Peng J, Korol A B, Fahima T, Röder M S, Ronin Y I, Li Y C, Nevo E
Institute of Evolution, University of Haifa, Mount Carmel, Haifa 31905, Israel.
Genome Res. 2000 Oct;10(10):1509-31. doi: 10.1101/gr.150300.
The main objectives of the study reported here were to construct a molecular map of wild emmer wheat, Triticum dicoccoides, to characterize the marker-related anatomy of the genome, and to evaluate segregation and recombination patterns upon crossing T. dicoccoides with its domesticated descendant Triticum durum (cultivar Langdon). The total map length exceeded 3000 cM and possibly covered the entire tetraploid genome (AABB). Clusters of molecular markers were observed on most of the 14 chromosomes. AFLP (amplified fragment length polymorphism) markers manifested a random distribution among homologous groups, but not among genomes and chromosomes. Genetic differentiation between T. dicoccoides and T. durum was attributed mainly to the B genome as revealed by AFLP markers. The segregation-distorted markers were mainly clustered on 4A, 5A, and 5B chromosomes. Homeoalleles, differentially conferring the vigor of gametes, might be responsible for the distortion on 5A and 5B chromosomes. Quasilinkage, deviation from free recombination between markers of nonhomologous chromosomes, was discovered. Massive negative interference was observed in most of the chromosomes (an excess of double crossovers in adjacent intervals relative to the expected rates on the assumption of no interference). The general pattern of distribution of islands of negative interference included near-centromeric location, spanning the centromere, and median/subterminal location. [An appendix describing the molecular marker loci is available as an online supplement at http://www.genome.org.]
本文报道的研究的主要目的是构建野生二粒小麦(Triticum dicoccoides)的分子图谱,描述基因组中与标记相关的结构,并评估野生二粒小麦与其驯化后代硬粒小麦(品种Langdon)杂交后的分离和重组模式。总图长度超过3000厘摩,可能覆盖了整个四倍体基因组(AABB)。在14条染色体中的大多数上都观察到了分子标记簇。AFLP(扩增片段长度多态性)标记在同源组之间呈随机分布,但在基因组和染色体之间并非如此。AFLP标记显示,野生二粒小麦和硬粒小麦之间的遗传分化主要归因于B基因组。分离扭曲的标记主要聚集在4A、5A和5B染色体上。同源等位基因对配子活力有不同的影响,可能是5A和5B染色体上出现分离扭曲的原因。发现了准连锁现象,即非同源染色体标记之间偏离自由重组。在大多数染色体中观察到大量负干扰(相对于无干扰假设下的预期速率,相邻区间的双交换过多)。负干扰岛的一般分布模式包括近着丝粒位置、跨越着丝粒以及中间/亚末端位置。[描述分子标记位点的附录可在http://www.genome.org上作为在线补充资料获取。]