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首页> 外文期刊>Proceedings of the National Academy of Sciences of the United States of America >Identification of an activator protein required for the induction of fruA, a gene essential for fruiting body development in Myxococcus xanthus.
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Identification of an activator protein required for the induction of fruA, a gene essential for fruiting body development in Myxococcus xanthus.

机译:鉴定了诱导fruA所需的激活蛋白,fruA是一种对黄色粘球菌子实体发育至关重要的基因。

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摘要

Myxococcus xanthus exhibits social behavior and multicellular development. FruA is an essential transcription factor for fruiting body development in M. xanthus. In the present study, the upstream promoter region was found to be necessary for the induction of fruA expression during development. A cis-acting element required for the induction was identified and was located between nucleotides -154 and -107 with respect to the transcription initiation site. In addition, it was found that two binding sites exist within this element of the fruA promoter. By using DNA affinity column chromatography containing the cis-acting element, a fruA promoter-binding protein was purified. The purified protein was shown by N-terminal sequence analysis to be identical to MrpC, a protein identified previously by transposon insertion mutagenesis as an essential locus for fruiting body development [Sun, H. & Shi, W. (2001) J. Bacteriol. 183, 4786-4795]. Furthermore, fruA mRNA was not detectable in the mrpC::km strain, demonstrating that MrpC is essential for fruA expression. Moreover, mutational analysis of the binding sites for MrpC in the fruA promoter indicates that binding of MrpC activates transcription of fruA in vivo. This report provides evidence for a direct molecular interaction involved in temporally regulated gene expression in M. xanthus.
机译:黄腐粘球菌表现出社交行为和多细胞发育。 FruA是黄连果子实体发育的重要转录因子。在本研究中,发现上游启动子区域对于发育期间诱导fruA表达是必需的。鉴定了诱导所需的顺式作用元件,其相对于转录起始位点位于核苷酸-154和-107之间。另外,发现在fruA启动子的这个元件内存在两个结合位点。通过使用含有顺式作用元件的DNA亲和柱色谱法,纯化了fruA启动子结合蛋白。通过N-末端序列分析显示纯化的蛋白质与MrpC相同,MrpC是先前通过转座子插入诱变鉴定的蛋白质,是子实体发育的必要位点[Sun,H。&Shi,W。(2001)J.Bacteriol。 183,4786-4795]。此外,在mrpC :: km菌株中未检测到fruA mRNA,这表明MrpC对于fruA表达至关重要。此外,对fruA启动子中MrppC结合位点的突变分析表明,MrppC的结合在体内激活了fruA的转录。该报告提供了证据,证明了黄单胞菌中与时间调控基因表达有关的直接分子相互作用。

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