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TILLING for allergen reduction and improvement of quality traits in peanut (Arachis hypogaea L.)

机译:降低花生中过敏原和改善品质性状的方法(花生)

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Background Allergic reactions to peanuts (Arachis hypogaea L.) can cause severe symptoms and in some cases can be fatal, but avoidance is difficult due to the prevalence of peanut-derived products in processed foods. One strategy of reducing the allergenicity of peanuts is to alter or eliminate the allergenic proteins through mutagenesis. Other seed quality traits could be improved by altering biosynthetic enzyme activities. Targeting Induced Local Lesions in Genomes (TILLING), a reverse-genetics approach, was used to identify mutations affecting seed traits in peanut. Results Two similar copies of a major allergen gene, Ara h 1, have been identified in tetraploid peanut, one in each subgenome. The same situation has been shown for major allergen Ara h 2. Due to the challenge of discriminating between homeologous genes in allotetraploid peanut, nested PCR was employed, in which both gene copies were amplified using unlabeled primers. This was followed by a second PCR using gene-specific labeled primers, heteroduplex formation, CEL1 nuclease digestion, and electrophoretic detection of labeled fragments. Using ethyl methanesulfonate (EMS) as a mutagen, a mutation frequency of 1 SNP/967 kb (3,420 M2 individuals screened) was observed. The most significant mutations identified were a disrupted start codon in Ara h 2.02 and a premature stop codon in Ara h 1.02. Homozygous individuals were recovered in succeeding generations for each of these mutations, and elimination of Ara h 2.02 protein was confirmed. Several Ara h 1 protein isoforms were eliminated or reduced according to 2D gel analyses. TILLING also was used to identify mutations in fatty acid desaturase AhFAD2 (also present in two copies), a gene which controls the ratio of oleic to linoleic acid in the seed. A frameshift mutation was identified, resulting in truncation and inactivation of AhFAD2B protein. A mutation in AhFAD2A was predicted to restore function to the normally inactive enzyme. Conclusions This work represents the first steps toward the goal of creating a peanut cultivar with reduced allergenicity. TILLING in peanut can be extended to virtually any gene, and could be used to modify other traits such as nutritional properties of the seed, as shown in this study.
机译:背景技术对花生(Arachis hypogaea L.)的过敏反应可引起严重症状,在某些情况下可能是致命的,但由于加工食品中普遍存在花生衍生产品,因此很难避免。降低花生过敏原性的一种策略是通过诱变改变或消除过敏原蛋白。其他种子品质性状可以通过改变生物合成酶的活性来改善。针对基因组中的诱导局部病变(TILLING)是一种反向遗传学方法,用于鉴定影响花生种子性状的突变。结果在四倍体花生中鉴定出两个相似的主要变应原基因拷贝Ara h 1,每个亚基因组一个。对于主要变应原Ara h 2,也显示出相同的情况。由于在异源四倍体花生中区分同源基因的挑战,因此采用了巢式PCR,其中两个基因的拷贝均使用未标记的引物扩增。随后进行第二次PCR,使用基因特异性标记引物,异源双链体形成,CEL1核酸酶消化和电泳检测标记片段。使用甲磺酸乙酯(EMS)作为诱变剂,观察到1 SNP / 967 kb的突变频率(筛选了3,420 M 2 个体)。鉴定出的最重要的突变是Ara h 2.02中的起始密码子被破坏和Ara h 1.02中的提前终止密码子。对于这些突变中的每一个,均在后代中恢复了纯合子个体,并证实消除了Ara h 2.02蛋白。根据2D凝胶分析,消除或减少了几种Ara h 1蛋白同工型。耕种还用于鉴定脂肪酸去饱和酶AhFAD2(也有两个拷贝)中的突变,该基因控制种子中油酸与亚油酸的比例。鉴定出移码突变,导致AhFAD2B蛋白被截短和失活。预测AhFAD2A中的突变可恢复正常失活的酶的功能。结论这项工作是朝着降低变应原性的花生品种迈出的第一步。如本研究所示,花生中的分ING几乎可以扩展到任何基因,并且可以用于修饰其他性状,例如种子的营养特性。

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