Bacterial Argonaute nucleases reveal different modes of DNA targeting in vitro and in vivo
Abstract
Prokaryotic Argonaute proteins (pAgos) are homologs of eukaryotic Argonautes (eAgos) that were similarly proposed to play a role in cell defense against invaders. However, pAgos are much more diverse than eAgos and very little is known about their functional activity and target specificity in vivo. Here, we describe five pAgo proteins from mesophilic bacteria that act as DNA-guided DNA endonucleases and analyze their ability to target chromosomal and invader DNA. In vitro, the analyzed proteins use small guide DNAs for precise cleavage of single-stranded DNA at a wide range of temperatures. Upon their expression in Escherichia coli, all five pAgos are loaded with small DNAs preferentially produced from plasmid DNA and from chromosomal regions of replication termination. One of the tested pAgos, EmaAgo from Exiguobacterium marinum can induce DNA interference between multicopy sequences resulting in targeted processing of homologous plasmid and chromosomal loci. EmaAgo also protects bacteria from bacteriophage infection and is preferentially loaded with phage guide DNAs suggesting that the ability of pAgos to target multicopy elements may be crucial for their protective function. The wide spectrum of pAgo activities suggests that they may have diverse functions in vivo and paves the way for their use in biotechnology.
Additional Information
The copyright holder for this preprint is the author/funder, who has granted bioRxiv a license to display the preprint in perpetuity. It is made available under a CC-BY-NC-ND 4.0 International license. We thank Dr. David Leach and Dr. Gerry Smith for insightful discussions, Dr. Anna Olina for help in preparation of smDNA libaries. This study was supported in part by the Russian Science Foundation (grant 20-74-10127 to AA, analysis of in vitro activities of pAgos; grant 19-14-00359 to DE, analysis of genomic DNA targeting by pAgos). Data Availability. The smDNA sequencing datasets generated in this study are available from the Sequence Read Archive (SRA) database under accession numbers PRJNA827032 and PRJNA827167. The code used for data analysis is available at the GitHub repository at https://github.com/AlekseiAgapov/5pAgos. The genomic sequence of phage P1 used in the experiments is available from GenBank under accession number OP279344. All primary data are available from the corresponding author upon request. The authors have declared no competing interest.Attached Files
Submitted - 2022.09.09.507302v1.full.pdf
Supplemental Material - media-1.pdf
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Additional details
- Eprint ID
- 120339
- Resolver ID
- CaltechAUTHORS:20230322-367657000.25
- Russian Science Foundation
- 20-74-10127
- Russian Science Foundation
- 19-14-00359
- Created
-
2023-03-27Created from EPrint's datestamp field
- Updated
-
2023-05-03Created from EPrint's last_modified field
- Caltech groups
- Division of Biology and Biological Engineering (BBE)