ARED: human AU-rich element-containing mRNA database reveals an unexpectedly diverse functional repertoire of encoded proteins

被引:338
作者
Bakheet, T
Frevel, M
Williams, BRG
Greer, W
Khabar, KSA
机构
[1] King Faisal Specialist Hosp & Res Ctr, Dept Biol & Med Res, Interferon & Cytokine Res Unit, Riyadh 11211, Saudi Arabia
[2] King Faisal Specialist Hosp & Res Ctr, Dept Biostat Epidemiol & Sci Comp, Bioinformat Sect, Riyadh 11211, Saudi Arabia
[3] Cleveland Clin Fdn, Lemer Res Inst, Dept Canc Biol, Cleveland, OH 44195 USA
关键词
D O I
10.1093/nar/29.1.246
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The adenylate uridylate-rich elements (AREs) mediate the rapid turnover of mRNAs encoding proteins that regulate cellular growth and body response to exogenous agents such as microbes, inflammatory and environmental stimuli. However, the full repertoire of ARE-containing mRNAs is unknown. Here, we explore the distribution of AREs in human mRNA sequences. Computational derivation of a 13-bp ARE pattern was performed using multiple expectation maximization for motif elicitations (MEME) and consensus analyses. This pattern was statistically Validated for the specificity towards the 3'-untranslated region and not coding region. The computationally derived ARE pattern is the basis of a database which contains non-redundant full-length ARE-mRNAs. The ARE-mRNA database (ARED; http:// rc.kfshrc.edu.sa/ared) reveals that ARE-mRNAs encode a wide repertoire of functionally diverse proteins that belong to different biological processes and are important in several disease states. Cluster analysis was performed using the ARE sequences to demonstrate potential relationships between the type and number of ARE motifs, and the functional characteristics of the proteins.
引用
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页码:246 / 254
页数:9
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