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

โœ Scribed by Richard Pelletier; David Mah; Suzanne Landry; Diamanto Matheos; Gerald B. Price; Maria Zannis-Hadjopoulos


Publisher
John Wiley and Sons
Year
1997
Tongue
English
Weight
330 KB
Volume
66
Category
Article
ISSN
0730-2312

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โœฆ Synopsis


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 DpnI 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.


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Ors12, a mammalian autonomously replicating sequence (812 bp), was previously isolated by extrusion of African green monkey (CV-1 cells) nascent DNA from active replication bubbles. It contains a region of โฃ-satellite extending 168-bp from the 5ะˆ-end, and a nonrepetitive portion extending from nucle