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Biology of Reproduction 60, 551-557 (1999)
©Copyright 1999 Society for the Study of Reproduction, Inc.

Canine Preprorelaxin: Nucleic Acid Sequence and Localization within the Canine Placenta

T. Klonisch1,a, S. Hombach-Klonischa, C. Froehlicha, J. Kauffoldb, K. Stegera, B.G. Steinetzc, and B. Fischera

a Department of Anatomy and Cell Biology, Faculty of Medicine, Martin-Luther-University Halle-Wittenberg, D-06097 Halle (Saale), Germany b Large Animal Clinic for Theriogenology and Ambulance Services, Faculty of Veterinary Medicine, University of Leipzig, Leipzig, Germany c Nelson Institute of Environmental Medicine, New York University Medical Center, Tuxedo, New York 10987

Employing uteroplacental tissue at Day 35 of gestation, we determined the nucleic acid sequence of canine preprorelaxin using reverse transcription- and rapid amplification of cDNA ends-polymerase chain reaction. Canine preprorelaxin cDNA consisted of 534 base pairs encoding a protein of 177 amino acids with a signal peptide of 25 amino acids (aa), a B domain of 35 aa, a C domain of 93 aa, and an A domain of 24 aa. The putative receptor binding region in the N'-terminal part of the canine relaxin B domain GRDYVR contained two substitutions from the classical motif (E->D and L->Y). Canine preprorelaxin shared highest homology with porcine and equine preprorelaxin. Northern analysis revealed a 1-kilobase transcript present in total RNA of canine uteroplacental tissue but not of kidney tissue. Uteroplacental tissue from two bitches each at Days 30 and 35 of gestation were studied by in situ hybridization to localize relaxin mRNA. Immunohistochemistry for relaxin, cytokeratin, vimentin, and von Willebrand factor was performed on uteroplacental tissue at Day 30 of gestation. The basal cell layer at the core of the chorionic villi was devoid of relaxin mRNA and immunoreactive relaxin or vimentin but was immunopositive for cytokeratin and identified as cytotrophoblast cells. The cell layer surrounding the chorionic villi displayed specific hybridization signals for relaxin mRNA and immunoreactivity for relaxin and cytokeratin but not for vimentin, and was identified as syncytiotrophoblast. Those areas of the chorioallantoic tissue with most intense relaxin immunoreactivity were highly vascularized as demonstrated by immunoreactive von Willebrand factor expressed on vascular endothelium. The uterine glands and nonplacental uterine areas of the canine zonary girdle placenta were devoid of relaxin mRNA and relaxin. We conclude that the syncytiotrophoblast is the source of relaxin in the canine placenta.

1 Correspondence: T. Klonisch, Department of Anatomy and Cell Biology, Martin-Luther-University Halle-Wittenberg, Grosse Steinstr. 52, D-06097 Halle (Saale), Germany. FAX: 0049 345 557 1700; thomas.klonisch{at}medizin.uni-halle.de




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