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Multiple transcription factors regulate the expression of genes for error prone DNA polymerases in Acinetobacter baumannii
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  • Brian Nguyen,
  • Carly Ching,
  • Ashley MacGuire,
  • Pranav Casula,
  • Connor Newman,
  • Faith Finley,
  • Veronica G. Godoy
Brian Nguyen
Northeastern University
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Carly Ching
Northeastern University
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Ashley MacGuire
Northeastern University
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Pranav Casula
Northeastern University
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Connor Newman
Northeastern University
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Faith Finley
Northeastern University
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Veronica G. Godoy
Northeastern University

Corresponding Author:v.godoycarter@northeastern.edu

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Abstract

Acinetobacter baumannii is an opportunistic pathogen causing several infections that are increasingly difficult to treat due to its ability to rapidly gain antibiotic resistances. These resistances can arise due to mutations during the DNA damage response (DDR), through the activity of error-prone DNA polymerases, such as DNA polymerase V (DNA Pol V). Currently, the DDR in A. baumannii is not well understood and the regulation of genes encoding multiple copies of DNA Pol V is not fully characterized. Through genome wide mutagenesis, we have identified a novel TetR-like family regulator of genes that encode DNA Pol V, which we have named E rror- p rone p olymerase r egulator, EppR. We have found that EppR represses the expression of the genes encoding DNA Pol V and itself through direct binding to a conserved EppR motif in their promoters. Lastly, we show that EppR also regulates UmuDAb, previously identified as a regulator of genes encoding DNA Pol V. These two gene products are functionally required to ensure regulation of expression of genes encoding DNA Pol Vs and umuDAb. With these results, we propose a co-repressor model for the regulation of genes encoding DNA Pol V and umuDAb.
01 Oct 2024Submitted to Molecular Microbiology
03 Oct 2024Submission Checks Completed
03 Oct 2024Assigned to Editor
08 Oct 2024Reviewer(s) Assigned
28 Oct 2024Review(s) Completed, Editorial Evaluation Pending
06 Nov 2024Editorial Decision: Revise Minor