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Probing nucleosome function: A highly versatile library of synthetic histone H3 and H4 mutants

机译:探测核小体功能:合成组蛋白H3和H4突变体的多功能库

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摘要

Nucleosome structural integrity underlies the regulation of DNA metabolism and transcription. Using a synthetic approach, a versatile library of 486 systematic histone H3 and H4 substitution and deletion mutants that probes the contribution of each residue to nucleosome function was generated in Saccharomyces cerevisiae. We probed fitness contributions of each residue to perturbations of chromosome integrity and transcription, mapping global patterns of chemical sensitivities and requirements for transcriptional silencing onto the nucleosome surface. Each histone mutant was tagged with unique molecular barcodes, facilitating identification of histone mutant pools through barcode amplification, labeling, and TAG microarray hybridization. Barcodes were used to score complex phenotypes such as competitive fitness in a chemostat, DNA repair proficiency, and synthetic genetic interactions, revealing new functions for distinct histone residues and new interdependencies among nucleosome components and their modifiers.
机译:核小体的结构完整性是DNA代谢和转录调控的基础。使用一种合成方法,在酿酒酵母中生成了一个由486个系统化组蛋白H3和H4取代和缺失突变体组成的通用库,该库可探测每个残基对核小体功能的贡献。我们探究了每个残基对染色体完整性和转录扰动的适应性贡献,绘制了化学敏感性的整体模式以及对核小体表面转录沉默的要求。每个组蛋白突变体都标记有独特的分子条形码,从而通过条形码扩增,标记和TAG微阵列杂交促进组蛋白突变体库的鉴定。条形码用于对复杂的表型进行评分,例如在恒化器中的竞争适应性,DNA修复能力和合成遗传相互作用,从而揭示了不同组蛋白残基的新功能以及核小体成分及其修饰物之间的新相互依赖性。

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