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真核 RNA 聚合酶 α 样亚基的不同相互作用模式。

Distinct Interaction Modes for the Eukaryotic RNA Polymerase Alpha-like Subunits.

机构信息

Department of Biochemistry and Molecular Biology, SUNY Upstate Medical University, Syracuse, New York, USA.

出版信息

Mol Cell Biol. 2023;43(6):269-282. doi: 10.1080/10985549.2023.2210023. Epub 2023 May 24.

Abstract

Eukaryotic DNA-dependent RNA polymerases (Pols I-III) encode two distinct alpha-like heterodimers where one is shared between Pols I and III, and the other is unique to Pol II. Human alpha-like subunit mutations are associated with several diseases including Treacher Collins Syndrome (TCS), 4H leukodystrophy, and primary ovarian sufficiency. Yeast is commonly used to model human disease mutations, yet it remains unclear whether the alpha-like subunit interactions are functionally similar between yeast and human homologs. To examine this, we mutated several regions of the yeast and human small alpha-like subunits and used biochemical and genetic assays to establish the regions and residues required for heterodimerization with their corresponding large alpha-like subunits. Here we show that different regions of the small alpha-like subunits serve differential roles in heterodimerization, in a polymerase- and species-specific manner. We found that the small human alpha-like subunits are more sensitive to mutations, including a "humanized" yeast that we used to characterize the molecular consequence of the TCS-causingPOLR1D G52E mutation. These findings help explain why some alpha subunit associated disease mutations have little to no effect when made in their yeast orthologs and offer a better yeast model to assess the molecular basis of POLR1D associated disease mutations.

摘要

真核生物依赖 DNA 的 RNA 聚合酶(Pols I-III)编码两种不同的α样异二聚体,其中一种存在于 Pols I 和 III 之间,另一种则是 Pol II 所特有的。人类α样亚基突变与多种疾病有关,包括特雷彻·柯林斯综合征(TCS)、4H 脑白质营养不良和原发性卵巢功能不全。酵母通常被用于模拟人类疾病突变,但目前尚不清楚酵母和人类同源物之间的α样亚基相互作用在功能上是否相似。为了研究这一点,我们突变了酵母和人类小α样亚基的几个区域,并使用生化和遗传测定来确定与相应的大α样亚基形成异二聚体所需的区域和残基。在这里,我们表明小α样亚基的不同区域以聚合酶和物种特异性的方式在异二聚化中发挥不同的作用。我们发现,小的人类α样亚基对突变更敏感,包括我们用来表征引起 TCS 的 POLR1D G52E 突变的分子后果的“人源化”酵母。这些发现有助于解释为什么一些α亚基相关疾病突变在其酵母同源物中几乎没有影响,并提供了一个更好的酵母模型来评估 POLR1D 相关疾病突变的分子基础。

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