Affiliation:
1. Department of Biochemistry1 and
2. Department of Molecular and Medical Genetics,2 University of Toronto, Toronto, Ontario, Canada M5S 1A8
Abstract
ABSTRACT
Distinct classes of sporulation-specific genes are sequentially expressed during the process of spore formation in
Saccharomyces cerevisiae
. The transition from expression of early meiotic genes to expression of middle sporulation-specific genes occurs at about the time that cells exit from pachytene and form the meiosis I spindle. To identify genes encoding potential regulators of middle sporulation-specific gene expression, we screened for mutants that expressed early meiotic genes but failed to express middle sporulation-specific genes. We identified mutant alleles of
RPD3
,
SIN3
, and
NDT80
in this screen. Rpd3p, a histone deacetylase, and Sin3p are global modulators of gene expression. Ndt80p promotes entry into the meiotic divisions. We found that entry into the meiotic divisions was not required for activation of middle sporulation genes; these genes were efficiently expressed in a
clb1 clb3 clb4
strain, which fails to enter the meiotic divisions due to reduced Clb-dependent activation of Cdc28p kinase. In contrast, middle sporulation genes were not expressed in a
dmc1
strain, which fails to enter the meiotic divisions because a defect in meiotic recombination leads to a
RAD17
-dependent checkpoint arrest. Expression of middle sporulation genes, as well as entry into the meiotic divisions, was restored to a
dmc1
strain by mutation of
RAD17
. Our studies also revealed that
NDT80
was a temporally distinct, pre-middle sporulation gene and that its expression was reduced, but not abolished, on mutation of
DMC1
,
RPD3
,
SIN3
, or
NDT80
itself. In summary, our data indicate that Ndt80p is required for expression of middle sporulation genes and that the activity of Ndt80p is controlled by the meiotic recombination checkpoint. Thus, middle genes are expressed only on completion of meiotic recombination and subsequent generation of an active form of Ndt80p.
Publisher
American Society for Microbiology
Subject
Cell Biology,Molecular Biology
Cited by
144 articles.
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