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Nucleic Acids Research, 1985, Vol. 13, No. 22 8035-8052
© 1985


Articles

Thymine glycols and urea residues in M13 DNA constitute replicative blocks in vitro

Hiroshi Ide, Yoke Wah Kow and Susan S. Wallace

Department of Microbiology and Immunology, New York Medical College Valhalla, NY 10595, USA

Received August 20, 1985. Revised October 14, 1985. Accepted October 14, 1985.

Thymine glycols were produced in M13 DNA in a concentration dependent manner by treating the DNA with osmium tetroxide (OsO4). For the formation of urea-containing M13 DNA, OsO4-oxidized DNA was hydrolyzed in alkali (pH12) to convert the thymine glycols to urea residues. With both thymine glycol- and urea-containing M13 DNA, DNA synthesis catalyzed by Escherichia coli DNA polymerase I Klenow fragment was decreased in proportion to the number of damages present in the template DNA. Sequencing gel analysis of the products synthesized byE. coli DNA polymerase I and T4 DNA polymerase showed that DNA synthesis terminated opposite the putative thymine glycol site and at one nucleotide before the putative urea site. Substitution of manganese for magnesium in the reaction mix resulted in increased processivity of DNA synthesis so that a base was incorporated opposite urea. With thymine glycol-containing DNA, processivity in the presence of manganese was strongly dependent on the presence of a pyrimidine 5' to the thymine glycol in the template.


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