Johnston L H, Johnson A L
Division of Yeast Genetics, National Institute for Medical Research, London, UK.
Nucleic Acids Res. 1995 Jun 25;23(12):2147-52. doi: 10.1093/nar/23.12.2147.
The DNA repair genes RAD54 and UNG1 have MCB elements in their promoters and are shown to be cell cycle regulated. Their transcripts are coordinately expressed with RNR1, ribonucleotide reductase, a MCB-regulated gene known to be expressed in late G1. However, no evidence was obtained for a direct role of MCB elements in DNA repair. Of the proteins that bind and activate MCB elements, only mutations in SWI6 have a defect in DNA repair, showing significant sensitivity to methyl methane sulphonate. Furthermore, analysis of the CDC9 promoter indicates that MCB elements are not required for the induction of the gene by ultraviolet light irradiation. These promoter elements may not respond directly to DNA damage but may have a role in enhancing the induction response.
DNA修复基因RAD54和UNG1在其启动子中有MCB元件,并且已证明受细胞周期调控。它们的转录本与核糖核苷酸还原酶RNR1协同表达,RNR1是一个已知在G1晚期表达的受MCB调控的基因。然而,没有获得MCB元件在DNA修复中直接作用的证据。在结合并激活MCB元件的蛋白质中,只有SWI6中的突变在DNA修复中有缺陷,对甲基磺酸甲酯表现出显著的敏感性。此外,对CDC9启动子的分析表明,紫外线照射诱导该基因并不需要MCB元件。这些启动子元件可能不直接对DNA损伤作出反应,但可能在增强诱导反应中起作用。