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Markerless Escherichia coli rrn Deletion Strains for Genetic Determination of Ribosomal Binding Sites

Single-copy rrn strains facilitate genetic ribosomal studies in Escherichia coli. Consecutive markerless deletion of rrn operons resulted in slower growth upon inactivation of the fourth copy, which was reversed by supplying transfer RNA genes encoded in rrn operons in trans. Removal of the sixth, p...

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Autores principales: Quan, Selwyn, Skovgaard, Ole, McLaughlin, Robert E., Buurman, Ed T., Squires, Catherine L.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Genetics Society of America 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4683628/
https://www.ncbi.nlm.nih.gov/pubmed/26438293
http://dx.doi.org/10.1534/g3.115.022301
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author Quan, Selwyn
Skovgaard, Ole
McLaughlin, Robert E.
Buurman, Ed T.
Squires, Catherine L.
author_facet Quan, Selwyn
Skovgaard, Ole
McLaughlin, Robert E.
Buurman, Ed T.
Squires, Catherine L.
author_sort Quan, Selwyn
collection PubMed
description Single-copy rrn strains facilitate genetic ribosomal studies in Escherichia coli. Consecutive markerless deletion of rrn operons resulted in slower growth upon inactivation of the fourth copy, which was reversed by supplying transfer RNA genes encoded in rrn operons in trans. Removal of the sixth, penultimate rrn copy led to a reduced growth rate due to limited rrn gene dosage. Whole-genome sequencing of variants of single-copy rrn strains revealed duplications of large stretches of genomic DNA. The combination of selective pressure, resulting from the decreased growth rate, and the six identical remaining scar sequences, facilitating homologous recombination events, presumably leads to elevated genomic instability.
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spelling pubmed-46836282015-12-18 Markerless Escherichia coli rrn Deletion Strains for Genetic Determination of Ribosomal Binding Sites Quan, Selwyn Skovgaard, Ole McLaughlin, Robert E. Buurman, Ed T. Squires, Catherine L. G3 (Bethesda) Investigations Single-copy rrn strains facilitate genetic ribosomal studies in Escherichia coli. Consecutive markerless deletion of rrn operons resulted in slower growth upon inactivation of the fourth copy, which was reversed by supplying transfer RNA genes encoded in rrn operons in trans. Removal of the sixth, penultimate rrn copy led to a reduced growth rate due to limited rrn gene dosage. Whole-genome sequencing of variants of single-copy rrn strains revealed duplications of large stretches of genomic DNA. The combination of selective pressure, resulting from the decreased growth rate, and the six identical remaining scar sequences, facilitating homologous recombination events, presumably leads to elevated genomic instability. Genetics Society of America 2015-10-04 /pmc/articles/PMC4683628/ /pubmed/26438293 http://dx.doi.org/10.1534/g3.115.022301 Text en Copyright © 2015 Quan et al. http://creativecommons.org/licenses/by/4.0/ 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, provided the original work is properly cited.
spellingShingle Investigations
Quan, Selwyn
Skovgaard, Ole
McLaughlin, Robert E.
Buurman, Ed T.
Squires, Catherine L.
Markerless Escherichia coli rrn Deletion Strains for Genetic Determination of Ribosomal Binding Sites
title Markerless Escherichia coli rrn Deletion Strains for Genetic Determination of Ribosomal Binding Sites
title_full Markerless Escherichia coli rrn Deletion Strains for Genetic Determination of Ribosomal Binding Sites
title_fullStr Markerless Escherichia coli rrn Deletion Strains for Genetic Determination of Ribosomal Binding Sites
title_full_unstemmed Markerless Escherichia coli rrn Deletion Strains for Genetic Determination of Ribosomal Binding Sites
title_short Markerless Escherichia coli rrn Deletion Strains for Genetic Determination of Ribosomal Binding Sites
title_sort markerless escherichia coli rrn deletion strains for genetic determination of ribosomal binding sites
topic Investigations
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4683628/
https://www.ncbi.nlm.nih.gov/pubmed/26438293
http://dx.doi.org/10.1534/g3.115.022301
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