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Origin, Splicing, and Expression of Rodent Amelogenin Exon 8

¹ Department of Cytokine Biology,
³ Department of Immunology, Forsyth Institute &
² Department of Developmental Biology, Harvard School of Dental Medicine, Boston, MA 02115, and
⁴ Division of Aging and Geriatric Dentistry, Tohoku University Graduate School of Dentistry, Sendai, 980-8575, Japan; and
⁵ Michigan Dental Research Laboratory, Ann Arbor, MI 48108

^* corresponding author, jbartlett{at}forsyth.org

Amelogenin RNA transcripts undergo extensive alternative splicing, and MMP-20 processes the isoforms following their secretion. Since amelogenins have been ascribed cell-signaling activities, we asked if a lack of proteolytic processing by MMP-20 affects amelogenin signaling and consequently alters amelogenin splice site selection. RT-PCR analyses of amelogenin mRNA between control and Mmp20^–/–mice revealed no differences in the splicing pattern. We characterized 3 previously unidentified amelogenin alternatively spliced transcripts and demonstrated that exon-8-encoded amelogenin isoforms are processed by MMP-20. Transcripts with exon 8 were expressed approximately five-fold less than those with exon 7. Analyses of the mouse and rat amelogenin gene structures confirmed that exon 8 arose in a duplication of exons 4 through 5, with translocation of the copy downstream of exon 7. No downstream genomic sequences homologous to exons 4–5 were present in the bovine or human amelogenin genes, suggesting that this translocation occurred only in rodents.

KEY WORDS: enamelysin • enamel • amelogenin

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