Patterson M, Sclafani R A, Fangman W L, Rosamond J
Mol Cell Biol. 1986 May;6(5):1590-8. doi: 10.1128/mcb.6.5.1590-1598.1986.
The product of the CDC7 gene of Saccharomyces cerevisiae appears to have multiple roles in cellular physiology. It is required for the initiation of mitotic DNA synthesis. While it is not required for the initiation of meiotic DNA replication, it is necessary for genetic recombination during meiosis and for the formation of ascospores. It has also been implicated in an error-prone DNA repair pathway. Plasmids capable of complementing temperature-sensitive cdc7 mutations were isolated from libraries of yeast genomic DNA in the multicopy plasmid vectors YRp7 and YEp24. The complementing activity was localized within a 3.0-kilobase genomic DNA fragment. Genetic studies that included integration of the genomic insert at or near the CDC7 locus and marker rescue of four cdc7 alleles proved that the cloned fragment contains the yeast chromosomal CDC7 gene. The RNA transcript of CDC7 is about 1,700 nucleotides. Analysis of the nucleotide sequence of a 2.1-kilobase region of the cloned fragment revealed the presence of an open reading frame of 1,521 nucleotides that is presumed to encode the CDC7 protein. Depending on which of two possible ATG codons initiates translation, the calculated size of the CDC7 protein is 58.2 or 56 kilodaltons. Comparison of the predicted amino acid sequence of the CDC7 gene product with other known protein sequences suggests that CDC7 encodes a protein kinase.
酿酒酵母CDC7基因的产物似乎在细胞生理学中具有多种作用。它是有丝分裂DNA合成起始所必需的。虽然减数分裂DNA复制的起始不需要它,但它对于减数分裂期间的基因重组和子囊孢子的形成是必需的。它也与一种易出错的DNA修复途径有关。从多拷贝质粒载体YRp7和YEp24中的酵母基因组DNA文库中分离出了能够互补温度敏感型cdc7突变的质粒。互补活性定位于一个3.0千碱基的基因组DNA片段内。包括将基因组插入片段整合到CDC7基因座或其附近以及对四个cdc7等位基因进行标记拯救的遗传研究证明,克隆片段包含酵母染色体CDC7基因。CDC7的RNA转录本约为1700个核苷酸。对克隆片段2.1千碱基区域的核苷酸序列分析揭示了一个1521个核苷酸的开放阅读框,推测其编码CDC7蛋白。根据两个可能的ATG密码子中的哪一个启动翻译,计算出的CDC7蛋白大小为58.2或56千道尔顿。将CDC7基因产物的预测氨基酸序列与其他已知蛋白质序列进行比较表明,CDC7编码一种蛋白激酶。