DNA supercoiling in Escherichia coli: topA mutations can be suppressed by DNA amplifications involving the tolC locus

Dorman, C. J. ; Lynch, A. S. ; Bhriain, N. Ni ; Higgins, C. F.

Oxford, UK : Blackwell Publishing Ltd
Published 1989
ISSN:
1365-2958
Source:
Blackwell Publishing Journal Backfiles 1879-2005
Topics:
Biology
Medicine
Notes:
The level of DNA supercoiling is crucial for many cellular processes, Including gene expression, and is determined, primarily, by the opposing actions of two enzymes: topoisomerase I and DNA gyrase. Escherichia coli strains lacking topoisomerase I (topA mutants) normally fail to grow in the absence of compensatory mutations which are presumed to relax DNA. We have found that, in media of low osmolarity, topA mutants are viable in the absence of any compensatory mutation, consistent with the view that decreased extracellular osmolarity causes a relaxation of cellular DNA. At higher osmolarity most compensatory mutations, as expected, are in the gyrA and gyrB genes. The only other locus at which compensatory mutations arise, designated toc, is shown to involve the amplification of a region of chromosomal DNA which includes the tolC gene. However, amplification of tolC alone is insufficient to explain the phenotypes of toc mutants. tolC insertion mutations alter the distribution of plasmid topoisomers in vivo. This effect is probably indirect, possibly a result of altered membrane structure and an alteration in the cell's osmotic barrier. As tolC is a highly pleiotropic locus, affecting the expression of many genes, it is possible that some of the TolC phenotypes are a direct result of this topological change. The possible relationship between toe and tolC mutations, and the means by which tolC mutations might affect DNA supercoiling, are discussed.
Type of Medium:
Electronic Resource
URL:
_version_ 1798290416003448832
autor Dorman, C. J.
Lynch, A. S.
Bhriain, N. Ni
Higgins, C. F.
autorsonst Higgins, C. F.
book_url http://dx.doi.org/10.1111/j.1365-2958.1989.tb00199.x
datenlieferant nat_lic_papers
hauptsatz hsatz_simple
identnr NLZ241779987
insertion_date 2012-04-27
issn 1365-2958
journal_name Molecular microbiology
materialart 1
notes The level of DNA supercoiling is crucial for many cellular processes, Including gene expression, and is determined, primarily, by the opposing actions of two enzymes: topoisomerase I and DNA gyrase. Escherichia coli strains lacking topoisomerase I (topA mutants) normally fail to grow in the absence of compensatory mutations which are presumed to relax DNA. We have found that, in media of low osmolarity, topA mutants are viable in the absence of any compensatory mutation, consistent with the view that decreased extracellular osmolarity causes a relaxation of cellular DNA. At higher osmolarity most compensatory mutations, as expected, are in the gyrA and gyrB genes. The only other locus at which compensatory mutations arise, designated toc, is shown to involve the amplification of a region of chromosomal DNA which includes the tolC gene. However, amplification of tolC alone is insufficient to explain the phenotypes of toc mutants. tolC insertion mutations alter the distribution of plasmid topoisomers in vivo. This effect is probably indirect, possibly a result of altered membrane structure and an alteration in the cell's osmotic barrier. As tolC is a highly pleiotropic locus, affecting the expression of many genes, it is possible that some of the TolC phenotypes are a direct result of this topological change. The possible relationship between toe and tolC mutations, and the means by which tolC mutations might affect DNA supercoiling, are discussed.
package_name Blackwell Publishing
publikationsjahr_anzeige 1989
publikationsjahr_facette 1989
publikationsjahr_intervall 8014:1985-1989
publikationsjahr_sort 1989
publikationsort Oxford, UK
publisher Blackwell Publishing Ltd
reference 3 (1989), S. 0
search_space articles
shingle_author_1 Dorman, C. J.
Lynch, A. S.
Bhriain, N. Ni
Higgins, C. F.
shingle_author_2 Dorman, C. J.
Lynch, A. S.
Bhriain, N. Ni
Higgins, C. F.
shingle_author_3 Dorman, C. J.
Lynch, A. S.
Bhriain, N. Ni
Higgins, C. F.
shingle_author_4 Dorman, C. J.
Lynch, A. S.
Bhriain, N. Ni
Higgins, C. F.
shingle_catch_all_1 Dorman, C. J.
Lynch, A. S.
Bhriain, N. Ni
Higgins, C. F.
DNA supercoiling in Escherichia coli: topA mutations can be suppressed by DNA amplifications involving the tolC locus
Blackwell Publishing Ltd
The level of DNA supercoiling is crucial for many cellular processes, Including gene expression, and is determined, primarily, by the opposing actions of two enzymes: topoisomerase I and DNA gyrase. Escherichia coli strains lacking topoisomerase I (topA mutants) normally fail to grow in the absence of compensatory mutations which are presumed to relax DNA. We have found that, in media of low osmolarity, topA mutants are viable in the absence of any compensatory mutation, consistent with the view that decreased extracellular osmolarity causes a relaxation of cellular DNA. At higher osmolarity most compensatory mutations, as expected, are in the gyrA and gyrB genes. The only other locus at which compensatory mutations arise, designated toc, is shown to involve the amplification of a region of chromosomal DNA which includes the tolC gene. However, amplification of tolC alone is insufficient to explain the phenotypes of toc mutants. tolC insertion mutations alter the distribution of plasmid topoisomers in vivo. This effect is probably indirect, possibly a result of altered membrane structure and an alteration in the cell's osmotic barrier. As tolC is a highly pleiotropic locus, affecting the expression of many genes, it is possible that some of the TolC phenotypes are a direct result of this topological change. The possible relationship between toe and tolC mutations, and the means by which tolC mutations might affect DNA supercoiling, are discussed.
1365-2958
13652958
shingle_catch_all_2 Dorman, C. J.
Lynch, A. S.
Bhriain, N. Ni
Higgins, C. F.
DNA supercoiling in Escherichia coli: topA mutations can be suppressed by DNA amplifications involving the tolC locus
Blackwell Publishing Ltd
The level of DNA supercoiling is crucial for many cellular processes, Including gene expression, and is determined, primarily, by the opposing actions of two enzymes: topoisomerase I and DNA gyrase. Escherichia coli strains lacking topoisomerase I (topA mutants) normally fail to grow in the absence of compensatory mutations which are presumed to relax DNA. We have found that, in media of low osmolarity, topA mutants are viable in the absence of any compensatory mutation, consistent with the view that decreased extracellular osmolarity causes a relaxation of cellular DNA. At higher osmolarity most compensatory mutations, as expected, are in the gyrA and gyrB genes. The only other locus at which compensatory mutations arise, designated toc, is shown to involve the amplification of a region of chromosomal DNA which includes the tolC gene. However, amplification of tolC alone is insufficient to explain the phenotypes of toc mutants. tolC insertion mutations alter the distribution of plasmid topoisomers in vivo. This effect is probably indirect, possibly a result of altered membrane structure and an alteration in the cell's osmotic barrier. As tolC is a highly pleiotropic locus, affecting the expression of many genes, it is possible that some of the TolC phenotypes are a direct result of this topological change. The possible relationship between toe and tolC mutations, and the means by which tolC mutations might affect DNA supercoiling, are discussed.
1365-2958
13652958
shingle_catch_all_3 Dorman, C. J.
Lynch, A. S.
Bhriain, N. Ni
Higgins, C. F.
DNA supercoiling in Escherichia coli: topA mutations can be suppressed by DNA amplifications involving the tolC locus
Blackwell Publishing Ltd
The level of DNA supercoiling is crucial for many cellular processes, Including gene expression, and is determined, primarily, by the opposing actions of two enzymes: topoisomerase I and DNA gyrase. Escherichia coli strains lacking topoisomerase I (topA mutants) normally fail to grow in the absence of compensatory mutations which are presumed to relax DNA. We have found that, in media of low osmolarity, topA mutants are viable in the absence of any compensatory mutation, consistent with the view that decreased extracellular osmolarity causes a relaxation of cellular DNA. At higher osmolarity most compensatory mutations, as expected, are in the gyrA and gyrB genes. The only other locus at which compensatory mutations arise, designated toc, is shown to involve the amplification of a region of chromosomal DNA which includes the tolC gene. However, amplification of tolC alone is insufficient to explain the phenotypes of toc mutants. tolC insertion mutations alter the distribution of plasmid topoisomers in vivo. This effect is probably indirect, possibly a result of altered membrane structure and an alteration in the cell's osmotic barrier. As tolC is a highly pleiotropic locus, affecting the expression of many genes, it is possible that some of the TolC phenotypes are a direct result of this topological change. The possible relationship between toe and tolC mutations, and the means by which tolC mutations might affect DNA supercoiling, are discussed.
1365-2958
13652958
shingle_catch_all_4 Dorman, C. J.
Lynch, A. S.
Bhriain, N. Ni
Higgins, C. F.
DNA supercoiling in Escherichia coli: topA mutations can be suppressed by DNA amplifications involving the tolC locus
Blackwell Publishing Ltd
The level of DNA supercoiling is crucial for many cellular processes, Including gene expression, and is determined, primarily, by the opposing actions of two enzymes: topoisomerase I and DNA gyrase. Escherichia coli strains lacking topoisomerase I (topA mutants) normally fail to grow in the absence of compensatory mutations which are presumed to relax DNA. We have found that, in media of low osmolarity, topA mutants are viable in the absence of any compensatory mutation, consistent with the view that decreased extracellular osmolarity causes a relaxation of cellular DNA. At higher osmolarity most compensatory mutations, as expected, are in the gyrA and gyrB genes. The only other locus at which compensatory mutations arise, designated toc, is shown to involve the amplification of a region of chromosomal DNA which includes the tolC gene. However, amplification of tolC alone is insufficient to explain the phenotypes of toc mutants. tolC insertion mutations alter the distribution of plasmid topoisomers in vivo. This effect is probably indirect, possibly a result of altered membrane structure and an alteration in the cell's osmotic barrier. As tolC is a highly pleiotropic locus, affecting the expression of many genes, it is possible that some of the TolC phenotypes are a direct result of this topological change. The possible relationship between toe and tolC mutations, and the means by which tolC mutations might affect DNA supercoiling, are discussed.
1365-2958
13652958
shingle_title_1 DNA supercoiling in Escherichia coli: topA mutations can be suppressed by DNA amplifications involving the tolC locus
shingle_title_2 DNA supercoiling in Escherichia coli: topA mutations can be suppressed by DNA amplifications involving the tolC locus
shingle_title_3 DNA supercoiling in Escherichia coli: topA mutations can be suppressed by DNA amplifications involving the tolC locus
shingle_title_4 DNA supercoiling in Escherichia coli: topA mutations can be suppressed by DNA amplifications involving the tolC locus
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source_archive Blackwell Publishing Journal Backfiles 1879-2005
timestamp 2024-05-06T08:16:23.097Z
titel DNA supercoiling in Escherichia coli: topA mutations can be suppressed by DNA amplifications involving the tolC locus
titel_suche DNA supercoiling in Escherichia coli: topA mutations can be suppressed by DNA amplifications involving the tolC locus
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WW-YZ
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