Lima-Brito J, Carvalho A, Martin A, Heslop-Harrison J S, Guedes-Pinto H
Department of Genetics and Biotechnology, CGB-ICETA / University of Trás-os-Montes and Alto Douro, Apt. 1013, 5000-911 Vila Real, Portugal.
J Genet. 2006 Aug;85(2):123-31. doi: 10.1007/BF02729018.
The morphological, yield, cytological and molecular characteristics of bread wheat x tritordeum F(1) hybrids (2n = 6x = 42; AABBDH(ch)) and their parents were analysed. Morphologically, these hybrids resembled the wheat parent. They were slightly bigger than both parents, had more spikelets per spike, and tillered more profusely. The hybrids are self-fertile but a reduction of average values of yield parameters was observed. For the cytological approach we used a double-target fluorescence in situ hybridization performed with total genomic DNA from Hordeum chilense L. and the ribosomal sequence pTa71. This technique allowed us to confirm the hybrid nature and to analyse chromosome pairing in this material. Our results showed that the expected complete homologous pairing (14 bivalents plus 14 univalents) was only observed in 9.59% of the pollen mother cells (PMCs) analysed. Some PMCs presented autosyndetic pairing of H(ch) and A, B or D chromosomes. The average number of univalents was higher in the wheat genome (6.8) than in the H(ch) genome (5.4). The maximum number of univalents per PMC was 20. We only observed wheat multivalents (one per PMC) but the frequency of trivalents (0.08) was higher than that of quadrivalents (0.058). We amplified 50 RAPD bands polymorphic between the F(1) hybrid and one of its parents, and 31 ISSR polymorphic bands. Both sets of markers proved to be reliable for DNA fingerprinting. The complementary use of morphological and yield analysis, molecular cytogenetic techniques and molecular markers allowed a more accurate evaluation and characterization of the hybrids analysed here.
对面包小麦×三角麦F(1)杂种(2n = 6x = 42;AABBDH(ch))及其亲本的形态学、产量、细胞学和分子特征进行了分析。在形态学上,这些杂种与小麦亲本相似。它们比双亲略大,每穗小穗数更多,分蘖更旺盛。这些杂种可自交结实,但观察到产量参数的平均值有所降低。对于细胞学方法,我们使用了用智利大麦的总基因组DNA和核糖体序列pTa71进行的双靶标荧光原位杂交。该技术使我们能够确认杂种性质并分析该材料中的染色体配对。我们的结果表明,预期的完全同源配对(14个二价体加14个单价体)仅在9.59%的分析花粉母细胞(PMC)中观察到。一些PMC呈现H(ch)与A、B或D染色体的同源配对。小麦基因组中的单价体平均数(6.8)高于H(ch)基因组中的单价体平均数(5.4)。每个PMC的单价体最大数为20。我们仅观察到小麦多价体(每个PMC一个),但三价体的频率(0.08)高于四价体的频率(0.058)。我们扩增了50个在F(1)杂种与其亲本之一之间多态的RAPD条带和31个ISSR多态条带。两组标记都被证明可用于DNA指纹分析。形态学和产量分析、分子细胞遗传学技术和分子标记的互补使用,使得对这里分析的杂种能够进行更准确的评估和表征。