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Studies of Telomere Structure Using Yeast Model Systems

Studies of Telomere Structure Using Yeast Model Systems
使用酵母模型系统研究端粒结构
批准号:
7337130
负责人:
JACK D GRIFFITH
金额:
$3.06万
依托单位国家:
美国
项目类别:
财政年份:
2001
资助国家:
美国
项目状态:
已结题
起止时间:
2001-08-01 至 2010-12-31

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中文摘要
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英文摘要
Over the past three years work in the laboratory of Dr. Lubomir Tomaska at Comenius University in the Slovak Republic has been supported by a FIRCA award (TWO 5654) under the parent grant GM31819 to Dr. Jack Griffith at the University of North Carolina. The FIRCA support has resulted in 14 publications and 10 meeting abstracts from the Tomaska laboratory in the past 3 years with two high profile papers just published in TheJournalof Biological Chemistry. These studies have laid the foundation for investigations of telomere structure which are being seen as very significant by investigators both in the US and internationally. The work has been done primarily at Comenius University with 1to 3 month visits each year by Dr. Tomaska and his students to UNC. All funds from the award have gone to his laboratory. In Aim I, the development of the yeast S. cerevisciae minichromosome system will allow the isolation of native minichromosomes for examination by electron microscopy (EM) providing an important new tool that will directly benefit the goals of the parent grant and the objectives of the Griffith laboratory. This minichromosome system will be used by the Tomaska laboratory to continue their examination of the architecture of yeast telomeres. In Aim II, work also initiated under the FIRCA award will continue on the reconstitution of a yeast telosome in vitro using the S. pombe system. In the past funding period the telomere binding protein, Taz1 was shown to form loops at the ends of model S. pombe telomeres. This now places us in a position to understand how Taz1 protein interacts with Pot1 and other telomere binding proteins to form a native telosome. The parent NIH grant has supported the development of methods for examining DNA-protein complexes by EM, and transferring these methods to other laboratories. This technology transfer has now begun with Dr. Tomaska's students learning these EM methods. It is critical that we continue this highly productive international collaboration.
期刊论文(19)
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会议论文
Search for protein partners of mitochondrial single-stranded DNA-binding protein Rim1p using a yeast two-hybrid system.
使用酵母双杂交系统寻找线粒体单链 DNA 结合蛋白 Rim1p 的蛋白伴侣。
DOI: 10.1007/bf02930953
发表时间: 2003
期刊: Folia microbiologica
影响因子: 2.6
作者: [Kucejová,B, Foury,F]
通讯作者: Foury,F
Telomere heterogeneity: taking advantage of stochastic events.
端粒异质性:利用随机事件。
DOI: 10.1016/j.febslet.2009.02.032
发表时间: 2009
期刊: FEBS letters
影响因子: 3.5
作者: [Tomaska,Lubomir, Nosek,Jozef]
通讯作者: Nosek,Jozef
A collection of yeast mutants selectively resistant to ionophores acting on mitochondrial inner membrane.
一组选择性抵抗作用于线粒体内膜的离子载体的酵母突变体。
DOI: 10.1016/j.mito.2007.10.003
发表时间: 2008
期刊: Mitochondrion
影响因子: 4.4
作者: [Petrezselyova,Silvia, Lalakova,Jana, Abelovska,Lenka, Klobucnikova,Vlasta, Tomaska,Lubomir]
通讯作者: Tomaska,Lubomir
DOI: 10.1016/j.mito.2012.07.109
发表时间: 2012-09
期刊: Mitochondrion
影响因子: 4.4
作者: [M. Valach;Leszek P. Pryszcz;L. Tomáška;A. Gácser;T. Gabaldón;J. Nosek]
通讯作者: M. Valach;Leszek P. Pryszcz;L. Tomáška;A. Gácser;T. Gabaldón;J. Nosek
8
    R-loops at the telomere as a toxic source of genomic instability
    R-loops at the telomere as a toxic source of genomic instability
    R-loops at the telomere as a toxic source of genomic instability
    Instrumentation for upgrading cryoEM and single particle analysis capabilities
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