Agricultural Research Institute of the Hungarian Academy of Sciences, POB 19, Martonvásár, 2462, Hungary.
Theor Appl Genet. 2010 May;120(8):1535-45. doi: 10.1007/s00122-010-1274-0. Epub 2010 Feb 10.
The main objective of the present work was to develop a wheat genotype containing both the recessive crossability alleles (kr1kr1kr2kr2), allowing high crossability between 6x wheat and diploid rye, and the 1BL.1RS wheat/rye translocation chromosome. This wheat genotype could be used as a recipient partner in wheat-rye crosses for the efficient introduction of new allelic variation into 1RS in translocation wheats. After crossing the wheat cultivars 'Mv Magdaléna' and 'Mv Béres', which carry the 1BL.1RS translocation involving the 1RS chromosome arm from 'Petkus', with the line 'Mv9 kr1', 117 F(2) plants were analysed for crossability, ten of which had higher than 50% seed set with rye and thus presumably carried the kr1kr1kr2kr2 alleles. Four of the ten plants contained the 1BL.1RS translocation in the disomic condition as detected by genomic in situ hybridization (GISH). The wheat x rye F(1) hybrids produced between these lines and the rye cultivar 'Kriszta' were analysed in meiosis using GISH. 1BL.1RS/1R chromosome pairing was detected in 62.4% of the pollen mother cells. The use of fluorescent in situ hybridization (FISH) with the repetitive DNA probes pSc119.2, Afa family and pTa71 allowed the 1R and 1BL.1RS chromosomes to be identified. The presence of the 1RS arm from 'Kriszta' besides that of 'Petkus' was demonstrated in the F(1) hybrids using the rye SSR markers RMS13 and SCM9. In four of the 22 BC(1) progenies analysed, only 'Kriszta'-specific bands were observed with these markers, though the presence of the 1BL.1RS translocation was detected using GISH. It can be concluded that recombination occurred between the 'Petkus' and 'Kriszta' 1RS chromosome arms in the translocated chromosome in these plants.
本研究的主要目的是开发一个同时含有隐性可交配性等位基因(kr1kr1kr2kr2)的小麦基因型,该基因型允许 6x 小麦与二倍体黑麦之间具有高的可交配性,并含有 1BL.1RS 小麦/黑麦易位染色体。该小麦基因型可用作小麦-黑麦杂交的受体亲本,以有效地将新的等位基因变异导入易位小麦的 1RS 中。在与携带来自‘Petkus’的 1RS 染色体臂的 1BL.1RS 易位的小麦品种‘Mv Magdaléna’和‘Mv Béres’与品系‘Mv9 kr1’杂交后,对 117 个 F(2)植株进行了可交配性分析,其中 10 个植株与黑麦的结实率高于 50%,因此可能携带 kr1kr1kr2kr2 等位基因。在这 10 个植株中,有 4 个植株在二体状态下含有 1BL.1RS 易位,这是通过基因组原位杂交(GISH)检测到的。用这些品系与黑麦品种‘Kriszta’之间产生的小麦-黑麦 F(1)杂种进行减数分裂分析,使用 GISH 检测 1BL.1RS/1R 染色体配对。在 62.4%的花粉母细胞中检测到 1BL.1RS/1R 染色体配对。使用重复 DNA 探针 pSc119.2、Afa 家族和 pTa71 的荧光原位杂交(FISH)可以鉴定 1R 和 1BL.1RS 染色体。在 F(1)杂种中,使用黑麦 SSR 标记 RMS13 和 SCM9 可以证明除了‘Petkus’之外,还有来自‘Kriszta’的 1RS 臂。在分析的 22 个 BC(1)后代中,尽管使用 GISH 检测到 1BL.1RS 易位,但只有这 4 个后代观察到与这些标记特异性的‘Kriszta’条带。可以得出结论,在这些植株中,易位染色体上的‘Petkus’和‘Kriszta’1RS 染色体臂之间发生了重组。