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c-myc复制起点的多个起始事件与染色体位置无关。

Multiple initiations in the c-myc replication origin independent of chromosomal location.

作者信息

Trivedi A, Waltz S E, Kamath S, Leffak M

机构信息

Department of Biochemistry and Molecular Biology, Wright State University, Dayton, OH 45435, USA.

出版信息

DNA Cell Biol. 1998 Oct;17(10):885-96. doi: 10.1089/dna.1998.17.885.

DOI:10.1089/dna.1998.17.885
PMID:9809750
Abstract

At supramolecular resolution, DNA synthesis begins at preferred replication origins in the chromosomes of metazoan cells. To characterize one of these origins in detail, the initiation of replication was examined in the HeLa c-myc origin. Polymerase chain reaction (PCR) amplification of size-fractionated nascent chromosomal DNAs revealed multiple replication initiation sites over a 12-kb region spanning the c-myc origin, including the transcribed region and the 5' and 3' flanking DNA of the gene. Two of the start sites for chromosomal replication occurred inside a 2.4-kb region of the origin that exhibits autonomously replicating sequence (ARS) activity. When a plasmid containing the 2.4-kb ARS region was transfected into HeLa cells, PCR mapping of nascent plasmid DNA confirmed that the plasmid replicated semiconservatively and autonomously and that replication did not initiate at random sites but rather began at multiple sites in a limited zone overlapping the c-myc DNA insert. Within the resolution of the PCR assay, the same sites that were used in the chromosomal c-myc origin were used in the 2.4-kb ARS fragment. The locations of replication start sites determined by PCR are considered in the context of other functional and structural elements of the c-myc origin.

摘要

在超分子分辨率下,DNA合成始于后生动物细胞染色体中优先选择的复制起点。为了详细表征其中一个这样的起点,我们在HeLa细胞的c-myc起点处研究了复制起始情况。对大小分级的新生染色体DNA进行聚合酶链反应(PCR)扩增,结果显示在跨越c-myc起点的12kb区域内有多个复制起始位点,包括该基因的转录区域以及基因的5'和3'侧翼DNA。染色体复制的两个起始位点位于该起点的一个2.4kb区域内,该区域具有自主复制序列(ARS)活性。当将含有2.4kb ARS区域的质粒转染到HeLa细胞中时,对新生质粒DNA进行PCR定位证实该质粒进行半保留自主复制,并且复制并非在随机位点起始,而是在与c-myc DNA插入片段重叠的有限区域内的多个位点起始。在PCR检测的分辨率范围内,染色体c-myc起点中使用的相同位点也在2.4kb ARS片段中被使用。我们结合c-myc起点的其他功能和结构元件来考虑通过PCR确定的复制起始位点的位置。

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