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* Department of Molecular Biology, University of Texas Southwestern
Medical Center, Dallas, TX 75390-9148; and § Institute for
Cellular and Molecular Biology, Department of Chemistry and
Biochemistry, and Section of Molecular Genetics and Microbiology,
University of Texas, Austin, TX 78712
Communicated by Marlene Belfort, New York State Department of
Health, Albany, NY, September 19, 2001 (received for review July 23, 2001)
Group II introns, the presumed ancestors of nuclear pre-mRNA
introns, are site-specific retroelements. In addition to
"homing" to unoccupied sites in intronless alleles, group II
introns transpose at low frequency to ectopic sites that resemble the
normal homing site. Two general mechanisms have been proposed for group
II intron transposition, one involving reverse splicing of the intron
RNA directly into an ectopic DNA site, and the other involving reverse splicing into a site in RNA followed by reverse transcription and
integration of the resulting cDNA by homologous recombination. Here, by
using an "inverted-site" strategy, we show that the yeast mtDNA group II intron aI1 retrotransposes by reverse splicing directly
into an ectopic DNA site. This same mechanism could account for other
previously described ectopic transposition events in fungi and bacteria
and may have contributed to the dispersal of group II introns into
different genes.
Genetics
Retrotransposition of a yeast group II intron occurs by reverse
splicing directly into ectopic DNA sites
,
,
,
L.D. and H.-R.H. contributed equally to this work.
Present address: Pacific Northwest Research
Institute, 720 Broadway, Seattle, WA 98122.
¶
Present address: National Institute of Advanced
Industrial Science and Technology, Tsukuba, Ibaraki, Japan, 305-8562.
To whom reprint requests should be addressed.
E-mail: philip.perlman{at}utsouthwestern.edu.
www.pnas.org/cgi/doi/10.1073/pnas.231494498
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