结核分枝杆菌H37有毒株与无毒株的代谢相关基因pabB和lpdA启动子活性分析

Comparative study of the promoter activity of metabolism-related pabB and lpdA genes between Mycobacterium tuberculosis strains H37Rv and H37Ra

摘要:

摘要：【目的】通过分析结核分枝杆菌无毒株 H37Ra 的全基因组序列，并与 H37Rv 基因组序列比较，发现 pabB 和 lpdA 预测的启动子区发生了突变。我们利用报告基因，确认启动子突变与其基因转录水平的关系，探索结核分枝杆菌 H37Ra 毒力丧失的内在原因。【方法】利用生物信息学方法预测这两对基因的启动子区，采用 PCR 技术克隆这两对基因的启动子，与分枝杆菌启动子探针载体 pMC210 相连，DNA测序证实连接片段正确后，用电穿孔法将重组质粒转化至耻垢分枝杆菌 mc2155。利用 Quantit

Abstract:

Abstract: [Objective] Comparative genomic study revealed mutations at the promoter regions of pabB and lpdA in avirulent Mycobacterium tuberculosis strain H37Ra compared to its virulent counterpart strain H37Rv. LacZ reporter system was used to test whether those mutations will affect promoter activity and its potential relationship to virulence attenuation of H37Ra. [Methods] Promoter regions of pabB and lpdA were predicted by the “Neural Network Promoter Prediction” method (http://www.fruitfly.org/seq_tools/promoter.html). Promoter sequences were PCR amplified and cloned into mycobacterial promoterless probe vector pMC210. Resultant recombinant plasmids were transformed into M. smegmatis by electroporation. The transcription activity of lacZ under the control of cloned promoters were monitored by Quantitative Real-Time RT-PCR. [Results] Quantitative Real Time PCR results showed that the promoter activity of H37Ra pabB was six times more than that of H37Rv pabB (p < 0.05), while the promoter activity of the H37Rv lpdA was two fold of that of H37Ra lpdA (p < 0.05). [Conclusion] The mutations in pabB and lpdA promoters affect its expression activity. The T-A mutation in lpdA promoter may be related to virulence attenuation of H37Ra.