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Bulk Segregant Analysis Reveals the Genetic Basis of a Natural Trait Variation in Fission Yeast

机译:大量分离分析揭示了裂殖酵母自然性状变异的遗传基础

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Although the fission yeast Schizosaccharomyces pombe is a well-established model organism, studies of natural trait variations in this species remain limited. To assess the feasibility of segregant-pool-based mapping of phenotype-causing genes in natural strains of fission yeast, we investigated the cause of a maltose utilization defect (Mal-) of the S. pombe strain CBS5557 (originally known as Schizosaccharomyces malidevorans). Analyzing the genome sequence of CBS5557 revealed 955 nonconservative missense substitutions, and 61 potential loss-of-function variants including 47 frameshift indels, 13 early stop codons, and 1 splice site mutation. As a side benefit, our analysis confirmed 146 sequence errors in the reference genome and improved annotations of 27 genes. We applied bulk segregant analysis to map the causal locus of the Mal- phenotype. Through sequencing the segregant pools derived from a cross between CBS5557 and the laboratory strain, we located the locus to within a 2.23-Mb chromosome I inversion found in most S. pombe isolates including CBS5557. To map genes within the inversion region that occupies 18% of the genome, we created a laboratory strain containing the same inversion. Analyzing segregants from a cross between CBS5557 and the inversion-containing laboratory strain narrowed down the locus to a 200-kb interval and led us to identify agl1, which suffers a 5-bp deletion in CBS5557, as the causal gene. Interestingly, loss of agl1 through a 34-kb deletion underlies the Mal- phenotype of another S. pombe strain CGMCC2.1628. This work adapts and validates the bulk segregant analysis method for uncovering trait-gene relationship in natural fission yeast strains.
机译:尽管裂变酵母粟酒裂殖酵母是一种成熟的模式生物,但对该物种自然性状变异的研究仍然有限。为了评估裂殖酵母天然菌株中基于分离子池的表型致病基因作图的可行性,我们调查了粟酒裂殖酵母菌株CBS5557的麦芽糖利用缺陷(Mal -)的原因。 (最初称为Schizosaccharomyces malidevorans)。分析CBS5557的基因组序列显示955个非保守错义取代和61个潜在的功能丧失变异体,包括47个移码插入缺失,13个早期终止密码子和1个剪接位点突变。作为附带好处,我们的分析确认了参考基因组中的146个序列错误,并改进了27个基因的注释。我们应用大量分离子分析来绘制Mal -表型的因果基因座。通过对源自CBS5557与实验室菌株之间杂交的分离子库进行测序,我们将基因座定位于在大多数包括CBS5557的粟酒裂殖酵母分离物中发现的2.23-Mb染色体I倒位内。为了在占基因组18%的反向区域内绘制基因图,我们创建了一个包含相同反向的实验室菌株。分析来自CBS5557和含倒置的实验室菌株之间杂交的分离物,将基因座范围缩小到200kb,并导致我们鉴定agl1,它是CBS5557中缺失5bp的原因基因。有趣的是,通过缺失34kb缺失agl1是另一株粟酒裂殖酵母CGMCC2.1628的Mal -表型的基础。这项工作适应并验证了用于在自然裂变酵母菌株中发现性状-基因关系的本体分离分析方法。

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