Bingbing Duan, Chenxi Qiu, Steve W Lockless, Sing-Hoi Sze, Craig D Kaplan
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引用次数: 0
Abstract
RNA polymerase II (Pol II) has a highly conserved domain, the trigger loop (TL), that controls transcription fidelity and speed. We previously probed pairwise genetic interactions between residues within and surrounding the TL for the purpose of understand functional interactions between residues and to understand how individual mutants might alter TL function. We identified widespread incompatibility between TLs of different species when placed in the Saccharomyces cerevisiae Pol II context, indicating species-specific interactions between otherwise highly conserved TLs and its surroundings. These interactions represent epistasis between TL residues and the rest of Pol II. We sought to understand why certain TL sequences are incompatible with S. cerevisiae Pol II and to dissect the nature of genetic interactions within multiply substituted TLs as a window on higher order epistasis in this system. We identified both positive and negative higher-order residue interactions within example TL haplotypes. Intricate higher-order epistasis formed by TL residues was sometimes only apparent from analysis of intermediate genotypes, emphasizing complexity of epistatic interactions. Furthermore, we distinguished TL substitutions with distinct classes of epistatic patterns, suggesting specific TL residues that potentially influence TL evolution. Our examples of complex residue interactions suggest possible pathways for epistasis to facilitate Pol II evolution.
RNA 聚合酶 II(Pol II)有一个高度保守的结构域,即触发环(TL),它控制着转录的保真度和速度。我们以前曾探究过 TL 内部和周围残基之间的成对遗传相互作用,目的是了解残基之间的功能性相互作用,并了解单个突变体可能如何改变 TL 的功能。我们发现,当把不同物种的 TL 放在酿酒酵母 Pol II 上下文中时,它们之间普遍存在不相容性,这表明原本高度保守的 TL 与其周围环境之间存在物种特异性相互作用。这些相互作用代表了 TL 残基与 Pol II 其他部分之间的外显性。我们试图了解某些 TL 序列与 S. cerevisiae Pol II 不兼容的原因,并剖析多重置换 TL 内遗传相互作用的性质,以此作为了解该系统中高阶表观性的窗口。我们在示例 TL 单倍型中发现了正向和负向的高阶残基相互作用。由 TL 残基形成的错综复杂的高阶表观性有时只能从中间基因型的分析中看出,这强调了表观相互作用的复杂性。此外,我们还区分了具有不同表观模式类别的 TL 替代,这表明特定的 TL 残基可能会影响 TL 的进化。我们列举的复杂残基相互作用的例子表明了表观作用促进 Pol II 进化的可能途径。
期刊介绍:
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