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Impact of genetic structures on haploid genome-based quantification of genetically modified DNA: theoretical considerations, experimental data in MON 810 maize kernels (Zea mays L.) and some practical applications

机译:遗传结构对基于单倍体基因组的转基因DNA定量的影响:理论考虑,MON 810玉米粒(Zea mays L.)中的实验数据和一些实际应用

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Real-time Polymerase Chain Reaction (PCR) based assays are widely used to estimate the content of genetically modified (GM) materials in food, feed and seed. It has been known that the genetic structures of the analyte can significantly influence the GM content expressed by the haploid genome (HG) % estimated using real-time PCR assays; this kind of influence is also understood as the impact of biological factors. The influence was first simulated at theoretical level using maize as a model. We then experimentally assessed the impact of biological factors on quantitative results, analysing by quantitative real-time PCR six maize MON 810 hybrid kernels with different genetic structures: (1) hemizygous from transgenic male parent, (2) hemizygous from transgenic female parent and (3) homozygous at the transgenic locus. The results obtained in the present study showed clear influences of biological factors on GM DNA quantification: 1% of GM materials by weight (wt) for the three genetic structures contained 0.39, 0.55 and 1.0% of GM DNA by HG respectively, from quantitative real-time PCR analyses. The relationships between GM wt% and GM HG% can be empirically established as: (1) in the case of the presence of a single GM trait: GM HG% = GM wt% × (0.5 ± 0.167Y), where Y is the endosperm DNA content (%) in the total DNA of a maize kernel, (2) in the case of the presence of multiple GM traits: GM HG% = N × GM wt% × (0.5 ± 0.167Y), where N is the number of GM traits (stacked or not) present in an unknown sample. This finding can be used by stakeholders related to GMO for empirical prediction from one unit of expression to another in the monitoring of seed and grain production chains. Practical equations have also been suggested for haploid copy number calculations, using hemizygous GM materials for calibration curves.
机译:基于实时聚合酶链反应(PCR)的测定法被广泛用于估算食品,饲料和种子中转基因(GM)材料的含量。众所周知,分析物的遗传结构会显着影响由单倍体基因组(HG)%表示的GM含量,这些单倍体基因组是使用实时PCR测定法估算的;这种影响也可以理解为生物因素的影响。首先以玉米为模型在理论水平上模拟了这种影响。然后,我们通过实验方法评估了生物学因素对定量结果的影响,通过实时定量PCR分析了六种具有不同遗传结构的玉米MON 810杂种仁:(1)来自转基因雄性亲本的半合子,(2)来自转基因雌性亲本的半合子和( 3)在转基因位点纯合的。在本研究中获得的结果表明,生物学因素对GM DNA定量有明显影响:按重量比,三个基因结构的GM物质按重量(wt)计分别占三个基因结构的HG DNA的0.39%,0.55%和1.0%。时PCR分析。 GM wt%和GM HG%之间的关系可以凭经验建立:(1)在存在单个GM性状的情况下:GM HG%= GM wt%×(0.5±0.167Y),其中Y为玉米籽粒总DNA中的胚乳DNA含量(%),(2)在存在多个GM特性的情况下:GM HG%= N×GM wt%×(0.5±0.167Y),其中N为未知样品中存在的GM性状数量(是否堆叠)。与转基因生物有关的利益相关者可以利用这一发现进行实证预测,从一个表达单位到另一个表达单位,以监测种子和谷物生产链。对于半单倍体GM量的校正曲线,还提出了用于单倍体拷贝数计算的实用方程式。

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