Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
21
pubmed:dateCreated
1994-6-29
pubmed:abstractText
The INO4 gene encodes a protein required for derepression of a number of structural genes encoding enzymes involved in phospholipid biosynthesis in the yeast Saccharomyces cerevisiae. Ino4p shows structural similarity to the basic helix-loop-helix (bHLH) family of regulatory proteins (Hoshizaki, D. K., Hill, J. E., and Henry, S. A. (1990) J. Biol Chem. 265, 4736-4745). In this report we demonstrate that Ino4p translated in vitro forms a complex with Ino2p, another positive regulator of phospholipid biosynthesis that contains a bHLH domain. The Ino2p.Ino4p complex binds to a fragment of the INO1 promoter containing two copies of the consensus binding site for the bHLH family of proteins. The complex formed when this DNA fragment is incubated with in vitro translated Ino2p and Ino4p is identical in mobility to the complex formed when this DNA fragment is incubated with whole cell extracts. The binding of DNA by the Ino2p.Ino4p complex is competed by an oligonucleotide containing the consensus binding sequence for bHLH proteins. Neither Ino2p nor Ino4p translated alone is capable of forming a complex with the INO1 promoter fragment. The two products, translated separately and mixed, show only reduced capability to form a complex compared with cotranslated proteins. Immunoprecipitation experiments demonstrate that Ino2p and Ino4p interact in the absence of DNA. Ino2p and Ino4p are, thus, both necessary and sufficient for formation of a complex with the INO1 promoter.
pubmed:grant
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
http://linkedlifedata.com/resource/pubmed/chemical/Basic Helix-Loop-Helix..., http://linkedlifedata.com/resource/pubmed/chemical/DNA, Fungal, http://linkedlifedata.com/resource/pubmed/chemical/DNA-Binding Proteins, http://linkedlifedata.com/resource/pubmed/chemical/Fungal Proteins, http://linkedlifedata.com/resource/pubmed/chemical/INO2 protein, S cerevisiae, http://linkedlifedata.com/resource/pubmed/chemical/INO4 protein, S cerevisiae, http://linkedlifedata.com/resource/pubmed/chemical/Phospholipids, http://linkedlifedata.com/resource/pubmed/chemical/Repressor Proteins, http://linkedlifedata.com/resource/pubmed/chemical/Saccharomyces cerevisiae Proteins, http://linkedlifedata.com/resource/pubmed/chemical/Trans-Activators, http://linkedlifedata.com/resource/pubmed/chemical/Transcription Factors
pubmed:status
MEDLINE
pubmed:month
May
pubmed:issn
0021-9258
pubmed:author
pubmed:issnType
Print
pubmed:day
27
pubmed:volume
269
pubmed:geneSymbol
INO1, INO2, INO4
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
15344-9
pubmed:dateRevised
2009-11-19
pubmed:meshHeading
pubmed-meshheading:8195172-Base Sequence, pubmed-meshheading:8195172-Basic Helix-Loop-Helix Transcription Factors, pubmed-meshheading:8195172-Binding Sites, pubmed-meshheading:8195172-DNA, Fungal, pubmed-meshheading:8195172-DNA-Binding Proteins, pubmed-meshheading:8195172-Fungal Proteins, pubmed-meshheading:8195172-Genes, Fungal, pubmed-meshheading:8195172-Helix-Loop-Helix Motifs, pubmed-meshheading:8195172-Molecular Sequence Data, pubmed-meshheading:8195172-Phospholipids, pubmed-meshheading:8195172-Promoter Regions, Genetic, pubmed-meshheading:8195172-Protein Binding, pubmed-meshheading:8195172-Protein Biosynthesis, pubmed-meshheading:8195172-Repressor Proteins, pubmed-meshheading:8195172-Saccharomyces cerevisiae, pubmed-meshheading:8195172-Saccharomyces cerevisiae Proteins, pubmed-meshheading:8195172-Trans-Activators, pubmed-meshheading:8195172-Transcription Factors
pubmed:year
1994
pubmed:articleTitle
INO2 and INO4 gene products, positive regulators of phospholipid biosynthesis in Saccharomyces cerevisiae, form a complex that binds to the INO1 promoter.
pubmed:affiliation
Department of Biological Sciences, Carnegie Mellon University, Pittsburgh, Pennsylvania 15213.
pubmed:publicationType
Journal Article, Research Support, U.S. Gov't, P.H.S.