RESUMO
A novel series of charge-modified, dye-labeled 2',3'-dideoxynucleoside-triphosphate terminators were synthesized and evaluated as reagents for DNA sequencing. These terminators possess an advantage over existing reagents in that no purification is required to remove unreacted nucleotide or associated breakdown products prior to electrophoretic separation of the sequencing fragments. This obviates the need for a time consuming post-reaction work up, allowing direct loading of DNA sequencing reaction mixtures onto a slab gel. Thermo Sequenase II DNA polymerase poorly incorporates the charge-modified terminators compared with regular dye-labeled terminators. However, extending the linker arm between dye and nucleotide and using a mutant form of a related DNA polymerase can in part mitigate the decrease in substrate efficiency. We also present evidence that these charge-modified terminators can relieve gel compression artefacts when used with dGTP in sequencing reactions.
Assuntos
DNA/química , Desoxirribonucleotídeos/química , Análise de Sequência de DNA/métodos , Corantes/química , DNA/genética , DNA/metabolismo , Eletroforese/métodos , Mutação , Reprodutibilidade dos Testes , Taq Polimerase/genética , Taq Polimerase/metabolismoRESUMO
A series of charge-modified, dye-labeled 2', 3'-dideoxynucleoside-5'-triphosphates have been synthesized and evaluated as reagents for dye-terminator DNA sequencing. Unlike the commonly used dye-labeled terminators, these terminators possess a net positive charge and migrate in the opposite direction to dye-labeled Sanger fragments during electrophoresis. Post-sequencing reaction purification is not required to remove unreacted nucleotide or associated breakdown products prior to electrophoresis. Thus, DNA sequencing reaction mixtures can be loaded directly onto a separating medium such as a sequencing gel. The charge-modified nucleotides have also been shown to be more efficiently incorporated by a number of DNA polymerases than regular dye-labeled dideoxynucleotide terminators or indeed normal dideoxynucleoside-5'-triphosphates.
Assuntos
DNA Polimerase Dirigida por DNA/metabolismo , Didesoxinucleosídeos/química , Lisina/análogos & derivados , Nucleotídeos/metabolismo , Análise de Sequência de DNA/métodos , Sequência de Bases , Cromatografia Líquida de Alta Pressão/métodos , Corantes/química , DNA/química , DNA/genética , Lisina/química , Dados de Sequência Molecular , Estrutura Molecular , Nucleotídeos/química , Nucleotídeos/genética , Reprodutibilidade dos Testes , Sensibilidade e EspecificidadeRESUMO
A number of terminal phosphate-labeled nucleotides with three or more phosphates and with varied length linkers attached between the terminal phosphate and the dye have been synthesized. These nucleotides have been tested as substrates for different DNA and RNA polymerases. We have also explored their utility in DNA sequencing, SNP analysis, nucleic acid amplification, quantitative PCR, and other biochemical assays.
Assuntos
DNA Polimerase Dirigida por DNA/química , Técnicas Genéticas , Nucleotídeos/química , Nucleotídeos/síntese química , Corantes/farmacologia , DNA/química , Primers do DNA/química , Modelos Químicos , Fosfatos/química , Reação em Cadeia da Polimerase , Polimorfismo de Nucleotídeo Único , Análise de Sequência de DNA , Fatores de TempoRESUMO
A four-color set of negatively charged, single dye as well as energy transfer dye labeled-ddNTPs were synthesized and evaluated in combination with a novel polymerase in a "direct-load" DNA sequencing, obviating the laborious and time consuming post-reaction work-up.
Assuntos
Corantes , DNA/química , Desoxirribonucleotídeos/síntese química , Didesoxinucleosídeos/síntese química , Sequência de Bases , Transferência de Energia , Indicadores e ReagentesRESUMO
A number of different energy transfer dye labeled-cassettes were synthesized using aminoacid based trifunctional linkers and coupled to the propargylamino-substituted dideoxynucleoside-5'-triphosphates (ddNTPs). These terminators were evaluated for their energy transfer efficiency and DNA sequencing potential using thermostable DNA polymerase.