利用基因组比对EST序列进行UTR重建和分析。

Z Kan, W Gish, E Rouchka, J Glasscock, D States
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摘要

非翻译区(UTR)在mRNA加工的转录后调控中发挥重要作用。从快速积累的EST集合中可以挖掘出大量与utr相关的信息。一种计算工具,UTR-extender,已经开发出来,从基因组比对的est推断UTR序列。使用908个功能克隆转录本,可以完整准确地重建72%的3' utr和15%的5' utr。此外,它还预测了11%的5' utr和28%的3' utr的延长。通过检查剪接频率和保护水平来验证这些扩展区域。我们还开发了一种称为聚腺苷化位点扫描(PASS)的方法来精确地绘制人类基因组序列中的聚腺苷化位点。对908个基因区进行的PASS分析估计,40-50%的人类基因经历了选择性聚腺苷化。使用EST冗余来评估表达水平,我们还发现具有短3' utr的基因倾向于高表达。
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UTR reconstruction and analysis using genomically aligned EST sequences.

Untranslated regions (UTR) play important roles in the posttranscriptional regulation of mRNA processing. There is a wealth of UTR-related information to be mined from the rapidly accumulating EST collections. A computational tool, UTR-extender, has been developed to infer UTR sequences from genomically aligned ESTs. It can completely and accurately reconstruct 72% of the 3' UTRs and 15% of the 5' UTRs when tested using 908 functionally cloned transcripts. In addition, it predicts extensions for 11% of the 5' UTRs and 28% of the 3' UTRs. These extension regions are validated by examining splicing frequencies and conservation levels. We also developed a method called polyadenylation site scan (PASS) to precisely map polyadenylation sites in human genomic sequences. A PASS analysis of 908 genic regions estimates that 40-50% of human genes undergo alternative polyadenylation. Using EST redundancy to assess expression levels, we also find that genes with short 3' UTRs tend to be highly expressed.

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