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一种与酵母DNA复制基因的Mlu I细胞周期盒结合的因子的鉴定与纯化。

Identification and purification of a factor that binds to the Mlu I cell cycle box of yeast DNA replication genes.

作者信息

Verma R, Patapoutian A, Gordon C B, Campbell J L

机构信息

Braun Laboratories, California Institute of Technology, Pasaden 91125.

出版信息

Proc Natl Acad Sci U S A. 1991 Aug 15;88(16):7155-9. doi: 10.1073/pnas.88.16.7155.

Abstract

In Saccharomyces cerevisiae, the genes encoding at least 10 enzymes involved in DNA replication are periodically expressed in the late G1 and S phases of the cell cycle. All of these genes have one copy or more of the sequence ACGCGT, which conforms to the recognition site for the Mlu I restriction endonuclease. For the CDC21, CDC9, and POL1 genes, the Mlu I site has been shown to be absolutely required for periodic transcription. Using nuclear extracts fractionated by conventional and oligonucleotide affinity chromatography, we have purified a 17-kDa protein that recognizes the Mlu I motif. Synthetic oligonucleotides containing mutated Mlu I sites do not bind the protein. In contrast, synthetic oligonucleotides derived from the CDC2, CDC6, and CDC21 genes, which are expressed with the same timing as POL1, bind purified protein efficiently.

摘要

在酿酒酵母中,编码至少10种参与DNA复制的酶的基因在细胞周期的G1晚期和S期周期性表达。所有这些基因都有一个或多个ACGCGT序列,该序列符合Mlu I限制性内切酶的识别位点。对于CDC21、CDC9和POL1基因,已证明Mlu I位点是周期性转录绝对必需的。利用通过常规和寡核苷酸亲和色谱分级分离的核提取物,我们纯化了一种识别Mlu I基序的17 kDa蛋白质。含有突变Mlu I位点的合成寡核苷酸不与该蛋白质结合。相反,源自与POL1同时表达的CDC2、CDC6和CDC21基因的合成寡核苷酸能有效地结合纯化的蛋白质。

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