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Volume 272, Number 24, Issue of June 13, 1997 pp. 15313-15322
©1997 by The American Society for Biochemistry and Molecular Biology, Inc.

Targeting of Endopeptidase 24.16 to Different Subcellular Compartments by Alternative Promoter Usage

(Received for publication, February 28, 1997)

Akira Kato , Naoaki Sugiura § , Yohko Saruta , Takehiko Hosoiri , Hiroshi Yasue and Shigehisa Hirose

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'-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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