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Genetic Dissection of Ethanol Tolerance in the Budding Yeast Saccharomyces cerevisiae

机译:酵母发酵酵母中乙醇耐性的遗传解剖

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摘要

Uncovering genetic control of variation in ethanol tolerance in natural populations of yeast Saccharomyces cerevisiae is essential for understanding the evolution of fermentation, the dominant lifestyle of the species, and for improving efficiency of selection for strains with high ethanol tolerance, a character of great economic value for the brewing and biofuel industries. To date, as many as 251 genes have been predicted to be involved in influencing this character. Candidacy of these genes was determined from a tested phenotypic effect following gene knockout, from an induced change in gene function under an ethanol stress condition, or by mutagenesis. This article represents the first genomics approach for dissecting genetic variation in ethanol tolerance between two yeast strains with a highly divergent trait phenotype. We developed a simple but reliable experimental protocol for scoring the phenotype and a set of STR/SNP markers evenly covering the whole genome. We created a mapping population comprising 319 segregants from crossing the parental strains. On the basis of the data sets, we find that the tolerance trait has a high heritability and that additive genetic variance dominates genetic variation of the trait. Segregation at five QTL detected has explained ∼50% of phenotypic variation; in particular, the major QTL mapped on yeast chromosome 9 has accounted for a quarter of the phenotypic variation. We integrated the QTL analysis with the predicted candidacy of ethanol resistance genes and found that only a few of these candidates fall in the QTL regions.
机译:揭示酿酒酵母自然种群中乙醇耐受性变异的遗传控制,对于理解发酵的进化,该物种的主要生活方式以及提高对具有较高经济价值特征的乙醇耐受性高的菌株的选择效率至关重要。用于酿造和生物燃料行业。迄今为止,已经预测多达251个基因参与影响该字符。这些基因的候选资格是根据基因敲除后测试的表型效应,乙醇胁迫条件下诱导的基因功能变化或诱变来确定的。本文代表了第一个基因组学方法,用于剖析两个具有高度差异性状表型的酵母菌株之间乙醇耐受性的遗传变异。我们开发了一种简单但可靠的实验方案来对表型进行评分,并使用一组STR / SNP标记均匀覆盖整个基因组。我们创建了一个包含319个来自亲代菌株的分离子的作图种群。根据数据集,我们发现耐性性状具有较高的遗传力,加性遗传方差主导了该性状的遗传变异。在五个QTL处的分离解释了〜50%的表型变异。尤其是,定位在酵母9号染色体上的主要QTL占表型变异的四分之一。我们将QTL分析与预测的乙醇抗性候选基因整合在一起,发现只有少数候选基因属于QTL区域。

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