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The use of thymidine analogs to improve the replication of an extra DNA base pair: a synthetic biological system
Synthetic biology based on a six-letter genetic alphabet that includes the two non-standard nucleobases isoguanine (isoG) and isocytosine (isoC), as well as the standard A, T, G and C, is known to suffer as a consequence of a minor tautomeric form of isoguanine that pairs with thymine, and therefore...
Autores principales: | , |
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Formato: | Texto |
Lenguaje: | English |
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Oxford University Press
2005
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1236980/ https://www.ncbi.nlm.nih.gov/pubmed/16192575 http://dx.doi.org/10.1093/nar/gki873 |
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author | Sismour, A. Michael Benner, Steven A. |
author_facet | Sismour, A. Michael Benner, Steven A. |
author_sort | Sismour, A. Michael |
collection | PubMed |
description | Synthetic biology based on a six-letter genetic alphabet that includes the two non-standard nucleobases isoguanine (isoG) and isocytosine (isoC), as well as the standard A, T, G and C, is known to suffer as a consequence of a minor tautomeric form of isoguanine that pairs with thymine, and therefore leads to infidelity during repeated cycles of the PCR. Reported here is a solution to this problem. The solution replaces thymidine triphosphate by 2-thiothymidine triphosphate (2-thioTTP). Because of the bulk and hydrogen bonding properties of the thione unit in 2-thioT, 2-thioT does not mispair effectively with the minor tautomer of isoG. To test whether this might allow PCR amplification of a six-letter artificially expanded genetic information system, we examined the relative rates of misincorporation of 2-thioTTP and TTP opposite isoG using affinity electrophoresis. The concentrations of isoCTP and 2-thioTTP were optimal to best support PCR amplification using thermostable polymerases of a six-letter alphabet that includes the isoC–isoG pair. The fidelity-per-round of amplification was found to be ∼98% in trial PCRs with this six-letter DNA alphabet. The analogous PCR employing TTP had a fidelity-per-round of only ∼93%. Thus, the A, 2-thioT, G, C, isoC, isoG alphabet is an artificial genetic system capable of Darwinian evolution. |
format | Text |
id | pubmed-1236980 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2005 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-12369802005-09-30 The use of thymidine analogs to improve the replication of an extra DNA base pair: a synthetic biological system Sismour, A. Michael Benner, Steven A. Nucleic Acids Res Article Synthetic biology based on a six-letter genetic alphabet that includes the two non-standard nucleobases isoguanine (isoG) and isocytosine (isoC), as well as the standard A, T, G and C, is known to suffer as a consequence of a minor tautomeric form of isoguanine that pairs with thymine, and therefore leads to infidelity during repeated cycles of the PCR. Reported here is a solution to this problem. The solution replaces thymidine triphosphate by 2-thiothymidine triphosphate (2-thioTTP). Because of the bulk and hydrogen bonding properties of the thione unit in 2-thioT, 2-thioT does not mispair effectively with the minor tautomer of isoG. To test whether this might allow PCR amplification of a six-letter artificially expanded genetic information system, we examined the relative rates of misincorporation of 2-thioTTP and TTP opposite isoG using affinity electrophoresis. The concentrations of isoCTP and 2-thioTTP were optimal to best support PCR amplification using thermostable polymerases of a six-letter alphabet that includes the isoC–isoG pair. The fidelity-per-round of amplification was found to be ∼98% in trial PCRs with this six-letter DNA alphabet. The analogous PCR employing TTP had a fidelity-per-round of only ∼93%. Thus, the A, 2-thioT, G, C, isoC, isoG alphabet is an artificial genetic system capable of Darwinian evolution. Oxford University Press 2005 2005-09-28 /pmc/articles/PMC1236980/ /pubmed/16192575 http://dx.doi.org/10.1093/nar/gki873 Text en © The Author 2005. Published by Oxford University Press. All rights reserved |
spellingShingle | Article Sismour, A. Michael Benner, Steven A. The use of thymidine analogs to improve the replication of an extra DNA base pair: a synthetic biological system |
title | The use of thymidine analogs to improve the replication of an extra DNA base pair: a synthetic biological system |
title_full | The use of thymidine analogs to improve the replication of an extra DNA base pair: a synthetic biological system |
title_fullStr | The use of thymidine analogs to improve the replication of an extra DNA base pair: a synthetic biological system |
title_full_unstemmed | The use of thymidine analogs to improve the replication of an extra DNA base pair: a synthetic biological system |
title_short | The use of thymidine analogs to improve the replication of an extra DNA base pair: a synthetic biological system |
title_sort | use of thymidine analogs to improve the replication of an extra dna base pair: a synthetic biological system |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1236980/ https://www.ncbi.nlm.nih.gov/pubmed/16192575 http://dx.doi.org/10.1093/nar/gki873 |
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