Catlett Michael G, Forsburg Susan L
Molecular & Cell Biology Laboratory, The Salk Institute, La Jolla, California 92037, USA.
Mol Biol Cell. 2003 Nov;14(11):4707-20. doi: 10.1091/mbc.e03-05-0288. Epub 2003 Aug 7.
We report the characterization of rdh54+, the second fission yeast Schizosaccharomyces pombe Rad54 homolog. rdh54+ shares sequence and functional homology to budding yeast RDH54/TID1. Rdh54p is present during meiosis with appropriate timing for a meiotic recombination factor. It interacts with Rhp51 and the meiotic Rhp51 homolog Dmc1 in yeast two-hybrid assays. Deletion of rdh54+ has no effect on DNA damage repair during the haploid vegetative cell cycle. In meiosis, however, rdh54Delta shows decreased spore viability and homologous recombination with a concomitant increase in sister chromatid exchange. The rdh54Delta single mutant repairs meiotic breaks with similar timing to wild type, suggesting redundancy of meiotic recombination factors. Consistent with this, the rdh54Delta rhp54Delta double mutant fails to repair meiotic double strand breaks. Live cell analysis shows that rdh54Delta rhp54Delta asci do not arrest, but undergo both meiotic divisions with near normal timing, suggesting that failure to repair double strand breaks in S. pombe meiosis does not result in checkpoint arrest.
我们报道了粟酒裂殖酵母(Schizosaccharomyces pombe)中第二个Rad54同源物rdh54+的特性。rdh54+与芽殖酵母RDH54/TID1具有序列和功能同源性。Rdh54p在减数分裂过程中适时出现,作为一个减数分裂重组因子。在酵母双杂交实验中,它与Rhp51以及减数分裂的Rhp51同源物Dmc1相互作用。缺失rdh54+对单倍体营养细胞周期中的DNA损伤修复没有影响。然而,在减数分裂中,rdh54Δ显示出孢子活力下降以及同源重组减少,同时姐妹染色单体交换增加。rdh54Δ单突变体修复减数分裂双链断裂的时间与野生型相似,这表明减数分裂重组因子存在冗余。与此一致的是,rdh54Δ rhp54Δ双突变体无法修复减数分裂双链断裂。活细胞分析表明,rdh54Δ rhp54Δ的子囊不会停滞,而是以接近正常的时间进行两次减数分裂,这表明粟酒裂殖酵母减数分裂中双链断裂未能修复不会导致检查点停滞。