FAST DB: a website resource for the study of the expression regulation of human gene products

被引:67
作者
de la Grange, P [1 ]
Dutertre, M [1 ]
Martin, N [1 ]
Auboeuf, D [1 ]
机构
[1] Hop St Louis, Inst Univ Hematol, Ctr G Hayem, INSERM,U685,AVENIR, F-75010 Paris, France
关键词
D O I
10.1093/nar/gki738
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
Human genes use various mechanisms to generate different transcripts having different exon content, which in turn generate multiple protein isoforms having differential and even opposite biological activities. To understand the biological consequences of gene transcriptional activity modulation, it is necessary to integrate the capability of genes to generate distinct functional products, particularly because transcriptional stimuli also affect the exon content of their target gene products. For this purpose, we have developed a bioinformatics suite, FAST DB, which defines easily and accurately the exon content of all known transcripts produced by human genes. In addition, several tools have been developed, including a graphical presentation of all gene products, a sequence multi-alignment of all gene transcripts and an in silico PCR computer program. The FAST DB interface also offers extensive links to website resources for promoter analysis and transcription factor binding site prediction, splicing regulatory sequence prediction, as well as 5'- and 3'-untranslated region analysis. FAST DB has been designed to facilitate studies that integrate transcriptional and post-transcriptional events to investigate the expression regulation of human gene products.
引用
收藏
页码:4276 / 4284
页数:9
相关论文
共 55 条
[1]   How did alternative splicing evolve? [J].
Ast, G .
NATURE REVIEWS GENETICS, 2004, 5 (10) :773-782
[2]   Differential recruitment of nuclear receptor coactivators may determine alternative RNA splice site choice in target genes [J].
Auboeuf, D ;
Dowhan, DH ;
Kang, YK ;
Larkin, K ;
Lee, JW ;
Berget, SM ;
O'Malley, BW .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2004, 101 (08) :2270-2274
[3]   CoAA, a nuclear receptor coactivator protein at the interface of transcriptional coactivation and RNA splicing [J].
Auboeuf, D ;
Dowhan, DH ;
Li, XT ;
Larkin, K ;
Ko, L ;
Berget, SM ;
O'Malley, BW .
MOLECULAR AND CELLULAR BIOLOGY, 2004, 24 (01) :442-453
[4]   Coordinate regulation of transcription and splicing by steroid receptor coregulators [J].
Auboeuf, D ;
Hönig, A ;
Berget, SM ;
O'Malley, BW .
SCIENCE, 2002, 298 (5592) :416-419
[5]   Dragon Promoter Finder: recognition of vertebrate RNA polymerase II promoters [J].
Bajic, VB ;
Seah, SH ;
Chong, A ;
Zhang, GL ;
Koh, JLY ;
Brusic, V .
BIOINFORMATICS, 2002, 18 (01) :198-199
[6]   Identification of alternate polyadenylation sites and analysis of their tissue distribution using EST data [J].
Beaudoing, E ;
Gautheret, D .
GENOME RESEARCH, 2001, 11 (09) :1520-1526
[7]   SiteSeer: visualisation and analysis of transcription factor binding sites in nucleotide sequences [J].
Boardman, PE ;
Oliver, SG ;
Hubbard, SJ .
NUCLEIC ACIDS RESEARCH, 2003, 31 (13) :3572-3575
[8]   Improving promoter prediction Improving promoter prediction for the NNPP2.2 algorithm:: a case study using Escherichia coli DNA sequences [J].
Burden, S ;
Lin, YX ;
Zhang, R .
BIOINFORMATICS, 2005, 21 (05) :601-607
[9]   ESEfinder: a web resource to identify exonic splicing enhancers [J].
Cartegni, L ;
Wang, JH ;
Zhu, ZW ;
Zhang, MQ ;
Krainer, AR .
NUCLEIC ACIDS RESEARCH, 2003, 31 (13) :3568-3571
[10]   Functional association between promoter structure and transcript alternative splicing [J].
Cramer, P ;
Pesce, CG ;
Baralle, FE ;
Kornblihtt, AR .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1997, 94 (21) :11456-11460