Elise Miedlar, Grace E Hamilton, Samuel R Witus, Sara J Gonske, Michael Riffle, Alex Zelter, Rachel E Klevit, Charles L Asbury, Yoana N Dimitrova, Trisha N Davis
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引用次数: 0
摘要
在此之前,我们用重组的酿酒葡萄孢蛋白重组了一个最小功能的动转子,它能够将力从动态微管传递到含有中心粒特异性组蛋白变体 Cse4 的核小体上(Hamilton 等,2020 年)。这项工作揭示了通过内动点传递力的两条路径:通过 Mif2 和通过 Okp1/Ame1 复合物(OA)。在这里,我们利用含有芽殖酵母点中心粒的关键中心粒决定元件的嵌合 DNA 序列,证明在含有 Cse4 的核小体中存在中心粒 DNA 序列能显著加强 OA 介导的连接。我们的研究结果表明,中心粒序列对于将基于微管的力传递到染色体非常重要。
Force transmission through the inner kinetochore is enhanced by centromeric DNA sequences.
Previously, we reconstituted a minimal functional kinetochore from recombinant S. cerevisiae proteins that was capable of transmitting force from dynamic microtubules to nucleosomes containing the centromere-specific histone variant Cse4 (Hamilton et al. 2020). This work revealed two paths of force transmission through the inner kinetochore: through Mif2 and through the Okp1/Ame1 complex (OA). Here, using a chimeric DNA sequence that contains crucial centromere-determining elements of the budding yeast point centromere, we demonstrate that the presence of centromeric DNA sequences in Cse4-containing nucleosomes significantly strengthens OA-mediated linkages. Our findings indicate that centromeric sequences are important for the transmission of microtubule-based forces to the chromosome.