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Molecular and Cellular Biology, November 1998, p. 6839-6852, Vol. 18, No. 11
Department of Molecular Biology and Genetics,
Johns Hopkins University School of Medicine, Baltimore, Maryland
21205,1 and
Laboratory of Eukaryotic
Gene Regulation, National Institutes of Child Health and Human
Development, National Institutes of Health, Bethesda, Maryland
208922
Received 20 March 1998/Returned for modification 25 May
1998/Accepted 19 August 1998
The Tf2 retrotransposon, found in the fission yeast
Schizosaccharomyces pombe, is nearly identical to its
sister element, Tf1, in its reverse transcriptase-RNase H and integrase
domains but is very divergent in the gag domain, the
protease, the 5' untranslated region, and the U3 domain of the long
terminal repeats. It has now been demonstrated that a
neo-marked copy of Tf2 overexpressed from a heterologous
promoter can mobilize into the S. pombe genome and produce
true transposition events. However, the Tf2-neo
mobilization frequency is 10- to 20-fold lower than that of
Tf1-neo, and 70% of the Tf2-neo events are
homologous recombination events generated independently of a functional
Tf2 integrase. Thus, the Tf2 element is primarily dependent on
homologous recombination with preexisting copies of Tf2 for its
propagation. Finally, production of Tf2-neo proteins and
cDNA was also analyzed; surprisingly, Tf2 was found to produce its
reverse transcriptase as a single species in which it is fused to
protease, unlike all other retroviruses and retrotransposons.
0270-7306/98/$04.00+0
Copyright © 1998, American Society for Microbiology. All rights reserved.
Schizosaccharomyces pombe
Retrotransposon Tf2 Mobilizes Primarily through Homologous cDNA
Recombination
*
Corresponding author. Mailing address: Dept. of
Molecular Biology and Genetics, Hunterian Bldg., Rm. 617, Johns Hopkins
University School of Medicine, 725 N. Wolfe St., Baltimore, MD 21205. Phone: (410) 955-2481. Fax: (410) 614-2987. E-mail:
jboekejhmi.edu.
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