Laboratório de Bacteriologia, Centro de Referência Prof. Hélio Fraga, Escola Nacional de Saúde Pública Sergio Arouca, Fiocruz. Estr. de Curicica 2000, Jacarepaguá, 22780-194 Rio de Janeiro, RJ, Brazil.
Laboratório de Genômica Funcional e Bioinformática, Instituto Oswaldo Cruz, Fiocruz. Av. Brasil 4365, Manguinhos, 21040-900 Rio de Janeiro, RJ, Brazil.
Tuberculosis (Edinb). 2014 Jan;94(1):26-33. doi: 10.1016/j.tube.2013.11.004. Epub 2013 Nov 26.
The Brazilian anti-tuberculosis vaccine strain Mycobacterium bovis bacillus Calmette-Guérin (BCG) BCG Moreau is unique in having a deletion of 7608 bp (RD16) that results in the truncation of a putative TetR transcriptional regulator, the ortholog of Mycobacterium tuberculosis rv3405c, BCG_M3439c. We investigated the effect of this truncation on the expression of the rv3406 ortholog (BCG_M3440), lying 81 bp downstream in the opposite orientation. RT-PCR and western blot experiments show that rv3406 mRNA and Rv3406 accumulate in BCG Moreau but not in BCG Pasteur (strain that bears an intact rv3405c), suggesting this to be a result of rv3405c truncation. Recombinant Rv3405c forms a complex with the rv3405c-rv3406 intergenic region, which contains a characteristic transcription factor binding site, showing it to have DNA binding activity. Complementation of M. bovis BCG Moreau with an intact copy of rv3405c abolishes Rv3406 accumulation. These results show that Rv3405c is a DNA binding protein that acts as a transcriptional repressor of rv3406.
巴西抗结核疫苗株牛分枝杆菌卡介苗(BCG)BCG Moreau 是独一无二的,它缺失了 7608bp(RD16),导致假定的 TetR 转录调节剂截断,与结核分枝杆菌 rv3405c 的同源物,BCG_M3439c。我们研究了这种截断对位于相反方向下游 81bp 的 rv3406 同源物(BCG_M3440)表达的影响。RT-PCR 和 Western blot 实验表明,rv3406 mRNA 和 Rv3406 在 BCG Moreau 中积累,但在 BCG Pasteur(携带完整 rv3405c 的菌株)中不积累,表明这是 rv3405c 截断的结果。重组 Rv3405c 与 rv3405c-rv3406 基因间区形成复合物,该区域包含特征性转录因子结合位点,表明其具有 DNA 结合活性。用完整的 rv3405c 基因对 M. bovis BCG Moreau 进行互补,消除了 Rv3406 的积累。这些结果表明,Rv3405c 是一种 DNA 结合蛋白,作为 rv3406 的转录阻遏物。