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酵母 DNA 解旋酶的遗传和生化相互作用。

Genetic and biochemical interactions of yeast DNA helicases.

机构信息

Molecular & Cellular Biochemistry Department, Indiana University, Bloomington, IN 47405 USA.

Molecular & Cellular Biochemistry Department, Indiana University, Bloomington, IN 47405 USA.

出版信息

Methods. 2022 Aug;204:234-240. doi: 10.1016/j.ymeth.2022.04.014. Epub 2022 Apr 26.

Abstract

DNA helicases function in many types of nucleic acid transactions, and as such, they are vital for genome integrity. Although they are often considered individually, work from many groups demonstrates that these enzymes often genetically and biochemically interact in vivo. Here, we highlight methods to interrogate such interactions among the PIF1 (Pif1 and Rrm3) and RecQ (Hrq1 and Sgs1) family helicases in Saccharomyces cerevisiae. The interactions among these enzymes were investigated in vivo using deletion and inactivation alleles with a gross-chromosomal rearrangement (GCR) assay. Further, wild-type and inactive recombinant proteins were used to determine the effects of the helicases on telomerase activity in vitro. We found that synergistic increases in GCR rates often occur in double vs. single mutants, suggesting that the helicases function in distinct genome integrity pathways. Further, the recombinant helicases can function together in vitro to modulate telomerase activity. Overall, the data suggest that the interactions among the members of these DNA helicase families are multipartite and argue for a comprehensive systems biology approach to fully elucidate the physiological interplay between these enzymes.

摘要

DNA 解旋酶在多种类型的核酸代谢中发挥作用,因此对基因组完整性至关重要。尽管它们通常被单独考虑,但许多研究小组的工作表明,这些酶在体内通常具有遗传和生化相互作用。在这里,我们重点介绍了在酿酒酵母中研究 PIF1(Pif1 和 Rrm3)和 RecQ(Hrq1 和 Sgs1)家族解旋酶之间相互作用的方法。使用带有大片段染色体重排(GCR)测定的缺失和失活等位基因在体内研究了这些酶之间的相互作用。此外,还使用野生型和无活性的重组蛋白来确定解旋酶对体外端粒酶活性的影响。我们发现,与单突变体相比,双突变体中的 GCR 率通常协同增加,这表明这些解旋酶在不同的基因组完整性途径中发挥作用。此外,重组解旋酶可以在体外协同作用以调节端粒酶活性。总的来说,这些数据表明这些 DNA 解旋酶家族成员之间的相互作用是多方面的,并支持采用全面的系统生物学方法来充分阐明这些酶之间的生理相互作用。

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