非翻译区外显子的非量子化最小自由能

K. Knapp, A. Rahaman, Y.-P.P. Chen
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引用次数: 1

摘要

为了提高基因非翻译区域的自动基因预测,我们完成了对8,689个亚遗传DNA序列的最小自由能的深入分析。我们扩展了Zhang的分类模型,并将每个亚基因序列分类为27个可能的基序之一。我们计算了每个基序的最小自由能,以探索与生物学相关的亚基因序列相关的统计特征。如果生物学上相关的亚基因序列落入不同的自由能量子,则有可能根据其最小自由能来表征基序。正确描述基序可以更好地理解自动基因发现、基因变异和DNA结构在基因网络调控中的作用。我们的分析确定:(1)外显子、内含子和其他与生物学相关的亚遗传序列的平均自由能值;(2)这些子序列不存在于不同的能量量子中;(3)与所有其他与生物学相关的亚遗传序列类型相比,内含子存在于紧密耦合的平均最小自由能量子中;(4)单外显子基因比跨整个编码序列作为多外显子基因的一部分的外显子表现出更高的稳定性;(5)所有基序类型在达到平台之前在大约核苷酸位置1000处包含自由能全局最小值。这些结果应该与生物化学家和生物信息学家寻求理解亚基因序列及其背后信息之间的关系有关。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Non-quantized minimum free energy in untranslated region exons
In an attempt to improve automated gene prediction in the untranslated region of a gene, we completed an in-depth analysis of the minimum free energy for 8,689 sub-genetic DNA sequences. We expanded Zhang's classification model and classified each sub-genetic sequence into one of 27 possible motifs. We calculated the minimum free energy for each motif to explore statistical features that correlate to biologically relevant sub-genetic sequences. If biologically relevant sub-genetic sequences fall into distinct free energy quanta it may be possible to characterize a motif based on its minimum free energy. Proper characterization of motifs can lead to greater understanding in automated genefinding, gene variability and the role DNA structure plays in gene network regulation. Our analysis determined: (1) the average free energy value for exons, introns and other biologically relevant sub-genetic sequences, (2) that these subsequences do not exist in distinct energy quanta, (3) that introns exist however in a tightly coupled average minimum free energy quantum compared to all other biologically relevant sub-genetic sequence types, (4) that single exon genes demonstrate a higher stability than exons which span the entire coding sequence as part of a multi-exon gene and (5) that all motif types contain a free energy global minimum at approximately nucleotide position 1,000 before reaching a plateau. These results should be relevant to the biochemist and bioinformatician seeking to understand the relationship between sub-genetic sequences and the information behind them.
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