Hepworth S R, Friesen H, Segall J
Department of Biochemistry, University of Toronto, Toronto, Ontario, Canada M5S 1A8.
Mol Cell Biol. 1998 Oct;18(10):5750-61. doi: 10.1128/MCB.18.10.5750.
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.
在酿酒酵母的孢子形成过程中,不同类别的孢子形成特异性基因会被顺序表达。从早期减数分裂基因的表达过渡到中期孢子形成特异性基因的表达,大约发生在细胞离开粗线期并形成减数分裂I纺锤体的时候。为了鉴定编码中期孢子形成特异性基因表达潜在调节因子的基因,我们筛选了那些表达早期减数分裂基因但未能表达中期孢子形成特异性基因的突变体。在这个筛选过程中,我们鉴定出了RPD3、SIN3和NDT80的突变等位基因。Rpd3p是一种组蛋白去乙酰化酶,Sin3p是基因表达的全局调节因子。Ndt80p促进进入减数分裂。我们发现,进入减数分裂对于中期孢子形成基因的激活并非必需;这些基因在clb1 clb3 clb4菌株中能有效表达,该菌株由于Cdc28p激酶的Clb依赖性激活降低而无法进入减数分裂。相比之下,中期孢子形成基因在dmc1菌株中不表达,该菌株由于减数分裂重组缺陷导致RAD17依赖性检查点停滞而无法进入减数分裂。通过RAD17突变,dmc1菌株恢复了中期孢子形成基因的表达以及进入减数分裂的能力。我们的研究还表明,NDT80是一个时间上不同的、孢子形成前期的基因,并且在DMC1、RPD3、SIN3或NDT80自身发生突变时,其表达会降低但不会被消除。总之,我们的数据表明Ndt80p是中期孢子形成基因表达所必需的,并且Ndt80p的活性受减数分裂重组检查点的控制。因此,只有在减数分裂重组完成并随后产生活性形式的Ndt80p后,中期基因才会表达。