Abstract
We describe here a transposon-based DNA sequencing strategy that allows the introduction of sequencing priming sites throughout a target sequence by bacterial mating. A miniplasmid was designed to select against transposon insertions into the vector. Sites of transposon insertion are mapped by the polymerase chain reaction with bacterial overnight cultures providing the templates. A small set of plasmids with transposons spaced several hundred base pairs apart can then be sequenced. Sequencing primers corresponding to the transposon ends allow sequencing in both directions. Thus, the entire sequence of both strands can be easily determined.
Dates
Type | When |
---|---|
Created | 19 years, 2 months ago (May 31, 2006, 7:53 a.m.) |
Deposited | 3 years, 4 months ago (April 13, 2022, 1:18 p.m.) |
Indexed | 3 weeks, 4 days ago (Aug. 5, 2025, 8:19 a.m.) |
Issued | 34 years, 6 months ago (Feb. 15, 1991) |
Published | 34 years, 6 months ago (Feb. 15, 1991) |
Published Online | 34 years, 6 months ago (Feb. 15, 1991) |
Published Print | 34 years, 6 months ago (Feb. 15, 1991) |
@article{Strathmann_1991, title={Transposon-facilitated DNA sequencing.}, volume={88}, ISSN={1091-6490}, url={http://dx.doi.org/10.1073/pnas.88.4.1247}, DOI={10.1073/pnas.88.4.1247}, number={4}, journal={Proceedings of the National Academy of Sciences}, publisher={Proceedings of the National Academy of Sciences}, author={Strathmann, M and Hamilton, B A and Mayeda, C A and Simon, M I and Meyerowitz, E M and Palazzolo, M J}, year={1991}, month=feb, pages={1247–1250} }