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Predicate | Object |
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rdf:type | |
lifeskim:mentions |
umls-concept:C0009015,
umls-concept:C0017262,
umls-concept:C0017362,
umls-concept:C0017366,
umls-concept:C0020792,
umls-concept:C0036025,
umls-concept:C0185117,
umls-concept:C0205147,
umls-concept:C0851285,
umls-concept:C1176140,
umls-concept:C1413745,
umls-concept:C1413865,
umls-concept:C1418799,
umls-concept:C1446409,
umls-concept:C1519249,
umls-concept:C1521840,
umls-concept:C1668248,
umls-concept:C1705261,
umls-concept:C1705794,
umls-concept:C1706113,
umls-concept:C2911684
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pubmed:issue |
3
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pubmed:dateCreated |
1985-10-11
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pubmed:abstractText |
CYP1 is a trans acting regulatory locus modulating both iso 1- and iso 2-cytochrome c synthesis. Genetical analysis of various mutated alleles has allowed us to identify the gene product as a positive regulatory element. The region of the target sequence of the CYP1 product on the iso 2-cytochrome c structural gene was located by molecular and genetic analysis of two cis acting mutations located at the CYP3 locus: CYP3-36 and CYP3-4, which have been shown to arise from the integration of TY1 elements near the promoter site. Determination of the amount of iso 2-cytochrome c synthesized by strains bearing various genetic constructions, in which the cis acting mutations were associated with different alleles of the CYP1 trans acting locus, showed that TY1 inserted into CYP3-36 extinguishes the activation function due to a mutated overproducer allele CYP1-18, while CYP3-4 amplifies this function. This result identifies at least a part of the target sequence of the CYP1 product within the region separating the two TY1 insertions. To clone the CYP1 gene, we took advantage of the iso 2-cytochrome c overproducer phenotype of the mutated allele CYP1-18, which confers a Lactate+ phenotype on an iso 1-cytochrome c-deficient strain. Such a phenotype allowed the isolation of a recombinant plasmid YEpJFM1 carrying the mutated allele, able to complement on lactate medium a lactate- recipient strain. The identity of the YEpJFM1 sequence with the chromosomal gene was confirmed by homologous recombination at the CYP1 locus.
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pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical | |
pubmed:status |
MEDLINE
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pubmed:issn |
0026-8925
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:volume |
199
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
524-33
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pubmed:dateRevised |
2006-11-15
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pubmed:meshHeading |
pubmed-meshheading:2993801-Alleles,
pubmed-meshheading:2993801-Base Sequence,
pubmed-meshheading:2993801-Cloning, Molecular,
pubmed-meshheading:2993801-Cytochrome c Group,
pubmed-meshheading:2993801-Cytochromes c,
pubmed-meshheading:2993801-DNA Restriction Enzymes,
pubmed-meshheading:2993801-Genes,
pubmed-meshheading:2993801-Genes, Fungal,
pubmed-meshheading:2993801-Genes, Regulator,
pubmed-meshheading:2993801-Mutation,
pubmed-meshheading:2993801-Nucleic Acid Hybridization,
pubmed-meshheading:2993801-Plasmids,
pubmed-meshheading:2993801-Protein Biosynthesis,
pubmed-meshheading:2993801-Saccharomyces cerevisiae
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pubmed:year |
1985
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pubmed:articleTitle |
Regulation of the expression of iso 2-cytochrome c gene in S. cerevisiae: cloning of the positive regulatory gene CYP1 and identification of the region of its target sequence on the structural gene CYP3.
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pubmed:publicationType |
Journal Article
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