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Differentially Active Origins of DNA Replication in Tumor versus Normal Cells

Domenic Di Paola^1,2, Gerald B. Price^1, and Maria Zannis-Hadjopoulos^1,2

¹ McGill Cancer Center and ² Department of Biochemistry, McGill University, Montreal, Quebec, Canada

Requests for reprints: Maria Zannis-Hadjopoulos, McGill Cancer Center, 3655 Promenade Sir William Osler, Room 710, Montreal, Quebec, Canada H3G 1Y6. Phone: 514-398-3536; Fax: 514-398-6769; E-mail: maria.zannis{at}mcgill.ca.

Previously, a degenerate 36 bp human consensus sequence was identified as a determinant of autonomous replication in eukaryotic cells. Random mutagenesis analyses further identified an internal 20 bp of the 36 bp consensus sequence as sufficient for acting as a core origin element. Here, we have located six versions of the 20 bp consensus sequence (20mer) on human chromosome 19q13 over a region spanning 211 kb and tested them for ectopic and in situ replication activity by transient episomal replication assays and nascent DNA strand abundance analyses, respectively. The six versions of the 20mer alone were capable of supporting autonomous replication of their respective plasmids, unlike random genomic sequence of the same length. Furthermore, comparative analyses of the endogenous replication activity of these 20mers at their respective chromosomal sites, in five tumor/transformed and two normal cell lines, done by in situ chromosomal DNA replication assays, involving preparation of nascent DNA by the exonuclease method and quantification by real-time PCR, showed that these sites coincided with chromosomal origins of DNA replication in all cell lines. Moreover, a 2- to 3-fold higher origin activity in the tumor/transformed cells by comparison to the normal cells was observed, suggesting a higher activation of these origins in tumor/transformed cell lines. (Cancer Res 2006; 66(10): 5094-103)