Hayashi M, Miyahara A, Sato S, Kato T, Yoshikawa M, Taketa M, Hayashi M, Pedrosa A, Onda R, Imaizumi-Anraku H, Bachmair A, Sandal N, Stougaard J, Murooka Y, Tabata S, Kawasaki S, Kawaguchi M, Harada K
Faculty of Horticulture, Chiba University, Matsudo, Japan.
DNA Res. 2001 Dec 31;8(6):301-10. doi: 10.1093/dnares/8.6.301.
Among leguminous plants, the model legume Lotus japonicus (Regel) Larsen has many biological and genetic advantages. We have developed a genetic linkage map of L. japonicus based on amplified fragment length polymorphism (AFLP), simple sequence repeat polymorphism (SSRP) and derived cleaved amplified polymorphic sequence (dCAPS). The F2 mapping population used was derived from a cross between two L. japonicus accessions Gifu B-129 and Miyakojima MG-20. These parental accessions showed remarkable cytological differences, particularly with respect to size and morphology of chromosomes 1 and 2. Using fluorescence in situ hybridization (FISH) with BAC clones from Gifu B-129 and TAC (Transformation-competent Artificial Chromosome) clones from Miyakojima MG-20, a reciprocal translocation was found to be responsible for the cytological differences between chromosomes 1 and 2. The borders of the translocations were identified by FISH and by alignment toward the L. filicaulis x L. japonicus Gifu B-129 linkage map. The markers from the main translocated region were located on linkage groups 1 and 2 of the two accessions, Gifu B-129 and Miyakojima MG-20, respectively. The framework of the linkage map was constructed based on codominant markers, and then dominant markers were integrated separately in each linkage group of the parents. The resulting linkage groups correspond to the six pairs of chromosomes of L. japonicus and consist of 287 markers with 487.3 cM length in Gifu B-129 and 277 markers with 481.6 cM length in Miyakojima MG-20. The map and marker information is available through the World Wide Web at http://www.kazusa.or.jp/lotus/.
在豆科植物中,模式豆科植物百脉根(Lotus japonicus (Regel) Larsen)具有许多生物学和遗传学优势。我们基于扩增片段长度多态性(AFLP)、简单序列重复多态性(SSRP)和衍生酶切扩增多态性序列(dCAPS)构建了百脉根的遗传连锁图谱。所用的F2作图群体来自两个百脉根种质系Gifu B - 129和宫古岛MG - 20的杂交。这些亲本种质系在细胞学上表现出显著差异,特别是在第1和第2号染色体的大小和形态方面。通过使用来自Gifu B - 129的BAC克隆和来自宫古岛MG - 20的TAC(可转化人工染色体)克隆进行荧光原位杂交(FISH),发现一个相互易位是导致第1和第2号染色体细胞学差异的原因。通过FISH以及与丝状百脉根×百脉根Gifu B - 129连锁图谱的比对确定了易位的边界。来自主要易位区域的标记分别位于两个种质系Gifu B - 129和宫古岛MG - 20的连锁群1和连锁群2上。基于共显性标记构建了连锁图谱的框架,然后将显性标记分别整合到亲本的每个连锁群中。所得的连锁群对应于百脉根的六对染色体,在Gifu B - 129中由287个标记组成,长度为487.3 cM,在宫古岛MG - 20中由277个标记组成,长度为481.6 cM。该图谱和标记信息可通过万维网在http://www.kazusa.or.jp/lotus/获取。