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Journal of Virology, July 2001, p. 6337-6347, Vol. 75, No. 14
Graduate Program in Biochemistry and
Molecular Biology, Robert Wood Johnson Medical School, University
of Medicine and Dentistry of New Jersey,1 and
Department of Molecular Biology and Biochemistry, Rutgers
University,2 Piscataway, New Jersey 08854
Received 28 December 2000/Accepted 12 April 2001
Reverse transcriptases (RTs) are found in a wide variety of mobile
genetic elements including viruses, retrotransposons, and infectious
organellar introns. An invariant triad of aspartates is thought to be
required for the catalytic function of RTs. We generated RT mutants in
the yeast retrotransposon Ty1, changing each of these active-site
aspartates to asparagine or glutamate. All but one of the mutants
lacked detectable polymerase activity. The novel exception,
D211N, retained near wild-type in vitro polymerase activity
within virus-like particles but failed to carry out in vivo
transposition. For this mutant, minus-strand synthesis is impaired and
formation of the plus-strand strong-stop intermediate is eliminated.
Intragenic second-site suppressor mutations of the transposition defect
map to the RNase H domain of the enzyme. Our results demonstrate that
one of the three active-site aspartates in a retrotransposon RT is not
catalytically critical. This implies a basic difference in the
polymerase active-site geometry of Ty1 and human immunodeficiency virus
RT and shows that subtle mutations in one domain can cause dramatic
functional effects on a distant domain of the same enzyme.
0022-538X/01/$04.00+0 DOI: 10.1128/JVI.75.14.6337-6347.2001
Copyright © 2001, American Society for Microbiology. All rights reserved.
A Ty1 Reverse Transcriptase Active-Site Aspartate
Mutation Blocks Transposition but Not Polymerization

*
Corresponding author. Mailing address: Department of
Molecular Biology and Biochemistry, Rutgers University, CABM 306, 679 Hoes Lane, Piscataway, NJ 08854. Phone: (732) 235-5097. Fax: (732) 235-4880. E-mail: gabriel{at}cabm.rutgers.edu.
Dedicated to the memory of Esther M. Gabriel.
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