Structural basis of antiphage defence by an ATPase-associated reverse transcriptase

Jerrin Thomas George(Montana State University), Nathaniel Burman(Montana State University), Royce A. Wilkinson(Montana State University), Senuri de Silva(Montana State University), Quynh McKelvey-Pham(Montana State University), Murat Buyukyoruk(Montana State University), Adelaide Dale(Montana State University), Hannah Landman(Montana State University), Ava B. Graham(Montana State University), Steven Z. DeLuca(Montana State University), Blake Wiedenheft(Montana State University)
Nature Communications
September 26, 2025
Cited by 8Open Access
Full Text

Abstract

Reverse transcriptases (RTs) have well-established roles in the replication and spread of retroviruses and retrotransposons. However, recent evidence suggests that RTs have been conscripted by cells for diverse roles in antiviral defence. Here we determine structures of a type I-A retron, which explain how RNA, DNA, RT, HNH-nuclease and four molecules of a structure maintenance of chromosome (SMC)-family ATPase assemble into a 364 kDa complex that provides phage defence. We show that phage-encoded nucleases trigger degradation of the retron-associated DNA, leading to activation of the HNH nuclease. The HNH nuclease cleaves tRNASer, stalling protein synthesis and arresting viral replication. Taken together, these data reveal diverse and paradoxical roles for RTs in the perpetuation and elimination of genetic parasites. In this study, the authors determine the structure of a Type I-A retron from E. coli FORC82 and reveal the functional interplay between Reverse Transcriptases (RTs) and Structural Maintenance of Chromosomes (SMC) ATPases.’


Related Papers

No related papers found

Powered by citation graph analysis