ARED 3.0: the large and diverse AU-rich transcriptome

被引:264
作者
Bakheet, Tala
Williams, Bryan R. G.
Khabar, Khalid S. A. [1 ]
机构
[1] King Faisal Specialist Hosp & Res Ctr, Dept Biostat Epidemiol & Sci Comp, Bioinformat Sect, Riyadh 11211, Saudi Arabia
[2] King Faisal Specialist Hosp & Res Ctr, Dept Biol & Med Res, Riyadh 11211, Saudi Arabia
[3] Cleveland Clin Fdn, Lerner Res Inst, Dept Canc Biol, Cleveland, OH 44195 USA
关键词
D O I
10.1093/nar/gkj052
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
A comprehensive search that utilized a large set of mRNA data from human genome databases and additionally, expressed sequence tag (EST) database characterized this latest update of AU-rich elements (AREs) containing mRNA database (ARED). A large number of ARE-mRNA, as much as 4000, were recovered and include many of ARE alternative forms. This number represents as much as 5-8% of the human genes depending on the entire number of genes. The new ARED does not contain only larger and diverse number of ARE-mRNAs but additional functionality and enhanced search capabilities are given in the database website http://rc.kfshrc.edu.sa/ared/. These include class and cluster of AREs, source mRNAs, EST evidence, buildup information, retrieval of lists of genes, and integration with current and new NCBI data, such as Entrez ID and Unigene. Gene Ontology analysis shows there are significant differences in functional diversity of ARED when compared with the overall genome. Many of ARE-genes mediate regulatory processes, reactions to outside stimuli, RNA metabolism, and developmental processes particularly those of early and transient responses. The wide interest in mRNA turnover and importance of AREs in health and disease signify the compilation of ARE-genes.
引用
收藏
页码:D111 / D114
页数:4
相关论文
共 16 条
[1]   FatiGO:: a web tool for finding significant associations of Gene Ontology terms with groups of genes [J].
Al-Shahrour, F ;
Díaz-Uriarte, R ;
Dopazo, J .
BIOINFORMATICS, 2004, 20 (04) :578-580
[2]   ARED 2.0: an update of AU-rich element mRNA database [J].
Bakheet, T ;
Williams, BRG ;
Khabar, KSA .
NUCLEIC ACIDS RESEARCH, 2003, 31 (01) :421-423
[3]   ARED: human AU-rich element-containing mRNA database reveals an unexpectedly diverse functional repertoire of encoded proteins [J].
Bakheet, T ;
Frevel, M ;
Williams, BRG ;
Greer, W ;
Khabar, KSA .
NUCLEIC ACIDS RESEARCH, 2001, 29 (01) :246-254
[4]   GOstat: find statistically overrepresented Gene Ontologies within a group of genes [J].
Beissbarth, T ;
Speed, TP .
BIOINFORMATICS, 2004, 20 (09) :1464-1465
[5]   SELECTIVE DEGRADATION OF EARLY-RESPONSE-GENE MESSENGER-RNAS - FUNCTIONAL ANALYSES OF SEQUENCE FEATURES OF THE AU-RICH ELEMENTS [J].
CHEN, CYA ;
SHYU, AB .
MOLECULAR AND CELLULAR BIOLOGY, 1994, 14 (12) :8471-8482
[6]   AU-RICH ELEMENTS - CHARACTERIZATION AND IMPORTANCE IN MESSENGER-RNA DEGRADATION [J].
CHEN, CYA ;
SHYU, AB .
TRENDS IN BIOCHEMICAL SCIENCES, 1995, 20 (11) :465-470
[7]   Association of nucleotide patterns with gene function classes:: application to human 3′ untranslated sequences [J].
Conklin, D ;
Jonassen, I ;
Aasland, R ;
Taylor, WR .
BIOINFORMATICS, 2002, 18 (01) :182-189
[8]   The role of the AU-rich elements of mRNAs in controlling translation [J].
Espel, E .
SEMINARS IN CELL & DEVELOPMENTAL BIOLOGY, 2005, 16 (01) :59-67
[9]   p38 mitogen-activated protein kinase-dependent and -independent signaling of mRNA stability of AU-rich element-containing transcripts [J].
Frevel, MAE ;
Bakheet, T ;
Silva, AM ;
Hissong, JG ;
Khabar, KSA ;
Williams, BRG .
MOLECULAR AND CELLULAR BIOLOGY, 2003, 23 (02) :425-436
[10]   The AU-rich transcriptome: More than interferons and cytokines, and its role in disease [J].
Khabar, KSA .
JOURNAL OF INTERFERON AND CYTOKINE RESEARCH, 2005, 25 (01) :1-10