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对ors12进行缺失分析,ors12是一种着丝粒的、早期激活的哺乳动物DNA复制起点。

Deletion analysis of ors12, a centromeric, early activated, mammalian origin of DNA replication.

作者信息

Pelletier R, Mah D, Landry S, Matheos D, Price G B, Zannis-Hadjopoulos M

机构信息

McGill Cancer Centre, McGill University, Montréal, Québec, Canada.

出版信息

J Cell Biochem. 1997 Jul 1;66(1):87-97.

PMID:9215531
Abstract

We have generated a panel of deletion mutants of ors12 (812-bp), a mammalian origin of DNA replication previously isolated by nascent strand extrusion from early replicating African Green monkey (CV-1) DNA. The deletion mutants were tested for their replication activity in vivo by the bromodeoxyuridine substitution assay, after transfection into HeLa cells, and in vitro by the Dpnl resistance assay, using extracts from HeLa cells. We identified a 215-bp internal fragment as essential for the autonomous replication activity of ors12. When subcloned into the vector pML2 and similarly tested, this subfragment was capable of autonomous replication in vivo and in vitro. Several repeated sequence motifs are present in this 215-bp fragment, such as TGGG(A) and G(A)AG (repeated four times each); TTTC, AGG, and CTTA (repeated 3 times each); the motifs CACACA and CTCTCT, and two imperfect inverted repeats. 22 and 16 bp long, respectively. The overall sequence of the 215-bp fragment is G/C-rich (50.2%), by comparison to the 186-bp (33.5% G/C-rich) minimal sequence required for the autonomous replication activity of ors8, another functional ors that was similarly isolated and characterized.

摘要

我们构建了一组ors12(812碱基对)的缺失突变体,ors12是先前通过新生链挤出法从早期复制的非洲绿猴(CV-1)DNA中分离出的哺乳动物DNA复制起点。将这些缺失突变体转染到HeLa细胞后,通过溴脱氧尿苷替代试验在体内测试其复制活性,并使用HeLa细胞提取物通过DpnI抗性试验在体外进行测试。我们鉴定出一个215碱基对的内部片段对ors12的自主复制活性至关重要。当亚克隆到载体pML2中并进行类似测试时,该亚片段能够在体内和体外自主复制。在这个215碱基对的片段中存在几个重复序列基序,例如TGGG(A)和G(A)AG(各重复四次);TTTC、AGG和CTTA(各重复三次);基序CACACA和CTCTCT,以及两个分别长22和16碱基对的不完全反向重复序列。与ors8(另一个通过类似方法分离和表征的功能性ors)自主复制活性所需的186碱基对(富含33.5%的G/C)最小序列相比,这个215碱基对片段的总体序列富含G/C(50.2%)。

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