Hawley R S, Marcus C H, Cameron M L, Schwartz R L, Zitron A E
Proc Natl Acad Sci U S A. 1985 Dec;82(23):8095-9. doi: 10.1073/pnas.82.23.8095.
We have examined rDNA magnification in Drosophila melanogaster males carrying one of 11 recombination- or repair-defective mutations representing seven loci. We show that mutations defined by a defect in postreplication repair (mus-101, mei-41, and mus-108) are also defective in rDNA magnification, whereas mutations that do not affect postreplication repair have little or no effect on magnification. mei-41 inhibits only premeiotic magnification events, while mus-108 blocks both premeiotic and meiotic events. This suggests that meiotic and premeiotic events share some but not all functions. A molecular analysis of rDNA magnification reveals that in mus-108 males, changes in the rDNA restriction pattern can occur within one or a few generations under magnifying conditions. We interpret these data in terms of the role of DNA repair systems in rDNA magnification and in terms of stable maintenance of tandemly repeated genes.
我们研究了携带代表七个基因座的11种重组或修复缺陷突变之一的黑腹果蝇雄性个体中的核糖体DNA(rDNA)扩增情况。我们发现,由复制后修复缺陷(mus-101、mei-41和mus-108)所定义的突变在rDNA扩增方面也存在缺陷,而不影响复制后修复的突变对扩增几乎没有影响。mei-41仅抑制减数分裂前的扩增事件,而mus-108则阻断减数分裂前和减数分裂事件。这表明减数分裂和减数分裂前事件有一些共同功能,但并非全部。对rDNA扩增的分子分析表明,在mus-108雄性个体中,在扩增条件下,rDNA限制图谱的变化可在一代或几代内发生。我们从DNA修复系统在rDNA扩增中的作用以及串联重复基因的稳定维持方面来解释这些数据。