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  5. The major subunit of widespread competence pili exhibits a novel and conserved type IV pilin fold
 
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The major subunit of widespread competence pili exhibits a novel and conserved type IV pilin fold
File(s)
J. Biol. Chem.-2020-Sheppard-6594-604.pdf (2.31 MB)
Published version
Author(s)
Sheppard, Devon
Berry, Jamie-Lee
Denise, Rémi
Rocha, Eduardo PC
Matthews, Steve
more
Type
Journal Article
Abstract
<jats:p>Type IV filaments (T4F), which are helical assemblies of type IV pilins, constitute a superfamily of filamentous nanomachines virtually ubiquitous in prokaryotes that mediate a wide variety of functions. The competence (Com) pilus is a widespread T4F, mediating DNA uptake (the first step in natural transformation) in bacteria with one membrane (monoderms), an important mechanism of horizontal gene transfer. Here, we report the results of genomic, phylogenetic, and structural analyses of ComGC, the major pilin subunit of Com pili. By performing a global comparative analysis, we show that Com pili genes are virtually ubiquitous in Bacilli, a major monoderm class of Firmicutes. This also revealed that ComGC displays extensive sequence conservation, defining a monophyletic group among type IV pilins. We further report ComGC solution structures from two naturally competent human pathogens, <jats:italic>Streptococcus sanguinis</jats:italic> (ComGC<jats:sub>SS</jats:sub>) and <jats:italic>Streptococcus pneumoniae</jats:italic> (ComGC<jats:sub>SP</jats:sub>), revealing that this pilin displays extensive structural conservation. Strikingly, ComGC<jats:sub>SS</jats:sub> and ComGC<jats:sub>SP</jats:sub> exhibit a novel type IV pilin fold that is purely helical. Results from homology modeling analyses suggest that the unusual structure of ComGC is compatible with helical filament assembly. Because ComGC displays such a widespread distribution, these results have implications for hundreds of monoderm species.</jats:p>
Date Issued
2020-05-08
Date Acceptance
2020-04-09
Citation
Journal of Biological Chemistry, 2020, 295 (19), pp.6594-6604
URI
http://hdl.handle.net/10044/1/79128
DOI
https://www.dx.doi.org/10.1074/jbc.ra120.013316
ISSN
0021-9258
Publisher
American Society for Biochemistry & Molecular Biology (ASBMB)
Start Page
6594
End Page
6604
Journal / Book Title
Journal of Biological Chemistry
Volume
295
Issue
19
Copyright Statement
© 2020 Sheppard et al. Published by The American Society for Biochemistry and Molecular Biology, Inc. Final version open access under the terms of the Creative
Commons CC-BY license (https://creativecommons.org/licenses/by/4.0/).
Sponsor
Medical Research Council (MRC)
Grant Number
MR/P022197/1
Subjects
DNA transformation
DNA uptake
Streptococcus sanguinis
nuclear magnetic resonance (NMR)
phylogenetics
protein structure
type IV filaments
type IV pili
type IV pilin
03 Chemical Sciences
06 Biological Sciences
11 Medical and Health Sciences
Biochemistry & Molecular Biology
Publication Status
Published
Date Publish Online
2020-04-09
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