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首页> 外文期刊>Journal of Microbiological Methods >Single-cell analysis of aneuploidy events using yeast whole chromosome painting probes (WCPPs)
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Single-cell analysis of aneuploidy events using yeast whole chromosome painting probes (WCPPs)

机译:使用酵母全染色体绘画探针(WCPP)对非整倍性事件进行单细胞分析

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Aneuploidy is considered a widespread genetic variation in such cell populations as yeast strains, cell lines and cancer cells, and spontaneous changes in the chromosomal copy number may have implications for data interpretation. Thus, aneuploidy monitoring is essential during routine laboratory practice, especially while conducting biochemical and/or gene expression analyses. In the present study, we constructed a panel of whole chromosome painting probes (WCPPs) to monitor aneuploidy in a single yeast Saccharomyces cerevisiae cell. The WCPP-based system was validated using "normal" haploid and diploid cells, as well as disomic cells both with and without cell synchronisation. FISH that utilised WCPPs was combined with DNA cell cycle analysis (imaging cytometry) to provide a detailed analysis of signal variability during the cell cycle. Chromosome painting can be utilised to detect spontaneously formed disomic chromosomes and study aneuploidy-promoting conditions. For example, the frequency of disomic chromosomes was increased in cells lacking NAD(+)-dependent histone deacetylase Sir2p compared with wild-type cells (p < 0.05). In conclusion, WCPPs may be considered to be a powerful molecular tool to identify individual genomic differences. Moreover, the WCPP-based system may be used at the single-cell level of analysis to supplement array-based techniques and high-throughput analyses at the population scale. (C) 2015 Elsevier B.V. All rights reserved.
机译:非整倍性被认为是在诸如酵母菌株,细胞系和癌细胞的细胞群体中广泛的遗传变异,并且染色体拷贝数的自发改变可能对数据解释有影响。因此,非整倍性监测在常规实验室实践中至关重要,尤其是在进行生化和/或基因表达分析时。在本研究中,我们构建了一个完整的染色体绘画探针(WCPPs)面板,以监控单个酵母酿酒酵母细胞中的非整倍性。基于WCPP的系统已使用“正常”的单倍体和二倍体细胞以及带有和不带有细胞同步功能的二体细胞进行了验证。利用WCPPs的FISH与DNA细胞周期分析(成像细胞计数)相结合,以提供细胞周期期间信号变异性的详细分析。染色体绘画可用于检测自发形成的二体染色体并研究非整倍性促进条件。例如,与野生型细胞相比,缺乏NAD(+)依赖的组蛋白脱乙酰基酶Sir2p的细胞的染色体组染色体频率增加(p <0.05)。总之,WCPPs可以被认为是鉴定个体基因组差异的强大分子工具。此外,基于WCPP的系统可用于单细胞分析,以补充人口规模的基于阵列的技术和高通量分析。 (C)2015 Elsevier B.V.保留所有权利。

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