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The PSO4 gene is responsible for an error-prone recombinational DNA repair pathway in Saccharomyces cerevisiae
Authors:H H de Andrade  E K Marques  A C Schenberg  J A Henriques
Affiliation:(1) Instituto de Biociências, Departmento de Genética, Universidade Federal do Rio Grande do Sul, Rua. Prof. Annes Dias, 112/15° andar, 90001 Porto Alegre, RS, Brazil;(2) Instituto de Ciências Biomédicas, Departamento de Microbiologia, Universidade de S?o Paulo, Av. Prof. Lineu Prestes No. 1374, Cidade Universitária, 05434 S?o Paulo, Brazil;(3) Instituto de Biociências, Departamento de Fisiologia, Farmacologia e Biofisica, Universidade Federal do Rio Grande do Sul, Rua. Prof. Sarmento Leite, 500, 90049 Porto Alegre, RS, Brazil
Abstract:Summary The induction of mitotic gene conversion and crossing-over inSaccharomyces cerevisiae diploid cells homozygous for thepso4-1 mutation was examined in comparison to the corresponding wild-type strain. Thepso4-1 mutant strain was found to be completely blocked in mitotic recombination induced by photoaddition of mono- and bifunctional psoralen derivatives as well as by mono- (HN1) and bifunctional (HN2) nitrogen mustards or 254 nm UV radiation in both stationary and exponential phases of growth. Concerning the lethal effect, diploids homozygous for thepso4-1 mutation are more sensitive to all agents tested in any growth phase. However, this effect is more pronounced in the G2 phase of the cell cycle. These results imply that the ploidy effect and the resistance of budding cells are under the control of thePSO4 gene. On the other hand, thepso4-1 mutant is mutationally defective for all agents used. Therefore, thepso4-1 mutant has a generalized block in both recombination and mutation ability. This indicates that thePSO4 gene is involved in an error-prone repair pathway which relies on a recombinational mechanism, strongly suggesting an analogy between thepso4-1 mutation and theRecA orLexA mutation ofEscherichia coli.
Keywords:pso4-1 mutation   Saccharomyces cerevisiae   Error-prone recombinational repair  Mitotic recombination
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