An exact method for finding short motifs in sequences, with application to the ribosome binding site problem.

M Tompa
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Abstract

This is an investigation of methods for finding short motifs that only occur in a fraction of the input sequences. Unlike local search techniques that may not reach a global optimum, the method proposed here is guaranteed to produce the motifs with greatest z-scores. This method is illustrated for the Ribosome Binding Site Problem, which is to identify the short mRNA 5' untranslated sequence that is recognized by the ribosome during initiation of protein synthesis. Experiments were performed to solve this problem for each of fourteen sequenced prokaryotes, by applying the method to the full complement of genes from each. One of the interesting results of this experimentation is evidence that the recognized sequence of the thermophilic archaea A. fulgidus, M. jannaschii, M. thermoautotrophicum, and P. horikoshii may be somewhat different than the well known Shine-Dalgarno sequence.

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寻找序列中短基序的精确方法,并应用于核糖体结合位点问题。
这是一项调查的方法,以寻找短基序,只出现在一小部分的输入序列。与局部搜索技术可能无法达到全局最优不同,本文提出的方法保证产生具有最大z分数的图案。该方法用于解决核糖体结合位点问题,即识别在蛋白质合成起始阶段被核糖体识别的短mRNA 5'未翻译序列。通过将该方法应用于每个原核生物的完整基因补体,对14个测序的原核生物中的每一个进行了实验,以解决这个问题。该实验的一个有趣结果是,已知的嗜热古细菌A. fulgidus、M. jannaschii、M. thermoautotrophicum和P. horikoshii的序列可能与众所周知的Shine-Dalgarno序列有所不同。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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