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复杂的修饰符景观基础上的遗传背景效应。

Complex modifier landscape underlying genetic background effects.

机构信息

Donnelly Centre for Cellular and Biomolecular Research, University of Toronto, Toronto, ON M5S 3E1, Canada;

Donnelly Centre for Cellular and Biomolecular Research, University of Toronto, Toronto, ON M5S 3E1, Canada.

出版信息

Proc Natl Acad Sci U S A. 2019 Mar 12;116(11):5045-5054. doi: 10.1073/pnas.1820915116. Epub 2019 Feb 25.

DOI:10.1073/pnas.1820915116
PMID:30804202
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6421401/
Abstract

The phenotypic consequence of a given mutation can be influenced by the genetic background. For example, conditional gene essentiality occurs when the loss of function of a gene causes lethality in one genetic background but not another. Between two individual strains, S288c and Σ1278b, ∼1% of yeast genes were previously identified as "conditional essential." Here, in addition to confirming that some conditional essential genes are modified by a nonchromosomal element, we show that most cases involve a complex set of genomic modifiers. From tetrad analysis of S288C/Σ1278b hybrid strains and whole-genome sequencing of viable hybrid spore progeny, we identified complex sets of multiple genomic regions underlying conditional essentiality. For a smaller subset of genes, including and , each of which encodes components of the cysteine biosynthesis pathway, we observed a segregation pattern consistent with a single modifier associated with conditional essentiality. In natural yeast isolates, we found that the / conditional essentiality can be caused by variation in two independent modifiers, and , each with roles associated with cellular cysteine physiology. Interestingly, the allelic variation appears to have arisen independently from separate lineages, with rare allele frequencies below 0.5%. Thus, while conditional gene essentiality is usually driven by genetic interactions associated with complex modifier architectures, our analysis also highlights the role of functionally related, genetically independent, and rare variants.

摘要

给定突变的表型后果可能受到遗传背景的影响。例如,当一个基因的功能丧失导致在一种遗传背景下致死,但在另一种遗传背景下不致死时,就会出现条件性基因必需性。在两个个体菌株 S288c 和 Σ1278b 之间,以前约有 1%的酵母基因被鉴定为“条件必需”。在这里,除了证实一些条件必需基因受到非染色体元件的修饰外,我们还表明,大多数情况涉及一组复杂的基因组修饰因子。通过 S288C/Σ1278b 杂种菌株的四分体分析和可育杂种孢子后代的全基因组测序,我们确定了条件必需性的多个基因组区域的复杂组合。对于一小部分基因,包括 和 ,它们分别编码半胱氨酸生物合成途径的组成部分,我们观察到与条件必需性相关的单个修饰因子的分离模式。在天然酵母分离株中,我们发现 / 条件必需性可能是由两个独立的修饰因子 和 引起的,每个修饰因子都与细胞半胱氨酸生理学有关。有趣的是, 等位基因变异似乎是由与复杂修饰因子结构相关的遗传相互作用独立产生的,其罕见等位基因频率低于 0.5%。因此,虽然条件基因必需性通常是由与复杂修饰因子结构相关的遗传相互作用驱动的,但我们的分析也突出了功能相关的、遗传独立的和罕见变异的作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f8ff/6421401/45cf1b0fed40/pnas.1820915116fig05.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f8ff/6421401/57934e53d05a/pnas.1820915116fig01.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f8ff/6421401/382c5083236e/pnas.1820915116fig02.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f8ff/6421401/16f5046f6f83/pnas.1820915116fig03.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f8ff/6421401/05d4581a0a37/pnas.1820915116fig04.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f8ff/6421401/45cf1b0fed40/pnas.1820915116fig05.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f8ff/6421401/57934e53d05a/pnas.1820915116fig01.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f8ff/6421401/382c5083236e/pnas.1820915116fig02.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f8ff/6421401/16f5046f6f83/pnas.1820915116fig03.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f8ff/6421401/05d4581a0a37/pnas.1820915116fig04.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f8ff/6421401/45cf1b0fed40/pnas.1820915116fig05.jpg

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