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大豆类黄酮3'-羟化酶基因中的单碱基缺失与灰色茸毛色相关。

A single-base deletion in soybean flavonoid 3'-hydroxylase gene is associated with gray pubescence color.

作者信息

Toda Kyoko, Yang Daijun, Yamanaka Naoki, Watanabe Satoshi, Harada Kyuya, Takahashi Ryoji

机构信息

National Institute of Crop Science, Tsukuba, Ibaraki, Japan.

出版信息

Plant Mol Biol. 2002 Sep;50(2):187-96. doi: 10.1023/a:1016087221334.

Abstract

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.

摘要

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。

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