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A34.5 a nonessential component of yeast RNA polymerase I cooperates with subunit A14 and DNA topoisomerase I to produce a functional rRNA synthesis machine.

机译:酵母RNA聚合酶I的非必需成分A34.5与亚基A14和DNA拓扑异构酶I共同产生功能性rRNA合成机。

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摘要

A34.5, a phosphoprotein copurifying with RNA polymerase I (Pol I), lacks homology to any component of the Pol II or Pol III transcription complexes. Cells devoid of A34.5 hardly affect growth and rRNA synthesis and generate a catalytically active but structurally modified enzyme also lacking subunit A49 upon in vitro purification. Other Pol I-specific subunits (A49, A14, and A12.2) are nonessential for growth at 30 degrees C but are essential (A49 and A12.2) or helpful (A14) at 25 or 37 degrees C. Triple mutants without A34.5, A49, and A12.2 are viable, but inactivating any of these subunits together with A14 is lethal. Lethality is rescued by expressing pre-rRNA from a Pol II-specific promoter, demonstrating that these subunits are collectively essential but individually dispensable for rRNA synthesis. A14 and A34.5 single deletions affect the subunit composition of the purified enzyme in pleiotropic but nonoverlapping ways which, if accumulated in the double mutants, provide a structural explanation for their strict synthetic lethality. A34.5 (but not A14) becomes quasi-essential in strains lacking DNA topoisomerase I, suggesting a specific role of this subunit in helping Pol I to overcome the topological constraints imposed on ribosomal DNA by transcription.
机译:与RNA聚合酶I(Pol I)共纯化的磷蛋白A34.5与Pol II或Pol III转录复合物的任何成分均缺乏同源性。不含A34.5的细胞几乎不影响生长和rRNA合成,并且在体外纯化后几乎不具有A49亚基的催化活性但结构修饰的酶。其他Pol I特异的亚基(A49,A14和A12.2)对于在30摄氏度下的生长是不必要的,但在25摄氏度或37摄氏度下是必需的(A49和A12.2)或有用的(A14)。没有A34的三重突变体.5,A49和A12.2是可行的,但是与A14一起使这些亚基失活是致命的。通过从Pol II特异性启动子表达pre-rRNA可以挽救致命性,这表明这些亚基是集体必需的,但对于rRNA合成而言可单独分配。 A14和A34.5单一缺失以多效性但非重叠的方式影响纯化酶的亚基组成,如果这些积累在双突变体中,则为其严格的合成杀伤力提供了结构性解释。在缺乏DNA拓扑异构酶I的菌株中,A34.5(而不是A14)成为准必需蛋白,这表明该亚基在帮助Pol I克服转录对核糖体DNA施加的拓扑约束方面具有特殊作用。

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