Publication Detail
The publication detail shows the title, authors (with indicators showing other profiled authors), information on the publishing organization, abstract and a link to the article in PubMed. This abstract is what is used to create the fingerprint of the publication. If any grants are referenced by the publication, they will be listed here as well.
Domains required for transcriptional activation show conservation in the mga family of virulence gene regulators.
Cheryl M Vahling; Kevin S McIver (Profiled Author: Kevin S. McIver)
Department of Microbiology, University of Texas Southwestern Medical Center, 5323 Harry Hines Blvd., Dallas, TX 75390-9048, USA.
Journal of bacteriology 2006;188(3):863-73.
Mga, or the multigene regulator of the group A streptococcus (GAS) (Streptococcus pyogenes), is a transcriptional regulator of virulence genes important for colonization and immune evasion. All serotypes of the GAS possess one of two divergent mga alleles (mga-1 or mga-2), and orthologues of Mga have also been identified in other pathogenic streptococci. To date, the only functional motifs established within Mga are two amino-terminal DNA-binding domains (HTH-3 and HTH-4). To uncover novel domains, a random mutagenesis screen using an M6 Mga (mga-1) was undertaken to find mutations leading to a defect in transcriptional activation of the Mga-regulated emm gene. In addition to mutations in the established DNA-binding domains, the screen also revealed mutations in a region conserved among several Mga orthologues. Alanine scanning helped resolve the boundaries of this conserved Mga domain (CMD-1) spanning from residues 10 to 15 of the protein, with the two flanking amino acid residues likely involved in protein stability. Transcriptional reporter analyses demonstrated the importance of CMD-1 for activation of Pemm and autoactivation of Pmga in the serotype M6 Mga. Mutational analyses showed that both CMD-1 and HTH-4 are also necessary for activation of the promoter target Pmrp in a divergent serotype M4 Mga (mga-2), suggesting a conserved functionality. However, in contrast to M6, the M4 Mga mutants did not show a defect in autoregulation. Mutation of similar conserved residues in the Mga-like regulator DmgB from S. dysgalactiae subsp. dysgalactiae showed that CMD-1 and HTH-4 are critical for transcriptional activation in this orthologue, implying that a common mechanism of virulence gene activation may exist for members of the Mga family of regulators.
1 Originating Grant
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1.
MCIVER, KEVIN S.
PRD-Containing Virulence Regulators of Pathogenic Streptococci
1 July 2000 - 31 January 2017
NATIONAL INSTITUTE OF ALLERGY AND INFECTIOUS DISEASES
Scientific Context
This section shows information related to the publication - computed using the fingerprint of the publication - including related publications, related experts and related grants with fingerprints representing significant amounts of overlap between their fingerprint and this publication. The red dots indicate whether those experts or terms appear within the publication, thereby showing potential and actual connections.
Related Publications
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1.
2002Kevin S McIver; Rhonda L Myles
Molecular microbiology 2002;43(6):1591-601. -
2.
2012Elise R Hondorp; Sherry C Hou; Andrew D Hempstead; Lara L Hause; Dorothy M Beckett; Kevin S McIver
Molecular microbiology 2012;83(5):953-67. -
3.
2008Traci L Kinkel; Kevin S McIver
CcpA-mediated repression of streptolysin S expression and virulence in the group A streptococcus.
Infection and immunity 2008;76(8):3451-63.
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