支原体
电泳迁移率测定
生物
泰特
抄写(语言学)
基因
转录组
细胞生物学
核糖核酸
基因表达
遗传学
分子生物学
抑制因子
病理
哲学
医学
语言学
结核分枝杆菌
肺结核
作者
Parul Singh,Arbind Kumar,Ravindresh Chhabra,Kashmir Singh,Jagdeep Kaur
标识
DOI:10.2217/fmb-2022-0238
摘要
Aim: To decipher the role of MSMEG_5850 in the physiology of mycobacteria. Methods: MSMEG_5850 was knocked out and RNA sequencing was performed. MSMEG_5850 protein was purified from the Escherichia coli pET28a system. Electrophoretic mobility shift assay and size exclusion chromatography were used to determine the binding of MSMEG_5850 to its motif and binding stoichiometry. The effect of nutritional stress was monitored. Results: Transcriptome analysis revealed the differential expression of 148 genes in an MSMEG_5850 knockout strain. MSMEG_5850 had control over 50 genes because those genes had a binding motif upstream of their sequence. The electrophoretic mobility shift assay showed MSMEG_5850 bound to its motif as a monomer. MSMEG_5850 was upregulated under nutritional stress and promoted the survival of mycobacteria. Conclusion: The study confirms the role of MSMEG_5850 in global transcriptional regulation.
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