Cargando…

The Structural Basis for Promoter −35 Element Recognition by the Group IV σ Factors

The control of bacterial transcription initiation depends on a primary σ factor for housekeeping functions, as well as alternative σ factors that control regulons in response to environmental stresses. The largest and most diverse subgroup of alternative σ factors, the group IV extracytoplasmic func...

Descripción completa

Detalles Bibliográficos
Autores principales: Lane, William J, Darst, Seth A
Formato: Texto
Lenguaje:English
Publicado: Public Library of Science 2006
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1540707/
https://www.ncbi.nlm.nih.gov/pubmed/16903784
http://dx.doi.org/10.1371/journal.pbio.0040269
_version_ 1782129173974745088
author Lane, William J
Darst, Seth A
author_facet Lane, William J
Darst, Seth A
author_sort Lane, William J
collection PubMed
description The control of bacterial transcription initiation depends on a primary σ factor for housekeeping functions, as well as alternative σ factors that control regulons in response to environmental stresses. The largest and most diverse subgroup of alternative σ factors, the group IV extracytoplasmic function σ factors, directs the transcription of genes that regulate a wide variety of responses, including envelope stress and pathogenesis. We determined the 2.3-Å resolution crystal structure of the −35 element recognition domain of a group IV σ factor, Escherichia coli σ(E) (4), bound to its consensus −35 element, GGAACTT. Despite similar function and secondary structure, the primary and group IV σ factors recognize their −35 elements using distinct mechanisms. Conserved sequence elements of the σ(E) −35 element induce a DNA geometry characteristic of AA/TT-tract DNA, including a rigid, straight double-helical axis and a narrow minor groove. For this reason, the highly conserved AA in the middle of the GGAACTT motif is essential for −35 element recognition by σ(E) (4), despite the absence of direct protein–DNA interactions with these DNA bases. These principles of σ(E) (4)/−35 element recognition can be applied to a wide range of other group IV σ factors.
format Text
id pubmed-1540707
institution National Center for Biotechnology Information
language English
publishDate 2006
publisher Public Library of Science
record_format MEDLINE/PubMed
spelling pubmed-15407072006-09-21 The Structural Basis for Promoter −35 Element Recognition by the Group IV σ Factors Lane, William J Darst, Seth A PLoS Biol Research Article The control of bacterial transcription initiation depends on a primary σ factor for housekeeping functions, as well as alternative σ factors that control regulons in response to environmental stresses. The largest and most diverse subgroup of alternative σ factors, the group IV extracytoplasmic function σ factors, directs the transcription of genes that regulate a wide variety of responses, including envelope stress and pathogenesis. We determined the 2.3-Å resolution crystal structure of the −35 element recognition domain of a group IV σ factor, Escherichia coli σ(E) (4), bound to its consensus −35 element, GGAACTT. Despite similar function and secondary structure, the primary and group IV σ factors recognize their −35 elements using distinct mechanisms. Conserved sequence elements of the σ(E) −35 element induce a DNA geometry characteristic of AA/TT-tract DNA, including a rigid, straight double-helical axis and a narrow minor groove. For this reason, the highly conserved AA in the middle of the GGAACTT motif is essential for −35 element recognition by σ(E) (4), despite the absence of direct protein–DNA interactions with these DNA bases. These principles of σ(E) (4)/−35 element recognition can be applied to a wide range of other group IV σ factors. Public Library of Science 2006-09 2006-08-15 /pmc/articles/PMC1540707/ /pubmed/16903784 http://dx.doi.org/10.1371/journal.pbio.0040269 Text en © 2006 Lane and Darst. http://creativecommons.org/licenses/by/4.0/ 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 author and source are properly credited.
spellingShingle Research Article
Lane, William J
Darst, Seth A
The Structural Basis for Promoter −35 Element Recognition by the Group IV σ Factors
title The Structural Basis for Promoter −35 Element Recognition by the Group IV σ Factors
title_full The Structural Basis for Promoter −35 Element Recognition by the Group IV σ Factors
title_fullStr The Structural Basis for Promoter −35 Element Recognition by the Group IV σ Factors
title_full_unstemmed The Structural Basis for Promoter −35 Element Recognition by the Group IV σ Factors
title_short The Structural Basis for Promoter −35 Element Recognition by the Group IV σ Factors
title_sort structural basis for promoter −35 element recognition by the group iv σ factors
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1540707/
https://www.ncbi.nlm.nih.gov/pubmed/16903784
http://dx.doi.org/10.1371/journal.pbio.0040269
work_keys_str_mv AT lanewilliamj thestructuralbasisforpromoter35elementrecognitionbythegroupivsfactors
AT darstsetha thestructuralbasisforpromoter35elementrecognitionbythegroupivsfactors
AT lanewilliamj structuralbasisforpromoter35elementrecognitionbythegroupivsfactors
AT darstsetha structuralbasisforpromoter35elementrecognitionbythegroupivsfactors