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Determinants of Centromere Identity in Drosophila

Determinants of Centromere Identity in Drosophila
果蝇着丝粒身份的决定因素
批准号:
7100270
负责人:
Gary H KARPEN
金额:
$34.1万
依托单位国家:
美国
项目类别:
财政年份:
2004
资助国家:
美国
项目状态:
已结题
起止时间:
2004-08-01 至 2008-07-31

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中文摘要
翻译
描述(由申请人提供):染色体复制和传递对于遗传性状的遗传至关重要,但在多细胞真核生物中对这些过程的机制仍知之甚少。着丝粒在有丝分裂和减数分裂中与动粒相连,是连接纺锤体的关键部位。在着丝粒领域的一个紧迫的问题,今天是如何在多细胞真核生物中的着丝粒身份是从一代到下一代传播。阐明着丝粒的身份,繁殖和功能的决定因素,需要确定的基因产物,促进着丝粒的形成和反式功能,并最终确定它们如何与顺式作用元件进行交互,以执行其基本功能。从本质上讲,我们需要了解着丝粒染色质的组织,复制和修饰。 在高等真核生物中解决这些复杂问题所需的多方面遗传、分子、细胞生物学和生物化学方法很可能在果蝇中取得成功。有超过世纪的实验分析使用果蝇,这有利于复杂的体内分析。在这里,我们提出了遗传,分子,细胞生物学和生物化学实验,旨在识别和表征基因产物,促进着丝粒染色质的组装和繁殖,并确定其属性和功能。我们进入着丝粒染色质的切入点将是一个保守的组蛋白H3样蛋白(CID,为着丝粒标识符),专门定位于功能性着丝粒。我们将使用遗传筛选和生化分离来鉴定与CID相互作用的基因和蛋白质,然后使用各种方法来确定它们在着丝粒功能中的作用。这些研究将解决特定的假设,并为未来分析果蝇和其他高等真核生物(如人类)的遗传和着丝粒功能提供基础。
英文摘要
DESCRIPTION (provided by applicant): Chromosome replication and transmission are essential for the inheritance of genetic traits, but the mechanisms responsible for these processes remain poorly understood in multicellular eukaryotes. The centromere, which appears as a constriction in metaphase chromosomes, is associated with the kinetochore and serves as the key attachment site to the spindle during mitosis and meiosis. A pressing question in the centromere field today is how centromere identity is propagated from one generation to the next in multicellular eukaryotes. Elucidating the determinants of centromere identity, propagation and function requires identification of the gene products that promote centromere formation and function in trans, and ultimately determining how they interact with the cis-acting elements to perform their essential functions. In essence, we need to understand the organization, replication, and modification of centromeric chromatin. The multifaceted genetic, molecular, cell biological and biochemical approaches required to address these complex questions in higher eukaryotes are likely to succeed in Drosophila. There is over a century of experimental analyses using the fruit fly, which facilitates sophisticated in vivo analyses. Here, we propose genetic, molecular, cell biological and biochemical experiments designed to identify and characterize gene products that promote the assembly and propagation of centromeric chromatin, and to determine their properties and functions. Our entry point into centromeric chromatin will be a conserved histone H3-like protein (CID, for Centromere IDentifier) that localizes exclusively to functional centromeres. We will use genetic screens and biochemical isolations to identify genes and proteins that interact with CID, then use a variety of approaches to determine their roles in centromere function. These studies will address specific hypotheses and provide the groundwork for future analysis of inheritance and centromere function in Drosophila and other higher eukaryotes, such as humans.
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