首页> 美国卫生研究院文献>Proceedings of the National Academy of Sciences of the United States of America >A cell cycle-responsive transcriptional control element and a negative control element in the gene encoding DNA polymerase alpha in Saccharomyces cerevisiae.
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A cell cycle-responsive transcriptional control element and a negative control element in the gene encoding DNA polymerase alpha in Saccharomyces cerevisiae.

机译:酿酒酵母中编码DNA聚合酶α的基因中的细胞周期响应转录控制元件和阴性控制元件。

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摘要

Transcription of the POL1 gene of Saccharomyces cerevisiae, which encodes DNA polymerase alpha, the DNA polymerase required for the initiation of DNA replication, has previously been shown to be cell cycle regulated. To understand how the POL1 gene senses cell cycle position, we have investigated the cis-acting elements that respond to the factors that govern cell cycle progression. In this report we demonstrate that a region of 54 nucleotides containing the repeated element ACGCGT, which conforms to an Mlu I restriction endonuclease recognition site, contains all information necessary for transcriptional activation and cell cycle responsiveness. Although oligonucleotides lacking either one or both of the repeated Mlu I sites can function as an upstream activating sequence, the presence of at least one Mlu I site stimulates expression and, moreover, is absolutely essential for cell cycle regulation. A synthetic oligonucleotide corresponding to a 19-base-pair sequence in the POL1 promoter containing one Mlu I site can function as an autonomous cell cycle-responsive upstream element (upstream activation sequence) with temporal regulation indistinguishable from that previously described for the POL1 gene. Thus, the Mlu I site is an essential part of a cis-acting element responsible for the observed periodic activation. This sequence differs from previously defined cell cycle-responsive transcriptional control elements in the yeast HO endonuclease and histone genes. We also present evidence for a negative regulatory element in the 5' flanking region of the Mlu I upstream activation sequence.
机译:酿酒酵母的POL1基因的转录,其编码DNA聚合酶α(DNA复制起始所需的DNA聚合酶),以前已被证明是受细胞周期调节的。为了了解POL1基因如何感测细胞周期位置,我们研究了对控制细胞周期进程的因素有反应的顺式作用元件。在此报告中,我们证明了一个包含重复元素ACGCGT的54个核苷酸的区域,该区域符合Mlu I限制性核酸内切酶识别位点,包含转录激活和细胞周期响应性所需的所有信息。尽管缺少一个或两个重复的Mlu I位点的寡核苷酸可以起上游激活序列的作用,但是至少一个Mlu I位点的存在刺激了表达,此外,对于细胞周期调控绝对必要。对应于含有一个Mlu I位点的POL1启动子中的19个碱基对序列的合成寡核苷酸可作为自主细胞周期响应性上游元件(上游激活序列),其时间调控与先前针对POL1基因所述的调控没有区别。因此,Mlu I位点是负责观察到的周期性激活的顺式作用元件的重要组成部分。该序列不同于酵母HO核酸内切酶和组蛋白基因中先前定义的细胞周期响应转录控制元件。我们还提供证据表明在Mlu I上游激活序列的5'侧翼区域中存在负调控元件。

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