PromoLign: A database for upstream region analysis and SNPs

被引:24
作者
Zhao, T
Chang, LW
McLeod, HL
Stormo, GD
机构
[1] Washington Univ, Sch Med, Dept Genet, St Louis, MO 63110 USA
[2] Washington Univ, Sch Med, Dept Biomed Engn, St Louis, MO 63110 USA
[3] Washington Univ, Sch Med, Dept Med, St Louis, MO 63110 USA
关键词
PromoLign; SNP; transcription regulation; orthology; sequence alignment; database; pharmacogenomics;
D O I
10.1002/humu.20049
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
The study of transcriptional regulation at the genomic level has been hindered by the lack of functional annotation in the putative regulatory regions. Phylogenetic footprinting, in which cross-species sequence alignment among orthologous genes is applied to locate conserved sequence blocks, is an effective strategy to attack this problem. Single nucleotide polymorphisms (SNPs) in transcription factor (TF) binding sites contribute to the heterogeneity of TIF binding sites and might disrupt or enhance their regulatory activity. The correlation of SNPs with the TF sites will not only help in functional evaluation of SNPs, but will also help in the study of transcription regulation by focusing attention on specific TF sites. PromoLign (http:// polly.wustl:edu/promolign/main.html) is an online database application that presents SNPs and TF binding profiles in the context of human-mouse orthologous sequence alignment with a hyperlinked graphical interface. PromoLign could be applied to a variety of SNPs and transcription related studies, including association genetics; population genetics, and pharmacogenetics. (C) 2004 Wiley-Liss, Inc.
引用
收藏
页码:534 / 539
页数:6
相关论文
共 28 条
[1]  
[Anonymous], ISMB
[2]  
Ansari-Lari MA, 1998, GENOME RES, V8, P29
[3]  
Antonarakis SE, 1998, HUM MUTAT, V11, P1
[4]   LAGAN and Multi-LAGAN: Efficient tools for large-scale multiple alignment of genomic DNA [J].
Brudno, M ;
Do, CB ;
Cooper, GM ;
Kim, MF ;
Davydov, E ;
Green, ED ;
Sidow, A ;
Batzoglou, S .
GENOME RESEARCH, 2003, 13 (04) :721-731
[5]   Alignment of whole genomes [J].
Delcher, AL ;
Kasif, S ;
Fleischmann, RD ;
Peterson, J ;
White, O ;
Salzberg, SL .
NUCLEIC ACIDS RESEARCH, 1999, 27 (11) :2369-2376
[6]  
den Dunnen JT, 2000, HUM MUTAT, V15, P7
[7]   CORG: a database for COmparative Regulatory Genomics [J].
Dieterich, C ;
Wang, H ;
Rateitschak, K ;
Luz, H ;
Vingron, M .
NUCLEIC ACIDS RESEARCH, 2003, 31 (01) :55-57
[8]   Searching for regulatory elements in human noncoding sequences [J].
Duret, L ;
Bucher, P .
CURRENT OPINION IN STRUCTURAL BIOLOGY, 1997, 7 (03) :399-406
[9]   Drug therapy - Pharmacogenomics - Drug disposition, drug targets, and side effects [J].
Evans, WE ;
McLeod, HL .
NEW ENGLAND JOURNAL OF MEDICINE, 2003, 348 (06) :538-549
[10]   HGVbase:: a human sequence variation database emphasizing data quality and a broad spectrum of data sources [J].
Fredman, D ;
Siegfried, M ;
Yuan, YP ;
Bork, P ;
Lehväslaiho, H ;
Brookes, AJ .
NUCLEIC ACIDS RESEARCH, 2002, 30 (01) :387-391