Methods to replicate DNA in vitro using PRD1-catalyzed DNA repli

Chemistry: molecular biology and microbiology – Measuring or testing process involving enzymes or... – Involving nucleic acid

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435 911, 435 912, 4351721, 536 231, 536 241, 935 1, 935 16, 935 17, C12Q 168, C12P 1934, C07H 1700, C12N 1500

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053895312

ABSTRACT:
This invention relates to artificial DNAs which are useful in the fields of genetic engineering and medical science and to a method for DNA replication using said DNAs as the replication origin. In one embodiment, this invention provides single- or double-stranded, artificial DNAs having, at the 3' end, a DNA sequence represented by the following general formula:

REFERENCES:
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Savilahti et al., Gene 57 (1987) 121-130.
Yoo et al. J. Mol. Biol. 218: 779-789 '91 (Mar. 20, 1991).
Tamanoi et al. P.N.A.S. 80: 6446-6450 '83.
"Protein-Primed Replication of Bacteriophage PRD1 Genomie in Vitro", by Seung-Ku Yoo and Junetsu Ito, 170 Virology, pp. 442-449 (1989).
"Bacteriophage PRD1 DNA polymerase: Evolution of DNA polymerases", by Guhung Jung, Mark C. Leavitt, Jui-Cheng Hsieh, and Junetsu Ito, 84 Proc. Nat. Acad. Sci., U.S.A., pp. 8287-8291 (1987).
"Primary Structure of the DNA terminal protein of bacteriophage PRD1", by Jui-Cheng Hsieh, Guhung Jung, Mark C. Leavitt, and Junetsu Ito, 15 Nucl. Acids. Res., pp. 8999-9009.
"The complete nucleotide sequence of the left very early region of Escherichia coli bacteriophage PRD1 coding for the terminal protein and the DNA polymerase", 57 Gene, pp. 121-130 (1987).
"Molecular Cloning of Bacteriophage PRD1 Genomic Fragments", Mol. Gen. Genet., pp. 233-236 (1983).

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