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大豆种子脂氧合酶基因:分子特征和分子标记分析的开发。

Soybean seed lipoxygenase genes: molecular characterization and development of molecular marker assays.

机构信息

Division of Plant Sciences, University of Missouri, 108 Waters Hall, Columbia, MO 65211, USA.

出版信息

Theor Appl Genet. 2010 Apr;120(6):1139-49. doi: 10.1007/s00122-009-1241-9.

DOI:10.1007/s00122-009-1241-9
PMID:20058147
Abstract

Soybean seeds contain three lipoxygenase (Lox) enzymes that are controlled by separate genes, Lox1, Lox2 and Lox3. Lipoxygenases play a role in the development of unpleasant flavors in foods containing soybean by oxidation of polyunsaturated fatty acids. Null alleles for all three enzymes have been identified, lox1, lox2 and lox3, and are known to be inherited as simple recessive alleles. Previous studies determined that a missense mutation rendered Lox2 inactive; however, the genetic cause of either lox1 or lox3 mutation was not known. The objectives of this study were the molecular characterization of both lox1 and lox3 mutant alleles and the development of molecular markers to accelerate breeding for Lox-free soybean varieties. We identified two independent mutant alleles as the genetic causes of the lack of Lox1 in seeds of two lox1 mutant soybean lines. Similarly, a mutant allele that truncates Lox3 in a lox3 mutant soybean line was identified. Molecular markers were designed and confirmed to distinguish mutant, wild type, and heterozygous individuals for Lox1, Lox2 and Lox3 genes. Genotype and Lox phenotype analysis showed a perfect association between the inheritance of homozygous lox mutant alleles and the lack of Lox activity. Molecular characterization of a seed-lipoxygenase-free soybean line led to the discovery that an induced recombination event within the Lox1 gene was responsible for breaking the tight linkage in repulsion phase between mutant alleles at the Lox1 and Lox2 loci. The molecular resources developed in this work should accelerate the inclusion of the lipoxygenase-free trait in soybean varieties.

摘要

大豆种子含有三种脂肪氧合酶(Lox),它们分别由不同的基因控制,分别是 Lox1、Lox2 和 Lox3。脂肪氧合酶通过氧化多不饱和脂肪酸在含有大豆的食品中发挥作用,导致不愉快的味道。已经鉴定出三种酶的缺失等位基因,lox1、lox2 和 lox3,并且已知它们作为简单的隐性等位基因遗传。先前的研究确定,错义突变使 Lox2 失去活性;然而,lox1 或 lox3 突变的遗传原因尚不清楚。本研究的目的是对 lox1 和 lox3 突变等位基因进行分子特征分析,并开发分子标记,以加速无脂肪氧合酶大豆品种的选育。我们确定了两个独立的突变等位基因,是两个 lox1 突变大豆系种子中 Lox1 缺失的遗传原因。同样,在 lox3 突变大豆系中,截短 Lox3 的突变等位基因也被鉴定出来。设计并验证了分子标记,以区分 Lox1、Lox2 和 Lox3 基因的突变型、野生型和杂合个体。基因型和 Lox 表型分析表明,纯合 lox 突变等位基因的遗传与 Lox 活性缺失之间存在完美的相关性。无种子脂肪氧合酶大豆系的分子特征分析表明,lox1 基因内诱导的重组事件是导致 Lox1 和 Lox2 基因座上突变等位基因在排斥相中断紧密连锁的原因。本研究开发的分子资源应加速将无脂肪氧合酶特性纳入大豆品种。

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