Kramer W, Fartmann B, Ringbeck E C
Institut für Molekulare Genetik, Georg-August-Universität, Göttingen, Germany.
Mol Gen Genet. 1996 Sep 13;252(3):275-83. doi: 10.1007/BF02173773.
Transcription of the Saccharomyces cerevisiae DNA mismatch repair genes PMS1, MSH2, and MSH6, a recently discovered homolog of the Escherichia coli mutS gene, was shown to be cell cycle regulated. In contrast, transcription of the MSH1, MSH3 and MLH1 genes was not regulated during the cell cycle. The MSH1 gene, which is thought to be involved in DNA mismatch repair in mitochondria, was also not induced under aerobic growth conditions. Regulation of the PMS1 gene was dependent on intact MluI cell cycle boxes, as demonstrated by analysis of a promoter mutant. Both reduced and increased expression of PMS1 resulted in a mitotic mutator phenotype. Analysis of mRNA levels was performed with a newly developed reverse transcription-PCR (polymerase chain reaction) approach using fluorescently labeled primers and an automated DNA sequencer for detection of PCR products.
酿酒酵母DNA错配修复基因PMS1、MSH2和MSH6(最近发现的大肠杆菌mutS基因的一个同源物)的转录显示受细胞周期调控。相比之下,MSH1、MSH3和MLH1基因的转录在细胞周期中不受调控。据认为参与线粒体DNA错配修复的MSH1基因在有氧生长条件下也未被诱导。如对一个启动子突变体的分析所示,PMS1基因的调控依赖于完整的MluI细胞周期框。PMS1表达的降低和增加均导致有丝分裂突变体表型。使用荧光标记引物和用于检测PCR产物的自动DNA测序仪,通过新开发的逆转录PCR(聚合酶链反应)方法对mRNA水平进行了分析。