栽培花生的高油酸性状[arachhis hypogaea L]。2该性状的分子基础和遗传学。

S Jung, G Powell, K Moore, A Abbott
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引用次数: 144

摘要

以前曾报道过一种油酸含量高的花生品种。选用该高油质品种进行选育时,根据选用的正常油质品种的不同,高油质与正常油质后代的F2分离比为3:1或15:1。这些数据表明,高油酸性状由两个隐性基因控制,一些花生品种与高油酸品种的差异是由一个基因突变引起的,而另一些品种则是由两个基因突变引起的。本研究的目的是了解高油酸性状的分子性质和各种分离模式。在本刊之前的文章中,我们报道了两个同源基因中的一个(ahFAD2B)在栽培花生中表达的油酰- pc去饱和酶的转录本水平在高油酸品种中显著降低。在这篇报道中,我们通过RT-PCR/限制性酶切检测了一个高油酸性状的单基因分离模式的基因表达。我们的数据显示,严重降低的ahFAD2B转录水平与该杂交的高油酸表型绝对相关,表明单基因差异与ahFAD2B转录水平相关。通过在酵母中表达ahFAD2A和ahFAD2B基因的克隆序列,检测ahFAD2A和ahFAD2B基因编码蛋白的酶活性,只有ahFAD2B基因产物表现出显著的油酰pc去饱和酶活性。这些数据,结合ahFAD2A在其他去饱和酶中绝对保守的残基上的变化(D150N)的观察,提出了ahFAD2A在这些正常和高油酸系中是突变等位基因的可能性。为了支持这一假设,我们发现另一个ahFAD2A等位基因在一个正常的油酸花生品系中没有D150N的变化。该花生品系表现出高油酸性状的双基因分离模式。总之,我们的研究结果表明,ahFAD2A的突变和ahFAD2B转录物水平的显著降低共同导致花生品种的高油酸表型,并且编码功能酶的表达基因似乎足以实现正常的油酸表型。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
The high oleate trait in the cultivated peanut [Arachis hypogaea L]. II. Molecular basis and genetics of the trait.

A peanut variety with high oleate content has previously been described. When this high oleate variety was used in breeding crosses, the F2 segregation ratio of high oleate to normal oleate progeny was 3:1 or 15:1 depending on the normal oleate varieties used in the crosses. These data suggested that the high oleate trait is controlled by two recessive genes, and some peanut varieties differ from the high oleate variety by mutations in one gene, while others differ by mutations in two genes. The objective of this study was to understand the molecular nature of the high oleate trait and the various segregation patterns. In the previous paper in this issue, we reported that the level of transcripts expressed by one (ahFAD2B) of two homoeologous genes for oleoyl-PC desaturases in cultivated peanut is significantly reduced in high oleate varieties. In this report, we examined gene expression by RT-PCR/restriction digestion in a cross that shows a one-gene segregation pattern for the high oleate trait. Our data showed that the severely reduced level of ahFAD2B transcript correlates absolutely with the high oleate phenotype in this cross, suggesting that the single gene difference is correlated with the ahFAD2B transcript level. When we tested the enzyme activity of the proteins encoded by ahFAD2A and ahFAD2B by expression of the cloned sequences in yeast, only the ahFAD2B gene product showed significant oleoyl-PC desaturase activity. These data, combined with the observation that ahFAD2A shows a change (D150N) in a residue that is absolutely conserved among other desaturases, raised the possibility that the ahFAD2A in these normal and high oleate lines is a mutant allele. In support of this hypothesis, we found that another ahFAD2A allele in a normal oleate peanut line does not have the D150N change. This peanut line displays a two-gene-segregation pattern for the high oleate trait. In conclusion, our results suggest that a mutation in ahFAD2A and a significant reduction in levels of the ahFAD2B transcript together cause the high oleate phenotype in peanut varieties, and that one expressed gene encoding a functional enzyme appears to be sufficient for the normal oleate phenotype.

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