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Vol. 12, Issue 5, 1381-1392, May 2001
and
Department of Biochemistry and Molecular Biology, Pennsylvania
State University College of Medicine, Hershey, Pennsylvania 17033
Reports of nuclear tRNA aminoacylation and its role in tRNA nuclear
export (Lund and Dahlberg, 1998; Sarkar et al., 1999; Grosshans et al., 2000a) have led to the prediction that
there should be nuclear pools of aminoacyl-tRNA synthetases. We report that in budding yeast there are nuclear pools of tyrosyl-tRNA synthetase, Tys1p. By sequence alignments we predicted a Tys1p nuclear
localization sequence and showed it to be sufficient for nuclear
location of a passenger protein. Mutations of this nuclear localization
sequence in endogenous Tys1p reduce nuclear Tys1p pools, indicating
that the motif is also important for nucleus location. The mutations do
not significantly affect catalytic activity, but they do cause defects
in export of tRNAs to the cytosol. Despite export defects, the cells
are viable, indicating that nuclear tRNA aminoacylation is not required
for all tRNA nuclear export paths. Because the tRNA nuclear exportin,
Los1p, is also unessential, we tested whether tRNA aminoacylation and Los1p operate in alternative tRNA nuclear export paths. No genetic interactions between aminoacyl-tRNA synthetases and Los1p were detected, indicating that tRNA nuclear aminoacylation and Los1p operate
in the same export pathway or there are more than two pathways for tRNA
nuclear export.
Department of Cellular and Molecular
Medicine, Howard Hughes Medical Institution, University of California,
San Diego, School of Medicine, La Jolla, California 9209.
Corresponding author. E-mail address:
ahopper{at}psu.edu
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