Organization and Regulation of Eukaryotic Centromeres

真核着丝粒的组织和调控

• 批准号: 7919764
• 负责人: BETH A SULLIVAN
• 金额: $ 4.68万
• 依托单位: DUKE UNIVERSITY
• 依托单位国家: 美国
• 财政年份: 2009
• 资助国家: 美国
• 起止时间: 2009-09-29 至 2010-01-31
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/7919764
• 关键词: Address; Affect; Aneuploidy; Biological Assay; Cells; Centromere; Chromatin; Chromatin Modeling; Chromatin Structure; Chromosomal Stability; Chromosome Segregation; Chromosome abnormality; Chromosomes; Complex; Congenital Abnormality; DNA; DNA Sequence; Defect; Down Syndrome; Drosophila genus; Ensure; Epigenetic Process; Fission Yeast; Foundations; Genetic; Genome Stability; Genomics; Goals; Health; Heterochromatin; Histone Code; Histones; Human; Human Chromosomes; Kinetochores; Lead; Maps; Metaphase; Modification; Mus; Nucleosomes; Organism; Post-Translational Protein Processing; Process; Property; Proteins; RNA Interference; Reagent; Regulation; Research Personnel; Role; Saccharomycetales; Sister Chromatid; Spontaneous abortion; Structure; System; Tail; Techniques; Testing; Yeasts; cancer type; centromere protein A; cohesion; comparative; design; fly; functional genomics; histone modification; knock-down; novel; programs; research study; transmission process; tumor

DESCRIPTION (provided by applicant): Chromosome inheritance ensures transmission of genetic information. Abnormal chromosome segregation severely affects the health and viability of all cells and organisms. Errors in chromosome inheritance lead to chromosome abnormalities (aneuploidy) that cause many birth defects, such as Down Syndrome and miscarriages, and are the hallmarks of almost all types of cancers. The centromere, a complex of DNA and proteins, is central to the chromosome inheritance process and contributes to formation of the kinetochore, heterochromatin and sister chromatid cohesion. Defects in centromere functions lead to aneuploidy or tumor formation in yeast, flies and mice. CENP-A, a conserved H3-1ike histone that replaces H3 in centromeric nucleosomes, is the structural and functional foundation of the kinetochore and adjacent centromeric region. We have shown that kinetochore chromatin is uniquely arranged as interspersed domains of CENP-A and H3 nucleosomes that promote a specialized cylindrical structure on metaphase chromosomes. This special structure is formed on divergent DNA sequences, and it is not known how centromeric chromatin is established and maintained, nor the structural and functional aspects if it is altered. The goal of this proposal is to apply an integrative, dual-system approach, using novel reagents and techniques that I have developed in my former lab, to test key organizational and functional aspects of centromeric chromatin in Drosophila and humans. We propose to investigate the roles of genomic structure and chromatin organization and dynamics in assembly and regulation of CENP-A chromatin, centromeric domains, and metaphase kinetochore structure.

描述（申请人提供）：染色体遗传保证了遗传信息的传递。异常的染色体分离严重影响所有细胞和生物体的健康和生存能力。染色体遗传错误导致染色体异常（非整倍体），导致许多出生缺陷，如唐氏综合症和流产，并且是几乎所有类型癌症的标志。着丝粒是DNA和蛋白质的复合体，是染色体遗传过程的核心，并有助于着丝点、异染色质和姐妹染色单体内聚的形成。在酵母、果蝇和小鼠中，着丝粒功能缺陷导致非整倍体或肿瘤形成。CENP-A是一种保守的H3-1样组蛋白，取代着丝粒核小体中的H3，是着丝粒和相邻着丝粒区域的结构和功能基础。我们已经证明，着丝粒染色质以独特的方式排列为CENP-A和H3核小体的穿插结构域，促进中期染色体上的特化圆柱形结构。这种特殊的结构是在不同的DNA序列上形成的，我们不知道着丝粒染色质是如何建立和维持的，也不知道如果它被改变了，它的结构和功能方面。本提案的目标是应用一种综合的双系统方法，使用我在以前的实验室开发的新试剂和技术，来测试果蝇和人类着丝粒染色质的关键组织和功能方面。我们建议研究基因组结构、染色质组织和动力学在CENP-A染色质、着丝粒结构域和中期着丝粒结构的组装和调控中的作用。

项目成果

Human gamma-satellite DNA maintains open chromatin structure and protects a transgene from epigenetic silencing

• DOI: 10.1101/gr.086496.108
• 发表时间: 2009-04-01
• 期刊: GENOME RESEARCH
• 影响因子: 7
• 作者: Kim, Jung-Hyun;Ebersole, Thomas;Larionov, Vladimir
• 通讯作者: Larionov, Vladimir

Genomic size of CENP-A domain is proportional to total alpha satellite array size at human centromeres and expands in cancer cells.

CENP-A结构域的基因组大小与人centromeres的总α卫星阵列大小成正比，并在癌细胞中扩展。

• DOI: 10.1007/s10577-011-9208-5
• 发表时间: 2011-05
• 期刊: CHROMOSOME RESEARCH
• 影响因子: 2.6
• 作者: Sullivan, Lori L.;Boivin, Christopher D.;Mravinac, Brankica;Song, Ihn Young;Sullivan, Beth A.
• 通讯作者: Sullivan, Beth A.

Human centromere repositioning within euchromatin after partial chromosome deletion.

• DOI: 10.1007/s10577-016-9536-6
• 发表时间: 2016-12
• 期刊: Chromosome research : an international journal on the molecular, supramolecular and evolutionary aspects of chromosome biology
• 作者: Sullivan LL;Maloney KA;Towers AJ;Gregory SG;Sullivan BA
• 通讯作者: Sullivan BA