TY - JOUR
T1 - Selfish restriction modification genes
T2 - Resistance of a resident R/M plasmid to displacement by an incompatible plasmid mediated by host killing
AU - Naito, Yasuhiro
AU - Naito, Taku
AU - Kobayashi, Ichizo
N1 - Funding Information:
This work was supported by grants from Ministry ofEducation, Science, Sports, and Culture ofJapan, Nagase Science Foundation and theTakeda Science Foundation.
PY - 1998
Y1 - 1998
N2 - Previous work from this laboratory demonstrated that plasmids carrying a type II restriction-modification gene complex are not easily lost from their bacterial host because plasmid-free segregant cells are killed through chromosome cleavage. Here, we have followed the course of events that takes place when an Escherichia coli recBC sbcA strain carrying a plasmid coding for the PaeR71 restriction-modification (R/M) gene complex is transformed by a plasmid with an identical origin of replication. The number of transformants that appeared was far fewer than with the restriction-minus (r-) control. Most of the transformants were very small. After prolonged incubation, the number and the size of the colonies increased, but this increase never attained the level of the r- control. Most of the transformed colonies retained the drug-resistance of the resident, r+ m+ plasmid. These results indicate that post-segregational host killing occurs when a plasmid bearing an R/M gene complex is displaced by an incompatible plasmid. Such cell killing eliminates the competitor plasmid along with the host and, thus, would allow persistence of the R/M plasmid in the neighboring, clonal host cells in nature. This phenomenon is reminiscent of mammalian apoptosis and other forms of altruistic cell death strategy against infection. This type of resistance to displacement was also studied in a wild type Escherichia coli strain that was normal for homologous recombination (rec+). A number of differences between the recBC sbcA strain and the rec+ strain were observed and these will be discussed.
AB - Previous work from this laboratory demonstrated that plasmids carrying a type II restriction-modification gene complex are not easily lost from their bacterial host because plasmid-free segregant cells are killed through chromosome cleavage. Here, we have followed the course of events that takes place when an Escherichia coli recBC sbcA strain carrying a plasmid coding for the PaeR71 restriction-modification (R/M) gene complex is transformed by a plasmid with an identical origin of replication. The number of transformants that appeared was far fewer than with the restriction-minus (r-) control. Most of the transformants were very small. After prolonged incubation, the number and the size of the colonies increased, but this increase never attained the level of the r- control. Most of the transformed colonies retained the drug-resistance of the resident, r+ m+ plasmid. These results indicate that post-segregational host killing occurs when a plasmid bearing an R/M gene complex is displaced by an incompatible plasmid. Such cell killing eliminates the competitor plasmid along with the host and, thus, would allow persistence of the R/M plasmid in the neighboring, clonal host cells in nature. This phenomenon is reminiscent of mammalian apoptosis and other forms of altruistic cell death strategy against infection. This type of resistance to displacement was also studied in a wild type Escherichia coli strain that was normal for homologous recombination (rec+). A number of differences between the recBC sbcA strain and the rec+ strain were observed and these will be discussed.
KW - Apoptosis
KW - Homologous recombination
KW - Plasmid
KW - Programmed cell death
KW - Selfish gene
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U2 - 10.1515/bchm.1998.379.4-5.429
DO - 10.1515/bchm.1998.379.4-5.429
M3 - Article
C2 - 9628334
AN - SCOPUS:0031981856
SN - 1431-6730
VL - 379
SP - 429
EP - 436
JO - Biological Chemistry
JF - Biological Chemistry
IS - 4-5
ER -