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Using sequence logos and information analysis of Lrp DNA binding sites to investigate discrepancies between natural selection and SELEX
Author(s) -
Ryan K. Shultzaberger,
Thomas D. Schneider
Publication year - 1999
Publication title -
nucleic acids research
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 9.008
H-Index - 537
eISSN - 1362-4954
pISSN - 0305-1048
DOI - 10.1093/nar/27.3.882
Subject(s) - systematic evolution of ligands by exponential enrichment , biology , dna , computational biology , sequence (biology) , binding site , dna binding site , genetics , selection (genetic algorithm) , gene , artificial intelligence , rna , computer science , gene expression , promoter
In vitro experiments that characterize DNA-protein interactions by artificial selection, such as SELEX,are often performed with the assumption that the experimental conditions are equivalent to natural ones. To test whether SELEX gives natural results, we compared sequence logos composed from naturally occurring leucine-responsive regulatory protein (Lrp) binding sites with those composed from SELEX-generated binding sites. The sequence logos were significantly different, indicating that the binding conditions are disparate. A likely explanation is that the SELEX experiment selected for a dimeric or trimeric Lrp complex bound to DNA. In contrast, natural sites appear to be bound by a monomer. This discrepancy suggests that in vitro selections do not necessarily give binding site sets comparable with the natural binding sites.

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