Selective processing of submandibular rat 1 protein at dibasic cleavage sites

Salivary and bloodstream secretion products

Authors

  • Catherine ROUGEOT,

    1. Unité de Génétique et Biochimie du Développement, Unité de Recherche Associée 361 Centre National de la Recherche Scientifique, Département d'Immunologie, Institut Pasteur, Paris, France
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  • Isabelle ROSINSKI-CHUPIN,

    1. Unité de Génétique et Biochimie du Développement, Unité de Recherche Associée 361 Centre National de la Recherche Scientifique, Département d'Immunologie, Institut Pasteur, Paris, France
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  • Elisabeth NJAMKEPO,

    1. Unité de Génétique et Biochimie du Développement, Unité de Recherche Associée 361 Centre National de la Recherche Scientifique, Département d'Immunologie, Institut Pasteur, Paris, France
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  • François ROUGEON

    Corresponding author
    1. Unité de Génétique et Biochimie du Développement, Unité de Recherche Associée 361 Centre National de la Recherche Scientifique, Département d'Immunologie, Institut Pasteur, Paris, France
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Correspondence to F. Rougeon, Unité de Génétique et Biochimie du Développement, Unité de Recherche Associée 361 Centre National de la Recherche Scientifique, Département d'Immunologie, Institut Pasteur, 25 rue du Dr Roux, F-75724 Paris Cédex 15, France
Fax: + 33 1 45 68 86 39.

Abstract

The amino acid sequence of submandibular rat 1 (SMR1) protein, deduced from its cDNA sequence, led to the prediction that the SMR1 gene encodes a hormone-like precursor [Rosinski-Chupin, I., Tronik, D. & Rougeon, F. (1988) Proc. Natl Acad. Sci. USA 85, 8553–8557]. SMR1 contains an N-terminal putative secretory signal sequence and a tetrapeptide (QHNP), located between dibasic amino acids which constitute the most common signal for prohormone processing.

We have isolated and characterized from the male rat submandibular gland and its secretions three structurally related peptides, namely an undecapeptide (VRGPRRQHNPR), a hexapeptide (RQHNPR) and a pentapeptide (QHNPR) generated from SMR1 by selective proteolytic cleavages at pairs of arginine residues.

The biosynthesis of these peptides is subjected to distinct regulatory pathways depending on the organ, sex and age of the rat. Furthermore, the peptides are differentially distributed in the submandibular gland and in resting or epinephrine-elicited submandibular salivary secretions, suggesting distinct proteolytic pathways for their maturation. The undecapeptide is generated in the gland of both male and female rats, but under basal conditions it is only released into the saliva in male animals. The hexapeptide is produced in large amounts in the gland of adult male rats and released into the saliva in both resting and stimulated conditions. The pentapeptide appears only in the male saliva and is present mostly under stimulated conditions. In addition, administration of epinephrine induces the release of the hexapeptide from the submandibular gland into the bloodstream. The evidence indicates that the rat submandibular gland can function as a dual exocrine and endocrine organ for the SMR1-derived hexapeptide, as has been reported for nerve growth factor, epidermal growth factor, renin and kallikrein.

Although the biological activities of the SMR1-derived peptides are not yet known, their high production and adrenergic-induced release only into the saliva and bloodstream of adult male rats, suggest a physiological involvement in some male-specific processes.

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