Abstract
We analyzed DNA fingerprints in the chestnut blight fungus, Cryphonectria parasitica, for stability, inheritance, linkage and variability in a natural population. DNA fingerprints resulting from hybridization with a dispersed moderately repetitive DNA sequence of C. parasitica in plasmid pMS5.1 hybridized to 6-17 restriction fragments per individual isolate. In a laboratory cross and from progeny from a single perithecium collected from a field population, the presence/absence of 11 fragments in the laboratory cross and 12 fragments in the field progeny set segregated in 1:1 ratios. Two fragments in each progeny set cosegregated; no other linkage was detected among the segregating fragments. Mutations, identified by missing bands, were detected for only one fragment in which 4 of 43 progeny lacked a band present in both parents; no novel fragments were detected in any progeny. All other fragments appeared to be stably inherited. Hybridization patterns did not change during vegetative growth or sporulation. However, fingerprint patterns of single conidial isolates of strains EP155 and EP67 were found to be heterogenous due to mutations that occurred during culturing in the laboratory since these strains were first isolated in 1976-1977. In a population sample of 39 C. parasitica isolates, we found 33 different fingerprint patterns with pMS5.1. Most isolates differed from all other isolates by the presence or absence of several fragments. Six fingerprint patterns each occurred twice. Isolates with identical fingerprints occurred in cankers on the same chestnut stems three times; isolates within the other three pairs were isolated from cankers more than 5 m apart. The null hypothesis of random mating in this population could not be rejected if the six putative clones were removed from the analysis. Thus, a rough estimate of the clonal fraction of this population is 6 in 39 isolates (15.4%).
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Selected References
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- Burke T., Bruford M. W. DNA fingerprinting in birds. Nature. 1987 May 14;327(6118):149–152. doi: 10.1038/327149a0. [DOI] [PubMed] [Google Scholar]
- Chu G., Vollrath D., Davis R. W. Separation of large DNA molecules by contour-clamped homogeneous electric fields. Science. 1986 Dec 19;234(4783):1582–1585. doi: 10.1126/science.3538420. [DOI] [PubMed] [Google Scholar]
- Hamer J. E., Farrall L., Orbach M. J., Valent B., Chumley F. G. Host species-specific conservation of a family of repeated DNA sequences in the genome of a fungal plant pathogen. Proc Natl Acad Sci U S A. 1989 Dec;86(24):9981–9985. doi: 10.1073/pnas.86.24.9981. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Hamer J. E., Givan S. Genetic mapping with dispersed repeated sequences in the rice blast fungus: mapping the SMO locus. Mol Gen Genet. 1990 Sep;223(3):487–495. doi: 10.1007/BF00264458. [DOI] [PubMed] [Google Scholar]
- Jeffreys A. J., Wilson V., Thein S. L. Hypervariable 'minisatellite' regions in human DNA. Nature. 1985 Mar 7;314(6006):67–73. doi: 10.1038/314067a0. [DOI] [PubMed] [Google Scholar]
- Jeffreys A. J., Wilson V., Thein S. L. Individual-specific 'fingerprints' of human DNA. Nature. 1985 Jul 4;316(6023):76–79. doi: 10.1038/316076a0. [DOI] [PubMed] [Google Scholar]
- Lynch M. Estimation of relatedness by DNA fingerprinting. Mol Biol Evol. 1988 Sep;5(5):584–599. doi: 10.1093/oxfordjournals.molbev.a040518. [DOI] [PubMed] [Google Scholar]
- Orbach M. J., Vollrath D., Davis R. W., Yanofsky C. An electrophoretic karyotype of Neurospora crassa. Mol Cell Biol. 1988 Apr;8(4):1469–1473. doi: 10.1128/mcb.8.4.1469. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Powell W. A., Van Alfen N. K. Differential accumulation of poly(A)+ RNA between virulent and double-stranded RNA-induced hypovirulent strains of Cryphonectria (Endothia) parasitica. Mol Cell Biol. 1987 Oct;7(10):3688–3693. doi: 10.1128/mcb.7.10.3688. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Rogstad S. H., Patton J. C., 2nd, Schaal B. A. M13 repeat probe detects DNA minisatellite-like sequences in gymnosperms and angiosperms. Proc Natl Acad Sci U S A. 1988 Dec;85(23):9176–9178. doi: 10.1073/pnas.85.23.9176. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Scherer S., Stevens D. A. A Candida albicans dispersed, repeated gene family and its epidemiologic applications. Proc Natl Acad Sci U S A. 1988 Mar;85(5):1452–1456. doi: 10.1073/pnas.85.5.1452. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Stoddart J. A., Taylor J. F. Genotypic diversity: estimation and prediction in samples. Genetics. 1988 Apr;118(4):705–711. doi: 10.1093/genetics/118.4.705. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Turner B. J., Elder J. F., Jr, Laughlin T. F., Davis W. P. Genetic variation in clonal vertebrates detected by simple-sequence DNA fingerprinting. Proc Natl Acad Sci U S A. 1990 Aug;87(15):5653–5657. doi: 10.1073/pnas.87.15.5653. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Van Alfen N. K., Jaynes R. A., Anagnostakis S. L., Day P. R. Chestnut Blight: Biological Control by Transmissible Hypovirulence in Endothia parasitica. Science. 1975 Sep 12;189(4206):890–891. doi: 10.1126/science.189.4206.890. [DOI] [PubMed] [Google Scholar]
- Vassart G., Georges M., Monsieur R., Brocas H., Lequarre A. S., Christophe D. A sequence in M13 phage detects hypervariable minisatellites in human and animal DNA. Science. 1987 Feb 6;235(4789):683–684. doi: 10.1126/science.2880398. [DOI] [PubMed] [Google Scholar]
- Vollrath D., Davis R. W. Resolution of DNA molecules greater than 5 megabases by contour-clamped homogeneous electric fields. Nucleic Acids Res. 1987 Oct 12;15(19):7865–7876. doi: 10.1093/nar/15.19.7865. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Wetton J. H., Carter R. E., Parkin D. T., Walters D. Demographic study of a wild house sparrow population by DNA fingerprinting. Nature. 1987 May 14;327(6118):147–149. doi: 10.1038/327147a0. [DOI] [PubMed] [Google Scholar]
