Computational identification of cis-regulatory elements associated with groups of functionally related genes in Saccharomyces cerevisiae

被引:750
作者
Hughes, JD
Estep, PW
Tavazoie, S
Church, GM
机构
[1] Harvard Univ, Sch Med, Dept Genet, Boston, MA 02115 USA
[2] Harvard Univ, Grad Program Biophys, Boston, MA 02115 USA
关键词
bioinformatics; computational biology; genomics; DNA regulatory motifs; yeast;
D O I
10.1006/jmbi.2000.3519
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
ALignACE is a Gibbs sampling algorithm for identifying motifs that are over-represented in a set of DNA sequences. When used to search upstream of apparently coregulated genes, AlignACE finds motifs that often correspond to the DNA binding preferences of transcription factors. We previously used ALignACE to analyze whole genome mRNA expression data. Here, we present a more detailed study of its effectiveness as applied to a variety of groups of genes in the Saccharomyces cerevisiae genome. Published functional catalogs of genes and sets of genes grouped by common name provided 248 groups, resulting in 3311 motifs. In conjunction with this analysis, we present measures for gauging the tendency of a motif to target a given set of genes relative to all other genes in the genome and for gauging the degree to which a motif is preferentially located in a certain distance range upstream of translational start sites. We demonstrate improved methods for comparing and clustering sequence motifs. Many previously identified cis-regulatory elements were found. We also describe previously unidentified motifs, one of which has been verified by experiments in our laboratory. An extensive set of AlignACE runs on randomly selected sets of genes and on sets of genes whose upstream regions contain known transcription factor binding sites serve as controls. (C) 2000 Academic Press.
引用
收藏
页码:1205 / 1214
页数:10
相关论文
共 39 条
[1]  
ALTSCHUL SF, 1990, J MOL BIOL, V215, P403, DOI 10.1006/jmbi.1990.9999
[2]   Cooperative binding interactions required for function of the Ty1 sterile responsive element [J].
Baur, M ;
Esch, RK ;
Errede, B .
MOLECULAR AND CELLULAR BIOLOGY, 1997, 17 (08) :4330-4337
[3]   A nonameric core sequence is required upstream of the LYS genes of Saccharomyces cerevisiae for Lys14p-mediated activation and apparent repression by lysine [J].
Becker, B ;
Feller, A ;
El Alami, M ;
Dubois, E ;
Piérard, A .
MOLECULAR MICROBIOLOGY, 1998, 29 (01) :151-163
[4]   SELECTION OF DNA-BINDING SITES BY REGULATORY PROTEINS - STATISTICAL-MECHANICAL THEORY AND APPLICATION TO OPERATORS AND PROMOTERS [J].
BERG, OG ;
VONHIPPEL, PH .
JOURNAL OF MOLECULAR BIOLOGY, 1987, 193 (04) :723-743
[5]   Met31p and Met32p, two related zinc finger proteins, are involved in transcriptional regulation of yeast sulfur amino acid metabolism [J].
Blaiseau, PL ;
Isnard, AD ;
SurdinKerjan, Y ;
Thomas, D .
MOLECULAR AND CELLULAR BIOLOGY, 1997, 17 (07) :3640-3648
[6]   Predicting gene regulatory elements in silico on a genomic scale [J].
Brazma, A ;
Jonassen, I ;
Vilo, J ;
Ukkonen, E .
GENOME RESEARCH, 1998, 8 (11) :1202-1215
[7]   Constitutive and carbon source-responsive promoter elements are involved in the regulated expression of the Saccharomyces cerevisiae malate synthase gene MLS1 [J].
Caspary, F ;
Hartig, A ;
Schuller, HJ .
MOLECULAR & GENERAL GENETICS, 1997, 255 (06) :619-627
[8]  
DELAHODDE A, 1995, MOL CELL BIOL, V15, P4043
[9]  
DEQUARDCHABLAT M, 1991, J BIOL CHEM, V266, P15300
[10]   SINGLE AMINO-ACID SUBSTITUTIONS ALTER HELIX LOOP HELIX PROTEIN SPECIFICITY FOR BASES FLANKING THE CORE CANNTG MOTIF [J].
FISHER, F ;
GODING, CR .
EMBO JOURNAL, 1992, 11 (11) :4103-4109