While methods for the detection of point mutations and small insertions or deletions in genomic DNA are well established, the detection of larger (>100 bp) genomic duplications or deletions can be more difficult. Most mutation scanning methods use PCR as a first step, but the subsequent analyses are
A technique for the detection of large DNA alterations in complex genomes
✍ Scribed by G. Hintermann; R. Crameri; T. Kieser; R. Hütter
- Publisher
- Elsevier Science
- Year
- 1982
- Tongue
- English
- Weight
- 332 KB
- Volume
- 121
- Category
- Article
- ISSN
- 0003-2697
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✦ Synopsis
As part of our effort to understand the chromosomal organization of streptomycetes, we have developed a method for detecting large alterations in the DNA, in particular to visualize insertions, transpositions, and deletions. The method involves the labeling of the DNA of two strains with ['Hlthymidine or ['%]thymidine, extraction and purification of the DNA, digestion with restriction endonucleases, and one-dimensional agarose gel electrophoresis of the two samples in the same slot. Following electrophoresis, the gel is cut into thin slices, and the "C/ 'H ratio is measured in each slice. Deviations from the average standard ratio are caused by differences in the restriction site arrangement in the DNA of the two strains, which may be caused by rearrangements in the DNA. The method has a high resolution of one restriction fragment change.
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