Marahrens Y, Stillman B
Cold Spring Harbor Laboratory, NY 11724.
Science. 1992 Feb 14;255(5046):817-23. doi: 10.1126/science.1536007.
Although it has been demonstrated that discrete origins of DNA replication exist in eukaryotic cellular chromosomes, the detailed organization of a eukaryotic cellular origin remains to be determined. Linker substitution mutations were constructed across the entire Saccharomyces cerevisiae chromosomal origin, ARS1. Functional studies of these mutants revealed one essential element (A), which includes a match to the ARS consensus sequence, and three additional elements (B1, B2, and B3), which collectively are also essential for origin function. These four elements arranged exactly as in ARS1, but surrounded by completely unrelated sequence, functioned as an efficient origin. Element B3 is the binding site for the transcription factor-origin binding protein ABF1. Other transcription factor binding sites substitute for the B3 element and a trans-acting transcriptional activation domain is required. The multipartite nature of a chromosomal replication origin and the role of transcriptional activators in its function present a striking similarity to the organization of eukaryotic promoters.
尽管已经证明真核细胞染色体中存在离散的DNA复制起点,但真核细胞起点的详细组织仍有待确定。构建了跨越酿酒酵母染色体起点ARS1的接头置换突变体。对这些突变体的功能研究揭示了一个必需元件(A),其包含与ARS共有序列的匹配,以及另外三个元件(B1、B2和B3),这三个元件共同对于起点功能也是必需的。这四个元件的排列与ARS1完全相同,但被完全不相关的序列包围,却能作为一个有效的起点发挥作用。元件B3是转录因子——起点结合蛋白ABF1的结合位点。其他转录因子结合位点可替代B3元件,并且需要一个反式作用转录激活结构域。染色体复制起点的多部分性质以及转录激活因子在其功能中的作用与真核启动子的组织呈现出惊人的相似性。