首页> 美国卫生研究院文献>G3: GenesGenomesGenetics >Whole-Genome Sequencing of Suppressor DNA Mixtures Identifies Pathways That Compensate for Chromosome Segregation Defects in Schizosaccharomyces pombe
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Whole-Genome Sequencing of Suppressor DNA Mixtures Identifies Pathways That Compensate for Chromosome Segregation Defects in Schizosaccharomyces pombe

机译:抑制基因DNA混合物的全基因组测序确定补偿粟酒裂殖酵母染色体分离缺陷的途径。

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摘要

Suppressor screening is a powerful method to identify genes that, when mutated, rescue the temperature sensitivity of the original mutation. Previously, however, identification of suppressor mutations has been technically difficult. Due to the small genome size of Schizosaccharomyces pombe, we developed a spontaneous suppressor screening technique, followed by a cost-effective sequencing method. Genomic DNAs of 10 revertants that survived at the restrictive temperature of the original temperature sensitive (ts) mutant were mixed together as one sample before constructing a library for sequencing. Responsible suppressor mutations were identified bioinformatically based on allele frequency. Then, we isolated a large number of spontaneous extragenic suppressors for three ts mutants that exhibited defects in chromosome segregation at their restrictive temperature. Screening provided new insight into mechanisms of chromosome segregation: loss of Ufd2 E4 multi-ubiquitination activity suppresses defects of an AAA ATPase, Cdc48. Loss of Wpl1, a releaser of cohesin, compensates for the Eso1 mutation, which may destabilize sister chromatid cohesion. The segregation defect of a ts histone H2B mutant is rescued if it fails to be deubiquitinated by the SAGA complex, because H2B is stabilized by monoubiquitination.
机译:抑制子筛选是一种强大的方法,可识别突变后可挽救原始突变的温度敏感性的基因。然而,以前,鉴定抑制子突变在技术上是困难的。由于粟酒裂殖酵母的基因组较小,我们开发了自发性抑制子筛选技术,然后开发了一种经济高效的测序方法。在构建用于测序的文库之前,将在原始温度敏感(ts)突变体的限制性温度下存活的10个回复子的基因组DNA作为一个样品混合在一起。根据等位基因频率通过生物信息学鉴定负责任的抑制基因突变。然后,我们分离出了三个ts突变体的大量自发外源抑制子,这些ts突变体在其限制性温度下表现出染色体分离缺陷。筛选为染色体分离的机制提供了新的见识:Ufd2 E4多泛素化活性的丧失抑制了AAA ATPase Cdc48的缺陷。 Wpl1(黏附素的释放剂)的丢失补偿了Eso1突变,这可能会使姐妹染色单体的黏附作用不稳定。如果ts组蛋白H2B突变体未能被SAGA复合物去泛素化,则可以挽救其分离缺陷,因为H2B通过单泛素化作用得以稳定。

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