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1.
Nucleic Acids Res ; 30(22): 4993-5003, 2002 Nov 15.
Artículo en Inglés | MEDLINE | ID: mdl-12434004

RESUMEN

The conditionally-lethal pso4-1 mutant allele of the spliceosomal-associated PRP19 gene allowed us to study this gene's influence on pre-mRNA processing, DNA repair and sporulation. Phenotypes related to intron-containing genes were correlated to temperature. Splicing reporter systems and RT-PCR showed splicing efficiency in pso4-1 to be inversely correlated to growth temperature. A single amino acid substitution, replacing leucine with serine, was identified within the N-terminal region of the pso4-1 allele and was shown to affect the interacting properties of Pso4-1p. Amongst 24 interacting clones isolated in a two-hybrid screening, seven could be identified as parts of the RAD2, RLF2 and DBR1 genes. RAD2 encodes an endonuclease indispensable for nucleotide excision repair (NER), RLF2 encodes the major subunit of the chromatin assembly factor I, whose deletion results in sensitivity to UVC radiation, while DBR1 encodes the lariat RNA splicing debranching enzyme, which degrades intron lariat structures during splicing. Characterization of mutagen-sensitive phenotypes of rad2Delta, rlf2Delta and pso4-1 single and double mutant strains showed enhanced sensitivity for the rad2Delta pso4-1 and rlf2Delta pso4-1 double mutants, suggesting a functional interference of these proteins in DNA repair processes in Saccharomyces cerevisiae.


Asunto(s)
Proteínas Fúngicas/genética , Proteínas Fúngicas/fisiología , Saccharomyces cerevisiae/genética , Saccharomyces cerevisiae/fisiología , Alelos , Secuencia de Aminoácidos , Sustitución de Aminoácidos , Daño del ADN , Reparación del ADN , Proteínas Fúngicas/química , Genes Fúngicos , Datos de Secuencia Molecular , Mutación , Fenotipo , Precursores del ARN/metabolismo , Empalme del ARN , Factores de Empalme de ARN , ARN de Hongos/metabolismo , Saccharomyces cerevisiae/efectos de la radiación , Proteínas de Saccharomyces cerevisiae/metabolismo , Homología de Secuencia de Aminoácido , Empalmosomas , Esporas Bacterianas , Temperatura , Técnicas del Sistema de Dos Híbridos , Rayos Ultravioleta
2.
Mutat Res ; 486(3): 195-206, 2001 Aug 09.
Artículo en Inglés | MEDLINE | ID: mdl-11459632

RESUMEN

The interaction trap method was used to isolate putative binding partners of Rad16/Pso5, a protein responsible for repair of silent DNA. One of the interactors found was Sgs1, a DNA helicase influencing the life span of Saccharomyces cerevisiae, with homology to the human BLM, WRN and RECQL4 proteins. Using the same fusion proteins from the two-hybrid screening, we show evidence that both proteins also interact in vitro. We tested isogenic strains, containing mutant alleles of the two genes in single and double mutant combination, for phenotypic similarity. Life span in sgs1Delta single and sgs1Delta rad16Delta double mutants is about 40% of that of WT, and the rad16/pso5Delta single mutant also had its life span reduced to 75%. Sensitivity to different mutagens, whose lesions are poorly repaired in rad16/pso5Delta mutants, was tested in sgs1Delta mutants. The sgs1Delta conferred sensitivity to MMS, H2O2 and was moderately sensitive to UV(254nm) (UVC) and 4-NQO. An epistatic interaction between rad16 and sgs1 mutations after UVC, 4-NQO and H2O2 was observed. Moreover, we found that in a top3 background, functional Sgs1p and Rad16p apparently channel MMS, 4-NQO and H2O2 induced lesions into aberrant DNA repair. Our results demonstrate that Sgs1 is not only involved in genome stability, somatic recombination and aging, but is also implicated, together with Rad16/Pso5, in the repair of specific DNA damage.


Asunto(s)
Adenosina Trifosfatasas , ADN Helicasas/metabolismo , Reparación del ADN , Proteínas Fúngicas/metabolismo , Proteínas de Saccharomyces cerevisiae , Saccharomyces cerevisiae/metabolismo , ADN Helicasas/genética , Reparación del ADN/genética , ADN de Hongos/efectos de los fármacos , ADN de Hongos/genética , ADN de Hongos/metabolismo , ADN de Hongos/efectos de la radiación , Proteínas Fúngicas/genética , Genes Fúngicos , Humanos , Mutágenos/toxicidad , Mutación , RecQ Helicasas , Proteínas Recombinantes de Fusión/genética , Proteínas Recombinantes de Fusión/metabolismo , Saccharomyces cerevisiae/genética , Saccharomyces cerevisiae/crecimiento & desarrollo , Técnicas del Sistema de Dos Híbridos , Rayos Ultravioleta/efectos adversos
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