Toda Kyoko, Yang Daijun, Yamanaka Naoki, Watanabe Satoshi, Harada Kyuya, Takahashi Ryoji
National Institute of Crop Science, Tsukuba, Ibaraki, Japan.
Plant Mol Biol. 2002 Sep;50(2):187-96. doi: 10.1023/a:1016087221334.
The T locus of soybean (Glycine max (L.) Merr.) controls pubescence and seed coat color and is presumed to encode flavonoid 3'-hydroxylase (F3'H). The dominant T and the recessive t allele of the locus produce brown and gray pubescence, respectively. PCR primers were constructed based on the sequence of a soybean EST clone homologous to the F3'H gene. A putative full-length cDNA, sf3'h1 was isolated by 3' and 5' RACE. Sequence analysis revealed that sf3'h1 consists of 1690 nucleotides encoding 513 amino acids. It had 68% and 66% homology with corresponding F3'H protein sequences of petunia and Arabidopsis, respectively. A conserved amino acid sequence of F3'H proteins, GGEK, was found in the deduced polypeptide. Sequence analysis of the gene from a pair of near-isogenic lines for T, To7B (TT, brown) and To7G (tt, gray) revealed that they differed by a single C deletion in the coding region of To7G. The deletion changed the subsequent reading frame resulting in a truncated polypeptide lacking the GGEK consensus sequence and the heme-binding domain. Genomic Southern analysis probed by sf3'h1 revealed restriction fragment length polymorphisms between cultivars with different pubescence color. Further, sf3'h1 was mapped at the same position with T locus on LG3(c2). PCR-RFLP analysis was performed to detect the single-base deletion. To7B and three cultivars with brown pubescence exhibited shorter fragments, while To7G and three cultivars with gray pubescence had longer fragments due to the single-base deletion. The PCR-RFLP marker co-segregated with genotypes at the T locus in a F2 population segregating for the T locus. The above results strongly suggest that sJ3'h1 represents the T gene of soybean responsible for pubescence color and that the single-base deletion may be responsible for gray pubescence color.
大豆(Glycine max (L.) Merr.)的T位点控制着茸毛和种皮颜色,推测其编码类黄酮3'-羟化酶(F3'H)。该位点的显性T等位基因和隐性t等位基因分别产生棕色和灰色茸毛。基于与F3'H基因同源的大豆EST克隆序列构建了PCR引物。通过3'和5' RACE分离出一个推定的全长cDNA,即sf3'h1。序列分析表明,sf3'h1由1690个核苷酸组成,编码513个氨基酸。它与矮牵牛和拟南芥相应的F3'H蛋白序列分别具有68%和66%的同源性。在推导的多肽中发现了F3'H蛋白的保守氨基酸序列GGEK。对T的一对近等基因系To7B(TT,棕色)和To7G(tt,灰色)的基因进行序列分析,结果显示它们在To7G的编码区存在一个单碱基C缺失。该缺失改变了后续的阅读框,导致产生一个截短的多肽,该多肽缺乏GGEK共有序列和血红素结合结构域。用sf3'h1进行基因组Southern分析,揭示了不同茸毛颜色品种之间的限制性片段长度多态性。此外,sf3'h1被定位在LG3(c2)上与T位点相同的位置。进行了PCR-RFLP分析以检测单碱基缺失。由于单碱基缺失,To7B和三个棕色茸毛品种表现出较短的片段,而To7G和三个灰色茸毛品种具有较长的片段。在T位点分离的F2群体中,PCR-RFLP标记与T位点的基因型共分离。上述结果强烈表明,sJ3'h1代表了控制大豆茸毛颜色的T基因,单碱基缺失可能是导致灰色茸毛颜色的原因。