Coulon Stéphane, Gaillard Pierre-Henri L, Chahwan Charly, McDonald William Hayes, Yates John R, Russell Paul
Department of Molecular Biology, The Scripps Research Institute, La Jolla, California 92037, USA.
Mol Biol Cell. 2004 Jan;15(1):71-80. doi: 10.1091/mbc.e03-08-0586. Epub 2003 Oct 3.
In most eukaryotes, genes encoding ribosomal RNAs (rDNA) are clustered in long tandem head-to-tail repeats. Studies of Saccharomyces cerevisiae have indicated that rDNA copy number is maintained through recombination events associated with site-specific blockage of replication forks (RFs). Here, we describe two Schizosaccharomyces pombe proteins, homologs of S. cerevisiae Slx1 and Slx4, as subunits of a novel type of endonuclease that maintains rDNA copy number. The Slx1-Slx4-dependent endonuclease introduces single-strand cuts in duplex DNA on the 3' side of junctions with single-strand DNA. Deletion of Slx1 or Rqh1 RecQ-like DNA helicase provokes rDNA contraction, whereas simultaneous elimination of Slx1-Slx4 endonuclease and Rqh1 is lethal. Slx1 associates with chromatin at two foci characteristic of the two rDNA repeat loci in S. pombe. We propose a model in which the Slx1-Slx4 complex is involved in the control of the expansion and contraction of the rDNA loci by initiating recombination events at stalled RFs.
在大多数真核生物中,编码核糖体RNA(rDNA)的基因以长串联头对头重复的形式聚集在一起。对酿酒酵母的研究表明,rDNA拷贝数通过与复制叉(RFs)位点特异性阻断相关的重组事件得以维持。在此,我们描述了粟酒裂殖酵母中的两种蛋白质,它们是酿酒酵母Slx1和Slx4的同源物,作为一种维持rDNA拷贝数的新型核酸内切酶的亚基。依赖Slx1 - Slx4的核酸内切酶在与单链DNA连接的双链DNA的3'侧引入单链切口。缺失Slx1或Rqh1 RecQ样DNA解旋酶会引发rDNA收缩,而同时消除Slx1 - Slx4核酸内切酶和Rqh1则是致命的。Slx1在粟酒裂殖酵母中两个rDNA重复位点特有的两个位点与染色质结合。我们提出了一个模型,其中Slx1 - Slx4复合物通过在停滞的RFs处启动重组事件参与rDNA位点扩增和收缩的控制。