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Prokaryotic genome regulation: A revolutionary paradigm

After determination of the whole genome sequence, the research frontier of bacterial molecular genetics has shifted to reveal the genome regulation under stressful conditions in nature. The gene selectivity of RNA polymerase is modulated after interaction with two groups of regulatory proteins, 7 si...

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Autor principal: ISHIHAMA, Akira
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Japan Academy 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3511978/
https://www.ncbi.nlm.nih.gov/pubmed/23138451
http://dx.doi.org/10.2183/pjab.88.485
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author ISHIHAMA, Akira
author_facet ISHIHAMA, Akira
author_sort ISHIHAMA, Akira
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description After determination of the whole genome sequence, the research frontier of bacterial molecular genetics has shifted to reveal the genome regulation under stressful conditions in nature. The gene selectivity of RNA polymerase is modulated after interaction with two groups of regulatory proteins, 7 sigma factors and 300 transcription factors. For identification of regulation targets of transcription factors in Escherichia coli, we have developed Genomic SELEX system and subjected to screening the binding sites of these factors on the genome. The number of regulation targets by a single transcription factor was more than those hitherto recognized, ranging up to hundreds of promoters. The number of transcription factors involved in regulation of a single promoter also increased to as many as 30 regulators. The multi-target transcription factors and the multi-factor promoters were assembled into complex networks of transcription regulation. The most complex network was identified in the regulation cascades of transcription of two master regulators for planktonic growth and biofilm formation.
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spelling pubmed-35119782012-12-21 Prokaryotic genome regulation: A revolutionary paradigm ISHIHAMA, Akira Proc Jpn Acad Ser B Phys Biol Sci Review After determination of the whole genome sequence, the research frontier of bacterial molecular genetics has shifted to reveal the genome regulation under stressful conditions in nature. The gene selectivity of RNA polymerase is modulated after interaction with two groups of regulatory proteins, 7 sigma factors and 300 transcription factors. For identification of regulation targets of transcription factors in Escherichia coli, we have developed Genomic SELEX system and subjected to screening the binding sites of these factors on the genome. The number of regulation targets by a single transcription factor was more than those hitherto recognized, ranging up to hundreds of promoters. The number of transcription factors involved in regulation of a single promoter also increased to as many as 30 regulators. The multi-target transcription factors and the multi-factor promoters were assembled into complex networks of transcription regulation. The most complex network was identified in the regulation cascades of transcription of two master regulators for planktonic growth and biofilm formation. The Japan Academy 2012-11-09 /pmc/articles/PMC3511978/ /pubmed/23138451 http://dx.doi.org/10.2183/pjab.88.485 Text en © 2012 The Japan Academy This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Review
ISHIHAMA, Akira
Prokaryotic genome regulation: A revolutionary paradigm
title Prokaryotic genome regulation: A revolutionary paradigm
title_full Prokaryotic genome regulation: A revolutionary paradigm
title_fullStr Prokaryotic genome regulation: A revolutionary paradigm
title_full_unstemmed Prokaryotic genome regulation: A revolutionary paradigm
title_short Prokaryotic genome regulation: A revolutionary paradigm
title_sort prokaryotic genome regulation: a revolutionary paradigm
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3511978/
https://www.ncbi.nlm.nih.gov/pubmed/23138451
http://dx.doi.org/10.2183/pjab.88.485
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