DNA content of a functioning chicken kinetochore

被引:8
作者
Ribeiro, Susana Abreu [1 ,2 ]
Vagnarelli, Paola [1 ,3 ]
Earnshaw, William C. [1 ]
机构
[1] Univ Edinburgh, Wellcome Trust Ctr Cell Biol, Edinburgh EH9 3JR, Midlothian, Scotland
[2] Univ Calif San Francisco, Howard Hughes Med Inst, Dept Cellular & Mol Pharmacol, San Francisco, CA USA
[3] Brunel Univ, Div Biosci, London UB8 3PH, England
基金
英国惠康基金; 英国生物技术与生命科学研究理事会;
关键词
Kinetochores; Heterochromatin; Centromere; Condensin; Chromosome; CENP-A; HUMAN CENTROMERE; MICROTUBULE INTERFACE; NEOCENTROMERES; ORGANIZATION; CHROMOSOME; CHROMATIN; ARCHITECTURE; CONDENSIN; CELLS;
D O I
10.1007/s10577-014-9410-3
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
In order to understand the three-dimensional structure of the functional kinetochore in vertebrates, we require a complete list and stoichiometry for the protein components of the kinetochore, which can be provided by genetic and proteomic experiments. We also need to know how the chromatin-containing CENP-A, which makes up the structural foundation for the kinetochore, is folded, and how much of that DNA is involved in assembling the kinetochore. In this MS, we demonstrate that functioning metaphase kinetochores in chicken DT40 cells contain roughly 50 kb of DNA, an amount that corresponds extremely closely to the length of chromosomal DNA associated with CENP-A in ChIP-seq experiments. Thus, during kinetochore assembly, CENP-A chromatin is compacted into the inner kinetochore plate without including significant amounts of flanking pericentromeric heterochromatin.
引用
收藏
页码:7 / 13
页数:7
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