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Molecular and Cellular Biology, November 2000, p. 8001-8007, Vol. 20, No. 21
0270-7306/00/$04.00+0
Copyright © 2000, American Society for Microbiology. All rights reserved.
Replication past
O6-Methylguanine by Yeast and Human DNA
Polymerase
Lajos
Haracska,
Satya
Prakash, and
Louise
Prakash*
University of Texas Medical Branch, Sealy
Center for Molecular Science, Galveston, Texas 77555-1061
Received 1 August 2000/Returned for modification 11 August
2000/Accepted 16 August 2000
O6-Methylguanine (m6G) is formed by the
action of alkylating agents such as
N-methyl-N'-nitro-N-nitrosoguanidine
(MNNG) on DNA. m6G is a highly mutagenic and carcinogenic lesion, and
it presents a block to synthesis by DNA polymerases. Here, we provide genetic and biochemical evidence for the involvement of yeast and human
DNA polymerase
(Pol
) in the replicative bypass of m6G lesions in
DNA. The formation of MNNG-induced mutations is almost abolished in the
rad30
pol32
double mutant of yeast, which lacks the
RAD30 gene that encodes Pol
and the Pol32 subunit of DNA
polymerase
(Pol
). Although Pol
can function in the mutagenic
bypass of m6G lesions, our biochemical studies indicate that Pol
is
much more efficient in replicating through m6G than Pol
. Both Pol
and Pol
insert a C or a T residue opposite from m6G; Pol
,
however, is more accurate, as it inserts a C about twice as frequently
as Pol
. Alkylating agents are used in the treatment of malignant
tumors, including lymphomas, brain tumors, melanomas, and
gastrointestinal carcinomas, and the clinical effectiveness of these
agents derives at least in part from their ability to form m6G in DNA.
Inactivation of Pol
could afford a useful strategy for enhancing the
effectiveness of these agents in cancer chemotherapy.
*
Corresponding author. Mailing address: University of
Texas Medical Branch, Sealy Center for Molecular Science, 6.104 Medical Research Building, 11th and Mechanic Streets, Galveston, TX 77555-1061. Phone: (409) 747-8601. Fax: (409) 747-8608. E-mail:
lprakash{at}scms.utmb.edu.
Molecular and Cellular Biology, November 2000, p. 8001-8007, Vol. 20, No. 21
0270-7306/00/$04.00+0
Copyright © 2000, American Society for Microbiology. All rights reserved.
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