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Restriction Enzyme Body Doubles and PCR Cloning: On the General Use of Type IIS Restriction Enzymes for Cloning
The procedure described here allows the cloning of PCR fragments containing a recognition site of the restriction endonuclease (Type IIP) used for cloning in the sequence of the insert. A Type IIS endonuclease - a Body Double of the Type IIP enzyme - is used to generate the same protruding palindrom...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3949710/ https://www.ncbi.nlm.nih.gov/pubmed/24618593 http://dx.doi.org/10.1371/journal.pone.0090896 |
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author | Tóth, Eszter Huszár, Krisztina Bencsura, Petra Kulcsár, Péter István Vodicska, Barbara Nyeste, Antal Welker, Zsombor Tóth, Szilvia Welker, Ervin |
author_facet | Tóth, Eszter Huszár, Krisztina Bencsura, Petra Kulcsár, Péter István Vodicska, Barbara Nyeste, Antal Welker, Zsombor Tóth, Szilvia Welker, Ervin |
author_sort | Tóth, Eszter |
collection | PubMed |
description | The procedure described here allows the cloning of PCR fragments containing a recognition site of the restriction endonuclease (Type IIP) used for cloning in the sequence of the insert. A Type IIS endonuclease - a Body Double of the Type IIP enzyme - is used to generate the same protruding palindrome. Thus, the insert can be cloned to the Type IIP site of the vector without digesting the PCR product with the same Type IIP enzyme. We achieve this by incorporating the recognition site of a Type IIS restriction enzyme that cleaves the DNA outside of its recognition site in the PCR primer in such a way that the cutting positions straddle the desired overhang sequence. Digestion of the PCR product by the Body Double generates the required overhang. Hitherto the use of Type IIS restriction enzymes in cloning reactions has only been used for special applications, the approach presented here makes Type IIS enzymes as useful as Type IIP enzymes for general cloning purposes. To assist in finding Body Double enzymes, we summarised the available Type IIS enzymes which are potentially useful for Body Double cloning and created an online program (http://group.szbk.u-szeged.hu/welkergr/body_double/index.html) for the selection of suitable Body Double enzymes and the design of the appropriate primers. |
format | Online Article Text |
id | pubmed-3949710 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-39497102014-03-12 Restriction Enzyme Body Doubles and PCR Cloning: On the General Use of Type IIS Restriction Enzymes for Cloning Tóth, Eszter Huszár, Krisztina Bencsura, Petra Kulcsár, Péter István Vodicska, Barbara Nyeste, Antal Welker, Zsombor Tóth, Szilvia Welker, Ervin PLoS One Research Article The procedure described here allows the cloning of PCR fragments containing a recognition site of the restriction endonuclease (Type IIP) used for cloning in the sequence of the insert. A Type IIS endonuclease - a Body Double of the Type IIP enzyme - is used to generate the same protruding palindrome. Thus, the insert can be cloned to the Type IIP site of the vector without digesting the PCR product with the same Type IIP enzyme. We achieve this by incorporating the recognition site of a Type IIS restriction enzyme that cleaves the DNA outside of its recognition site in the PCR primer in such a way that the cutting positions straddle the desired overhang sequence. Digestion of the PCR product by the Body Double generates the required overhang. Hitherto the use of Type IIS restriction enzymes in cloning reactions has only been used for special applications, the approach presented here makes Type IIS enzymes as useful as Type IIP enzymes for general cloning purposes. To assist in finding Body Double enzymes, we summarised the available Type IIS enzymes which are potentially useful for Body Double cloning and created an online program (http://group.szbk.u-szeged.hu/welkergr/body_double/index.html) for the selection of suitable Body Double enzymes and the design of the appropriate primers. Public Library of Science 2014-03-11 /pmc/articles/PMC3949710/ /pubmed/24618593 http://dx.doi.org/10.1371/journal.pone.0090896 Text en © 2014 Tóth et al 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 Tóth, Eszter Huszár, Krisztina Bencsura, Petra Kulcsár, Péter István Vodicska, Barbara Nyeste, Antal Welker, Zsombor Tóth, Szilvia Welker, Ervin Restriction Enzyme Body Doubles and PCR Cloning: On the General Use of Type IIS Restriction Enzymes for Cloning |
title | Restriction Enzyme Body Doubles and PCR Cloning: On the General Use of Type IIS Restriction Enzymes for Cloning |
title_full | Restriction Enzyme Body Doubles and PCR Cloning: On the General Use of Type IIS Restriction Enzymes for Cloning |
title_fullStr | Restriction Enzyme Body Doubles and PCR Cloning: On the General Use of Type IIS Restriction Enzymes for Cloning |
title_full_unstemmed | Restriction Enzyme Body Doubles and PCR Cloning: On the General Use of Type IIS Restriction Enzymes for Cloning |
title_short | Restriction Enzyme Body Doubles and PCR Cloning: On the General Use of Type IIS Restriction Enzymes for Cloning |
title_sort | restriction enzyme body doubles and pcr cloning: on the general use of type iis restriction enzymes for cloning |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3949710/ https://www.ncbi.nlm.nih.gov/pubmed/24618593 http://dx.doi.org/10.1371/journal.pone.0090896 |
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