Groundbreaking Discovery by Indian Scientists on Bacterial Gene Regulation in TB
Synopsis
Key Takeaways
New Delhi, April 2 (NationPress) Tuberculosis ranks among the most lethal infectious diseases globally. Recently, a group of researchers has identified a critical flaw in a long-held theory regarding bacterial gene expression regulation. This breakthrough could pave the way for novel tactics to tackle tuberculosis and other bacterial infections, as stated in an official announcement on Thursday.
Traditionally, it was understood that a protein named ‘σ factor’ binds to RNA polymerase, triggering bacterial transcription and subsequently detaching once the enzyme starts elongating RNA.
This concept, termed the ‘σ-cycle’, was thought to be a standard mechanism across all bacteria, including those causing TB.
However, new research conducted by Bose Institute in Kolkata, an autonomous institute under the Department of Science and Technology (DST), challenges this long-standing belief.
Researchers Dr. Jayanta Mukhopadhyay and Dr. N. Hazra have discovered that while certain σ factors in M. tuberculosis detach from RNA polymerase during transcription, others stay closely attached throughout.
Their findings, published in the international journal Nucleic Acids Research, indicate that the widely accepted “universal σ-cycle” does not apply universally to all bacteria or regulatory proteins.
“This study concentrates on Mycobacterium tuberculosis, the bacterium responsible for tuberculosis, revealing that different σ (sigma) factors—proteins that direct RNA polymerase to specific genes—exhibit markedly different behaviors during transcription, the initial stage of gene expression,” explained the Ministry of Science and Technology.
The revelation that σF remains bound to RNA polymerase implies a previously unknown mechanism by which the bacterium maintains expression of stress-response genes, providing crucial insights into TB biology.
With drug-resistant strains increasingly threatening treatment efficacy, M. tuberculosis navigates within the human host by meticulously regulating gene expression under severe stress conditions.