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A RecB-family nuclease motif in the Type I restriction endonuclease EcoR124I
The Type I restriction-modification enzyme EcoR124I is an ATP-dependent endonuclease that uses dsDNA translocation to locate and cleave distant non-specific DNA sites. Bioinformatic analysis of the HsdR subunits of EcoR124I and related Type I enzymes showed that in addition to the principal PD-(E/D)...
Autores principales: | , , , |
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Formato: | Texto |
Lenguaje: | English |
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Oxford University Press
2008
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2475608/ https://www.ncbi.nlm.nih.gov/pubmed/18511464 http://dx.doi.org/10.1093/nar/gkn333 |
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author | Šišáková, Eva Stanley, Louise K. Weiserová, Marie Szczelkun, Mark D. |
author_facet | Šišáková, Eva Stanley, Louise K. Weiserová, Marie Szczelkun, Mark D. |
author_sort | Šišáková, Eva |
collection | PubMed |
description | The Type I restriction-modification enzyme EcoR124I is an ATP-dependent endonuclease that uses dsDNA translocation to locate and cleave distant non-specific DNA sites. Bioinformatic analysis of the HsdR subunits of EcoR124I and related Type I enzymes showed that in addition to the principal PD-(E/D)xK Motifs, I, II and III, a QxxxY motif is also present that is characteristic of RecB-family nucleases. The QxxxY motif resides immediately C-terminal to Motif III within a region of predicted α-helix. Using mutagenesis, we examined the role of the Q and Y residues in DNA binding, translocation and cleavage. Roles for the QxxxY motif in coordinating the catalytic residues or in stabilizing the nuclease domain on the DNA are discussed. |
format | Text |
id | pubmed-2475608 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2008 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-24756082008-07-21 A RecB-family nuclease motif in the Type I restriction endonuclease EcoR124I Šišáková, Eva Stanley, Louise K. Weiserová, Marie Szczelkun, Mark D. Nucleic Acids Res Nucleic Acid Enzymes The Type I restriction-modification enzyme EcoR124I is an ATP-dependent endonuclease that uses dsDNA translocation to locate and cleave distant non-specific DNA sites. Bioinformatic analysis of the HsdR subunits of EcoR124I and related Type I enzymes showed that in addition to the principal PD-(E/D)xK Motifs, I, II and III, a QxxxY motif is also present that is characteristic of RecB-family nucleases. The QxxxY motif resides immediately C-terminal to Motif III within a region of predicted α-helix. Using mutagenesis, we examined the role of the Q and Y residues in DNA binding, translocation and cleavage. Roles for the QxxxY motif in coordinating the catalytic residues or in stabilizing the nuclease domain on the DNA are discussed. Oxford University Press 2008-07 2008-05-29 /pmc/articles/PMC2475608/ /pubmed/18511464 http://dx.doi.org/10.1093/nar/gkn333 Text en © 2008 The Author(s) http://creativecommons.org/licenses/by-nc/2.0/uk/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/2.0/uk/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Nucleic Acid Enzymes Šišáková, Eva Stanley, Louise K. Weiserová, Marie Szczelkun, Mark D. A RecB-family nuclease motif in the Type I restriction endonuclease EcoR124I |
title | A RecB-family nuclease motif in the Type I restriction endonuclease EcoR124I |
title_full | A RecB-family nuclease motif in the Type I restriction endonuclease EcoR124I |
title_fullStr | A RecB-family nuclease motif in the Type I restriction endonuclease EcoR124I |
title_full_unstemmed | A RecB-family nuclease motif in the Type I restriction endonuclease EcoR124I |
title_short | A RecB-family nuclease motif in the Type I restriction endonuclease EcoR124I |
title_sort | recb-family nuclease motif in the type i restriction endonuclease ecor124i |
topic | Nucleic Acid Enzymes |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2475608/ https://www.ncbi.nlm.nih.gov/pubmed/18511464 http://dx.doi.org/10.1093/nar/gkn333 |
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