首页> 外文期刊>Pakistan journal of botany >EVALUATION AND SCREENING OF RESISTANCE TO REPLANT IN GERMPLASM OF GRAPE AND PHYSIOLOGICAL MECHANISMS OF ITS RESISTANCE
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EVALUATION AND SCREENING OF RESISTANCE TO REPLANT IN GERMPLASM OF GRAPE AND PHYSIOLOGICAL MECHANISMS OF ITS RESISTANCE

机译:抗葡萄种质抗性抗性的评价及筛选及其抵抗力的生理机制

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Assessment of genotoxins-induced DNA damage and mutations at molecular level is important in ecogenotoxicology.Treatment with Peganum harmala crude extract can result in cytotoxic, carcinogenic and mutagenic effects. Mutagenesis isindicative of genetic instability and can be assayed using microsatellites or simple sequence repeats (SSRs). The application ofSSR marker analysis using capillary electrophoresis (CE) apparatus showed differences in SSR profiles within the extract aswell as between the two extracts. All the 12 SSR primer pairs used produced amplification products which showed 100%polymorphism. The total number of scoreable loci obtained with the 12 used primers were 112 alleles. Of the 112 allelesdetected 12 alleles (10.7 %) were considered as zero alleles. Three alleles produced by various primers were detected at locusVfG_22 to 15 at locus VfG_693 and VfG_873, with an average of 9.3 bands/SSR. The discrimination power of each SSR locuswas estimated by the PIC, which ranged from 0.47 for locus VfG_22 to 0.88 for locus VfG_693 with a mean of 0.70. About83.3% of the 18 alleles observed in untreated samples using the 12 primers disappeared from almost all the treatments withwater and ethanol extracts. Statistical analysis of morphometric traits showed significant differences between the two extractsin all studied traits except the percentage of germination and root dry weight which were non significant. However, on the otherhand significant differences were observed between treatments and the control for all the traits studied.
机译:评估遗传毒素诱导的DNA损伤和分子水平突变在生态毒理学中是重要的。与Peganum Hymala粗提物的处理可以导致细胞毒性,致癌和致突变性的效果。诱变遗传缺陷的诱导,可以使用微卫星或简单的序列重复(SSR)测定。使用毛细管电泳(CE)装置的SSR标记分析施用在提取物之间的SSR曲线中显示出SSR曲线的差异。所有12 SSR引物对使用产生的扩增产物,该扩增产物显示为100%多态性。用12二手引物获得的可批量基因座的总数为112个等位基因。在112个等位基因中,12个等位基因(10.7%)被认为是零等位基因。在LocuSVFG_22至15处以洛卡斯VFG_693和VFG_873检测各种引物产生的三个等位基因,平均为9.3带/ SSR。由PIC估计的每个SSR基因座的判别能力为轨迹VFG_22的0.47,对于轨迹VFG_693,均值为0.70。使用12个引物在未处理样品中观察到的18个等位基因的约83.3%从含水和乙醇提取物中的几乎所有处理中消失。形态测量性状的统计分析显示出两种提取物之间的显着差异,除了非显着的萌发和根系干重的百分比之外的所有研究的特征。然而,在治疗和对所研究所有特征的治疗之间观察到的其他方面的显着差异。

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