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通过连锁分子标记验证大麦种子休眠基因座。

Verification of barley seed dormancy loci via linked molecular markers.

机构信息

Department of Crop and Soil Sciences, Washington State University, 99164-6420, Pullman, WA, USA.

出版信息

Theor Appl Genet. 1996 Jan;92(1):87-91. doi: 10.1007/BF00222956.

DOI:10.1007/BF00222956
PMID:24166121
Abstract

Seed dormancy is a relatively complex trait in barley (Hordeum vulgare L.). Several dormancy loci were identified previously by quantitative trait locus analysis. Three reciprocal crosses were made in the present study between parents carrying specific dormancy alleles via linked molecular markers to verify individual dormancy locus effects and potential expression. Analyses of F2 progenies revealed that the dormancy allele at the locus flanked by the markers Ale and ABC302 on the long arm of chromosome 7 had a major effect on dormancy, and was at least partly epistatic to the dormancy locus in the ABC309-MWG851 interval near the telomere of the long arm of chromosome 7. In the absence of the dormancy allele in the Ale-ABC302 interval, the allele in the ABC309-MWG851 interval exerted moderate to large effects on dormancy. Cytoplasmic effects on dormancy were also observed. The germination percentages of progeny with relatively high levels of dormancy were more variable than those of non-dormant or less-dormant progeny, apparently due to environmental effects. Removal of the dormancy allele in the Ale-ABC302 interval, or introducing the dormancy allele in the ABC309-MWG851 interval, should suffice for adjusting dormancy levels in breeding programs to suit various production situations and end uses. The verification of dormancy loci via linked molecular markers allows manipulation of these loci in applied breeding programs.

摘要

种子休眠是大麦(Hordeum vulgare L.)的一个相对复杂的特性。先前通过数量性状位点分析鉴定了几个休眠位点。本研究通过连锁分子标记在携带特定休眠等位基因的亲本之间进行了三次相互杂交,以验证单个休眠位点效应和潜在表达。对 F2 后代的分析表明,7 号染色体长臂上标记 Ale 和 ABC302 之间位点的休眠等位基因对休眠有主要影响,并且至少部分与 7 号染色体长臂端粒附近的 ABC309-MWG851 区间的休眠位点上位性。在 Ale-ABC302 区间不存在休眠等位基因的情况下,ABC309-MWG851 区间的等位基因对休眠有中等至较大的影响。还观察到细胞质对休眠的影响。休眠水平较高的后代的发芽百分比比非休眠或休眠程度较低的后代更具变异性,显然是由于环境影响。在育种计划中,去除 Ale-ABC302 区间的休眠等位基因,或引入 ABC309-MWG851 区间的休眠等位基因,足以调节休眠水平,以适应各种生产情况和最终用途。通过连锁分子标记验证休眠位点可以在应用育种计划中操纵这些位点。

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本文引用的文献

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