Vlcek D, Slivková A, Podstavková S, Miadoková E
Department of Genetics, Faculty of Science, Comenius University, Bratislava, Slovak Republic.
Mutat Res. 1997 Dec;385(3):243-9. doi: 10.1016/s0921-8777(97)00052-9.
In this report, three DNA repair-deficient mutants of Chlamydomonas reinhardtii (uvs13, uvs14, uvs15) were characterized by using genetic, mutational and biochemical analyses. The mutant strain uvs15 belongs to the most sensitive repair-deficient mutants following exposure to all agents used. It is deficient in the nuclear excision-repair pathway, whereas uvs13 and uvs14 are not blocked in removal of pyrimidine dimers. Mutation study also revealed differences among strains. The mutant uvs15 does not mutate after UV and X-ray irradiation, and there is very low mutation rate after MNNG. These findings might indicate the involvement of UVS15 gene product in regulation of several repair pathways. Contrary to this, uvs14 showed higher mutation frequency, both spontaneous and induced after UV and MNNG treatments. Tetrad dissection proved that the uvs13 and uvs14 genes are located on the right arm of the linkage group I in the vicinity of the previously mapped uvs10 gene. Both mutants belong to the same repair pathway, which is different from that of uvs10 and uvs15.
在本报告中,通过遗传、突变和生化分析对莱茵衣藻的三个DNA修复缺陷型突变体(uvs13、uvs14、uvs15)进行了表征。突变菌株uvs15属于暴露于所有使用的试剂后最敏感的修复缺陷型突变体。它在核切除修复途径中存在缺陷,而uvs13和uvs14在嘧啶二聚体的去除方面没有受阻。突变研究还揭示了菌株之间的差异。突变体uvs15在紫外线和X射线照射后不会发生突变,在MNNG处理后的突变率非常低。这些发现可能表明UVS15基因产物参与了多种修复途径的调控。与此相反,uvs14在紫外线和MNNG处理后,自发和诱导的突变频率都更高。四分体分析证明,uvs13和uvs14基因位于连锁群I的右臂上,靠近先前定位的uvs10基因。这两个突变体属于相同的修复途径,与uvs10和uvs15的修复途径不同。