能力。