Abstract
Genetic and epigenetic modifications resulting from different genomes adjusting to a common nuclear environment have been observed in polyploids. Sequence restructuring within genomes involving retrotransposon/microsatellite-rich regions has been reported in triticale. The present study uses inter-retrotransposon amplified polymorphisms (IRAP) and retrotransposon microsatellite amplified polymorphisms (REMAP) to assess genome rearrangements in wheat–rye addition lines obtained by the controlled backcrossing of octoploid triticale to hexaploid wheat followed by self-fertilization. The comparative analysis of IRAP and REMAP banding profiles, involving a complete set of wheat–rye addition lines, and their parental species revealed in those lines the presence of wheat-origin bands absent in triticale, and the absence of rye-origin and triticale-specific bands. The presence in triticale × wheat backcrosses (BC) of rye-origin bands that were absent in the addition lines demonstrated that genomic rearrangement events were not a direct consequence of backcrossing, but resulted from further genome structural rearrangements in the BC plant progeny. PCR experiments using primers designed from different rye-origin sequences showed that the absence of a rye-origin band in wheat–rye addition lines results from sequence elimination rather than restrict changes on primer annealing sites, as noted in triticale. The level of genome restructuring events evaluated in all seven wheat–rye addition lines, compared to triticale, indicated that the unbalanced genome merger situation observed in the addition lines induced a new round of genome rearrangement, suggesting that the lesser the amount of rye chromatin introgressed into wheat the larger the outcome of genome reshuffling.
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References
Adams KL, Wendel JF (2005) Novel patterns of gene expression in polyploid plants. Trends Genet 21:539–543
Ainouche ML, Fortune PM, Salmon A, Parisod C, Grandbastien M-A, Fukunaga K, Ricou M, Misset M-T (2008) Hybridization, polyploidy and invasion: lessons from Spartina (Poaceae). Biol Invasions 11:1159–1173
Alkhimova AG, Heslop-Harrison JS, Shchapova AI, Vershinin AV (1999) Rye chromosome variability in wheat–rye addition and substitution lines. Chromosome Res 7:205–212
Bennett MD (1977) Heterochromatin, aberrant endosperm nuclei and grain shrivelling in wheat–rye genotypes. Heredity 39:411–419
Bento M, Pereira S, Rocheta M, Gustafson P, Viegas W, Silva M (2008) Polyploidization as a retraction force in plant genome evolution: sequence rearrangements in triticale. PLoS One 3:e1402
Charles M, Belcram H, Just J, Huneau C, Viollet A, Couloux A, Segurens B, Carter M, Huteau V, Coriton O, Appels R, Samain S, Chalhoub B (2008) Dynamics and differential proliferation of transposable elements during the evolution of the B and A genomes of wheat. Genetics 180:1071–1086
Chen M, Ha M, Lackey E, Wang JL, Chen ZJ (2008) RNAi of met1 reduces DNA methylation and induces genome-specific changes in gene expression and centromeric small RNA accumulation in Arabidopsis allopolyploids. Genetics 178:1845–1858
Gustafson JP, Lukaszewski AJ, Bennett MD (1983) Somatic deletion and redistribution of telomeric heterochromatin in the genus Secale and in Triticale. Chromosoma 88:293–298
Josefsson C, Dilkes B, Comai L (2006) Parent-dependent loss of gene silencing during interspecies hybridization. Curr Biol 16:1322–1328
Kalendar R, Grob T, Regina M, Suoniemi A, Schulman A (1999) IRAP and REMAP: two new retrotransposon-based DNA fingerprinting techniques. Theor Appl Genet 98:704–711
Kashkush K, Feldman M, Levy AA (2002) Gene loss, silencing and activation in a newly synthesized wheat allotetraploid. Genetics 160:1651–1659
Kashkush K, Feldman M, Levy AA (2003) Transcriptional activation of retrotransposons alters the expression of adjacent genes in wheat. Nat Genet 33:102–106
Leigh L, Kalendar R, Lea V, Lee D, Donini P, Schulman AH (2003) Comparison of the utility of barley retrotransposon families for genetic analysis by molecular marker techniques. Mol Genet Genomics 269:464–474
Liu B, Vega JM, Segal G, Abbo S, Rodova H, Feldman M (1998) Rapid genomic changes in newly synthesized amphiploids of Triticum and Aegilops I. Changes in low-copy noncoding DNA sequences. Genome 41:272–277
Ma XF, Gustafson JP (2005) Genome evolution of allopolyploids: a process of cytological and genetic diploidization. Cytogenet Genome Res 109(1–3):236–249
Ma XF, Gustafson JP (2006) Timing and rate of genome variation in triticale following allopolyploidization. Genome 49:950–958
Ma XF, Gustafson JP (2008) Allopolyploidization-accommodated genomic sequence changes in triticale. Ann Bot Lond 101:825–832
Ma XF, Fang P, Gustafson JP (2004) Polyploidization-induced genome variation in triticale. Genome 47(5):839–848
Madlung A, Tyagi AP, Watson B, Jiang HM, Kagochi T, Doerge RW, Martienssen R, Comai L (2005) Genomic changes in synthetic Arabidopsis polyploids. Plant J 41:221–230
Neves N, Silva M, Heslop-Harrison J, Viegas W (1997) Nucleolar dominance in triticale: control by unlinked genes. Chromosome Res 5:125–131
O’Mara JG (1940) Cytogenetic studies on triticale I. A method for determining the effects of individual secale chromosomes on Triticum. Genetics 25:401–408
Ozkan H, Tuna M, Arumuganathan K (2003) Nonadditive changes in genome size during allopolyploidization in the wheat (Aegilops-Triticum) group. J Hered 94:260–264
Pereira HS, Barao A, Delgado M, Morais-Cecilio L, Viegas W (2005) Genomic analysis of Grapevine Retrotransposon 1 (Gret1) in Vitis vinifera. Theor Appl Genet 111:871–878
Riley R (1960) The meiotic behavior, fertility and stability of wheat–rye chromosome addition lines. Heredity 14:89–100
Rocheta M, Cordeiro J, Oliveira M, Miguel C (2006) PpRT1: the first complete gypsy-like retrotransposon isolated in Pinus pinaster. Planta 225:551–562
Saghaimaroof MA, Soliman KM, Jorgensen RA, Allard RW (1984) Ribosomal DNA spacer-length polymorphisms in barley—Mendelian inheritance, chromosomal location, and population-dynamics. Proc Natl Acad Sci USA 81:8014–8018
Shaked H, Kashkush K, Ozkan H, Feldman M, Levy AA (2001) Sequence elimination and cytosine methylation are rapid and reproducible responses of the genome to wide hybridization and allopolyploidy in wheat. Plant Cell 13:1749–1759
Silva M, Pereira HS, Bento M, Santos AP, Shaw P, Delgado M, Neves N, Viegas W (2008) Interplay of ribosomal DNA loci in nucleolar dominance: dominant NORs are up-regulated by chromatin dynamics in the wheat–rye system. PLoS One 3:e3824
Smykal P (2006) Development of an efficient retrotransposon-based fingerprinting method for rapid pea variety identification. J Appl Genet 47:221–230
Tang ZX, Fu SL, Ren ZL, Zhou JP, Yan BJ, Zhang HQ (2008) Variations of tandem repeat, regulatory element, and promoter regions revealed by wheat–rye amphiploids. Genome 51:399–408
Vershinin AV, Alkhimova EG, HeslopHarrison JS (1996) Molecular diversification of tandemly organized DNA sequences and heterochromatic chromosome regions in some Triticeae species. Chromosome Res 4:517–525
Acknowledgments
Miguel Bento is funded by a doctoral scholarship (SFRH/BD/28657/2006) by Fundação para a Ciência e a Tecnologia, Portugal. This research was financed by Fundação para a Ciência e a Tecnologia (Projects PPCDT/BIABDE/57575/2004 and PTDC/BIA-BEC/101964/2008). We would like to thank Augusta Barão for her excellent technical assistance and Leonor Morais-Cecílio for her help in image processing.
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Communicated by A. Schulman.
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Fig. S1
Dimension of amplified fragments expected from the sequence pSc200 of S.cereale DNA sub-telomeric tandem repeat (accession number Z50039) that comprehends a repeat unit with 381 bp. (PDF 37 kb)
Fig. S2
Nikita IRAP banding profiles of wheat (W), rye (R), triticale (T) and wheat DNA + rye DNA test tubes (1-5). Test tubes correspond to reactions that used as DNA template the result from the mixture of wheat DNA plus decreasing quantities of rye DNA (1/3,1/4, 1/5, 1/6, and 1/7). b is an overexposed copy of a, reveling two rye-origin polymorphic bands, absent in wheat–rye addition lines, present in all rye dilutions used (arrowheads). A triticale-origin band is absent in all rye dilutions (arrowhead). Molecular weight marker: 1 kb+. (PDF 148 kb)
Fig. S3
Full multiple alignments obtained with ClustalW for the wheat-specific sequence MoB-11-1200W amplified from wheat and the equivalent sequences amplified from CS + 1R (MoB-11-1200W-1R) and amplified from CS + 7R (MoB-11-1200W-7R) addition lines. (PDF 20 kb)
Fig. S4
The alignment of the MoB-111-1000R [2] sequences amplified from wheat, rye, and triticale reveals that they are all analogous sequence. (PDF 14 kb)
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Bento, M., Gustafson, P., Viegas, W. et al. Genome merger: from sequence rearrangements in triticale to their elimination in wheat–rye addition lines. Theor Appl Genet 121, 489–497 (2010). https://doi.org/10.1007/s00122-010-1325-6
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DOI: https://doi.org/10.1007/s00122-010-1325-6