Blanco Antonio, Simeone Rosanna, Cenci Alberto, Gadaleta Agata, Tanzarella Oronzo A, Porceddu Enrico, Salvi Silvio, Tuberosa Roberto, Figliuolo Giovanni, Spagnoletti Pierluigi, Röder Marion S, Korzun Victor
Department of Environmental and Agro-Forestry Biology and Chemistry, University of Bari, via Amendola, 165/A, 70126 Bari, Italy.
Cell Mol Biol Lett. 2004;9(3):529-41.
A set of recombinant inbred lines (RIL) derived from a cross between the cultivar Messapia of durum wheat (Triticum turgidum var. durum) and the accession MG4343 of T. turgidum var. dicoccoides was analysed to increase the number of assigned markers and the resolution of the previously constructed genetic linkage map. An updated map of the durum wheat genome consisting of 458 loci was constructed. These loci include 261 Restriction Fragment Length Polymorphisms (RFLPs), 91 microsatellites (Simple Sequence Repeats, SSRs), 87 Amplified Fragment Length Polymorphisms (AFLPs), two ribosomal genes, and nine biochemical (seven seed storage proteins and two isozymes) and eight morphological markers. The loci were mapped on all 14 chromosomes of the A and B genomes, and covered a total distance of 3038.4 cM with an average distance of 6.7 cM between adjacent markers. The molecular markers were evenly distributed between the A and the B genomes (240 and 218 markers, respectively). An additional forty loci (8.8%) could not be assigned to a specific linkage group. A fraction (16.4%) of the markers significantly deviated from the expected Mendelian ratios; clusters of loci showing distorted segregation were found on the 1B, 2A, 2B, 3A, 4A, 7A and 7B chromosomes. The genetic lengths of the chromosomes range from 148.8 cM (chromosome 6B) to 318.0 cM (chromosome 2B) and approximately concur with their physical lengths. Chromosome 2B has the largest number of markers (47), while the chromosomes with the fewest markers are 3A and 6B (23). There are two gaps larger than 40 cM on chromosomes 2A and 3B. The durum wheat map was compared with the published maps of bread and durum wheats; the order of most common RFLP and SSR markers on the 14 chromosomes of the A and B genomes were nearly identical. A core-map can be extracted from the high-density Messapia x dicoccoides map and a subset of uniformly distributed markers can be used to detect and map quantitative trait loci.
分析了一组由硬粒小麦(Triticum turgidum var. durum)品种Messapia与野生二粒小麦(T. turgidum var. dicoccoides)材料MG4343杂交得到的重组自交系(RIL),以增加已定位标记的数量并提高先前构建的遗传连锁图谱的分辨率。构建了一张由458个位点组成的硬粒小麦基因组更新图谱。这些位点包括261个限制性片段长度多态性(RFLP)、91个微卫星(简单序列重复,SSR)、87个扩增片段长度多态性(AFLP)、两个核糖体基因,以及9个生化标记(7个种子贮藏蛋白和2个同工酶)和8个形态学标记。这些位点定位在A和B基因组的所有14条染色体上,覆盖的总距离为3038.4 cM,相邻标记之间的平均距离为6.7 cM。分子标记在A和B基因组之间均匀分布(分别为240个和218个标记)。另外40个位点(8.8%)无法定位到特定的连锁群。一部分标记(16.4%)显著偏离预期的孟德尔比率;在1B、2A、2B、3A、4A、7A和7B染色体上发现了显示偏分离的位点簇。染色体的遗传长度范围从148.8 cM(6B染色体)到318.0 cM(2B染色体),并且大致与其物理长度一致。2B染色体上的标记数量最多(47个),而标记数量最少的染色体是3A和6B(23个)。在2A和3B染色体上有两个大于40 cM的间隙。将硬粒小麦图谱与已发表的面包小麦和硬粒小麦图谱进行了比较;A和B基因组14条染色体上大多数常见RFLP和SSR标记的顺序几乎相同。可以从高密度的Messapia×dicoccoides图谱中提取核心图谱,并且可以使用一组均匀分布的标记子集来检测和定位数量性状位点。