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(Received for publication, February 28, 1997)
From the Department of Biological Sciences, Tokyo Institute of
Technology, 4259 Nagatsuta-cho, Midori-ku, Yokohama 226, Japan, the
§ Department of Biochemistry I, National Defense Medical
College, Tokorosawa, Saitama 359, Japan, and the ¶ Animal
Genome Research Group, National Institute of Animal Industry,
Inashiki-gun, Ibaraki 305, Japan
Endopeptidase 24.16 or mitochondrial
oligopeptidase, abbreviated here as EP 24.16 (MOP), is a thiol- and
metal-dependent oligopeptidase that is found in multiple
intracellular compartments in mammalian cells. From an analysis of the
corresponding gene, we found that the distribution of the enzyme to
appropriate subcellular locations is achieved by the use of alternative
sites for the initiation of transcription. The pig EP 24.16 (MOP) gene
spans over 100 kilobases and is organized into 16 exons. The core
protein sequence is encoded by exons 5-16 which match perfectly with
exons 2-13 of the gene for endopeptidase 24.15, another member of the
thimet oligopeptidase family. These two sets of 11 exons share the same
splice sites, suggesting a common ancestor. Multiple species of
mRNA for EP 24.16 (MOP) were detected by the 5
Volume 272, Number 24,
Issue of June 13, 1997
pp. 15313-15322
©1997 by The American Society for Biochemistry and Molecular Biology, Inc.
-rapid amplification
of cDNA ends and they were shown to have been generated from a
single gene by alternative choices of sites for the initiation of
transcription and splicing. Two types of transcript were prepared,
corresponding to transcription from distal and proximal sites. Their
expression in vitro in COS-1 cells indicated that they
encoded two isoforms (long and short) which differed only at their
amino termini: the long form contained a cleavable mitochondrial
targeting sequence and was directed to mitochondria; the short form,
lacking such a signal sequence, remained in the cytosol. The complex
structure of the EP 24.16 (MOP) gene thus allows, by alternative
promoter usage, a fine transcriptional regulation of coordinate
expression, in the different subcellular compartments, of the two
isoforms arising from a single gene.
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