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Identification of the Promoter in the Intergenic Region between orf1 and cry8Ea1 Controlled by Sigma H Factor

机译:Sigma H因子控制的orf1和cry8Ea1基因间区域启动子的鉴定

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摘要

Bacillus thuringiensis Cry8Ea toxin is specifically toxic to larvae of the Asian cockchafer, Holotrichia parallela. Here we investigated the mechanism of transcriptional regulation of the cry8Ea1 gene. Reverse transcription-PCR (RT-PCR) results indicated that cry8Ea1 and an upstream gene (orf1) were cotranscribed. Transcriptional fusions with the lacZ gene demonstrated that transcription of the cry8Ea1 gene started from two promoters: P-orf1 which is located upstream of the orf1 gene, and P-cry8E, located in the intergenic region mapping between orf1 and cry8Ea1. Of the known, similar orf1-cry operons, this is the first report of the existence of a promoter in the intergenic region between the orfl and cry genes. The transcriptional activity of P-orf1, was found during sporulation in B. thuringiensis subsp. kurstaki HD-73 and was almost abolished in the sigE mutant, while the transcriptional activity of P-cry8E was detected after the end of the exponential phase in HD-73 and was considerably lower in the sigH mutant. The transcription start sites generated by the two cry8Ea1 promoters were determined by the 5'-SMARTer rapid amplification of cDNA ends (RACE) method. The -35 and -10 regions of P-orf1 and P-cry8E showed high sequence similarity with the sigma(E) and sigma(H) promoters, respectively. These results indicated that P-orf1 is controlled by the sigma(E) factor and P-cry8E by the sigma(H) factor.
机译:苏云金芽孢杆菌Cry8Ea毒素对亚洲金龟子(Holotrichia parallela)的幼虫特别有毒。在这里,我们研究了cry8Ea1基因的转录调控机制。逆转录-PCR(RT-PCR)结果表明cry8Ea1和上游基因(orf1)被共转录。与lacZ基因的转录融合表明cry8Ea1基因的转录起始于两个启动子:位于orf1基因上游的P-orf1和位于orf1与cry8Ea1之间的基因间区域的P-cry8E。在已知的类似的orf1-cry操纵子中,这是在orf1和cry基因之间的基因间区域中存在启动子的第一个报道。在苏云金芽孢杆菌亚种的孢子形成过程中发现了P-orf1的转录活性。 urstaki HD-73并在sigE突变体中几乎被废除,而在HD-73的指数期结束后检测到P-cry8E的转录活性,而在sigH突变体中则显着降低。通过5'-SMARTer cDNA末端快速扩增(RACE)方法确定了两个cry8Ea1启动子产生的转录起始位点。 P-orf1和P-cry8E的-35和-10区分别显示与sigma(E)和sigma(H)启动子的高度序列相似性。这些结果表明,P-orf1受sigma(E)因子控制,P-cry8E受sigma(H)因子控制。

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