RESUMEN
AIM: To determine uncovered antifungal activity of lichen-derived compound, vulpinic acid, by using chemical-genetic analyses. METHODS AND RESULTS: Haploinsufficiency and homozygous-profiling assays were performed, revealing that strains lacking GLC7, MET4, RFC2, YAE1 and PRP18 were sensitive to three concentrations (12·5, 25 and 50% of inhibitory concentration) of vulpinic acid and independently validated. To verify inhibition of those genes, cell cycle analysis using flow cytometry was performed and relative expressions were measured. Under vulpinic acid-treated condition, cell cycle was arrested in S and G2/M phases and sensitive strains' relative expressions were significantly lower than the wild type yeast. CONCLUSIONS: Vulpinic acid mainly affects cell cycle, glycogen metabolism, transcription and translation to fungi. SIGNIFICANCE AND IMPACT OF THE STUDY: Although lichen-derived compounds are commercially valuable, few studies have determined their modes of action. This study used a chemogenomic approach to gain insight into the mechanisms of one of well-known lichen-derived compound, vulpinic acid.
Asunto(s)
Antifúngicos/farmacología , Furanos/farmacología , Líquenes/química , Fenilacetatos/farmacología , Ciclo Celular/efectos de los fármacos , Expresión Génica/efectos de los fármacos , Genómica , Glucógeno/metabolismo , Haploinsuficiencia , Homocigoto , Levaduras/efectos de los fármacos , Levaduras/genética , Levaduras/metabolismoRESUMEN
The recent completion of the deletion of essentially all of the ORFs in yeast is an important new resource for identifying the phenotypes of unknown genes. Each ORF is replaced with a cassette containing unique tag sequences that allow rapid parallel analysis of strains in a pool by using hybridization to a high-density oligonucleotide array. We examined the utility of this system to identify genes conferring resistance to UV irradiation by using a pool of 4,627 individual homozygous deletion strains (representing deletions of all nonessential genes). We identified most of the nonessential genes previously shown to be involved in nucleotide excision repair, in cell cycle checkpoints, in homologous recombination, and in postreplication repair after UV damage. We also identified and individually confirmed, by replacing the genes, three new genes, to our knowledge not previously reported to confer UV sensitivity when deleted. Two of these newly identified genes have human orthologs associated with cancer, demonstrating the potential of this system to uncover human genes affecting sensitivity to DNA-damaging agents and genes potentially involved in cancer formation.
Asunto(s)
Tolerancia a Radiación , Saccharomyces cerevisiae/genética , Saccharomyces cerevisiae/efectos de la radiación , Daño del ADN , Análisis de Secuencia por Matrices de Oligonucleótidos , Sistemas de Lectura Abierta , Rayos UltravioletaRESUMEN
The functions of many open reading frames (ORFs) identified in genome-sequencing projects are unknown. New, whole-genome approaches are required to systematically determine their function. A total of 6925 Saccharomyces cerevisiae strains were constructed, by a high-throughput strategy, each with a precise deletion of one of 2026 ORFs (more than one-third of the ORFs in the genome). Of the deleted ORFs, 17 percent were essential for viability in rich medium. The phenotypes of more than 500 deletion strains were assayed in parallel. Of the deletion strains, 40 percent showed quantitative growth defects in either rich or minimal medium.
Asunto(s)
Eliminación de Gen , Genes Esenciales , Genoma Fúngico , Sistemas de Lectura Abierta , Saccharomyces cerevisiae/genética , Medios de Cultivo , Regulación Fúngica de la Expresión Génica , Marcación de Gen , Genes Fúngicos , Fenotipo , Reacción en Cadena de la Polimerasa , Recombinación Genética , Saccharomyces cerevisiae/crecimiento & desarrolloRESUMEN
Lowering the dosage of a single gene from two copies to one copy in diploid yeast results in a heterozygote that is sensitized to any drug that acts on the product of this gene. This haploinsufficient phenotype thereby identifies the gene product of the heterozygous locus as the likely drug target. We exploited this finding in a genomic approach to drug-target identification. Genome sequence information was used to generate molecularly tagged heterozygous yeast strains that were pooled, grown competitively in drug and analysed for drug sensitivity using high-density oligonucleotide arrays. Individual heterozygous strain analysis verified six known drug targets. Parallel analysis identified the known target and two hypersensitive loci in a mixed culture of 233 strains in the presence of the drug tunicamycin. Our discovery that both drug target and hypersensitive loci exhibit drug-induced haploinsufficiency may have important consequences in pharmacogenomics and variable drug toxicity observed in human populations.
Asunto(s)
Haplotipos/efectos de los fármacos , Saccharomyces cerevisiae/efectos de los fármacos , Saccharomyces cerevisiae/genética , Antibacterianos/farmacología , Benomilo/farmacología , División Celular/efectos de los fármacos , División Celular/genética , Proteínas Fúngicas/efectos de los fármacos , Proteínas Fúngicas/genética , Fungicidas Industriales/farmacología , Dosificación de Gen , Genes Fúngicos , Heterocigoto , Hidroliasas/efectos de los fármacos , Hidroliasas/genética , Fenotipo , Saccharomyces cerevisiae/crecimiento & desarrollo , Tunicamicina/farmacologíaRESUMEN
The supercoiling of 2 micron DNA in yeast by a process or processes that generate positively and negatively supercoiled domains was shown by the use of yeast DNA topoisomerase mutants expressing Escherichia coli DNA topoisomerase I, an enzyme that relaxes negative supercoils specifically. Intracellular 2 micron DNA becomes positively supercoiled in yeast top1 top2 ts strains expressing the E. coli enzyme when neither one of the yeast DNA topoisomerases I and II is functional. Examination of the linking number distributions of plasmids bearing the inducible promoters of GAL1 and GAL10 genes indicates that the generation of supercoiled domains of opposite signs is related to transcription.
Asunto(s)
ADN de Hongos/ultraestructura , ADN Superhelicoidal , Plásmidos , Saccharomyces cerevisiae/genética , Transcripción Genética , ADN-Topoisomerasas de Tipo I/metabolismo , ADN de Hongos/fisiología , Electroforesis en Gel BidimensionalRESUMEN
A number of ways are known by which an event at one location on a DNA molecule can affect an event at a distant location on the same molecule. Three classes of mechanisms are described for such distal actions: tracking or translocation of a protein along a DNA, the association of two proteins bound at separate sites to form a DNA loop in between, and distal interactions that are affected by the topology of the DNA. The basic characteristics of each type of mechanism are discussed in terms of the known physicochemical properties of DNA. The various modes of action at a distance are often interrelated. Examples include the formation of positively and negatively supercoiled DNA loops by tracking and the strong effects of DNA topology on looping.
Asunto(s)
ADN , Conformación de Ácido Nucleico , ADN/genética , ADN/metabolismo , ADN Superhelicoidal , Desoxirribonucleoproteínas/metabolismo , Modelos MolecularesRESUMEN
DNA topoisomerase mutants of Escherichia coli and Saccharomyces cerevisiae were used to study the topological state of intracellular DNA. In E. coli, it is shown that switching off the gene topA encoding DNA topoisomerase I leads to an increase in the degree of negative supercoiling of intracellular DNA and inhibition of the growth of the cells: a d(pCpG)16.d(pCpG)16 sequence on a plasmid is also shown to flip from a right-handed B-helical structure to a left-handed Z-helical structure in vivo when topA is switched off. In S. cerevisiae, the topological state of intracellular DNA is little affected by the cellular levels of the topoisomerases.
Asunto(s)
ADN Superhelicoidal , Escherichia coli/genética , Conformación de Ácido Nucleico , Saccharomyces cerevisiae/genética , ADN-Topoisomerasas de Tipo I/metabolismo , ADN-Topoisomerasas de Tipo II/metabolismo , ADN Bacteriano , ADN de Hongos , Escherichia coli/enzimología , Mutación , Plásmidos , Saccharomyces cerevisiae/enzimología , TemperaturaRESUMEN
The nucleotide sequence of the gene TOP2 encoding DNA topoisomerase II of the yeast Saccharomyces cerevisiae has been determined. The entire coding sequence of the gene lies within an open reading frame, and there are 1429 amino acids in the single polypeptide protein if translation is assumed to start at the first ATG in this frame. The calculated subunit and molecular mass of the enzyme is 164,000 and 328,000 daltons, respectively. The transcriptional starts of the gene and a polyadenylation site of the message have also been mapped.
Asunto(s)
ADN-Topoisomerasas de Tipo II/genética , Genes , Saccharomyces cerevisiae/enzimología , Secuencia de Aminoácidos , Secuencia de Bases , Enzimas de Restricción del ADN/metabolismo , Peso Molecular , Poli A/metabolismo , Regiones Promotoras Genéticas , Saccharomyces cerevisiae/genéticaRESUMEN
The nucleotide sequence for the Saccharomyces cerevisiae gene TOP2, which encodes DNA topoisomerase II, was compared with the sequence for bacterial DNA gyrase. The amino and carboxyl terminal halves of the single-subunit yeast enzyme showed homologies with the B and A subunits of bacterial gyrase, respectively, at corresponding positions along the polypeptide chains. Although the two enzymes differ in both quaternary structure and activity, the homology between the two proteins indicates mechanistic as well as structural similarities, and a probable evolutionary relationship.