DNA fingerprinting by sampled sequencing.
Journal: 1989/December - Proceedings of the National Academy of Sciences of the United States of America
ISSN: 0027-8424
PUBMED: 2554336
Abstract:
We describe a method for characterizing DNA segments that combines limited sequencing with size separation of restriction fragments. As part of a multistep procedure, 5' overhangs of unknown sequence are generated by cleavage with a class IIS restriction enzyme. After labeling of these ends by using dideoxynucleotides tagged with distinctive fluorescent dyes, the restriction fragments are analyzed by polyacrylamide gel electrophoresis and detection of fluorescent emissions using a commercially available DNA sequencer. The nucleotide-specific fluorescent signatures permit determination of the terminal sequence for each labeled end. The set of labeled fragments, characterized by both size and terminal sequence, constitutes a fingerprint that can be used to compare DNA segments for overlap or relatedness. The inclusion of terminal sequence data dramatically increases the information content of the fingerprint, making comparisons more reliable and efficient than those based upon size alone.
Relations:
Content
Citations
(11)
References
(13)
Drugs
(2)
Chemicals
(2)
Organisms
(2)
Processes
(3)
Similar articles
Articles by the same authors
Discussion board
Proc Natl Acad Sci U S A 86(22): 8902-8906

DNA fingerprinting by sampled sequencing.

Abstract

We describe a method for characterizing DNA segments that combines limited sequencing with size separation of restriction fragments. As part of a multistep procedure, 5' overhangs of unknown sequence are generated by cleavage with a class IIS restriction enzyme. After labeling of these ends by using dideoxynucleotides tagged with distinctive fluorescent dyes, the restriction fragments are analyzed by polyacrylamide gel electrophoresis and detection of fluorescent emissions using a commercially available DNA sequencer. The nucleotide-specific fluorescent signatures permit determination of the terminal sequence for each labeled end. The set of labeled fragments, characterized by both size and terminal sequence, constitutes a fingerprint that can be used to compare DNA segments for overlap or relatedness. The inclusion of terminal sequence data dramatically increases the information content of the fingerprint, making comparisons more reliable and efficient than those based upon size alone.

Full text

Full text is available as a scanned copy of the original print version. Get a printable copy (PDF file) of the complete article (1.0M), or click on a page image below to browse page by page. Links to PubMed are also available for Selected References.

Images in this article

Click on the image to see a larger version.

Selected References

These references are in PubMed. This may not be the complete list of references from this article.
  • Coulson A, Sulston J, Brenner S, Karn J. Toward a physical map of the genome of the nematode Caenorhabditis elegans. Proc Natl Acad Sci U S A. 1986 Oct;83(20):7821–7825.[PMC free article] [PubMed] [Google Scholar]
  • Olson MV, Dutchik JE, Graham MY, Brodeur GM, Helms C, Frank M, MacCollin M, Scheinman R, Frank T. Random-clone strategy for genomic restriction mapping in yeast. Proc Natl Acad Sci U S A. 1986 Oct;83(20):7826–7830.[PMC free article] [PubMed] [Google Scholar]
  • Daniels DL, Blattner FR. Mapping using gene encyclopaedias. Nature. 325(6107):831–832. [PubMed] [Google Scholar]
  • Kohara Y, Akiyama K, Isono K. The physical map of the whole E. coli chromosome: application of a new strategy for rapid analysis and sorting of a large genomic library. Cell. 1987 Jul 31;50(3):495–508. [PubMed] [Google Scholar]
  • Lander ES, Waterman MS. Genomic mapping by fingerprinting random clones: a mathematical analysis. Genomics. 1988 Apr;2(3):231–239. [PubMed] [Google Scholar]
  • Prober JM, Trainor GL, Dam RJ, Hobbs FW, Robertson CW, Zagursky RJ, Cocuzza AJ, Jensen MA, Baumeister K. A system for rapid DNA sequencing with fluorescent chain-terminating dideoxynucleotides. Science. 1987 Oct 16;238(4825):336–341. [PubMed] [Google Scholar]
  • Birkmeyer RC, Diaco R, Hutson DK, Lau HP, Miller WK, Neelkantan NV, Pankratz TJ, Tseng SY, Vickery DK, Yang EK. Application of novel chromium dioxide magnetic particles to immunoassay development. Clin Chem. 1987 Sep;33(9):1543–1547. [PubMed] [Google Scholar]
  • Tartof KD, Hobbs CA. New cloning vectors and techniques for easy and rapid restriction mapping. Gene. 1988 Jul 30;67(2):169–182. [PubMed] [Google Scholar]
  • Birnboim HC, Doly J. A rapid alkaline extraction procedure for screening recombinant plasmid DNA. Nucleic Acids Res. 1979 Nov 24;7(6):1513–1523.[PMC free article] [PubMed] [Google Scholar]
  • Szybalski W. Universal restriction endonucleases: designing novel cleavage specificities by combining adapter oligodeoxynucleotide and enzyme moieties. Gene. 1985;40(2-3):169–173. [PubMed] [Google Scholar]
  • Sanger F, Coulson AR, Friedmann T, Air GM, Barrell BG, Brown NL, Fiddes JC, Hutchison CA, 3rd, Slocombe PM, Smith M. The nucleotide sequence of bacteriophage phiX174. J Mol Biol. 1978 Oct 25;125(2):225–246. [PubMed] [Google Scholar]
  • Carrano AV, Lamerdin J, Ashworth LK, Watkins B, Branscomb E, Slezak T, Raff M, de Jong PJ, Keith D, McBride L, et al. A high-resolution, fluorescence-based, semiautomated method for DNA fingerprinting. Genomics. 1989 Feb;4(2):129–136. [PubMed] [Google Scholar]
  • Robbins AK, Ryan JP, Whealy ME, Enquist LW. The gene encoding the gIII envelope protein of pseudorabies virus vaccine strain Bartha contains a mutation affecting protein localization. J Virol. 1989 Jan;63(1):250–258.[PMC free article] [PubMed] [Google Scholar]
Medical Research Council Molecular Genetics Unit, Cambridge, England.
Medical Research Council Molecular Genetics Unit, Cambridge, England.
Abstract
We describe a method for characterizing DNA segments that combines limited sequencing with size separation of restriction fragments. As part of a multistep procedure, 5' overhangs of unknown sequence are generated by cleavage with a class IIS restriction enzyme. After labeling of these ends by using dideoxynucleotides tagged with distinctive fluorescent dyes, the restriction fragments are analyzed by polyacrylamide gel electrophoresis and detection of fluorescent emissions using a commercially available DNA sequencer. The nucleotide-specific fluorescent signatures permit determination of the terminal sequence for each labeled end. The set of labeled fragments, characterized by both size and terminal sequence, constitutes a fingerprint that can be used to compare DNA segments for overlap or relatedness. The inclusion of terminal sequence data dramatically increases the information content of the fingerprint, making comparisons more reliable and efficient than those based upon size alone.
Collaboration tool especially designed for Life Science professionals.Drag-and-drop any entity to your messages.