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PHA-4和PEB-1转录因子在秀丽隐杆线虫咽形成过程中的相互干扰。

Interference between the PHA-4 and PEB-1 transcription factors in formation of the Caenorhabditis elegans pharynx.

作者信息

Kalb John M, Beaster-Jones Laura, Fernandez Anthony P, Okkema Peter G, Goszczynski Barbara, McGhee James D

机构信息

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.

出版信息

J Mol Biol. 2002 Jul 19;320(4):697-704. doi: 10.1016/s0022-2836(02)00555-7.

Abstract

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.

摘要

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。

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