DNA REPLICATION AND CHROMOSOME STRUCTURE IN YEAST

酵母中的 DNA 复制和染色体结构

• 批准号: 6329620
• 负责人: VIRGINIA A. ZAKIAN
• 金额: $ 45.49万
• 依托单位: PRINCETON UNIVERSITY
• 依托单位国家: 美国
• 财政年份: 1979
• 资助国家: 美国
• 起止时间: 1979-07-01 至 2004-11-30
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/6329620
• 关键词: DNA replication; Saccharomyces cerevisiae; cell cycle; chromosome aberrations; fungal genetics; gene mutation; genetic recombination; genetic transduction; helicase; microorganism culture; nucleic acid repetitive sequence; nucleic acid sequence; nucleic acid structure; plasmids; recombinant proteins; ribosomal DNA; telomerase; telomere

The long term goal of this project is to elucidate the process that ensures faithful maintenance of eukaryotic chromosomes, using the yeast Saccharomyces cerevisiae as a model system. The general goal of this funding period is to understand how telomere replication is regulated in Saccharomyces. The first and major aim focuses on two helicases, Pif1p and Rrm3p. These helicases are highly similar to each other and are members of a helicase sub-family that is conserved from yeast to humans. Pif1p and Rrm3p both influence telomeres but not in the same way. Rrm3p appears to act in a late step in telomere replication that is proposed to be important for generating a substrate for telomerase and hence promotes telomerase. Pif1p appears to act down stream of Rrm3p, and its actions inhibit telomerase. Aim 1 describes a series of genetic, biochemical, and DNA structural studies to understand how Pif1p and Rrm3p regulate telomerase. Wild type and mutant recombinant Pif1p and Rrm3p will be purified and used to determine substrate preferences. Both proteins will be tested for the effects on telomerase activity in vitro. In vivo analysis of the mutant alleles will determine if the helicase functions of Pif1p and Rrm3p are responsible for their effects on telomere replication. Chromatin immuno-precipitation (ChIP) will determine if Pif1p and/or Rrm3p are physically associated with telomeric DNA. Genetic approaches will identify genes that have overlapping functions with Rrm3p and to determine if lack of Rrm3p triggers a telomere-specific checkpoint. In vitro and in vivo approaches will determine if Pif1p inhibits telomerase by nucleolytic degradation of its substrate. The second aim is to understand how a very different type of telomerase regulator, a telomere structural protein, governs access of telomeres to telomerase. Rif1p and Rif2p are telomere binding proteins that act synergistically to limit telomere lengthening. ChIP will be used to determine if Rif proteins regulate access of telomeric DNA to telomerase by cell cycle or telomere length dependent binding. The effects of Rif proteins on replication timing of telomeres and on telomerase-independent, recombinational telomere maintenance will also be determined. The third aim is to identify additional genes whose mutation or over-expression increases telomerase mediated healing of broken chromosomes. There is increasing evidence that telomere replication has effects on both aging and cancer. As yeast telomeric DNA and the proteins that govern its properties are functionally and/or structurally conserved from yeast to humans, understanding telomere regulation in yeast is likely to be relevant to genetic instability in humans.

这个项目的长期目标是阐明这个过程