Brylawski B P, Cohen S M, Cordeiro-Stone M, Schell M J, Kaufman D G
Department of Pathology and Laboratory Medicine, University of North Carolina, Chapel Hill 27599-7525, USA.
Crit Rev Eukaryot Gene Expr. 2000;10(1):91-9.
The nuclear matrix is believed to contain sites of assembly of protein complexes that catalyze the initiation of DNA replication as well as DNA elongation. To explore this relationship, DNA replicated by human fibroblasts at the beginning of the S phase was purified and used to construct a cosmid library. Hybridization studies with a subgroup of clones (about one-sixth of the total clones in this library) showed that many of them were highlighted by probes prepared from early replicating DNA, as well as from nuclear matrix-associated DNA. Statistical analysis showed a positive correlation between these hybridization results. We seek to identify origins of replication that are activated early in the S phase of the cell cycle in human cells. Therefore, clones isolated from this library are being analyzed for the presence of structural motifs that have been found in other origins of replication and for potential sites of attachment to the nuclear matrix. This method of analysis is illustrated here using the published sequences for the origins of replication reported for the human lamin B2 and HPRT genes.
核基质被认为包含蛋白质复合物的组装位点,这些蛋白质复合物催化DNA复制的起始以及DNA延伸。为了探究这种关系,在S期开始时由人成纤维细胞复制的DNA被纯化,并用于构建黏粒文库。对一组克隆(该文库中总克隆数的约六分之一)的杂交研究表明,其中许多克隆被从早期复制DNA以及与核基质相关的DNA制备的探针所突出显示。统计分析表明这些杂交结果之间存在正相关。我们试图鉴定在人类细胞周期的S期早期被激活的复制起点。因此,正在分析从该文库中分离的克隆,以寻找在其他复制起点中发现的结构基序以及与核基质潜在的附着位点。这里使用已发表的人类层粘连蛋白B2和次黄嘌呤磷酸核糖转移酶(HPRT)基因复制起点的序列来说明这种分析方法。