Logsdon Glennis A, Barrey Evelyne J, Bassett Emily A, DeNizio Jamie E, Guo Lucie Y, Panchenko Tanya, Dawicki-McKenna Jennine M, Heun Patrick, Black Ben E
Department of Biochemistry and Biophysics, Graduate Program in Biochemistry and Molecular Biophysics, and Graduate Program in Cell and Molecular Biology, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA 19104 Department of Biochemistry and Biophysics, Graduate Program in Biochemistry and Molecular Biophysics, and Graduate Program in Cell and Molecular Biology, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA 19104.
Wellcome Trust Centre for Cell Biology, Institute of Cell Biology, School of Biological Sciences, University of Edinburgh, Edinburgh EH9 3QR, UK Faculty of Biology, Albert Ludwigs Universität Freiburg, 79104 Freiburg, Germany.
J Cell Biol. 2015 Mar 2;208(5):521-31. doi: 10.1083/jcb.201412011. Epub 2015 Feb 23.
The centromere-defined by the presence of nucleosomes containing the histone H3 variant, CENP-A-is the chromosomal locus required for the accurate segregation of chromosomes during cell division. Although the sequence determinants of human CENP-A required to maintain a centromere were reported, those that are required for early steps in establishing a new centromere are unknown. In this paper, we used gain-of-function histone H3 chimeras containing various regions unique to CENP-A to investigate early events in centromere establishment. We targeted histone H3 chimeras to chromosomally integrated Lac operator sequences by fusing each of the chimeras to the Lac repressor. Using this approach, we found surprising contributions from a small portion of the N-terminal tail and the CENP-A targeting domain in the initial recruitment of two essential constitutive centromere proteins, CENP-C and CENP-T. Our results indicate that the regions of CENP-A required for early events in centromere establishment differ from those that are required for maintaining centromere identity.
着丝粒由含有组蛋白H3变体CENP - A的核小体的存在所定义,是细胞分裂期间染色体精确分离所需的染色体位点。尽管已经报道了维持着丝粒所需的人类CENP - A的序列决定因素,但建立新着丝粒早期步骤所需的那些因素尚不清楚。在本文中,我们使用了含有CENP - A特有的各种区域的功能获得型组蛋白H3嵌合体来研究着丝粒建立的早期事件。我们通过将每个嵌合体与Lac阻遏物融合,将组蛋白H3嵌合体靶向染色体整合的Lac操纵序列。使用这种方法,我们发现N端尾巴的一小部分和CENP - A靶向结构域在两种必需的组成型着丝粒蛋白CENP - C和CENP - T的初始招募中做出了惊人的贡献。我们的结果表明,着丝粒建立早期事件所需的CENP - A区域与维持着丝粒身份所需的区域不同。