IDENTIFICATION AND CHARACTERIZATION OF NEW ELEMENTS INVOLVED IN CHECKPOINT AND FEEDBACK CONTROLS IN FISSION YEAST

Citation
F. Alkhodairy et al., IDENTIFICATION AND CHARACTERIZATION OF NEW ELEMENTS INVOLVED IN CHECKPOINT AND FEEDBACK CONTROLS IN FISSION YEAST, Molecular biology of the cell, 5(2), 1994, pp. 147-160
Citations number
30
Categorie Soggetti
Cytology & Histology",Biology
ISSN journal
10591524
Volume
5
Issue
2
Year of publication
1994
Pages
147 - 160
Database
ISI
SICI code
1059-1524(1994)5:2<147:IACONE>2.0.ZU;2-2
Abstract
To investigate the mechanisms that ensure the dependency relationships between cell cycle events and to investigate the checkpoints that pre vent progression through the cell cycle after DNA damage, we have isol ated mutants defective in the checkpoint and feedback control pathways . We report the isolation and characterization of 11 new loci that def ine distinct classes of mutants defective in one or more of the checkp oint and feedback control pathways. Two mutants, rad26.T12 and rad27.T 15, were selected for molecular analysis. The null allele of the rad26 gene (rad26.d) shares the phenotype reported for the ''checkpoint rad '' mutants rad1, rad3, rad9, rad17, and hus1, which are defective in t he radiation checkpoint and in the feedback controls that ensure the o rder of cell cycle events. The null allele of the rad27 gene (rad27.d) defines a new class of Schizosaccharomyces pombe mutant. The rad27 co mplementing gene codes for a putative protein kinase that is required for cell cycle arrest after DNA damage but not for the feedback contro l that links mitosis to the completion of prior DNA synthesis (the sam e gene has recently been described by Walworth et al. (1993) as chk1). These properties are similar to those of the rad9 gene of Saccharomyc es cerevisiae. A comparative analysis of the radiation responses in ra d26.d, rad26.T12, and rad27.d cells has revealed the existence of two separable responses to DNA damage controlled by the ''checkpoint rad'' genes. The first, G2 arrest, is defective in rad27.d and rad26.d but is unaffected in rad26.T12 cells. The second response is not associate d with G2 arrest after DNA damage and is defective in rad26.d and rad2 6.T12 but not rad27.d cells. A study of the radiation sensitivity of t hese mutants through the cell cycle suggests that this second response is associated with S phase and that the checkpoint rad mutants, in ad dition to an inability to arrest mitosis after radiation, are defectiv e in an S phase radiation checkpoint.