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Investigation on the Causes of Stoichiometric Error in Genome Size Estimation Using Heat Experiments: Consequences on Data Interpretation

机译:热实验估算基因组大小时化学计量误差的原因:数据解释的后果

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摘要

• Background and Aims In microdensitometry and flow cytometry, estimation of nuclear DNA content in a sample requires a standard with a known nuclear DNA content. It is assumed that dye accessibility to DNA is the same in the sample and standard nuclei. Stoichiometric error arises when dye accessibility is not proportional between the sample and standard. The aim of the present study was to compare the effects of standardization (external–internal) on nuclear fluorescence of two Coffea species and petunia when temperature increases, and the consequences on genome size estimation.• Methods Two coffee tree taxa, C. liberica subsp dewevrei (DEW) and C. pseudozanguebarieae (PSE), and Petunia hybrida were grown in a glasshouse in Montpellier, France. Nuclei were extracted by leaf chopping and at least 2 h after nuclei extraction they were stained with propidium iodide for approx. 3 min just before cytometer processing. In the first experiment, effects of heat treatment were observed in mixed (DEW + petunia) and unmixed extracts (petunia and DEW in separate extracts). Nine temperature treatments were carried out (21, 45, 55, 60, 65, 70, 75, 80 and 85 °C). In a second experiment, effects of heating on within-species genome size variations were investigated in DEW and PSE. Two temperatures (21 and 70 °C) were selected as representative of the maximal range of chromatin decondensation.• Key Results and Conclusions In coffee trees, sample and standard nuclei reacted differently to temperature according to the type of standardization (pseudo-internal vs. external). Cytosolic compounds released in the filtrate would modify chromatin sensitivity to decondensation. Consequently, the ‘genome size’ estimate depended on the temperature. Similarly, intraspecific variations in genome size changed between estimations at 21 °C and 70 °C. Consequences are discussed and stoichiometric error detection methods are proposed, along with proposals for minimizing them.
机译:•背景和目的在微光密度法和流式细胞仪中,估计样品中核DNA的含量需要具有已知核DNA含量的标准品。假定样品和标准核中染料对DNA的可及性相同。当样品和标准品之间的染料可及性不成比例时,就会出现化学计量误差。本研究的目的是比较标准化(外部-内部)对温度升高时两种咖啡和矮牵牛的核荧光的影响以及对基因组大小估计的影响。•方法两种咖啡树类群,C。liberica亚种dewevrei(DEW)和C. pseudozanguebarieae(PSE)和Petunia hybrida在法国蒙彼利埃的温室中生长。通过切叶来提取核,并且在核提取后至少2小时,将它们用碘化丙啶染色约2小时。在流式细胞仪处理前3分钟。在第一个实验中,混合(DEW +矮牵牛)和未混合提取物(矮牵牛和DEW在单独提取物中)均观察到热处理效果。进行了九种温度处理(21、45、55、60、65、70、75、80和85℃)。在第二个实验中,在DEW和PSE中研究了加热对物种内基因组大小变化的影响。选择了两个温度(21和70°C)作为染色质最大缩合范围的代表。•主要结果和结论在咖啡树中,样品和标准核根据标准品的类型对温度的反应不同(伪内部与外部)。外部)。滤液中释放的胞质化合物会改变染色质对缩合的敏感性。因此,“基因组大小”估计值取决于温度。同样,基因组大小的种内变异在21°C和70°C的估计之间变化。讨论了后果,并提出了化学计量误差检测方法,以及将其最小化的建议。

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