versão impressa ISSN 0100-204X
Pesq. agropec. bras. vol.46 no.7 Brasília jul. 2011
Genomic behavior of hybrid combinations between elephant grass and pearl millet
Comportamento genômico de combinações híbridas entre capim-elefante e milheto
Fernando Ferreira LeãoI; Lisete Chamma DavideII; José Marcello Salabert de CamposIII; Antonio Vander PereiraIV; Fernanda de Oliveira BustamanteII
IUniversidade Federal de Tocantins, Campus Gurupi, Caixa Postal 66, CEP 77402-970 Gurupi, TO, Brazil. E-mail: email@example.com
IIUniversidade Federal de Lavras, Departamento de Biologia, Caixa Postal 3037, CEP 37200-000 Lavras, MG, Brazil. E-mail: firstname.lastname@example.org, email@example.com
IIIUniversidade Federal de Juiz de Fora, Instituto de Ciências Biológicas, Departamento de Biologia, CEP 36036-900 Juiz de Fora, MG, Brazil. E-mail: firstname.lastname@example.org
IVEmbrapa Gado de Leite, Rua Eugênio do Nascimento, nº 610, CEP 36038-330 Juiz de Fora, MG, Brazil. E-mail: email@example.com
The objective of this work was to evaluate the genomic behavior of hybrid combinations between elephant grass (Pennisetum purpureum) and pearl millet (P. glaucum). Tetraploid (AAA'B) and pentaploid (AA'A'BB) chromosome races resulting from the backcross of the hexaploid hybrid to its parents elephant grass (A'A'BB) and pearl millet (AA) were analyzed as to chromosome number and DNA content. Genotypes of elephant grass, millet, and triploid and hexaploid induced hybrids were compared. Pentaploid and tetraploid genomic combinations showed high level of mixoploidy, in discordance with the expected somatic chromosome set. The pentaploid chromosome number ranged from 20 to 34, and the tetraploid chromosome number from 16 to 28. Chromosome number variation was higher in pentaploid genomic combinations than in tetraploid, and mixoploidy was observed among hexaploids. Genomic combinations 4x and 5x are mixoploid, and the variation of chromosome number within chromosomal race 5x is greater than in 4x.
Index terms: Pennisetum glaucum, Pennisetum purpureum, DNA content, interspecific hybrids, mixoploidy.
O objetivo deste trabalho foi avaliar o comportamento genômico de combinações híbridas resultantes do cruzamento entre capim-elefante (Pennisetum purpureum) e milheto (P. glaucum). Raças cromossômicas tetraploides (AAA'B) e pentaploides (AA'A'BB), resultantes do retrocruzamento do híbrido hexaploide com seus parentais capim-elefante (A'A'BB) e milheto (AA), foram avaliadas quanto ao número cromossômico e ao conteúdo de DNA. Foram comparados os genótipos de capim-elefante, milheto e de híbridos triploides e hexaploides induzidos. As combinações genômicas pentaploides e tetraploides mostraram elevado grau de mixoploidia, em desacordo com o complemento cromossômico somático esperado. O número cromossômico dos pentaploides variou de 20 a 34, e o dos tetraploides de 16 a 28. A variação do número cromossômico foi maior nas combinações genômicas pentaploides do que nas tetraploides, e a mixoploidia foi verificada entre hexaploides. As combinações genômicas 4x e 5x são mixoploides, e a variação do número de cromossomos na raça cromossômica 5x é maior do que na 4x.
Termos para indexação: Pennisetum glaucum, Pennisetum purpureum, conteúdo de DNA, híbridos interespecíficos, mixoploidia.
The genus Pennisetum is widely used in grass forage production. Among the species with an important role in forage grass production, elephant grass (Pennisetum purpureum Schumach; 2n = 4x = 28, A'A'BB) and pearl millet (P. glaucum L.R.Br.; 2n = 2x = 14, AA) are the ones of greatest economic importance within the genus. Hybrid production between these two species (2n = 3x = 21, AA'B) is a common strategy used in elephant grass breeding programs to combine the most favorable millet characteristics (resistance to drought, tolerance to diseases, and seed size) with the hardness, aggressiveness, and high dry matter production of elephant grass (Pereira et al., 2003). However, the sterility of the triploid hybrid is a limiting factor of this strategy.
Induction of chromosome duplication has been used as an alternative to restore hybrid fertility, producing fertile hexaploids with 2n = 6x = 42 (Abreu et al., 2006; Barbosa et al., 2007; Bustamante, 2009; Campos et al., 2009). Additionally, mixoploidy with cells containing between 14 and 42 chromosomes has been reported in these experiments.
New genomic combinations or chromosomal races have also been obtained by backcrossing the hexaploid hybrid with its tetraploid (elephant grass) and diploid (millet) parents, producing pentaploid (5x) and tetraploid (4x) hybrids, respectively. However, there is no known information on the cytogenetic behavior of the genotypes obtained. For instance, there is still the need to determine if hybrids 4x and 5x can be characterized as mixoploids or if there is the possibility to find genotypes with a more stable number of chromosomes.
Synthetic hybrids commonly display phenotypic and genetic instability as a result of nuclear conflicts, such as chromosome and DNA fragment elimination (Ozkan et al., 2003; Ma et al., 2004; Ma & Gustafson, 2006). Genome stability can be evaluated by chromosome counting, a very accurate method for the identification of the exact chromosome number of duplicated plants, and DNA content can be assessed by flow cytometry, a method frequently used to screen ploidy in a large number of plants (Bustamante, 2009; Campos et al., 2009).
The objective of this work was to evaluate the genomic behavior of hybrid combinations between elephant grass and pearl millet.
Materials and Methods
Fifteen genotypes of Pennisetum spp. provided by the active germplasm bank of Embrapa Gado de Leite, Juiz de Fora, MG, Brazil, were analyzed (Table 1). Thirteen genotypes were vegetatively propagated (clones), and M-36 millet and 'Paraíso' populations were propagated by seeds and by a seed mixture of seven different plants, respectively. Hexaploid genotypes were obtained by inducing chromosome duplication in the genomic combination HCM-6x-1, from six different clones, and HCM-6x-2, from seven different clones.
Chromosome counting was performed on genomic combinations 4x and 5x, and cultivar Paraíso and HCM-6x-2, both hexaploids, were used for comparison. All genotypes were evaluated by flow cytometry in order to determine DNA content.
The methodology proposed by Techio (2002) was used for chromosome counting. Slide analyses were performed using a bright field microscope (Leica DMLS, Wetzlar, Germany), equipped with a microcamera Nikon Digital Sight DS-Fi1, (Nikon Digital, Tokyo, Japan) for scanning images. Different metaphases (between 41 and 100) were obtained from at least five slides for each genotype. Analysis of variance was performed to estimate the significant differences between genomic combinations 4x and 5x.
For DNA content, three samples of each genotype were analyzed, and 20 to 30 mg of young leaf tissue were used for each sample. The same amount of young leaf material of Glycine max L. was used as an external standard reference. Nuclear suspension was stained with propidium iodide, and ten thousand nuclei were analyzed according to Doleel (1997). The analyses were performed on a FACSCalibur cytometer (BD Biosciences, San Jose, CA, USA), and the histograms were obtained using the CellQuest software (BD Biosciences, San Jose, CA, USA); the analyses were processed with WinMDI 2.8 (2009). Nuclear DNA content (pg) was normalized to the G1 peak of the standard reference G. max (2.50 pg) (Doleel et al., 2007).
The DNA content of elephant grass (4.54 pg) and pearl millet (4.75 pg) proposed by Campos et al. (2009) was used as a standard.
Results and Discussion
Since x = 7 is the basic number of chromosomes for elephant grass and millet, the expected chromosome number of tetraploid, pentaploid, and hexaploid hybrids was 28, 35 and 42, respectively. However, all genomic combinations showed variable levels of mixoploidy (Figure 1 and Table 2), and the number of cells observed with the full chromosome complement was reduced, although it was more frequent in the genomic combination HCM-6x-2.
The genomic combinations 4x and 5x were statistically different from each other regarding chromosome number (Table 3), and there is less variation on chromosomal race 4x than in 5x, especially when taking the modal number into consideration (Table 2). Genomic changes in interspecific crosses indicate that the presence of two or more different genomes in the same nucleus leads to chromosomal rearrangements and to changes in the number and the distribution of DNA sequences, which may cause intergenic conflicts and chromosome loss (Comai, 2000; Riddle & Birchler, 2003; Levy & Feldman, 2004; Adams & Wendel, 2005; Doyle et al., 2008; Bustamante, 2009; Campos et al., 2009).
Gernand et al. (2005), while evaluating hybrids from crosses between wheat and millet, observed uniparental chromosome elimination of millet with the formation of micronucleus and DNA heterochromatinization, with the chromosomes of pearl millet occupying a peripheral position in the interphase nuclei, being fragmented due to asynchrony during DNA replication. Likewise, Laurie & Bennett (1989) and Mochida et al. (2004) found that millet chromosome elimination began soon after fertilization, when studying hybrids from the same cross.
As in the present study, Abreu et al. (2006) also observed mixoploidy. The authors found that, for triploid hybrids between pearl millet and elephant grass treated with antimitotic agents, there was duplication followed by chromosome elimination, confirmed by chromosome aberrations. Furthermore, 86.4% of the cells analyzed had a chromosome number other than 21. Similarly, Barbosa et al. (2007) observed that the chromosome number in the metaphases ranged from 14 to 42 in samples in which chromosome duplication was induced by antimitotic agents. Campos et al. (2009) reported that, from 480 triploid seedlings (hybrids of elephant grass and pearl millet) treated with colchicine to obtain hexaploids, 115 of the 200 survivors were mixoploids.
The nuclear DNA content previously determined for millet and elephant grass is 4.75 and 4.54 pg, respectively (Campos et al., 2009). Therefore, the triploid hybrid has an intermediate DNA amount of its parents (4.65 pg), and chromosome duplication produces a hexaploid hybrid with 9.30 pg. The DNA content expected in genomic pentaploid combinations is derived from the sum of the parental gametic contents: 4.65 pg for hexaploid hybrids plus 2.27 pg for elephant grass, which totals 6.92 pg. For tetraploid genomic combinations, the expected value is 7.00 pg (4.65 pg for the hexaploid hybrid plus 2.38 pg for pearl millet).
Variation in the DNA amount of the different genotypes was also observed (Table 4 and Figure 2). Elephant grass, represented by cultivars Pioneiro and Cameroon (Table 1), millet, and triploid hybrids showed reduced loss of DNA content (0 to 2.16%) when compared to chromosomal races 4x, 5x, and to hybrids undergoing chromosome duplication (6x), which had loss in DNA content between 9.25 and 19%. These results show that triploid genotypes are genetically and evolutionarily well established in comparison to genomic combinations 4x, 5x, and 6x, whose greater reductions in DNA content indicate that they are still unstable and undergoing genomic reorganization, although it is likely that these new combinations may also achieve genotypic stability at some stage.
Different genomic combinations may also have influenced the differential loss on DNA content, since triploid genotypes and genomic combinations are clones, whereas hexaploids were obtained from a mixture of six and seven different clones of the elephant grass x pearl millet population (HCM-6x-1 and HCM-6x-2, respectively). The cultivar Paraíso was also obtained from a seed mixture of seven different plants, which may have contributed to the variation in DNA loss (Table 4).
The comparison between the genomic combinations 4x (AAA'B) and 5x (AA'A'BB) showed that the genomic constitution of pentaploids is very similar to that of elephant grass (A'A'BB), with only one extra dose of genome A, whereas tetraploids have two extra genomes (A' and B), having the AA genome as the diploid millet (Table 4). The greatest reduction in DNA observed in chromosomal race 4x is probably a consequence of the increased genomic imbalance, in comparison to 5x.
Since chromosomal race 4x showed less variation in chromosome number and greater loss of DNA when compared to chromosomal race 5x, it is possible to infer that losses of chromosome segments in 4x were greater than in 5x, and that more whole chromosomes were eliminated by chromosome race 5x.
Recent studies have attempted to explain the mechanism of chromosome elimination in Pennisetum hybrids (Andrade-Vieira, 2010). Preliminary results showed non-preferential chromosome elimination. The chromosome elimination process could be a consequence of the aneuploidizant effect of colchicine an alkaloid used for chromosome doubling , resulting in random chromosome losses (Schoenlein et al., 2003; Caperta et al., 2006).
DNA loss for hexaploid genotypes has been previously reported by Campos et al. (2009). A great difference in DNA amount was observed in comparison to the standards between repetitions 1 and 2 of genomic combinations HCM-6x-1 and HCM-6x-2 (Table 4), which could be explained by the fact that these combinations were obtained from a mixture of different clones. Therefore, the stability of genotypes with a smaller DNA loss (repetition 1 of genotype HCM-6x-1 and repetition 2 of genotype HCM-6x-2) is possibly higher, and genomic conflicts and sequence loss are probably still more intense in repetition 2 of genotype HCM-6x-1 and in repetition 1 of genotype HCM-6x-2.
Cultivar Paraíso, obtained from a seed mixture of seven different plants, also varied regarding DNA content loss. However, the constrast between the two repetitions was lower than the loss observed in genotypes HCM-6x-1 and HCM-6x-2 (Table 4). The greatest DNA losses (above 20%) occurred among hexaploids, i.e., between individuals with the highest ploidy. Similar results have been reported for species of Artemisia (Pellicer et al., 2010). The authors observed that the increase in 2C values in polyploids is not proportional to ploidy level, since the 1C genome size tends to decrease significantly when high ploidy levels are achieved.
These results indicate that the chromosome distribution of genomic combinations 4x and 5x is similar to that of their parental 6x, obtained by induced chromosome duplication. Mixoploidy, common to all these hybrids, confirms the difficulty in obtaining stable interspecific hybrids. However, the chromosome behavior of these genotypes does not decrease their forage potential, since the agronomic performance of chromosomal races 4x and, especially, 5x indicates that they have good potential use in breeding programs (Leão, 2009).
1. Genomic combinations 4x and 5x are mixoploid, and the variation of chromosome number within chromosomal race 5x is greater than in 4x.
2. Genomic changes occur in chromosomal race 4x, which lead to higher reduction in DNA amount when compared to 5x.
To Fundação de Amparo à Pesquisa do Estado de Minas Gerais, to Conselho Nacional de Desenvolvimento Científico e Tecnológico, and to Coordenação de Aperfeiçoamento de Pessoal de Nível Superior, for financial support.
ABREU, J.C. de; DAVIDE, L.C.; PEREIRA, A.V.; BARBOSA, S. Mixoploidia em híbridos de capim-elefante x milheto tratados com agentes antimitóticos. Pesquisa Agropecuária Brasileira, v.41, p.1629-1635, 2006. [ Links ]
ADAMS, K.L.; WENDEL, J.F. Polyploidy and genome evolution in plants. Current Opinion in Plant Biology, v.8, p.135-141, 2005. [ Links ]
ANDRADE-VIEIRA, L.F. Comportamento genômico em híbridos de capim-elefante e milheto (Pennisetum sp. Schum., Poaceae). 2010. 123p. Tese (Doutorado) - Universidade Federal de Lavras, Lavras. [ Links ]
BARBOSA, S.; DAVIDE, L.C.; PEREIRA, A.V.; ABREU, J.C. de. Duplicação cromossômica de híbridos triplóides de capim-elefante e milheto. Bragantia, v.66, p.365-372, 2007. [ Links ]
BUSTAMANTE, F.O. Variações cromossômicas associadas à poliploidização em híbridos de Pennisetum spp.: um estudo temporal e tecido específico. 2009. 53p. Dissertação (Mestrado) - Universidade Federal de Lavras, Lavras. [ Links ]
CAMPOS, J.M.S.; DAVIDE, L.C.; SALGADO, C.C.; SANTOS, F.C.; COSTA, P.N.; SILVA, P.S.; ALVES, C.C.S.; VICCINI, L.F.; PEREIRA, A.V. In vitro induction of hexaploid plants from triploid hybrids of Pennisetum purpureum and Pennisetum glaucum. Plant Breeding, v.128, p.101-104, 2009. [ Links ]
CAPERTA, A.D.; DELGADO, M.; RESSURREIÇÃO, F.; MEISTER, A.; JONES, R.N.; VIEGAS, W.; HOUBEN, A. Colchicine-induced polyploidization depends on tubulin polymerization in c-metaphase cells. Protoplasma, v.227, p.147-155, 2006. [ Links ]
COMAI, L. Genetic and epigenetic interactions in allopolyploid plants. Plant Molecular Biology, v.43, p.387-399, 2000. [ Links ]
DOLEEL, J. Application of flow cytometry for the study of plant genomes. Journal of Applied Genetics, v.38, p.285-302, 1997. [ Links ]
DOLEEL, J.; GREILHUBER, J.; SUDA, J. Estimation of nuclear DNA content in plants using flow cytometry. Nature Protocols, v.2, p.2233-2244, 2007. [ Links ]
DOYLE, J.J.; FLAGEL, L.E.; PATERSON, A.H.; RAPP, R.A.; SOLTIS, D.E.; SOLTIS, P.S.; JONATHAN, F.; WENDEL, J.F. Evolutionary genetics of genome merger and doubling in plants. Annual Review of Genetics, v.42, p.443-461, 2008. [ Links ]
GERNAND, D.; RUTTEN, T.; VARSHNEY, A.; RUBTSOVA, M.; PRODANOVIC, S.; BRÜB, C.; KUMLEHN, J.; MATZK, F.; HOUBEN, A. Uniparental chromosome elimination at mitosis and interphase in wheat and pearl millet crosses involves micronucleus formation, progressive heterochromatinization, and DNA fragmentation. Plant Cell, v.17, p.2431-2438, 2005. [ Links ]
LAURIE, D.A.; BENNETT, M.D. The timing of chromosome elimination in hexaploid wheat x maize crosses. Genome, v.32, p.953-961, 1989. [ Links ]
LEÃO, F.F. Citogenética e potencial forrageiro de combinações genômicas de capim-elefante e milheto. 2009. 112p. Tese (Doutorado) - Universidade Federal de Lavras, Lavras. [ Links ]
LEVY, A.A.; FELDMAN, M. Genetic and epigenetic reprogramming of the wheat genome upon allopolyploidization. Biological Journal of the Linnean Society, v.82, p.607-613, 2004. [ Links ]
MA, X.-F.; FANG, P.; GUSTAFSON, J.P. Polyploidization-induced genome variation in triticale. Genome, v.47, p.839-848, 2004. [ Links ]
MA, X.-F.; GUSTAFSON, J.P. Timing and rate of genome variation in triticale following allopolyploidization. Genome, v.49, p.950-958, 2006. [ Links ]
MOCHIDA, K.; TSUJIMOTO, H.; SASAKUMA, T. Confocal analysis of chromosome behaviour in wheat x maize zygotes. Genome, v.47, p.199-205, 2004. [ Links ]
OZKAN, H.; TUNA, M.; ARUMUGANATHAN, K. Nonadditive changes in genome size during allopolyploidization in the wheat (Aegilops-Triticum) group. Journal of Heredity, v.94, p.260-264, 2003. [ Links ]
PELLICER, J.; GARCIA, S.; CANELA, M.Á.; GARNATJE, T.; KOROBKOV, A.A.; TWIBELL, J.D.; VALLÈS, J. Genome size dynamics in Artemisia L. (Asteraceae): following the track of polyploidy. Plant Biology, v.12, p.820-830, 2010. [ Links ]
PEREIRA, A.V.; SOUZA SOBRINHO, F. de; SOUZA, F.H.D. de; LÉDO, F.J. da S. Tendências do melhoramento genético e produção de sementes forrageiras no Brasil. In: SIMPÓSIO DE ATUALIZAÇÃO EM GENÉTICA E MELHORAMENTO DE PLANTAS, 7., 2003, Lavras. Anais. Lavras: UFLA, 2003. p.36-63. [ Links ]
RIDDLE, N.C.; BIRCHLER, J.A. Effects of reunited diverged regulatory hierarchies in allopolyploids and species hybrids. Trends in Genetics, v.19, p.597-600, 2003. [ Links ]
SCHOENLEIN, P.V.; BARRETT, J.T.; KULHARYA, A.; DOHN, M.R.; SANCHEZ, A.; HOU, D.-Y.; MCCOY, J.B.S. Radiation therapy depletes extrachromosomally amplified drug resistance genes and oncogenes from tumor cells via micronuclear capture of episomes and double minute chromosomes. International Journal of Radiation Oncology, v.55, p.1051-1065, 2003. [ Links ]
TECHIO, V.H. Meiose e análise genômica em Pennisetum spp. 2002. 104p. Tese (Doutorado) - Universidade Federal de Lavras, Lavras. [ Links ]
Received on March 15, 2011 and accepted on June 2, 2011