State Key Laboratory for Agro-biotechnology, College of Biological Sciences, China Agricultural University, 100193, Beijing, China.
Mol Genet Genomics. 2010 Feb;283(2):123-33. doi: 10.1007/s00438-009-0502-2. Epub 2009 Dec 15.
The function of the regulatory protein AveR in Streptomyces avermitilis was examined. An aveR deletion mutant abolished avermectin production and produced more oligomycin, and its phenotype was complemented by a single copy of the aveR gene. Removal of the C-terminal HTH domain of AveR abolished avermectin biosynthesis, indicating the importance of HTH domain for AveR function. Promoter titration and promoter probe assays suggested that the transcription of aveA1, encoding polypeptide AVES1 of avermectin PKS, was activated by AveR. Chromatin immunoprecipitation (ChIP) assay showed that the predicted promoter regions of both the ave cluster and the olm cluster were target sites of AveR, and the DNA-binding activity of AveR was dependent on its HTH domain. RT-PCR analysis revealed that the transcriptions of ave structural genes were dependent on AveR, but that of olm structural genes and putative pathway-specific regulatory genes increased in the aveR mutants. Consistent with these observations, overexpression of aveR successfully increased avermectin production. These results indicated that aveR encodes a pathway-specific activator essential for avermectin biosynthesis and it also negatively affects oligomycin biosynthesis.
研究了调节蛋白 AveR 在链霉菌avermitilis 中的功能。aveR 缺失突变体消除了阿维菌素的产生并产生了更多的寡霉素,并且其表型可以通过单个 aveR 基因的拷贝来补充。AveR 的 C 末端 HTH 结构域的缺失消除了阿维菌素生物合成,表明 HTH 结构域对 AveR 功能的重要性。启动子滴定和启动子探针测定表明,编码阿维菌素 PKS 的多肽 AVES1 的 aveA1 的转录被 AveR 激活。染色质免疫沉淀(ChIP)实验表明,ave 簇和 olm 簇的预测启动子区域均为 AveR 的靶标位点,并且 AveR 的 DNA 结合活性依赖于其 HTH 结构域。RT-PCR 分析表明,ave 结构基因的转录依赖于 AveR,但 aveR 突变体中 olm 结构基因和假定途径特异性调节基因的转录增加。与这些观察结果一致,aveR 的过表达成功增加了阿维菌素的产量。这些结果表明,aveR 编码一种用于阿维菌素生物合成的途径特异性激活剂,它也会对寡霉素生物合成产生负面影响。