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Endocrinology Vol. 139, No. 12 5157-5163
Copyright © 1998 by The Endocrine Society


ARTICLES

A New Member of the Mouse Prolactin (PRL)-Like Protein-C Subfamily, PRL-Like Protein-C{alpha}: Structure and Expression1

Guoli Dai, Belinda M. Chapman, Bing Liu, Kyle E. Orwig2, Danhua Wang3, Robert A. White, Barry Preuett and Michael J. Soares

Department of Molecular & Integrative Physiology (G.D., B.M.C., B.L., K.E.O., D.W., M.J.S.), University of Kansas Medical Center, Kansas City, Kansas 66160; Section of Medical Genetics and Molecular Medicine (R.A.W., B.P.), Children’s Mercy Hospital, Kansas City, Missouri 64108

Address all correspondence and requests for reprints to: Michael J. Soares, Ph.D., Department of Molecular and Integrative Physiology, University of Kansas Medical Center, Kansas City, Kansas 66160-7401. E-mail: msoares{at}kumc.edu

In this study, we establish the presence of a unique member of the PRL-like protein-C (PLP-C) subfamily in the mouse, PLP-C{alpha}, characterize its complementary DNA and gene, and map its chromosomal location and pattern of expression during pregnancy. Mouse PLP-C{alpha} encodes for a 239 amino acid protein and possesses from 69–71% identity with rat PLP-C, PLP-Cv, PLP-D, and PLP-H. Another feature characteristic of PLP-C subfamily members that is also present in mouse PLP-C{alpha} is a 6-exon/5-intron gene structure including an aromatic domain encoded by exon 3. Southern analysis with mouse and rat PLP-C subfamily probes suggested the existence of a single mouse PLP-C{alpha} gene. Mouse PLP-C{alpha} maps to chromosome 13 along with other members of the mouse PRL family. Expression of mouse PLP-C{alpha} increases dramatically as gestation advances and is restricted to spongiotrophoblast and trophoblast giant cells of the junctional zone. In summary, we have established the presence of a new PLP-C subfamily member in the mouse and demonstrated its similarity in structure and expression to rat PLP-C subfamily members. This level of conservation between species expands the biological significance of the PLP-C subfamily and provides additional opportunities for genetically evaluating its function.




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