Acquiring new genetic traits by lateral gene transfer is a bacterial strategy for environmental adaptations. We previously showed that Escherichia coli laterally transmits nonconjugative plasmids in cocultures that contain strains with or without the plasmid. Using a pMB1-derived plasmid and the Keio collection, a comprehensive library of E. coli knockout mutants for nonessential genes, we recently screened for genes responsible for promoting or repressing cell-to-cell plasmid transfer in recipient cells. In this study, we used a pSC101-derived plasmid, instead of a pMB1-derived plasmid, to screen for repressing genes and identified 29 “transfer-up” mutants. Among these, four mutants are common to those previously screened using a pMB1-derived plasmid. Although the roles of the 29 gene products in plasmid transfer mechanism remain uncertain, it is interesting that 28 of the 29 screened genes map to two limited regions on the E. coli chromosome: 18 genes at 34.25–35.31 min and 10 genes at 12.62–13.35 min. Because these two regions commonly contain termination (Ter) sites for DNA replication (TerC: 34.64 min and TerH: 12.91 min), it is possible that chromosomal mutations around specific Ter sites may affect plasmid acquisition in the recipient cells.
Published in | American Journal of Life Sciences (Volume 2, Issue 6) |
DOI | 10.11648/j.ajls.20140206.13 |
Page(s) | 345-350 |
Creative Commons |
This is an Open Access article, distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution and reproduction in any medium or format, provided the original work is properly cited. |
Copyright |
Copyright © The Author(s), 2014. Published by Science Publishing Group |
Lateral Gene Transfer, Keio Collection, pSC101-Derived Plasmid, Ter Site, Escherichia coli
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APA Style
Yuka Shibata, Akiko Matsumoto, Mutsumi Horino, Akiko Hirabayashi, Kozue Shirota, et al. (2014). Genome-Wide Screen for Escherichia coli Genes Involved in Repressing Cell-To-Cell Transfer of a Nonconjugative pSC101-Derived Plasmid. American Journal of Life Sciences, 2(6), 345-350. https://doi.org/10.11648/j.ajls.20140206.13
ACS Style
Yuka Shibata; Akiko Matsumoto; Mutsumi Horino; Akiko Hirabayashi; Kozue Shirota, et al. Genome-Wide Screen for Escherichia coli Genes Involved in Repressing Cell-To-Cell Transfer of a Nonconjugative pSC101-Derived Plasmid. Am. J. Life Sci. 2014, 2(6), 345-350. doi: 10.11648/j.ajls.20140206.13
AMA Style
Yuka Shibata, Akiko Matsumoto, Mutsumi Horino, Akiko Hirabayashi, Kozue Shirota, et al. Genome-Wide Screen for Escherichia coli Genes Involved in Repressing Cell-To-Cell Transfer of a Nonconjugative pSC101-Derived Plasmid. Am J Life Sci. 2014;2(6):345-350. doi: 10.11648/j.ajls.20140206.13
@article{10.11648/j.ajls.20140206.13, author = {Yuka Shibata and Akiko Matsumoto and Mutsumi Horino and Akiko Hirabayashi and Kozue Shirota and Chinatsu Kawano and Sumio Maeda}, title = {Genome-Wide Screen for Escherichia coli Genes Involved in Repressing Cell-To-Cell Transfer of a Nonconjugative pSC101-Derived Plasmid}, journal = {American Journal of Life Sciences}, volume = {2}, number = {6}, pages = {345-350}, doi = {10.11648/j.ajls.20140206.13}, url = {https://doi.org/10.11648/j.ajls.20140206.13}, eprint = {https://article.sciencepublishinggroup.com/pdf/10.11648.j.ajls.20140206.13}, abstract = {Acquiring new genetic traits by lateral gene transfer is a bacterial strategy for environmental adaptations. We previously showed that Escherichia coli laterally transmits nonconjugative plasmids in cocultures that contain strains with or without the plasmid. Using a pMB1-derived plasmid and the Keio collection, a comprehensive library of E. coli knockout mutants for nonessential genes, we recently screened for genes responsible for promoting or repressing cell-to-cell plasmid transfer in recipient cells. In this study, we used a pSC101-derived plasmid, instead of a pMB1-derived plasmid, to screen for repressing genes and identified 29 “transfer-up” mutants. Among these, four mutants are common to those previously screened using a pMB1-derived plasmid. Although the roles of the 29 gene products in plasmid transfer mechanism remain uncertain, it is interesting that 28 of the 29 screened genes map to two limited regions on the E. coli chromosome: 18 genes at 34.25–35.31 min and 10 genes at 12.62–13.35 min. Because these two regions commonly contain termination (Ter) sites for DNA replication (TerC: 34.64 min and TerH: 12.91 min), it is possible that chromosomal mutations around specific Ter sites may affect plasmid acquisition in the recipient cells.}, year = {2014} }
TY - JOUR T1 - Genome-Wide Screen for Escherichia coli Genes Involved in Repressing Cell-To-Cell Transfer of a Nonconjugative pSC101-Derived Plasmid AU - Yuka Shibata AU - Akiko Matsumoto AU - Mutsumi Horino AU - Akiko Hirabayashi AU - Kozue Shirota AU - Chinatsu Kawano AU - Sumio Maeda Y1 - 2014/11/21 PY - 2014 N1 - https://doi.org/10.11648/j.ajls.20140206.13 DO - 10.11648/j.ajls.20140206.13 T2 - American Journal of Life Sciences JF - American Journal of Life Sciences JO - American Journal of Life Sciences SP - 345 EP - 350 PB - Science Publishing Group SN - 2328-5737 UR - https://doi.org/10.11648/j.ajls.20140206.13 AB - Acquiring new genetic traits by lateral gene transfer is a bacterial strategy for environmental adaptations. We previously showed that Escherichia coli laterally transmits nonconjugative plasmids in cocultures that contain strains with or without the plasmid. Using a pMB1-derived plasmid and the Keio collection, a comprehensive library of E. coli knockout mutants for nonessential genes, we recently screened for genes responsible for promoting or repressing cell-to-cell plasmid transfer in recipient cells. In this study, we used a pSC101-derived plasmid, instead of a pMB1-derived plasmid, to screen for repressing genes and identified 29 “transfer-up” mutants. Among these, four mutants are common to those previously screened using a pMB1-derived plasmid. Although the roles of the 29 gene products in plasmid transfer mechanism remain uncertain, it is interesting that 28 of the 29 screened genes map to two limited regions on the E. coli chromosome: 18 genes at 34.25–35.31 min and 10 genes at 12.62–13.35 min. Because these two regions commonly contain termination (Ter) sites for DNA replication (TerC: 34.64 min and TerH: 12.91 min), it is possible that chromosomal mutations around specific Ter sites may affect plasmid acquisition in the recipient cells. VL - 2 IS - 6 ER -