Halász, Júlia

Hegedűs, Attila

Kurilla, Anita

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 International Journal of Horticultural Science 2014, 20 (3–4): 23–26. Agroinform Publishing House, Budapest, Printed in Hungary  ISSN 1585-0404   Preliminary characterization of the self-incompatibility genotypes of European plum (Prunus domestica L.) cultivars  Halász, J., Kurilla, A. & Hegedûs, A.  Corvinus University of Budapest, Faculty of Horticultural Science, Department of Genetics and Plant Breeding, 1118 Budapest, Ménesi út 44., Hungary  E-mail: julia.halasz@uni-corvinus.hu  Summary: European plum is an important fruit crop with complex, hexaploid genome of unknown origin. The characterization of the self-incompatibility (S) locus of 16 European plum cultivars was carried out using the PaConsI-F primer in combination with the EM-PC1consRD primer for the first intron and the EM-PC2consFD and EM-PC3consRD primers for the second intron amplification. Altogether, 18 different alleles were scored indicating high genetic diversity. These alleles were labelled using alphabetical codes from SA to SS. We identified 5 different alleles in 9 cultivars, 4 alleles in 5 cultivars, while 3 alleles were shown in two of the assayed cultivars. A total of 16 different S-genotypes were assigned, and discrimination of all plum cultivars was successful based on their unique S-genotypes. However, further research is required to reliably identify the S-alleles based on their DNA sequence and clarify complete S-genotypes.    Keywords: self-incompatibility, S-allele, European plum, Prunus domestica L.    Introduction  European plum is an important fruit crop. The majority of world 10.7 million tons of ‘plums and sloe’ (as mentioned in the Faostat database) production quantity has been harvested in Asia (68%) while Europe ranks second with a value of 21% (Faostat, 2012). In Hungary, a total of 43,268 t was harvested in 2012, which makes it the second most important stone fruit crop in the country after sour cherry. Considering its economical prospects and naturally occurring wild and semi-wild populations throughout the country, the genetic characterization of the species may bring advantage through the exploitation and valorization of this fruit.  Throughout the world, several plant species are regarded and their fruit is marketed as “plum”. These include P. cerasifera Ehrh. (cherry plum), P. cocomilia Ten. (Italian plum), P. simonii Carr., P. spinosa L. (blackthorn or sloe),  P. insititia L., P. americana Marsh. (American plum), P. mexicana S.Watson (Mexican plum), P. nigra Ait. (Canada plum, Black plum) and others (Faust & Surányi, 1999). The species European plum (P. domestica) is grown in Hungary and other Central European countries. The species is characterized by a hexaploid genome (2n=6x=48) (Crane & Lawrence, 1929). Although hypotheses have been drawn pointing to both the allo- and autopolyploid origins of the species, no doubt clarification is still not available for either of the two.  Most Prunus species express gametophytic self-incompatibility (GSI) where the phenotype of the pollen is    determined by its own haploid genotype (de Nettancourt, 2001). In Rosaceae, GSI is controlled by the single polymorphic S-locus (named after the term, sterility) containing two genes, the  S-ribonuclease (S-RNase) and S-haplotype-specific F-box (SFB) (Hegedûs et al., 2012). Both genes exhibit high polymorphism and high sequence diversity. While self-incompatibility studies are common in case of diploid plum species (Halász et al., 2007; Guerra et al., 2009, 2012), information on the S-genotype of European plum cultivars is rather limited (Hegedûs & Halász, 2006). This might be explained by the fact that self-incompatibility occurs less frequently in polyploid than diploid plums and also by the hexaploid genome that makes allele identification a complex and elusive task. First study regarding the molecular genetics of self-incompatibility in domestic plum was published by Sutherland et al. (2004b).  Deduced polypeptide sequences of three myrobalan and three domestic plum S-RNases showed over 97% identity with S-RN-ases from other Prunus species, including almond, sweet cherry, Japanese apricot and Japanese plum (Sutherland et al., 2008). The second intron, which is generally highly polymorphic between alleles was also remarkably well conserved within these S-allele pairs. Degenerate consensus primers were developed and used to amplify and sequence the corresponding SFB alleles. Sequence comparisons also indicated high degrees of polypeptide sequence identity between three myrobalan and the three domestic plum SFB alleles and the corresponding Prunus SFB alleles supporting the trans-specific evolution of Prunus allele specificities.  24 Halász, J., Kurilla, A. & Hegedûs, A.  The applicability of six S-locus-specific markers previously used for other Prunus species were compared in the study of Kota-Dombrovska & Lacis (2013) for the characterization of 33 domestic plum cultivars. A range of 14–37 alleles was amplified for the markers used, the average observed heterozygosity was high. Applification of the tested primer pairs allowed discrimination of all plum cultivars by unique S-genotypes. Primer pairs EM-PC2consFD/ EM-PC3cons RD, PasPcons-F1/ PaC1cons-R1 and F-Box50A/ F-Box intronR provided the highest level of variability. The markers used did not distinguish plum cultivars according to self-compatible or –incompatible phenotype.  This study was aimed to obtain preliminary information regarding the self-incompatibility genotype of a range of important European plum cultivars grown in Hungary. We wanted to test the efficiency of the PCR markers developed for S-genotyping of diploid Prunus species and assess how many S-alleles of the hexaploid genome can be determined based on this approach.   Material and methods  Plant material  The study was performed on 16 domestic plum (Prunus domestica L.) cultivars (Table 1). Samples were obtained from the orchard of the Corvinus University of Budapest, Soroksár, Hungary.  Table 1. List of European plum cultivars with the S-genotype and their pedigree (Surányi & Erdôs, 2006)   Cultivar Provisional Pedigree   name S-genotype     1. Althann SFSKSOSP unknown  ringló      2. Bluefre SHSISK Stanley × President       3. Elena SBSGSISKSO Fellenberg × Stanley       4. Empress SASDSESHSN –       5. Haganta SCSHSISJSO Cacaks Beste × Valor       6. Hanita SHSISOSR President × Auerbacher       7. Haroma SHSISO (Ortenauer × Stanley 34) ×  Hanita      8. Jojo SISLSMSO Ortenauer × Stanley       9. Katinka SASKSLSO Ortenauer × Ruth Gerstetter       10. Presenta SCSHSKSMSP Ortenauer × President       11. President SCSDSHSISK unknown       12. Sermina SASFSISNSO old Italian cultivar       13. Stanley SHSISOSS Agen × Grand Duke       14. Topend Plus SCSISKSOSS Cacaks Beste × Valor       15. Topfive SISKSOSR Cacaks Beste × Auerbacher       16. Tophit SCSFSHSKSS Cacak’s Beste × President        DNA extraction and genomic PCR with S-RNase-specific primers  Genomic DNA was extracted from fully expanded young leaves using a DNeasy Plant Mini Kit (Qiagen, Hilden, Germany). PCR was conducted according to Sutherland et al. (2004a) using the degenerate primers EM-PC2consFD and EM-PC3consRD for the amplification of the second intron region of the S-RNase gene. To amplify the first intron, the fluorescently labelled (JOE) PaConsI-F primer (Sonneveld et al., 2003) was used in combination with the EM-PC1consRD primer (Ortega et al., 2005). PCR was carried out in a PTC 200 thermocycler (MJ Research, Budapest, Hungary) using the program described for the primers. Approximately 20–80 ng of genomic DNA were used for PCR amplification in a 25-µL reaction volume, containing 1 × PCR buffer (Sigma, Budapest, Hungary) with final concentrations of 10 mm Tris-HCl (pH 8.3), 50 mm KCl, 1.5 mm MgCl2, 0.2 mm of dNTPs, 0.4 µm of each primer and 0.625 U of Taq DNA polymerase (Sigma, Budapest, Hungary).  The PCR products were separated on 2% TAE agarose gels at 100 V for 2 h and DNA bands were stained with ethidium bromide. Fragment sizes were estimated by comparison with the 1 kb + DNA ladder (Promega, Madison, Wis.). For exact size determination of S-RNase first intron region fragments smaller than 500 bp, the fluorescently labeled products were run in an automated sequencer ABI Prism 3100 Genetic Analyzer (Applied Biosystems, Budapest, Hungary) using the GENOTYPER 3.7 software and GS500 LIZ size standard (Applied Biosystems, Budapest, Hungary).   Results and discussion  The characterization of the S-locus of 16 European plum cultivars was carried out using the PaConsI-F primer (Sonneveld et al., 2003) in combination with the EM-PC1consRD primer (Ortega et al., 2005) for the first intron and the EM-PC2consFD and EM-PC3consRD primers (Sutherland et al., 2004a) for the second intron amplification. Both primer pairs exhibited successful PCR amplification and yielded several amplification products for all assayed cultivars. Since domestic plum is hexaploid, a maximum of six amplification fragments can be found in one sample. Primer combination for the second intron region of the S-RNase gene amplified 4 to 6 bands for each of the cultivars. A total of 15 distinct bands were amplified. PCR products varied greatly in size, with bands ranging from 300 bp to 2500 bp in length. Kota-Dombrovska & Lacis (2013) tested six different primer combinations for S-genotyping of plum cultivars and the EM-PC2consFD and EM-PC3consRD primer pair was characterized by the highest number of amplified fragments per sample (4.0 in average).  To complete the S-genotype determination, precise first intron lengths were also measured for all cultivars using fluorescently labelled primers and automated sizing on a  Preliminary characterization of the self-incompatibility genotypes of European plum (Prunus domestica L.) cultivars 25  capillary sequencer. Analysis of the first intron in all 16 plums resulted in 4-5 fragments in each of the assayed cultivars, their sizes ranged between 232 and 416 bp. Altogether, 18 different alleles were scored indicating high genetic diversity. Due to the lack of any sequence information of the DNA fragments, we labelled these alleles using alphabetical codes from SA to SS. This provisional labelling system will be modified when DNA sequence of the corresponding alleles will allow reliable identification and harmonization, based on searching on a public sequence database. We identified 5 different alleles in 9 cultivars, 4 alleles in 5 cultivars, while 3 alleles were shown in two of the assayed cultivars (Table 1). It means that only partial S-genotypes were established. Analysis of these two regions of the S-RNase gene did not allow the identification of complete S-genotypes because two or more copies of the same allele (homozygosity) could not  be excluded based on these PCR assays. However, another explanation may be also relevant since certain alleles were not detected in some cases using DNA amplification with consensus primers due to the so-called preferential PCR amplification (Kodad et al., 2013). The most frequent alleles were SI and SO occurring in 11 cultivars, followed by SH and  SK (9), SC (5), SA, SF and SS (3), SD, SL, SM, SN, SP and SR (2), while each of the SB, SE, SG and SJ-alleles were found in only  one cultivar. Most of the cultivars share common S-alleles because of the same cultivars were used as parents for crosses in many cases (Figure 1), since breeding programmes attention has focussed on improvement of fruit quality and on resistance or tolerance to Plum pox virus (Hartmann & Neumuller, 2006). A total of 16 different S-genotypes were assigned, so discrimination of all plum cultivars was successful based on their unique S-genotypes.                                               Figure 1. Chromatogram of the fluorescently labelled first intron fragments of the S-RNase gene indicating S-alleles in 3 plum cultivars. Bluefre (SHSISK): Stanley (SHSISOSS) × President (SCSDSHSISK).  26 Halász, J., Kurilla, A. & Hegedûs, A.  Acknowledgements  This work was funded by the OTKA K 112554 project and also supported by the János Bolyai Research Scholarship of the Hungarian Academy of Sciences (J. Halász). The authors thank Róbert Rácz-Szabó for kindly providing plant material.   References  Crane, M.B. & Lawrence, W.J.C. (1929): Genetical and cytological aspects of incompatibility and sterility in cultivated fruits. J. Pomol. Hort. Sci., 7: 276–301.  de Nettancourt, D. (2001): Incompatibility and Incongruity in Wild and Cultivated Plants. Springer-Verlag, New York.  Faostat (2012): Agriculture data. http://apps.fao.org/page/ collections?subset = agriculture  Faust, M. & Suranyi, D. (1999): Origin and dissemination of plums. Hort. Rev., 23: 179–231.  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Preliminary characterization of the self-incompatibility genotypes of European plum (Prunus domestica L.) cultivars.

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