Vassilev L, Russev G
Biochim Biophys Acta. 1984 Feb 24;781(1-2):39-44. doi: 10.1016/0167-4781(84)90121-0.
The ability of EAT cells to initiate DNA synthesis in the presence of high doses of hydroxyurea was examined using the recently developed method for crosslinking DNA in vivo. Since crosslinking blocks elongation but has little effect on initiation (Russev and Vassilev (1982) J. Mol. Biol. 161, 77-87), this approach permits a separate study of the two stages of the DNA replication. We found out that hydroxyurea did not greatly affect the initiation of DNA replication but strongly inhibited the elongation of the already initiated new DNA chains. This resulted in the formation of short fragments enriched in sequences synthesized at and around the sites where DNA initiation began. These fragments were not ligated to the high molecular weight chromosomal DNA and could be released under denaturing conditions in single-stranded form. The reassociation and electrophoretic analysis showed that they contained about 200 nucleotides long interspersed DNA sequences repeated approx. 10(4) times per haploid genome, that probably served as replication origins.
使用最近开发的体内DNA交联方法,检测了EAT细胞在高剂量羟基脲存在下启动DNA合成的能力。由于交联会阻断延伸,但对起始作用影响很小(Russev和Vassilev(1982年)《分子生物学杂志》161卷,77 - 87页),这种方法允许对DNA复制的两个阶段进行单独研究。我们发现羟基脲对DNA复制的起始没有很大影响,但强烈抑制已起始的新DNA链的延伸。这导致形成了富含在DNA起始位点及周围合成的序列的短片段。这些片段没有与高分子量染色体DNA连接,并且在变性条件下可以以单链形式释放。重退火和电泳分析表明,它们包含约200个核苷酸长的散布DNA序列,每个单倍体基因组大约重复10⁴次,这些序列可能充当复制起点。