Laboratory of Biochemistry and Molecular Biology, National Cancer Institute, National Institutes of Health, Bethesda, MD, USA.
Laboratory of Membrane Proteins and Structural Biology, Biochemistry and Biophysics Center, National Heart, Lung, and Blood Institute, National Institutes of Health, Bethesda, MD, USA.
Nat Commun. 2021 Mar 19;12(1):1763. doi: 10.1038/s41467-021-21985-9.
Accurate chromosome segregation relies on the specific centromeric nucleosome-kinetochore interface. In budding yeast, the centromere CBF3 complex guides the deposition of CENP-A, an H3 variant, to form the centromeric nucleosome in a DNA sequence-dependent manner. Here, we determine the structures of the centromeric nucleosome containing the native CEN3 DNA and the CBF3core bound to the canonical nucleosome containing an engineered CEN3 DNA. The centromeric nucleosome core structure contains 115 base pair DNA including a CCG motif. The CBF3core specifically recognizes the nucleosomal CCG motif through the Gal4 domain while allosterically altering the DNA conformation. Cryo-EM, modeling, and mutational studies reveal that the CBF3core forms dynamic interactions with core histones H2B and CENP-A in the CEN3 nucleosome. Our results provide insights into the structure of the budding yeast centromeric nucleosome and the mechanism of its assembly, which have implications for analogous processes of human centromeric nucleosome formation.
准确的染色体分离依赖于特定的着丝粒核小体-动粒界面。在 budding yeast 中,着丝粒 CBF3 复合物指导 CENP-A(一种 H3 变体)的沉积,以 DNA 序列依赖性的方式形成着丝粒核小体。在这里,我们确定了含有天然 CEN3 DNA 的着丝粒核小体和与含有工程化 CEN3 DNA 的典型核小体结合的 CBF3core 的结构。着丝粒核小体核心结构包含 115 个碱基对 DNA,包括一个 CCG 基序。CBF3core 通过 Gal4 结构域特异性识别核小体 CCG 基序,同时改变 DNA 构象。冷冻电镜、建模和突变研究表明,CBF3core 在 CEN3 核小体中与核心组蛋白 H2B 和 CENP-A 形成动态相互作用。我们的结果为 budding yeast 着丝粒核小体的结构及其组装机制提供了深入了解,这对人类着丝粒核小体形成的类似过程具有重要意义。