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Meiotic induction of the yeast HOP1 gene is controlled by positive and negative regulatory sites.

机译:酵母HOP1基因的减数分裂诱导受阳性和阴性调节位点控制。

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摘要

The process of meiosis and sporulation in the yeast Saccharomyces cerevisiae is a highly regulated developmental pathway dependent on genetic as well as nutritional signals. The HOP1 gene, which encodes a component of meiotic chromosomes, is not expressed in mitotically growing cells, but its transcription is induced shortly after yeast cells enter the meiotic pathway. Through a series of deletions and mutations in the HOP1 promoter, we located two regulatory sites that are essential for proper regulation of HOP1. One site, called URS1H, brings about repression of HOP1 in mitotic cells and functions as an activator sequence in cells undergoing meiosis. The second site, which we designated UASH, acts as an activator sequence in meiotic cells and has similarity to the binding site of the mammalian CCAAT/enhancer binding protein (C/EBP). Both sites are required for full meiotic induction of the HOP1 promoter. We conclude that in mitotic yeast cells, the URS1H site maintains the repressed state of the HOP1 promoter, masking the effect of the UASH site. Upon entry into meiosis, repression is lifted, allowing the URS1H and UASH sites to activate high-level transcription.
机译:酵母酿酒酵母中的减数分裂和孢子形成过程是依赖基因和营养信号的高度调控的发育途径。编码减数分裂染色体组成部分的HOP1基因在有丝分裂生长的细胞中不表达,但在酵母细胞进入减数分裂途径后不久就诱导了其转录。通过在HOP1启动子中的一系列缺失和突变,我们找到了两个调节位点,这些位点对于正确调节HOP1是必不可少的。一个位点称为URS1H,可在有丝分裂细胞中抑制HOP1,并在减数分裂的细胞中起激活序列的作用。第二个位点,我们称为UASH,在减数分裂细胞中起激活序列的作用,与哺乳动物CCAAT /增强子结合蛋白(C / EBP)的结合位点相似。这两个位点对于HOP1启动子的完全减数分裂诱导都是必需的。我们得出结论,在有丝分裂酵母细胞中,URS1H位点保持HOP1启动子的受阻状态,掩盖了UASH位点的作用。进入减数分裂后,抑制被解除,允许URS1H和UASH位点激活高水平转录。

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