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首页> 外文期刊>Electrophoresis: The Official Journal of the International Electrophoresis Society >Evaluation of DNA bending models in their capacity to predict electrophoretic migration anomalies of satellite DNA sequences
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Evaluation of DNA bending models in their capacity to predict electrophoretic migration anomalies of satellite DNA sequences

机译:评估DNA弯曲模型预测卫星DNA序列电泳迁移异常的能力

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摘要

DNA containing a sequence that generates a local curvature exhibits a pronounced retardation in electrophoretic mobility. Various theoretical models have been proposed to explain relationship between DNA structural features and migration anomaly. Here, we studied the capacity of 15 static wedge-bending models to predict electrophoretic behavior of 69 satellite monomers derived from four divergent families. All monomers exhibited retarded mobility in PAGE corresponding to retardation factors ranging 1.02-1.54. The curvature varied both within and across the groups and correlated with the number, position, and lengths of A-tracts. Two dinucleotide models provided strong correlation between gel mobility and curvature prediction; two trinucleotide models were satisfactory while remaining dinucleotide models provided intermediate results with reliable prediction for subsets of sequences only. In some cases, similarly shaped molecules exhibited relatively large differences in mobility and vice versa. Generally less accurate predictions were obtained in groups containing less homogeneous sequences possessing distinct structural features. In conclusion, relatively universal theoretical models were identified suitable for the analysis of natural sequences known to harbor relatively moderate curvature. These models could be potentially applied to genome wide studies. However, in silico predictions should be viewed in context of experimental measurement of intrinsic DNA curvature.
机译:含有产生局部曲率的序列的DNA在电泳迁移率方面表现出明显的延迟。已经提出了各种理论模型来解释DNA结构特征和迁移异常之间的关系。在这里,我们研究了15种静态楔形弯曲模型预测来自四个不同家族的69个卫星单体的电泳行为的能力。所有单体均在PAGE中显示出延迟的迁移率,对应于1.02-1.54的延迟因子。曲率在组内和组之间均变化,并且与A形的数量,位置和长度相关。两种二核苷酸模型提供了凝胶迁移率和曲率预测之间的强相关性。两个三核苷酸模型令人满意,而其余的二核苷酸模型仅提供可靠的序列子集预测结果而提供了中间结果。在某些情况下,形状相似的分子在迁移率上表现出较大差异,反之亦然。通常,在包含具有不同结构特征的较少同源序列的组中获得的预测较不准确。总之,确定了相对通用的理论模型,适合于分析已知具有相对中等曲率的自然序列。这些模型可以潜在地应用于全基因组研究。但是,计算机模拟的预测应在对内在DNA曲率进行实验测量的背景下进行。

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