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(Received for publication, March 4, 1997, and in revised form, May 1, 1997)
From the Department of Molecular Biology, The University of
Medicine and Dentistry of New Jersey, School of Osteopathic
Medicine, Stratford, New Jersey 08084
We have previously identified distinct nuclear
and mitochondrial isoforms of dUTPase in human cells, reporting
the cDNA sequence of the nuclear isoform (DUT-N). We now
report a cDNA corresponding to the mitochondrial isoform (DUT-M).
The DUT-M cDNA contains an 252-amino acid open reading frame,
encoding a protein with a predicted Mr of
26,704. The amino-terminal region of the protein contains an
arginine-rich, 69-residue mitochondrial targeting presequence that is
absent in the mature protein. In vitro transcription and
translation of the DUT-M cDNA results in the production of a
precursor protein with an apparent molecular mass of 31 kDa as judged
by SDS-polyacrylamide gel electrophoresis. The DUT-M precursor is
enzymatically active and immunoreacts with a dUTPase-specific monoclonal antibody. Mitochondrial import and processing studies demonstrate that the DUT-M precursor is processed into a 23-kDa protein
and imported into mitochondria in vitro. Isoelectric
focusing experiments demonstrate that the DUT-N has a pI of 6.0, while the processed form of DUT-M has a more basic pI of 8.1, measurements that are in agreement with predicted values. Studies aimed at understanding the expression of these isoforms were performed utilizing
quiescent and replicating 34Lu human lung fibroblasts as a model cell
culture system. Northern blot analysis, employing an isoform-specific
probe, demonstrates that DUT-N and DUT-M are encoded by two distinct
mRNA species of 1.1 and 1.4 kilobases, respectively. Western and
Northern blot analysis reveal that DUT-M protein and mRNA are
expressed in a constitutive fashion, independent of cell cycle phase or
proliferation status. In contrast, DUT-N protein and mRNA levels
are tightly regulated to coincide with nuclear DNA replication status.
Because DUT-N and DUT-M have identical amino acid and cDNA
sequences in their overlapping regions, we set out to determine if they
were encoded by the same gene. The 5
Volume 272, Number 30,
Issue of July 25, 1997
pp. 19072-19080
©1997 by The American Society for Biochemistry and Molecular Biology, Inc.
DIFFERENTIAL EXPRESSION OF THE ISOFORMS AND CHARACTERIZATION OF
A cDNA ENCODING THE MITOCHONDRIAL SPECIES
region of the gene encoding
dUTPase was isolated and characterized by a combination of Southern
hybridization and DNA sequencing. These analyses demonstrate that the
dUTPase isoforms are encoded by the same gene with isoform-specific
transcripts arising through the use of alternative 5
exons. This
finding represents the first example in humans of alternative 5
exon
usage to generate differentially expressed nuclear and mitochondrial
specific protein isoforms.
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