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酿酒酵母复制起点的预测

Prediction of Saccharomyces cerevisiae replication origins.

作者信息

Breier Adam M, Chatterji Sourav, Cozzarelli Nicholas R

机构信息

Graduate Group in Biophysics, University of California-Berkeley, Berkeley, CA 94720-3204, USA.

出版信息

Genome Biol. 2004;5(4):R22. doi: 10.1186/gb-2004-5-4-r22. Epub 2004 Mar 4.

DOI:10.1186/gb-2004-5-4-r22
PMID:15059255
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC395781/
Abstract

BACKGROUND

Autonomously replicating sequences (ARSs) function as replication origins in Saccharomyces cerevisiae. ARSs contain the 17 bp ARS consensus sequence (ACS), which binds the origin recognition complex. The yeast genome contains more than 10,000 ACS matches, but there are only a few hundred origins, and little flanking sequence similarity has been found. Thus, identification of origins by sequence alone has not been possible.

RESULTS

We developed an algorithm, Oriscan, to predict yeast origins using similarity to 26 characterized origins. Oriscan used 268 bp of sequence, including the T-rich ACS and a 3' A-rich region. The predictions identified the exact location of the ACS. A total of 84 of the top 100 Oriscan predictions, and 56% of the top 350, matched known ARSs or replication protein binding sites. The true accuracy was even higher because we tested 25 discrepancies, and 15 were in fact ARSs. Thus, 94% of the top 100 predictions and an estimated 70% of the top 350 were correct. We compared the predictions to corresponding sequences in related Saccharomyces species and found that the ACSs of experimentally supported predictions show significant conservation.

CONCLUSIONS

The high accuracy of the predictions indicates that we have defined near-sufficient conditions for ARS activity, the A-rich region is a recognizable feature of ARS elements with a probable role in replication initiation, and nucleotide sequence is a reliable predictor of yeast origins. Oriscan detected most origins in the genome, demonstrating previously unrecognized generality in yeast replication origins and significant discriminatory power in the algorithm.

摘要

背景

自主复制序列(ARSs)在酿酒酵母中作为复制起点发挥作用。ARSs包含17bp的ARS共有序列(ACS),其与起点识别复合体结合。酵母基因组包含超过10000个ACS匹配序列,但只有几百个复制起点,并且几乎没有发现侧翼序列相似性。因此,仅通过序列来识别复制起点是不可能的。

结果

我们开发了一种算法Oriscan,利用与26个已表征的复制起点的相似性来预测酵母复制起点。Oriscan使用268bp的序列,包括富含T的ACS和一个3'富含A的区域。这些预测确定了ACS的确切位置。前100个Oriscan预测中有84个,前350个中有56%与已知的ARSs或复制蛋白结合位点匹配。实际准确率甚至更高,因为我们测试了25个差异,其中15个实际上是ARSs。因此,前100个预测中有94%,估计前350个中有70%是正确的。我们将这些预测与相关酿酒酵母物种中的相应序列进行比较,发现实验支持的预测中的ACSs显示出显著的保守性。

结论

预测的高精度表明我们已经定义了ARS活性的近乎充分条件,富含A的区域是ARS元件的一个可识别特征,可能在复制起始中起作用,并且核苷酸序列是酵母复制起点的可靠预测指标。Oriscan检测到了基因组中的大多数复制起点,证明了酵母复制起点中以前未被认识到的普遍性以及该算法具有显著的鉴别能力。

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