Weight matrix descriptions of four eukaryotic RNA polymerase II promoter elements derived from 502 unrelated promoter sequences
- PMID: 2329577
- DOI: 10.1016/0022-2836(90)90223-9
Weight matrix descriptions of four eukaryotic RNA polymerase II promoter elements derived from 502 unrelated promoter sequences
Abstract
Optimized weight matrices defining four major eukaryotic promoter elements, the TATA-box, cap signal, CCAAT-, and GC-box, are presented; they were derived by comparative sequence analysis of 502 unrelated RNA polymerase II promoter regions. The new TATA-box and cap signal descriptions differ in several respects from the only hitherto available base frequency Tables. The CCAAT-box matrix, obtained with no prior assumption but CCAAT being the core of the motif, reflects precisely the sequence specificity of the recently discovered nuclear factor NY-I/CP1 but does not include typical recognition sequences of two other purported CCAAT-binding proteins, CTF and CBP. The GC-box description is longer than the previously proposed consensus sequences but is consistent with Sp1 protein-DNA binding data. The notion of a CACCC element distinct from the GC-box seems not to be justified any longer in view of the new weight matrix. Unlike the two fixed-distance elements, neither the CCAAT- nor the GC-box occurs at significantly high frequency in the upstream regions of non-vertebrate genes. Preliminary attempts to predict promoters with the aid of the new signal descriptions were unexpectedly successful. The new TATA-box matrix locates eukaryotic transcription initiation sites as reliably as do the best currently available methods to map Escherichia coli promoters. This analysis was made possible by the recently established Eukaryotic Promoter Database (EPD) of the EMBL Nucleotide Sequence Data Library. In order to derive the weight matrices, a novel algorithm has been devised that is generally applicable to sequence motifs positionally correlated with a biologically defined position in the sequences. The signal must be sufficiently over-represented in a particular region relative to the given site, but need not be present in all members of the input sequence collection. The algorithm iteratively redefines the set of putative motif representatives from which a weight matrix is derived, so as to maximize a quantitative measure of local over-representation, an optimization criterion that naturally combines structural and positional constancy. A comprehensive description of the technique is presented in Methods and Data.
Similar articles
-
Inferring regulatory elements from a whole genome. An analysis of Helicobacter pylori sigma(80) family of promoter signals.J Mol Biol. 2000 Mar 24;297(2):335-53. doi: 10.1006/jmbi.2000.3576. J Mol Biol. 2000. PMID: 10715205
-
Predicting Pol II promoter sequences using transcription factor binding sites.J Mol Biol. 1995 Jun 23;249(5):923-32. doi: 10.1006/jmbi.1995.0349. J Mol Biol. 1995. PMID: 7791218
-
Isolation and characterization of the human A-myb promoter: regulation by NF-Y and Sp1.Oncogene. 2000 Aug 10;19(34):3931-40. doi: 10.1038/sj.onc.1203730. Oncogene. 2000. PMID: 10951586
-
Sequence signals in eukaryotic upstream regions.Crit Rev Biochem Mol Biol. 1990;25(3):185-224. doi: 10.3109/10409239009090609. Crit Rev Biochem Mol Biol. 1990. PMID: 2196161 Review.
-
A survey of 178 NF-Y binding CCAAT boxes.Nucleic Acids Res. 1998 Mar 1;26(5):1135-43. doi: 10.1093/nar/26.5.1135. Nucleic Acids Res. 1998. PMID: 9469818 Free PMC article. Review.
Cited by
-
Machine Learning to Advance Human Genome-Wide Association Studies.Genes (Basel). 2023 Dec 25;15(1):34. doi: 10.3390/genes15010034. Genes (Basel). 2023. PMID: 38254924 Free PMC article. Review.
-
Transcriptional regulation of brain gene expression in response to a territorial intrusion.Proc Biol Sci. 2012 Dec 22;279(1749):4929-38. doi: 10.1098/rspb.2012.2087. Epub 2012 Oct 24. Proc Biol Sci. 2012. PMID: 23097509 Free PMC article.
-
Transcription Factors as Important Regulators of Changes in Behavior through Domestication of Gray Rats: Quantitative Data from RNA Sequencing.Int J Mol Sci. 2022 Oct 14;23(20):12269. doi: 10.3390/ijms232012269. Int J Mol Sci. 2022. PMID: 36293128 Free PMC article.
-
Optimizing the GATA-3 position weight matrix to improve the identification of novel binding sites.BMC Genomics. 2012 Aug 22;13:416. doi: 10.1186/1471-2164-13-416. BMC Genomics. 2012. PMID: 22913572 Free PMC article.
-
Identification of cis-regulatory modules in promoters of human genes exploiting mutual positioning of transcription factors.Nucleic Acids Res. 2013 Oct;41(19):8822-41. doi: 10.1093/nar/gkt578. Epub 2013 Aug 2. Nucleic Acids Res. 2013. PMID: 23913413 Free PMC article.
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Other Literature Sources
Miscellaneous