首页> 美国卫生研究院文献>BMC Molecular Biology >DNA deformability changes of single base pair mutants within CDE binding sites in S. Cerevisiae centromere DNA correlate with measured chromosomal loss rates and CDE binding site symmetries
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DNA deformability changes of single base pair mutants within CDE binding sites in S. Cerevisiae centromere DNA correlate with measured chromosomal loss rates and CDE binding site symmetries

机译:酿酒酵母着丝粒DNA CDE结合位点内单碱基对突变体的DNA变形能力变化与测得的染色体丢失率和CDE结合位点对称性相关

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摘要

BackgroundThe centromeres in yeast (S. cerevisiae) are organized by short DNA sequences (125 bp) on each chromosome consisting of 2 conserved elements: CDEI and CDEIII spaced by a CDEII region. CDEI and CDEIII are critical sequence specific protein binding sites necessary for correct centromere formation and following assembly with proteins, are positioned near each other on a specialized nucleosome. Hegemann et al. BioEssays 1993, 15: 451–460 reported single base DNA mutants within the critical CDEI and CDEIII binding sites on the centromere of chromosome 6 and quantitated centromere loss of function, which they measured as loss rates for the different chromosome 6 mutants during cell division. Olson et al. Proc Natl Acad Sci USA 1998, 95: 11163–11168 reported the use of protein-DNA crystallography data to produce a DNA dinucleotide protein deformability energetic scale (PD-scale) that describes local DNA deformability by sequence specific binding proteins. We have used the PD-scale to investigate the DNA sequence dependence of the yeast chromosome 6 mutants' loss rate data. Each single base mutant changes 2 PD-scale values at that changed base position relative to the wild type. In this study, we have utilized these mutants to demonstrate a correlation between the change in DNA deformability of the CDEI and CDEIII core sites and the overall experimentally measured chromosome loss rates of the chromosome 6 mutants.
机译:背景酵母中的着丝粒由每个染色体上的短DNA序列(125 bp)组成,由2个保守元素组成:CDEI和CDEIII,由CDEII区隔开。 CDEI和CDEIII是正确的着丝粒形成和与蛋白质组装后所必需的关键序列特异性蛋白质结合位点,它们在专门的核小体上彼此靠近放置。 Hegemann等。 BioEssays 1993,15:451-460报告了在6号染色体着丝粒上关键CDEI和CDEIII结合位点内的单碱基DNA突变体,并定量了着丝粒功能丧失,他们将其测量为细胞分裂过程中不同6号染色体突变体的丧失率。 Olson等。 Proc Natl Acad Sci USA 1998,95:11163-11168报告了使用蛋白质DNA晶体学数据来产生DNA二核苷酸蛋白质可变形性能量表(PD量表),该量表通过序列特异性结合蛋白来描述局部DNA的可变形性。我们已使用PD量表来研究酵母6号染色体突变体的DNA序列依赖性丢失率数据。每个单个碱基突变体在相对于野生型改变的碱基位置上改变2个PD值。在这项研究中,我们利用这些突变体来证明CDEI和CDEIII核心位点的DNA变形能力的变化与6号染色体突变体的总体实验测得的染色体丢失率之间存在相关性。

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