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Assessing the Potential of Using the Langdon 5D(5B) Substitution Line for the Introgression of Aegilops Tauschii into Durum Wheat

Frontiers in plant science(2022)SCI 2区

Univ Nottingham

Cited 2|Views30
Abstract
Aegilops tauschii, the D-genome donor of hexaploid wheat, provides a source of genetic variation that could be used for tetraploid (durum) wheat improvement. In addition to the genes for wheat quality on the D-genome, which differentiate between bread and durum wheats in terms of end-use properties, genes coding for resistances to biotic and abiotic stresses are also present on the D-genome which would be useful in durum wheat. The introgression of Ae. tauschii into durum wheat, however, requires cytogenetic manipulation to induce homoeologous chromosome pairing to promote recombination. For this purpose, the introgression of Ae. tauschii into durum wheat was performed through a bridge cross of the wild species to the Langdon 5D(5B) disomic substitution line that lacks the Ph1 locus present on chromosome 5B, followed by a cross of the F1 to the durum wheat cultivar Om Rabi 5. Subsequent generations were self-fertilized, and these were screened for D-genome introgressions using (i) D-genome-specific Kompetitive Allele-Specific PCR (KASP) markers and (ii) KASP markers polymorphic between the 5D chromosomes of wheat, present in the Langdon 5D(5B) substitution line, and of Ae. tauschii. Homozygous introgression lines were confirmed using genomic and fluorescence in situ hybridization. The results showed that the use of the Langdon 5D(5B) disomic substitution line did not promote D-genome introgression across all linkage groups with only a limited success in the introgression of Ae. tauschii 5D segments into durum wheat.
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Aegilops tauschii,introgression,durum wheat,hexaploid wheat,chromosome-specific KASP markers
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要点】:该论文探讨了利用Langdon 5D(5B)异源染色体系列对硬质小麦进行D基因组导入的潜力,并成功导入了Ae. tauschii的D基因组片段,但成功率有限。

方法】:通过将野生物种与缺乏Ph1位点的Langdon 5D(5B)二倍体异源染色体系列进行桥接杂交,然后与硬质小麦品种Om Rabi 5进行杂交,接着进行自交,筛选出D基因组导入的后续代。

实验】:使用D基因组特异性KASP标记和5D染色体间多态性的KASP标记,结合基因组和荧光原位杂交代确认纯合导入系。结果显示,尽管利用Langdon 5D(5B)异源染色体系列进行了D基因组导入,但成功率只在有限的几段D基因组中得到确认。