A Subset of Exoribonucleases Serve as Degradative Enzymes for pGpG in c-di-GMP Signaling

Author:

Orr Mona W.1,Weiss Cordelia A.1,Severin Geoffrey B.2,Turdiev Husan1,Kim Soo-Kyoung1,Turdiev Asan1,Liu Kuanqing3,Tu Benjamin P.3,Waters Christopher M.4,Winkler Wade C.1,Lee Vincent T.1

Affiliation:

1. Department of Cell Biology and Molecular Genetics, University of Maryland, College Park, Maryland, USA

2. Department of Biochemistry & Molecular Biology, Michigan State University, East Lansing, Michigan, USA

3. Department of Biochemistry, University of Texas Southwestern Medical Center, Dallas, Texas, USA

4. Microbiology & Molecular Genetics, Michigan State University, East Lansing, Michigan, USA

Abstract

The bacterial bis-(3′-5′)-cyclic dimeric GMP (c-di-GMP) signaling molecule regulates complex processes, such as biofilm formation. c-di-GMP is degraded in two-steps, linearization into pGpG and subsequent cleavage to two GMPs. The 3′-to-5′ exonuclease oligoribonuclease (Orn) serves as the enzyme that degrades pGpG in Pseudomonas aeruginosa . Many phyla contain species that utilize c-di-GMP signaling but lack an Orn homolog, and the protein that functions to degrade pGpG remains uncharacterized. Here, systematic screening of genes encoding proteins containing domains found in exoribonucleases revealed a subset of genes encoded within the genomes of Bacillus anthracis and Vibrio cholerae that degrade pGpG to GMP and are functionally analogous to Orn. Feedback inhibition by pGpG is a conserved process, as strains lacking these genes accumulate c-di-GMP.

Funder

National Institutes of Health

HHS | National Institutes of Health

HHS | NIH | National Institute of Allergy and Infectious Diseases

National Science Foundation

Cystic Fibrosis Foundation

Publisher

American Society for Microbiology

Subject

Molecular Biology,Microbiology

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