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Updated: Oct 1, 2026

A Fluorescence-based Method to Study Bacterial Gene Regulation in Infected Tissues
Published on: February 19, 2019
Two DNA-binding domains of Mga are required for virulence gene activation in the group A streptococcus
Kevin S McIver1, Rhonda L Myles
1Department of Microbiology, University of Texas Southwestern Medical Center, Dallas, TX 75390-9048, USA. Kevin.Mciver@UTSouthwestern.edu
Abstract:
Mga is a DNA-binding protein that activates expression of several important virulence genes in the group A streptococcus (GAS), including those encoding M protein (emm), C5a peptidase (scpA) and Mga (mga). To determine the functionality of four potential helix-turn-helix DNA-binding motifs (HTH1-HTH4) identified within the amino-terminus of Mga, alanine substitutions were introduced within each domain in a MBP-Mga fusion allele and purified proteins were assayed for binding to Mga-specific promoter fragments (Pmga, PscpA and Pemm) in vitro. Although HTH-1 and HTH-2 mutations showed wild type DNA-binding activity, an altered HTH-3 domain resulted in reduced binding to the three promoters and an HTH-4 mutant was devoid of detectable binding activity. Plasmid-encoded expression of the HTH-3 and HTH-4 alleles from a constitutive promoter (Pspac) in the mga-deleted GAS strain JRS519 demonstrated that Mga-regulated emm expression correlated directly to the DNA-binding activity observed for each mutant protein in vitro. Single-copy expression of HTH-3 and HTH-4 from their native Pmga resulted in a dramatic reduction in autoregulated mga expression in both mutant strains. Thus, Mga appears to contain two DNA-binding domains (HTH-3 and HTH-4) that are required for direct activation of the Mga virulence regulon in vivo.
Insights
The Mga protein in group A Streptococcus utilizes two DNA-binding domains, HTH-3 and HTH-4, to activate crucial virulence genes. Mutations in these domains impair DNA binding and virulence gene expression.
Area of Science:
- Microbiology
- Molecular Biology
- Genetics
Background:
- Group A Streptococcus (GAS) is a significant human pathogen.
- The Mga protein regulates key GAS virulence factors, including M protein (emm) and C5a peptidase (scpA).
- Understanding Mga's DNA-binding mechanism is crucial for deciphering GAS pathogenesis.
Purpose of the Study:
- To investigate the function of four potential helix-turn-helix (HTH) DNA-binding motifs in the Mga protein.
- To determine which HTH domains are essential for Mga's DNA-binding activity and virulence gene regulation.
Main Methods:
- Alanine substitution mutations were introduced into the HTH1-HTH4 domains of Mga.
- Mutant Mga proteins were purified and tested for in vitro binding to Mga-specific promoter DNA.
- The functionality of mutant alleles was assessed in a GAS strain lacking mga.
Main Results:
- Mutations in HTH-3 and HTH-4 significantly reduced Mga's DNA-binding affinity.
- HTH-4 mutant Mga showed no detectable binding to promoter fragments.
- Altered HTH-3 and HTH-4 domains impaired Mga-regulated emm gene expression in vivo.
- Mutant strains exhibited reduced autoregulation of mga expression.
Conclusions:
- Mga possesses at least two functional DNA-binding domains, HTH-3 and HTH-4.
- These domains are essential for Mga's ability to bind DNA and activate the Mga virulence regulon in group A Streptococcus.
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