Everything OLD is new again: How structural, functional, and bioinformatic advances have redefined a neglected nuclease family

Author:

Dot Elena Wanvig1ORCID,Thomason Lynn C.2ORCID,Chappie Joshua S.1ORCID

Affiliation:

1. Department of Molecular Medicine Cornell University Ithaca New York USA

2. Molecular Control and Genetics Section, RNA Biology Laboratory National Cancer Institute at Frederick, National Institutes of Health Frederick Maryland USA

Abstract

AbstractOvercoming lysogenization defect (OLD) proteins are a conserved family of ATP‐powered nucleases that function in anti‐phage defense. Recent bioinformatic, genetic, and crystallographic studies have yielded new insights into the structure, function, and evolution of these enzymes. Here we review these developments and propose a new classification scheme to categorize OLD homologs that relies on gene neighborhoods, biochemical properties, domain organization, and catalytic machinery. This taxonomy reveals important similarities and differences between family members and provides a blueprint to contextualize future in vivo and in vitro findings. We also detail how OLD nucleases are related to PARIS and Septu anti‐phage defense systems and discuss important mechanistic questions that remain unanswered.

Funder

National Cancer Institute

National Institute of General Medical Sciences

Publisher

Wiley

Subject

Molecular Biology,Microbiology

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