@article{f87c2807a3674d6b910a83b74be946e6,
title = "Discovery of Functional Toxin/Antitoxin Systems in Bacteria by Shotgun Cloning",
abstract = "Toxin-antitoxin (TA) modules, composed of a toxic protein and a counteracting antitoxin, play important roles in bacterial physiology. We examined the experimental insertion of 1.5 million genes from 388 microbial genomes into an Escherichia coli host using more than 8.5 million random clones. This revealed hundreds of genes (toxins) that could only be cloned when the neighboring gene (antitoxin) was present on the same clone. Clustering of these genes revealed TA families widespread in bacterial genomes, some of which deviate from the classical characteristics previously described for such modules. Introduction of these genes into E. coli validated that the toxin toxicity is mitigated by the antitoxin. Infection experiments with T7 phage showed that two of the new modules can provide resistance against phage. Moreover, our experiments revealed an {"} antidefense{"} protein in phage T7 that neutralizes phage resistance. Our results expose active fronts in the arms race between bacteria and phage.",
author = "Hila Sberro and Azita Leavitt and Ruth Kiro and Eugene Koh and Yoav Peleg and Udi Qimron and Rotem Sorek",
note = "Funding Information: We thank Shany Doron, Eyal Weinstock, Daniel Dar, Uri Gophna, Omri Wurtzel, Tal Dagan, Gil Amitai, and Debbie Lindell for comments and stimulating discussions. We also thank Ada Dantes for excellent technical support. R.S. was supported, in part, by NIH grant R01AI082376-01, ISF-FIRST program (grant 1615/09), ISF (grant 1303/12), ERC-StG program (grant 260432), and the Leona M. and Harry B. Helmsley Charitable Trust, and by a DIP grant from the Deutsche Forschungsgemeinschaft. ",
year = "2013",
month = apr,
day = "11",
doi = "10.1016/j.molcel.2013.02.002",
language = "אנגלית",
volume = "50",
pages = "136--148",
journal = "Molecular Cell",
issn = "1097-2765",
publisher = "Cell Press",
number = "1",
}