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首页> 外文期刊>Molecular and Cellular Biology >Isolation of the gene encoding the Saccharomyces cerevisiae centromere-binding protein CP1.
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Isolation of the gene encoding the Saccharomyces cerevisiae centromere-binding protein CP1.

机译:编码啤酒酵母着丝粒结合蛋白CP1的基因的分离。

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CP1 is a sequence-specific DNA-binding protein of the yeast Saccharomyces cerevisiae which recognizes the highly conserved DNA element I (CDEI) of yeast centromeres. We cloned and sequenced the gene encoding CP1. The gene codes for a protein of molecular weight 39,400. When expressed in Escherichia coli, the CP1 gene directed the synthesis of a CDEI-binding protein having the same gel mobility as purified yeast CP1. We have given the CP1 gene the genetic designation CEP1 (centromere protein 1). CEP1 was mapped and found to reside on chromosome X, 2.0 centimorgans from SUP4. Strains were constructed in which most of CEP1 was deleted. Such strains lacked detectable CP1 activity and were viable; however, CEP1 gene disruption resulted in a 35% increase in cell doubling time and a ninefold increase in the rate of mitotic chromosome loss. An unexpected consequence of CP1 gene disruption was methionine auxotrophy genetically linked to cep1. This result and the recent finding that CDEI sites in the MET25 promoter are required to activate transcription (D. Thomas, H. Cherest, and Y. Surdin-Kerjan, J. Mol. Biol. 9:3292-3298, 1989) suggest that CP1 is both a kinetochore protein and a transcription factor.
机译:CP1是酿酒酵母(Saccharomyces cerevisiae)的序列特异性DNA结合蛋白,可识别酵母着丝粒的高度保守的DNA元素I(CDEI)。我们克隆并测序了编码CP1的基因。该基因编码分子量为39,400的蛋白质。当在大肠杆菌中表达时,CP1基因指导CDEI结合蛋白的合成,该蛋白具有与纯化酵母CP1相同的凝胶迁移率。我们已经给CP1基因指定了基因名称CEP1(着丝粒蛋白1)。映射CEP1,发现其位于X染色体上,即SUP4的2.0厘摩。构建了其中删除了大多数CEP1的菌株。这种菌株缺乏可检测的CP1活性并且是可行的。但是,CEP1基因破坏导致细胞倍增时间增加35%,有丝分裂染色体丢失率增加9倍。 CP1基因破坏的意外结果是与cep1遗传连锁的蛋氨酸营养缺陷型。该结果和最近发现MET25启动子中的CDEI位点是激活转录所必需的(D.Thomas,H.Cherest,和Y.Surdin-Kerjan,J.Mol.Biol.9:3292-3298,1989)表明: CP1既是动粒蛋白又是转录因子。

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