Multicopy suppressor screens reveal convergent evolution of single-gene lysis proteins

被引:0
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作者
Benjamin A. Adler
Karthik Chamakura
Heloise Carion
Jonathan Krog
Adam M. Deutschbauer
Ry Young
Vivek K. Mutalik
Adam P. Arkin
机构
[1] The UC Berkeley‐UCSF Graduate Program in Bioengineering,Department of Bioengineering
[2] University of California,Department of Biochemistry and Biophysics
[3] Berkeley,Environmental Genomics and Systems Biology Division
[4] Innovative Genomics Institute,undefined
[5] University of California,undefined
[6] Berkeley,undefined
[7] Center for Phage Technology,undefined
[8] Texas A&M University,undefined
[9] Lawrence Berkeley National Laboratory,undefined
[10] Armata Pharmaceuticals,undefined
[11] Inc.,undefined
来源
Nature Chemical Biology | 2023年 / 19卷
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摘要
Single-strand RNA (ssRNA) Fiersviridae phages cause host lysis with a product of single gene (sgl for single-gene lysis; product Sgl) that induces autolysis. Many different Sgls have been discovered, but the molecular targets of only a few have been identified. In this study, we used a high-throughput genetic screen to uncover genome-wide host suppressors of diverse Sgls. In addition to validating known molecular mechanisms, we discovered that the Sgl of PP7, an ssRNA phage of Pseudomonas aeruginosa, targets MurJ, the flippase responsible for lipid II export, previously shown to be the target of the Sgl of coliphage M. These two Sgls, which are unrelated and predicted to have opposite membrane topology, thus represent a case of convergent evolution. We extended the genetic screens to other uncharacterized Sgls and uncovered a common set of multicopy suppressors, suggesting that these Sgls act by the same or similar mechanism.
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页码:759 / 766
页数:7
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