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Segregation and linkage analyses in two complex populations derived from the citrus rootstock Cleopatra mandarin. Inheritance of seed reproductive traits

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Abstract

Two complex populations derived from the salt-tolerant citrus rootstock Cleopatra mandarin were used to investigate (1) the genomic regions affected by segregation distortion and (2) gene segregation heterogeneity and their causes and to obtain (3) a Citrus reshni linkage map to genetically analyze (4) the duration of the juvenility period and the seed embryony type. Both populations differed in the extent and origin of segregation distortion. The population derived from the cross between C. reshni and Poncirus trifoliata (R × Pr) showed 75 % of codominant markers with distorted segregation. The origin of this distortion was prezygotic in most cases. Meanwhile, 100 % of codominant markers in the self-pollinated population [F2(R × Pr)] showed genotypic distortion, and the origin of such distortion was mostly postzygotic, with the heterozygote being the most frequent genotype in all cases. In the R × Pr population, where two pollinator varieties were used, allele segregation was significantly heterogeneous not only in P. trifoliata (28.6 % of markers) but also in C. reshni (19.5 %). The results on segregation heterogeneity in the F2(R × Pr) suggest the presence at linkage group 4c of a postfertilization system of balanced lethal factors that reduces homozygosis in self-compatible hybrids. Four low to medium contributing quantitative trait loci (QTLs) were detected for the duration of juvenility period by both Kruskal–Wallis and interval mapping methodologies. For seed embryony type, three QTLs were detected by both methodologies, with the previously reported Apo2 being the QTL contributing the most. CR14,290 and TAA15 are good markers for early selection of polyembryonic rootstocks in progenies derived from C. reshni, Citrus aurantium, and Citrus volkameriana.

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References

  • Ahmad R, Struss D, Southwick SM (2003) Development and characterization of microsatellite markers in Citrus. J Amer Soc Hort Sci 128:584–590

    CAS  Google Scholar 

  • Aleza P, Juarez J, Ollitrault P, Navarro L (2010) Polyembryony in non-apomictic citrus genotypes. Ann Bot 106(4):533–454

    Article  PubMed  Google Scholar 

  • Arumuganathan K, Earle ED (1991) Nuclear DNA content of some important plant species. Plant Mol Biol Rep 9:208–218

    Article  CAS  Google Scholar 

  • Asins MJ, García MR, Ruiz C, Carbonell EA (2002) Molecular markers for the genetic analysis of apomixis. In: Jain SM, Brar DS, Ahloowalia BS (eds) Molecular techniques in crop improvement. Kluwer Academic Publishers, The Netherlands, pp 265–281

    Google Scholar 

  • Asins MJ, Bernet GP, Ruiz C, Cambra M, Guerri J, Carbonell EA (2004) QTL analysis of Citrus tristeza virus-citradia interaction. Theor Appl Genet 108:603–611

    Article  PubMed  CAS  Google Scholar 

  • Bacchi O (1943) Cytological observations in Citrus. III. Megasporogenesis, fertilization and polyembryony. Bot Gaz 105:221–225

    Article  Google Scholar 

  • Barkley NA, Roose ML, Krueger RR, Federici CT (2006) Assessing genetic diversity and population structure in a citrus germplasm collection utilizing simple sequence repeat markers (SSRs). Theor Appl Genet 112:1519–1531

    Article  PubMed  CAS  Google Scholar 

  • Bernet GP, Asins MJ (2003) Identification and genomic distribution of gypsy-like retrotransposons in Citrus and Poncirus. Theor Appl Genet 108:121–130

    Article  PubMed  CAS  Google Scholar 

  • Bernet GP, Fernandez-Ribacoba J, Raga V, Asins MJ (2008) Comparison of linkage maps among six citrus species: structural differences and genetic inferences. In: Deng X, Xu J, Lin S, Guan R (eds) Proceeding 11th international citrus congress, vol I. China Agriculture Press, Beijing, p 463

    Google Scholar 

  • Bernet GP, Fernandez-Ribacoba J, Carbonell EA, Asins MJ (2010) Comparative genome-wide segregation analysis and map construction using a reciprocal cross design to facilitate citrus germplasm utilization. Mol Breed 25:659–673

    Article  Google Scholar 

  • Bretó MP, Ruiz C, Pina JA, Asins MJ (2001) The diversification of Citrus clementina Hort. ex Tan., a vegetatively propagated crop species. Mol Phylogenet Evol 21(2):285–293

    Article  PubMed  Google Scholar 

  • Cameron JW (1979) Sexual and nucellar embryony in F1 hybrids and advanced crosses of Citrus with Poncirus. J Amer Soc Hort Sci 104:408–410

    Google Scholar 

  • Cameron JW, Frost HB (1968) Genetics, breeding and nucellar embryony. In: Reuther W, Batchelor LD, Webber HJ (eds) The citrus industry, vol II, Div Agr Sci. Univ California, Berkeley, pp 325–370

    Google Scholar 

  • Cameron JW, Garber MJ (1968) Identical-twin hybrids of Citrus × Poncirus from strictly sexual seed parents. Amer J Bot 55:199–205

    Article  Google Scholar 

  • Chen C, Bowman KD, Choi YA, Dang PM, Rao MN, Huang S, Soneji JR, McCollum TG, Gmitter FG Jr (2008) EST-SSR genetic maps for Citrus sinensis and Poncirus trifoliata. Tree Genet Genomes 4:1–10

    Article  Google Scholar 

  • Cooper WC (1961) Toxicity and accumulation of salts in Citrus trees on various rootstocks. P FL St Hortic Soc 74:95–104

    CAS  Google Scholar 

  • Edmé SJ, Glynn NG, Comstock JC (2006) Genetic segregation of microsatellite markers in Saccharum officinarum and S. spontaneum. Heredity 97:366–375

    Article  PubMed  Google Scholar 

  • Fang DQ, Roose ML, Krueger RR, Federici CT (1997) Fingerprinting trifoliate orange germ plasm accessions with isozymes, RFLPs, and inter-simple sequence repeat markers. Theor Appl Genet 95:211–219

    Article  CAS  Google Scholar 

  • Frost HB (1943) Seed reproduction: development of gametes and embryos. Chapter VIII. In: Webber HJ, Batchelor LD (eds) The citrus industry, vol I. University of California Press, Berkeley, pp 767–815

    Google Scholar 

  • García R, Asins MJ, Forner J, Carbonell EA (1999) Genetic analysis of apomixis in Citrus and Poncirus by molecular markers. Theor Appl Genet 99:511–518

    Article  PubMed  Google Scholar 

  • García MR, Bernet GP, Puchades J, Gómez I, Carbonell EA, Asins MJ (2002) Reliable and easy screening technique for salt tolerance of citrus rootstocks under controlled environments. Aust J Agric Res 53:653–662

    Article  Google Scholar 

  • Guerra M (1984) Cytogenetics of Rutaceae. II. Nuclear DNA content. Caryologia 37:219–226

    CAS  Google Scholar 

  • Jansen RC (2001) Quantitative trait loci in inbred lines. In: Balding DJ, Bishop M, Gannings G (eds) Handbook of statistical genetics. Wiley, New York, pp 567–597

    Google Scholar 

  • Kepiro JL, Roose ML (2010) AFLP markers closely linked to a major gene essential for nucellar embryony (apomixis) in Citrus maxima × Poncirus trifoliata. Tree Genet Genomics 6:1–11

    Article  Google Scholar 

  • Kijas JMH, Thomas MR, Fowler JCS, Roose ML (1997) Integration of trinucleotide microsatellites into a linkage map of Citrus. Theor Appl Genet 94:701–706

    Article  CAS  Google Scholar 

  • Melchinger AE, Utz HF, Schön CC (2004) QTL analyses of complex traits with cross validation, bootstrapping and other biometric methods. Euphytica 137:1–11

    Article  CAS  Google Scholar 

  • Nakano M, Shimizu T, Kuniga T, Nesumi H, Omura M (2008) Mapping and haplotyping of the flanking region of the polyembryony locus in Citrus unshiu Marcov. J Japan Soc Hort Sci 77(2):109–114

    Article  CAS  Google Scholar 

  • Ruiz C, Asins MJ (2003) Comparison between Poncirus and Citrus genetic linkage maps. Theor Appl Genet 106:826–836

    PubMed  CAS  Google Scholar 

  • Ruiz C, Bretó MP, Asins MJ (2000) An efficient methodology to identify sexual seedlings in citrus breeding programs using SSR markers. Euphytica 112:89–94

    Article  CAS  Google Scholar 

  • Van Ooijen JW, Maliepaard C (1996) MapQTL(tm) version 3: software for the calculation of QTL positions on genetic maps. CPRO-DLO, Wageningen

    Google Scholar 

  • Van Ooijen JW, Voorrips RE (2001) JoinMap version 3.0. software for the calculation of genetic linkage maps release 3.0. Plant Research International, Wageningen, The Netherlands

    Google Scholar 

Download references

Acknowledgments

This work has been partially supported by grants FP6-2003-INCO-MPC-2, RTA2006-0009-00-00, AGL2008-00197/AGR, Fondo Social Europeo (GPB), and IVIA (VR). We thank J. Puchades and P. Cirujeda for the technical assistance.

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Correspondence to M. J. Asins.

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Communicated by A. Dandekar

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Raga, V., Bernet, G.P., Carbonell, E.A. et al. Segregation and linkage analyses in two complex populations derived from the citrus rootstock Cleopatra mandarin. Inheritance of seed reproductive traits. Tree Genetics & Genomes 8, 1061–1071 (2012). https://doi.org/10.1007/s11295-012-0486-7

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  • DOI: https://doi.org/10.1007/s11295-012-0486-7

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