Cargando…
Recognition of dual symmetry by the controller protein C.Esp1396I based on the structure of the transcriptional activation complex
The controller protein C.Esp1396I regulates the timing of gene expression of the restriction–modification (RM) genes of the RM system Esp1396I. The molecular recognition of promoter sequences by such transcriptional regulators is poorly understood, in part because the DNA sequence motifs do not conf...
Autores principales: | , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2012
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3351150/ https://www.ncbi.nlm.nih.gov/pubmed/22210861 http://dx.doi.org/10.1093/nar/gkr1250 |
_version_ | 1782232735638618112 |
---|---|
author | McGeehan, J. E. Ball, N. J. Streeter, S. D. Thresh, S.-J. Kneale, G. G. |
author_facet | McGeehan, J. E. Ball, N. J. Streeter, S. D. Thresh, S.-J. Kneale, G. G. |
author_sort | McGeehan, J. E. |
collection | PubMed |
description | The controller protein C.Esp1396I regulates the timing of gene expression of the restriction–modification (RM) genes of the RM system Esp1396I. The molecular recognition of promoter sequences by such transcriptional regulators is poorly understood, in part because the DNA sequence motifs do not conform to a well-defined symmetry. We report here the crystal structure of the controller protein bound to a DNA operator site. The structure reveals how two different symmetries within the operator are simultaneously recognized by the homo-dimeric protein, underpinned by a conformational change in one of the protein subunits. The recognition of two different DNA symmetries through movement of a flexible loop in one of the protein subunits may represent a general mechanism for the recognition of pseudo-symmetric DNA sequences. |
format | Online Article Text |
id | pubmed-3351150 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-33511502012-05-14 Recognition of dual symmetry by the controller protein C.Esp1396I based on the structure of the transcriptional activation complex McGeehan, J. E. Ball, N. J. Streeter, S. D. Thresh, S.-J. Kneale, G. G. Nucleic Acids Res Structural Biology The controller protein C.Esp1396I regulates the timing of gene expression of the restriction–modification (RM) genes of the RM system Esp1396I. The molecular recognition of promoter sequences by such transcriptional regulators is poorly understood, in part because the DNA sequence motifs do not conform to a well-defined symmetry. We report here the crystal structure of the controller protein bound to a DNA operator site. The structure reveals how two different symmetries within the operator are simultaneously recognized by the homo-dimeric protein, underpinned by a conformational change in one of the protein subunits. The recognition of two different DNA symmetries through movement of a flexible loop in one of the protein subunits may represent a general mechanism for the recognition of pseudo-symmetric DNA sequences. Oxford University Press 2012-05 2011-12-29 /pmc/articles/PMC3351150/ /pubmed/22210861 http://dx.doi.org/10.1093/nar/gkr1250 Text en © The Author(s) 2011. Published by Oxford University Press. http://creativecommons.org/licenses/by-nc/3.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0), which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Structural Biology McGeehan, J. E. Ball, N. J. Streeter, S. D. Thresh, S.-J. Kneale, G. G. Recognition of dual symmetry by the controller protein C.Esp1396I based on the structure of the transcriptional activation complex |
title | Recognition of dual symmetry by the controller protein C.Esp1396I based on the structure of the transcriptional activation complex |
title_full | Recognition of dual symmetry by the controller protein C.Esp1396I based on the structure of the transcriptional activation complex |
title_fullStr | Recognition of dual symmetry by the controller protein C.Esp1396I based on the structure of the transcriptional activation complex |
title_full_unstemmed | Recognition of dual symmetry by the controller protein C.Esp1396I based on the structure of the transcriptional activation complex |
title_short | Recognition of dual symmetry by the controller protein C.Esp1396I based on the structure of the transcriptional activation complex |
title_sort | recognition of dual symmetry by the controller protein c.esp1396i based on the structure of the transcriptional activation complex |
topic | Structural Biology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3351150/ https://www.ncbi.nlm.nih.gov/pubmed/22210861 http://dx.doi.org/10.1093/nar/gkr1250 |
work_keys_str_mv | AT mcgeehanje recognitionofdualsymmetrybythecontrollerproteincesp1396ibasedonthestructureofthetranscriptionalactivationcomplex AT ballnj recognitionofdualsymmetrybythecontrollerproteincesp1396ibasedonthestructureofthetranscriptionalactivationcomplex AT streetersd recognitionofdualsymmetrybythecontrollerproteincesp1396ibasedonthestructureofthetranscriptionalactivationcomplex AT threshsj recognitionofdualsymmetrybythecontrollerproteincesp1396ibasedonthestructureofthetranscriptionalactivationcomplex AT knealegg recognitionofdualsymmetrybythecontrollerproteincesp1396ibasedonthestructureofthetranscriptionalactivationcomplex |