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. 1994 May;137(1):87–94. doi: 10.1093/genetics/137.1.87

Inheritance of Chromosome-Length Polymorphisms in Coprinus Cinereus

M E Zolan 1, N K Heyler 1, N Y Stassen 1
PMCID: PMC1205957  PMID: 7914506

Abstract

We have investigated the inheritance of chromosome-length polymorphisms in the basidiomycete Coprinus cinereus. The electrophoretic karyotypes of interfertile strains of C. cinereus are strikingly different, and crosses between strains with different karyotypes yield progeny with chromosomes of new sizes. Repeated backcrossing of a mutant to one parent often stabilizes the mutant chromosome at a unique size; this then becomes a chromosome-length polymorphism marker for that mutant gene. A comparison of mutant strains, their wild-type progenitor, and backcrossed strains revealed that these marker chromosomes are not caused by the initial mutagenic treatment and are found only in progeny of crosses between strains with polymorphic chromosomes. Thus, they are most likely formed by meiotic recombination. For the rad12 gene, the marker chromosome can further recombine to become the size of the homolog of the backcross parent. For the rad3 gene, both ectopic and homologous recombination events are likely involved in the generation of the marker chromosomes. As predicted by a recombination model, a cross to a new wild-type parent can change the size of a mutant marker chromosome. Therefore, changes in chromosome length are a common and prominent feature of the genome of this sexual fungus, and a variety of karyotypes is tolerated by the organism.

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Selected References

These references are in PubMed. This may not be the complete list of references from this article.

  1. Bidenne C., Blondin B., Dequin S., Vezinhet F. Analysis of the chromosomal DNA polymorphism of wine strains of Saccharomyces cerevisiae. Curr Genet. 1992 Jul;22(1):1–7. doi: 10.1007/BF00351734. [DOI] [PubMed] [Google Scholar]
  2. Binninger D. M., Skrzynia C., Pukkila P. J., Casselton L. A. DNA-mediated transformation of the basidiomycete Coprinus cinereus. EMBO J. 1987 Apr;6(4):835–840. doi: 10.1002/j.1460-2075.1987.tb04828.x. [DOI] [PMC free article] [PubMed] [Google Scholar]
  3. 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]
  4. Kinscherf T. G., Leong S. A. Molecular analysis of the karyotype of Ustilago maydis. Chromosoma. 1988;96(6):427–433. doi: 10.1007/BF00303036. [DOI] [PubMed] [Google Scholar]
  5. Montgomery E. A., Huang S. M., Langley C. H., Judd B. H. Chromosome rearrangement by ectopic recombination in Drosophila melanogaster: genome structure and evolution. Genetics. 1991 Dec;129(4):1085–1098. doi: 10.1093/genetics/129.4.1085. [DOI] [PMC free article] [PubMed] [Google Scholar]
  6. Ono B., Ishino-Arao Y. Inheritance of chromosome length polymorphisms in Saccharomyces cerevisiae. Curr Genet. 1988 Nov;14(5):413–418. doi: 10.1007/BF00521262. [DOI] [PubMed] [Google Scholar]
  7. Perkins D. D. The manifestation of chromosome rearrangements in unordered asci of Neurospora. Genetics. 1974 Jul;77(3):459–489. doi: 10.1093/genetics/77.3.459. [DOI] [PMC free article] [PubMed] [Google Scholar]
  8. Plummer K. M., Howlett B. J. Major chromosomal length polymorphisms are evident after meiosis in the phytopathogenic fungus Leptosphaeria maculans. Curr Genet. 1993 Jul-Aug;24(1-2):107–113. doi: 10.1007/BF00324673. [DOI] [PubMed] [Google Scholar]
  9. Pukkila P. J., Skrzynia C. Frequent changes in the number of reiterated ribosomal RNA genes throughout the life cycle of the basidiomycete Coprinus cinereus. Genetics. 1993 Feb;133(2):203–211. doi: 10.1093/genetics/133.2.203. [DOI] [PMC free article] [PubMed] [Google Scholar]
  10. Rustchenko-Bulgac E. P. Variations of Candida albicans electrophoretic karyotypes. J Bacteriol. 1991 Oct;173(20):6586–6596. doi: 10.1128/jb.173.20.6586-6596.1991. [DOI] [PMC free article] [PubMed] [Google Scholar]
  11. Tzeng T. H., Lyngholm L. K., Ford C. F., Bronson C. R. A restriction fragment length polymorphism map and electrophoretic karyotype of the fungal maize pathogen Cochliobolus heterostrophus. Genetics. 1992 Jan;130(1):81–96. doi: 10.1093/genetics/130.1.81. [DOI] [PMC free article] [PubMed] [Google Scholar]
  12. Walliker D., Quakyi I. A., Wellems T. E., McCutchan T. F., Szarfman A., London W. T., Corcoran L. M., Burkot T. R., Carter R. Genetic analysis of the human malaria parasite Plasmodium falciparum. Science. 1987 Jun 26;236(4809):1661–1666. doi: 10.1126/science.3299700. [DOI] [PubMed] [Google Scholar]
  13. Zakian V. A. Structure and function of telomeres. Annu Rev Genet. 1989;23:579–604. doi: 10.1146/annurev.ge.23.120189.003051. [DOI] [PubMed] [Google Scholar]
  14. Zolan M. E., Crittenden J. R., Heyler N. K., Seitz L. C. Efficient isolation and mapping of rad genes of the fungus Coprinus cinereus using chromosome-specific libraries. Nucleic Acids Res. 1992 Aug 11;20(15):3993–3999. doi: 10.1093/nar/20.15.3993. [DOI] [PMC free article] [PubMed] [Google Scholar]
  15. Zolan M. E., Tremel C. J., Pukkila P. J. Production and characterization of radiation-sensitive meiotic mutants of Coprinus cinereus. Genetics. 1988 Oct;120(2):379–387. doi: 10.1093/genetics/120.2.379. [DOI] [PMC free article] [PubMed] [Google Scholar]

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