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PMID: 3200828 Published · ppublish English Journal Article

DNA sequencing with Thermus aquaticus DNA polymerase and direct sequencing of polymerase chain reaction-amplified DNA.

Innis MA, Myambo KB, Gelfand DH, Brow MA

Abstract

The highly thermostable DNA polymerase from Thermus aquaticus (Taq) is ideal for both manual and automated DNA sequencing because it is fast, highly processive, has little or no 3'-exonuclease activity, and is active over a broad range of temperatures. Sequencing protocols are presented that produce readable extension products greater than 1000 bases having uniform band intensities. A combination of high reaction temperatures and the base analog 7-deaza-2'-deoxyguanosine was used to sequence through G + C-rich DNA and to resolve gel compressions. We modified the polymerase chain reaction (PCR) conditions for direct DNA sequencing of asymmetric PCR products without intermediate purification by using Taq DNA polymerase. The coupling of template preparation by asymmetric PCR and direct sequencing should facilitate automation for large-scale sequencing projects.

MeSH Terms
Autoanalysis Base Sequence DNA/analysis DNA-Directed DNA Polymerase/metabolism Deoxyguanosine/analogs & derivatives Electrophoresis, Polyacrylamide Gel Nucleotide Mapping/methods Temperature Templates, Genetic Thermus/enzymology
Chemicals
7-deaza-2'-deoxyguanosine DNA DNA-Directed DNA Polymerase Deoxyguanosine
Authors & Affiliations
4 authors, click to expand affiliations / ORCID
Innis M A
Department of Microbial Genetics, Cetus Corporation, Emeryville, CA 94608.
Myambo K B
Gelfand D H
Brow M A
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Article Info
Journal
Proceedings of the National Academy of Sciences of the United States of America
Abbr.
Proc Natl Acad Sci U S A
ISSN
0027-8424
Published
1988-12-00
Pages
9436-40
Language
English
Region
United States
NLM ID
7505876
PMCID
PMC282767
Subset
IM
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