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通过计算单个 tRNA 位置的平均判别能力来映射隐藏的潜在身份元素。

Mapping hidden potential identity elements by computing the average discriminating power of individual tRNA positions.

机构信息

Department of Biochemistry, Eötvös University, Budapest, Hungary.

出版信息

DNA Res. 2012 Jun;19(3):245-58. doi: 10.1093/dnares/dss008. Epub 2012 Feb 28.

DOI:10.1093/dnares/dss008
PMID:22378766
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3372374/
Abstract

The recently published discrete mathematical method, extended consensus partition (ECP), identifies nucleotide types at each position that are strictly absent from a given sequence set, while occur in other sets. These are defined as discriminating elements (DEs). In this study using the ECP approach, we mapped potential hidden identity elements that discriminate the 20 different tRNA identities. We filtered the tDNA data set for the obligatory presence of well-established tRNA features, and then separately for each identity set, the presence of already experimentally identified strictly present identity elements. The analysis was performed on the three kingdoms of life. We determined the number of DE, e.g. the number of sets discriminated by the given position, for each tRNA position of each tRNA identity set. Then, from the positional DE numbers obtained from the 380 pairwise comparisons of the 20 identity sets, we calculated the average excluding value (AEV) for each tRNA position. The AEV provides a measure on the overall discriminating power of each position. Using a statistical analysis, we show that positional AEVs correlate with the number of already identified identity elements. Positions having high AEV but lacking published identity elements predict hitherto undiscovered tRNA identity elements.

摘要

最近发表的离散数学方法,扩展共识分区(ECP),确定了在给定序列集中严格不存在但在其他集合中出现的每个位置的核苷酸类型。这些被定义为区分元素(DE)。在本研究中,我们使用 ECP 方法来映射潜在的隐藏身份元素,以区分 20 种不同的 tRNA 身份。我们对 tDNA 数据集进行了过滤,以强制存在已建立的 tRNA 特征,然后分别针对每个身份集,检查已经实验确定的严格存在的身份元素的存在。分析在生命的三个王国中进行。我们确定了 DE 的数量,例如,给定位置区分的集合数量,对于每个 tRNA 身份集的每个 tRNA 位置。然后,从 20 个身份集的 380 对两两比较中获得的位置 DE 数量,我们计算了每个 tRNA 位置的平均排除值(AEV)。AEV 提供了每个位置总体区分能力的衡量标准。通过统计分析,我们表明位置 AEV 与已确定的身份元素数量相关。具有高 AEV 但缺乏已发布身份元素的位置预测了迄今未发现的 tRNA 身份元素。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0cbb/3372374/eed2b7b66f45/dss00804.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0cbb/3372374/33722f0ce879/dss00801.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0cbb/3372374/7c215f7d9a08/dss00802.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0cbb/3372374/fb75873c7af2/dss00803.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0cbb/3372374/eed2b7b66f45/dss00804.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0cbb/3372374/33722f0ce879/dss00801.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0cbb/3372374/7c215f7d9a08/dss00802.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0cbb/3372374/fb75873c7af2/dss00803.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0cbb/3372374/eed2b7b66f45/dss00804.jpg

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