A Bacteriophage DNA Mimic Protein Employs a Non-specific Strategy to Inhibit the Bacterial RNA Polymerase

DNA mimicry by proteins is a strategy that employed by some proteins to occupy the binding sites of the DNA-binding proteins and deny further access to these sites by DNA. Such proteins have been found in bacteriophage, eukaryotic virus, prokaryotic, and eukaryotic cells to imitate non-coding functi...

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Main Authors: Zhihao Wang, Hongliang Wang, Nancy Mulvenna, Maximo Sanz-Hernandez, Peipei Zhang, Yanqing Li, Jia Ma, Yawen Wang, Steve Matthews, Sivaramesh Wigneshweraraj, Bing Liu
Format: Article
Language:English
Published: Frontiers Media S.A. 2021-06-01
Series:Frontiers in Microbiology
Subjects:
Online Access:https://www.frontiersin.org/articles/10.3389/fmicb.2021.692512/full
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spelling doaj-874cbe9f37da4d65834efeec2a5e52402021-06-02T05:45:46ZengFrontiers Media S.A.Frontiers in Microbiology1664-302X2021-06-011210.3389/fmicb.2021.692512692512A Bacteriophage DNA Mimic Protein Employs a Non-specific Strategy to Inhibit the Bacterial RNA PolymeraseZhihao Wang0Zhihao Wang1Hongliang Wang2Nancy Mulvenna3Maximo Sanz-Hernandez4Peipei Zhang5Yanqing Li6Jia Ma7Yawen Wang8Steve Matthews9Sivaramesh Wigneshweraraj10Bing Liu11Bing Liu12BioBank, The First Affiliated Hospital of Xi’an Jiaotong University, Xi’an, ChinaMRC Centre for Molecular Bacteriology and Infection, Imperial College London, London, United KingdomDepartment of Pathogen Biology and Immunology, School of Basic Medical Sciences, Xi’an Jiaotong University, Xi’an, ChinaMRC Centre for Molecular Bacteriology and Infection, Imperial College London, London, United KingdomMRC Centre for Molecular Bacteriology and Infection, Imperial College London, London, United KingdomBioBank, The First Affiliated Hospital of Xi’an Jiaotong University, Xi’an, ChinaBioBank, The First Affiliated Hospital of Xi’an Jiaotong University, Xi’an, ChinaBioBank, The First Affiliated Hospital of Xi’an Jiaotong University, Xi’an, ChinaBioBank, The First Affiliated Hospital of Xi’an Jiaotong University, Xi’an, ChinaMRC Centre for Molecular Bacteriology and Infection, Imperial College London, London, United KingdomMRC Centre for Molecular Bacteriology and Infection, Imperial College London, London, United KingdomBioBank, The First Affiliated Hospital of Xi’an Jiaotong University, Xi’an, ChinaInstrument Analysis Centre of Xi’an Jiaotong University, Xi’an, ChinaDNA mimicry by proteins is a strategy that employed by some proteins to occupy the binding sites of the DNA-binding proteins and deny further access to these sites by DNA. Such proteins have been found in bacteriophage, eukaryotic virus, prokaryotic, and eukaryotic cells to imitate non-coding functions of DNA. Here, we report another phage protein Gp44 from bacteriophage SPO1 of Bacillus subtilis, employing mimicry as part of unusual strategy to inhibit host RNA polymerase. Consisting of three simple domains, Gp44 contains a DNA binding motif, a flexible DNA mimic domain and a random-coiled domain. Gp44 is able to anchor to host genome and interact bacterial RNA polymerase via the β and β′ subunit, resulting in bacterial growth inhibition. Our findings represent a non-specific strategy that SPO1 phage uses to target different bacterial transcription machinery regardless of the structural variations of RNA polymerases. This feature may have potential applications like generation of genetic engineered phages with Gp44 gene incorporated used in phage therapy to target a range of bacterial hosts.https://www.frontiersin.org/articles/10.3389/fmicb.2021.692512/fullbacteriophageRNA polymeraseDNA binding abilityintrinsic disordered proteinDNA mimic protein
collection DOAJ
language English
format Article
sources DOAJ
author Zhihao Wang
Zhihao Wang
Hongliang Wang
Nancy Mulvenna
Maximo Sanz-Hernandez
Peipei Zhang
Yanqing Li
Jia Ma
Yawen Wang
Steve Matthews
Sivaramesh Wigneshweraraj
Bing Liu
Bing Liu
spellingShingle Zhihao Wang
Zhihao Wang
Hongliang Wang
Nancy Mulvenna
Maximo Sanz-Hernandez
Peipei Zhang
Yanqing Li
Jia Ma
Yawen Wang
Steve Matthews
Sivaramesh Wigneshweraraj
Bing Liu
Bing Liu
A Bacteriophage DNA Mimic Protein Employs a Non-specific Strategy to Inhibit the Bacterial RNA Polymerase
Frontiers in Microbiology
bacteriophage
RNA polymerase
DNA binding ability
intrinsic disordered protein
DNA mimic protein
author_facet Zhihao Wang
Zhihao Wang
Hongliang Wang
Nancy Mulvenna
Maximo Sanz-Hernandez
Peipei Zhang
Yanqing Li
Jia Ma
Yawen Wang
Steve Matthews
Sivaramesh Wigneshweraraj
Bing Liu
Bing Liu
author_sort Zhihao Wang
title A Bacteriophage DNA Mimic Protein Employs a Non-specific Strategy to Inhibit the Bacterial RNA Polymerase
title_short A Bacteriophage DNA Mimic Protein Employs a Non-specific Strategy to Inhibit the Bacterial RNA Polymerase
title_full A Bacteriophage DNA Mimic Protein Employs a Non-specific Strategy to Inhibit the Bacterial RNA Polymerase
title_fullStr A Bacteriophage DNA Mimic Protein Employs a Non-specific Strategy to Inhibit the Bacterial RNA Polymerase
title_full_unstemmed A Bacteriophage DNA Mimic Protein Employs a Non-specific Strategy to Inhibit the Bacterial RNA Polymerase
title_sort bacteriophage dna mimic protein employs a non-specific strategy to inhibit the bacterial rna polymerase
publisher Frontiers Media S.A.
series Frontiers in Microbiology
issn 1664-302X
publishDate 2021-06-01
description DNA mimicry by proteins is a strategy that employed by some proteins to occupy the binding sites of the DNA-binding proteins and deny further access to these sites by DNA. Such proteins have been found in bacteriophage, eukaryotic virus, prokaryotic, and eukaryotic cells to imitate non-coding functions of DNA. Here, we report another phage protein Gp44 from bacteriophage SPO1 of Bacillus subtilis, employing mimicry as part of unusual strategy to inhibit host RNA polymerase. Consisting of three simple domains, Gp44 contains a DNA binding motif, a flexible DNA mimic domain and a random-coiled domain. Gp44 is able to anchor to host genome and interact bacterial RNA polymerase via the β and β′ subunit, resulting in bacterial growth inhibition. Our findings represent a non-specific strategy that SPO1 phage uses to target different bacterial transcription machinery regardless of the structural variations of RNA polymerases. This feature may have potential applications like generation of genetic engineered phages with Gp44 gene incorporated used in phage therapy to target a range of bacterial hosts.
topic bacteriophage
RNA polymerase
DNA binding ability
intrinsic disordered protein
DNA mimic protein
url https://www.frontiersin.org/articles/10.3389/fmicb.2021.692512/full
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