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TmPrime: fast, flexible oligonucleotide design software for gene synthesis
Herein we present TmPrime, a computer program to design oligonucleotide sets for gene assembly by both ligase chain reaction (LCR) and polymerase chain reaction (PCR). TmPrime offers much flexibility with no constraints on the gene and oligonucleotide lengths. The program divides the long input DNA...
Autores principales: | , , , , |
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Formato: | Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2009
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2703938/ https://www.ncbi.nlm.nih.gov/pubmed/19515937 http://dx.doi.org/10.1093/nar/gkp461 |
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author | Bode, Marcus Khor, Samuel Ye, Hongye Li, Mo-Huang Ying, Jackie Y. |
author_facet | Bode, Marcus Khor, Samuel Ye, Hongye Li, Mo-Huang Ying, Jackie Y. |
author_sort | Bode, Marcus |
collection | PubMed |
description | Herein we present TmPrime, a computer program to design oligonucleotide sets for gene assembly by both ligase chain reaction (LCR) and polymerase chain reaction (PCR). TmPrime offers much flexibility with no constraints on the gene and oligonucleotide lengths. The program divides the long input DNA sequence based on the input desired melting temperature, and dynamically optimizes the length of oligonucleotides to achieve homologous melting temperatures. The output reports the melting temperatures, oligonucleotide sequences and potential formation of secondary structures. Our program also provides functions on sequence pooling to separate long genes into smaller pieces for multi-pool assembly and codon optimization for expression. The software has been successfully used in the design and synthesis of green fluorescent protein fragment (GFPuv) (760 bp), human protein kinase B-2 (PKB2) (1446 bp) and the promoter of human calcium-binding protein A4 (S100A4) (752 bp) using real-time PCR assembly with LCGreen I, which offers a novel approach to compare the efficiency of gene synthesis. The purity of assembled products is successfully estimated with the use of melting curve analysis, which would potentially eliminate the necessity for agarose gel electrophoresis. This program is freely available at http://prime.ibn.a-star.edu.sg. |
format | Text |
id | pubmed-2703938 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2009 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-27039382009-07-01 TmPrime: fast, flexible oligonucleotide design software for gene synthesis Bode, Marcus Khor, Samuel Ye, Hongye Li, Mo-Huang Ying, Jackie Y. Nucleic Acids Res Articles Herein we present TmPrime, a computer program to design oligonucleotide sets for gene assembly by both ligase chain reaction (LCR) and polymerase chain reaction (PCR). TmPrime offers much flexibility with no constraints on the gene and oligonucleotide lengths. The program divides the long input DNA sequence based on the input desired melting temperature, and dynamically optimizes the length of oligonucleotides to achieve homologous melting temperatures. The output reports the melting temperatures, oligonucleotide sequences and potential formation of secondary structures. Our program also provides functions on sequence pooling to separate long genes into smaller pieces for multi-pool assembly and codon optimization for expression. The software has been successfully used in the design and synthesis of green fluorescent protein fragment (GFPuv) (760 bp), human protein kinase B-2 (PKB2) (1446 bp) and the promoter of human calcium-binding protein A4 (S100A4) (752 bp) using real-time PCR assembly with LCGreen I, which offers a novel approach to compare the efficiency of gene synthesis. The purity of assembled products is successfully estimated with the use of melting curve analysis, which would potentially eliminate the necessity for agarose gel electrophoresis. This program is freely available at http://prime.ibn.a-star.edu.sg. Oxford University Press 2009-07-01 2009-06-10 /pmc/articles/PMC2703938/ /pubmed/19515937 http://dx.doi.org/10.1093/nar/gkp461 Text en © 2009 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 | Articles Bode, Marcus Khor, Samuel Ye, Hongye Li, Mo-Huang Ying, Jackie Y. TmPrime: fast, flexible oligonucleotide design software for gene synthesis |
title | TmPrime: fast, flexible oligonucleotide design software for gene synthesis |
title_full | TmPrime: fast, flexible oligonucleotide design software for gene synthesis |
title_fullStr | TmPrime: fast, flexible oligonucleotide design software for gene synthesis |
title_full_unstemmed | TmPrime: fast, flexible oligonucleotide design software for gene synthesis |
title_short | TmPrime: fast, flexible oligonucleotide design software for gene synthesis |
title_sort | tmprime: fast, flexible oligonucleotide design software for gene synthesis |
topic | Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2703938/ https://www.ncbi.nlm.nih.gov/pubmed/19515937 http://dx.doi.org/10.1093/nar/gkp461 |
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