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首页> 外文期刊>Journal of bacteriology >Combinatorial Regulation of the dev Operon by MrpC2 and FruA during Myxococcus xanthus Development
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Combinatorial Regulation of the dev Operon by MrpC2 and FruA during Myxococcus xanthus Development

机译:黄黏球菌发育过程中MrpC2和FruA对dev操纵子的组合调控。

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Proper expression of the dev operon is important for normal development of Myxococcus xanthus. When starved, these bacteria coordinate their gliding movements to build mounds that become fruiting bodies as some cells differentiate into spores. Mutations in the devTRS genes impair sporulation. Expression of the operon occurs within nascent fruiting bodies and depends in part on C signaling. Here, we report that expression of the dev operon, like that of several other C-signal-dependent genes, is subject to combinatorial control by the transcription factors MrpC2 and FruA. A DNA fragment upstream of the dev promoter was bound by a protein in an extract containing MrpC2, protecting the region spanning positions ?77 to ?54. Mutations in this region impaired binding of purified MrpC2 and abolished developmental expression of reporter fusions. The association of MrpC2 and/or its longer form, MrpC, with the dev promoter region depended on FruA in vivo, based on chromatin immunoprecipitation analysis, and purified FruA appeared to bind cooperatively with MrpC2 to DNA just upstream of the dev promoter in vitro. We conclude that cooperative binding of the two proteins to this promoter-proximal site is crucial for dev expression. 5′ deletion analysis implied a second upstream positive regulatory site, which corresponded to a site of weak cooperative binding of MrpC2 and FruA and boosted dev expression 24 h into development. This site is unique among the C-signal-dependent genes studied so far. Deletion of this site in the M. xanthus chromosome did not impair sporulation under laboratory conditions.
机译: dev 操纵子的正确表达对于粘球菌的正常发育很重要。饥饿时,这些细菌协调其滑行运动,形成一些果实分化为孢子的结实的果实。 devTRS 基因中的突变会削弱孢子形成。操纵子的表达发生在新生的子实体中,部分取决于C信号。在这里,我们报道 dev 操纵子的表达,与其他几个依赖C信号的基因一样,受到转录因子MrpC2和FruA的组合控制。 dev 启动子上游的DNA片段与含有MrpC2的提取物中的蛋白质结合,从而保护了跨越第77至第54位的区域。该区域中的突变削弱了纯化的MrpC2的结合并取消了报告融合蛋白的发育表达。根据染色质免疫沉淀分析,MrpC2和/或其较长形式的MrpC与 dev 启动子区域的关联取决于FruA 体内,并且纯化的FruA似乎可以结合与MrpC2协同作用于 dev 启动子体外上游的DNA。我们得出结论,这两个蛋白对此启动子附近位点的协同结合对于 dev 表达至关重要。 5'缺失分析暗示第二个上游阳性调控位点,其对应于MrpC2和FruA的弱合作结合位点,并在发育24小时内增强了 dev 表达。该位点是迄今为止研究的C信号依赖性基因中唯一的。在实验室条件下,在X. Xanthus染色体上删除该位点不会损害孢子形成。

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