Takahashi Tatsuro, Ohara Eri, Nishitani Hideo, Masukata Hisao
Department of Biology, Graduate School of Science, Osaka University, 1-1 Machikaneyama-cho, Toyonaka, Osaka 560-0043, Japan.
EMBO J. 2003 Feb 17;22(4):964-74. doi: 10.1093/emboj/cdg079.
In most eukaryotes, replication origins are composed of long chromosome regions, and the exact sequences required for origin recognition complex (ORC) and minichromosome maintenance (MCM) complex association remain elusive. Here, we show that two stretches of adenine/thymine residues are collectively essential for a fission yeast chromosomal origin. Chromatin immunoprecipitation assays revealed that the ORC subunits are located within a 1 kb region of ori2004. Analyses of deletion derivatives of ori2004 showed that adenine stretches are required for ORC binding in vivo. Synergistic interaction between ORC and adenine stretches was observed. On the other hand, MCM subunits were localized preferentially to a region near the initiation site, which is distant from adenine stretches. This association was dependent on adenine stretches and stimulated by a non-adenine element. Our results suggest that association of multiple ORC molecules with a replication origin is required for efficient MCM loading and origin firing in fission yeast.
在大多数真核生物中,复制起点由长染色体区域组成,而起始识别复合物(ORC)和微小染色体维持(MCM)复合物结合所需的精确序列仍不清楚。在此,我们表明两段腺嘌呤/胸腺嘧啶残基对于裂殖酵母染色体起点来说共同至关重要。染色质免疫沉淀分析显示,ORC亚基位于ori2004的1 kb区域内。对ori2004缺失衍生物的分析表明,腺嘌呤延伸序列是体内ORC结合所必需的。观察到ORC与腺嘌呤延伸序列之间存在协同相互作用。另一方面,MCM亚基优先定位于起始位点附近的一个区域,该区域与腺嘌呤延伸序列相距较远。这种结合依赖于腺嘌呤延伸序列,并受到一个非腺嘌呤元件的刺激。我们的结果表明,多个ORC分子与复制起点的结合是裂殖酵母中高效加载MCM和起始起点激活所必需的。