Andersen Marguerite P, Nelson Zara W, Hetrick Elizabeth D, Gottschling Daniel E
Division of Basic Sciences, Fred Hutchinson Cancer Research Center, Seattle, Washington 98109, USA.
Genetics. 2008 Jul;179(3):1179-95. doi: 10.1534/genetics.108.089250. Epub 2008 Jun 18.
Loss of heterozygosity (LOH) can be a driving force in the evolution of mitotic/somatic diploid cells, and cellular changes that increase the rate of LOH have been proposed to facilitate this process. In the yeast Saccharomyces cerevisiae, spontaneous LOH occurs by a number of mechanisms including chromosome loss and reciprocal and nonreciprocal recombination. We performed a screen in diploid yeast to identify mutants with increased rates of LOH using the collection of homozygous deletion alleles of nonessential genes. Increased LOH was quantified at three loci (MET15, SAM2, and MAT) on three different chromosomes, and the LOH events were analyzed as to whether they were reciprocal or nonreciprocal in nature. Nonreciprocal LOH was further characterized as chromosome loss or truncation, a local mutational event (gene conversion or point mutation), or break-induced replication (BIR). The 61 mutants identified could be divided into several groups, including ones that had locus-specific effects. Mutations in genes involved in DNA replication and chromatin assembly led to LOH predominantly via reciprocal recombination. In contrast, nonreciprocal LOH events with increased chromosome loss largely resulted from mutations in genes implicated in kinetochore function, sister chromatid cohesion, or relatively late steps of DNA recombination. Mutants of genes normally involved in early steps of DNA damage repair and signaling produced nonreciprocal LOH without an increased proportion of chromosome loss. Altogether, this study defines a genetic landscape for the basis of increased LOH and the processes by which it occurs.
杂合性缺失(LOH)可能是有丝分裂/体细胞二倍体细胞进化的驱动力,并且有人提出增加LOH发生率的细胞变化有助于这一过程。在酿酒酵母中,自发的LOH通过多种机制发生,包括染色体丢失以及相互和非相互重组。我们在二倍体酵母中进行了一项筛选,利用非必需基因的纯合缺失等位基因文库来鉴定LOH发生率增加的突变体。在三条不同染色体上的三个位点(MET15、SAM2和MAT)对增加的LOH进行了定量,并分析了LOH事件在本质上是相互的还是非相互的。非相互LOH进一步被表征为染色体丢失或截断、局部突变事件(基因转换或点突变)或断裂诱导复制(BIR)。鉴定出的61个突变体可分为几个组,包括具有位点特异性效应的组。参与DNA复制和染色质组装的基因中的突变主要通过相互重组导致LOH。相比之下,染色体丢失增加的非相互LOH事件主要是由涉及动粒功能、姐妹染色单体黏连或DNA重组相对后期步骤的基因中的突变引起的。通常参与DNA损伤修复和信号传导早期步骤的基因的突变体产生非相互LOH,但染色体丢失比例没有增加。总之,这项研究定义了增加LOH的基础及其发生过程的遗传格局。