Bio-Evaluation Center, Korea Research Institute of Bioscience and Biotechnology, Cheongwon, Chungbuk, Republic of Korea.
Theor Appl Genet. 2011 Mar;122(5):875-84. doi: 10.1007/s00122-010-1493-4. Epub 2010 Nov 23.
The rj1 mutation of soybean is a simple recessive allele in a single line that arose as a spontaneous mutation in a population; it exhibits non-nodulation with virtually all Bradyrhizobium and Sinorhizobium strains. Here, we described fine genetic and physical mapping of the rj1 locus on soybean chromosome 2. The initial mapping of the rj1 locus using public markers indicated that A343.p2, a sequence-based marker that contains sequence similar to a part of the LjNFR1 gene regulating nodule formation as a member of lysin motif-type receptor-like kinase (LYK) family, maps very close to or cosegregates with the rj1 locus. The sequence of A343.p2 is 100% identical to parts of two BAC clone sequences (GM_WBb0002O19 and GM_WBb098N11) that contain three members of the LYK family. We analyzed the sequence contig (262 kbp) of the two BAC clones by resequencing and subsequent fine genetic and physical mapping. The results indicated that rj1 is located in a gene-rich region with a recombination rate of 120 kbp/cM: several fold higher than the genome average. Among the LYK genes, NFR1α is most likely the gene encoded at the Rj1 locus. The non-nodulating rj1 allele was created by a single base-pair deletion that results in a premature stop codon. Taken together, the fine genetic and physical mapping of the Rj1-residing chromosomal region, combined with the unexpected observation of a putative recombination hotspot, allowed us to demonstrate that the Rj1 locus most likely encodes the NFR1α gene.
大豆的 rj1 突变是一个在单一线粒体中自发出现的简单隐性等位基因,它表现出与几乎所有 Bradyrhizobium 和 Sinorhizobium 菌株的非结瘤性。在这里,我们描述了大豆染色体 2 上 rj1 基因座的精细遗传和物理图谱。使用公共标记对 rj1 基因座的初步定位表明,A343.p2 是一个基于序列的标记,它包含类似于调控结瘤形成的 LjNFR1 基因的一部分序列,作为赖氨酸酶基序型受体样激酶(LYK)家族的成员,非常接近或与 rj1 基因座共分离。A343.p2 的序列与包含 LYK 家族三个成员的两个 BAC 克隆序列(GM_WBb0002O19 和 GM_WBb098N11)的部分序列完全相同。我们通过重新测序和随后的精细遗传和物理作图分析了这两个 BAC 克隆的序列连续体(262 kbp)。结果表明,rj1 位于一个基因丰富的区域,重组率为 120 kbp/cM:比基因组平均水平高几个数量级。在 LYK 基因中,NFR1α 最有可能是 Rj1 基因座编码的基因。无结瘤的 rj1 等位基因是由单个碱基对缺失引起的,导致过早的终止密码子。总之,Rj1 基因座所在染色体区域的精细遗传和物理图谱,加上对潜在重组热点的意外观察,使我们能够证明 Rj1 基因座最有可能编码 NFR1α 基因。