Burhans W C, Vassilev L T, Caddle M S, Heintz N H, DePamphilis M L
Department of Cell and Developmental Biology, Roche Institute of Molecular Biology, Nutley, New Jersey 07110.
Cell. 1990 Sep 7;62(5):955-65. doi: 10.1016/0092-8674(90)90270-o.
Mechanistically, an origin of bidirectional DNA replication (OBR) can be defined by the transition from discontinuous to continuous DNA synthesis that must occur on each template strand at the site where replication forks originate. This results from synthesis of Okazaki fragments predominantly on the retrograde arms of forks. We have identified these transitions at a specific site within a 0.45 kb sequence approximately 17 kb downstream from the 3' end of the dihydrofolate reductase gene in Chinese hamster ovary chromosomes. At least 80% of the replication forks in a 27 kb region emanated from this OBR. Thus, initiation of DNA replication in mammalian chromosomes uses the same replication fork mechanism previously described in a variety of prokaryotic and eukaryotic genomes, suggesting that mammalian chromosomes also utilize specific cis-acting sequences as origins of DNA replication.
从机制上讲,双向DNA复制起点(OBR)可通过从不连续到连续的DNA合成转变来定义,这种转变必定发生在复制叉起始位点的每条模板链上。这是由于冈崎片段主要在复制叉的逆行臂上合成所致。我们在中国仓鼠卵巢染色体中二氢叶酸还原酶基因3'端下游约17 kb处的一个0.45 kb序列内的特定位点鉴定到了这些转变。在一个27 kb区域中,至少80%的复制叉源自这个OBR。因此,哺乳动物染色体中DNA复制的起始采用了先前在各种原核和真核基因组中描述的相同复制叉机制,这表明哺乳动物染色体也利用特定的顺式作用序列作为DNA复制起点。