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Allele-specific PCR detection of sweet cherry self-incompatibility alleles S3, S4 and S9 using consensus and allele-specific primers in the Czech Republic

Author

Listed:
  • K. Sharma

    (Department of Genetics and Breeding, Faculty of Agrobiology, Food and Natural Resources, Czech University of Life Sciences Prague, Prague, Czech Republic)

  • P. Sedlák

    (Department of Genetics and Breeding, Faculty of Agrobiology, Food and Natural Resources, Czech University of Life Sciences Prague, Prague, Czech Republic)

  • D. Zeka

    (Department of Genetics and Breeding, Faculty of Agrobiology, Food and Natural Resources, Czech University of Life Sciences Prague, Prague, Czech Republic)

  • P. Vejl

    (Department of Genetics and Breeding, Faculty of Agrobiology, Food and Natural Resources, Czech University of Life Sciences Prague, Prague, Czech Republic)

  • J. Soukup

    (Department of Genetics and Breeding, Faculty of Agrobiology, Food and Natural Resources, Czech University of Life Sciences Prague, Prague, Czech Republic)

Abstract

Prunus avium species of the Rosaceae family exhibit gametophytic self-incompatibility. Determination of the self-incompatibility genotype of individuals is essential for genetic studies and the development of informed management strategies. The PCR-based detection of S-allele helps to promote and speed up traditional breeding activity and hence molecular analysis of the perspective genotypes has become more intensive in all cherry growing countries. The alleles S3, S4 and S9 from 34 accessions of Czech collections were determined using the polymerase chain reaction (PCR) method. Initially, DNA extracts were amplified with consensus primers that amplify across the first, second, or both introns of the S-ribonuclease gene which shows a considerable length polymorphism. The new allele specific primers were designed with the goal to overcome some occurring difficulties in the detection of expected alleles by previously published allele specific primers. S-alleles fragments of standard cultivars used in this study were PCR amplified, sequenced to validate the designed primers. The study demonstrates the advantage of newly designed primers application in testing of sweet cherry genotypes.

Suggested Citation

  • K. Sharma & P. Sedlák & D. Zeka & P. Vejl & J. Soukup, 2014. "Allele-specific PCR detection of sweet cherry self-incompatibility alleles S3, S4 and S9 using consensus and allele-specific primers in the Czech Republic," Horticultural Science, Czech Academy of Agricultural Sciences, vol. 41(4), pages 153-159.
  • Handle: RePEc:caa:jnlhor:v:41:y:2014:i:4:id:89-2014-hortsci
    DOI: 10.17221/89/2014-HORTSCI
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    Cited by:

    1. Josef Patzak & Alena Henychová & František Paprštein & Jiří Sedlák, 2019. "Molecular S-genotyping of sweet cherry (Prunus avium L.) genetic resources," Horticultural Science, Czech Academy of Agricultural Sciences, vol. 46(3), pages 146-152.
    2. Jitka Blažková & Adéla Skřivanová & Pavol Suran & Lubor Zelený & František Paprštein, 2020. "Long-term evaluation of rootstock effects on cropping and tree parameters of selected sweet cherry cultivars," Horticultural Science, Czech Academy of Agricultural Sciences, vol. 47(1), pages 13-20.

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