Foss M, McNally F J, Laurenson P, Rine J
Department of Molecular and Cellular Biology, University of California, Berkeley 94720.
Science. 1993 Dec 17;262(5141):1838-44. doi: 10.1126/science.8266071.
In Saccharomyces cerevisiae, the HMR-E silencer blocks site-specific interactions between proteins and their recognition sequences in the vicinity of the silencer. Silencer function is correlated with the firing of an origin of replication at HMR-E. An essential gene with a role in transcriptional silencing was identified by means of a screen for mutations affecting expression of HMR. This gene, known as ORC2, was shown to encode a component of the origin recognition complex that binds yeast origins of replication. A temperature-sensitive mutation in ORC2 disrupted silencing in cells grown at the permissive temperature. At the restrictive temperature, the orc2-1 mutation caused cell cycle arrest at a point in the cell cycle indicative of blocks in DNA replication. The orc2-1 mutation also resulted in the enhanced mitotic loss of a plasmid, suggestive of a defect in replication. These results provide strong evidence for an in vivo role of ORC in both chromosomal replication and silencing, and provide a link between the mechanism of silencing and DNA replication.
在酿酒酵母中,HMR-E沉默子可阻断蛋白质与其在沉默子附近识别序列之间的位点特异性相互作用。沉默子功能与HMR-E处复制起点的激活相关。通过筛选影响HMR表达的突变,鉴定出一个在转录沉默中起作用的必需基因。这个基因名为ORC2,已证明它编码与酵母复制起点结合的起点识别复合物的一个组分。ORC2中的一个温度敏感突变在允许温度下生长的细胞中破坏了沉默。在限制温度下,orc2-1突变导致细胞周期在细胞周期中的一个点停滞,这表明DNA复制受阻。orc2-1突变还导致质粒有丝分裂丢失增加,提示存在复制缺陷。这些结果为ORC在体内参与染色体复制和沉默提供了有力证据,并在沉默机制与DNA复制之间建立了联系。