One of the fundamental differences among mammals is the mechanism of maintaining the corpus luteum of pregnancy. Placentation in primates is associated with the production of the glycoprotein hormone chorionic gonadotropin (CG), which is secreted into the maternal serum and stimulates progesterone synthesis from the corpus luteum, which is essential for early development of the embryo. CG together with the pituitary hormones lutropin (LH), follitropin, and thyrotropin constitute the family of glycoprotein hormones comprised of a common ␣ subunit and a hormone-specific  subunit. The LH and CG subunits share 85% amino acid sequence identity, and functionally LH and CG are interchangeable. CG evolved by a recent gene duplication event from the LH locus, and despite the close relationship between them, their modes of secretion are quite different. CG release from the placenta is apically directed, whereas LH is released from the basal side of the cell, and the determinant(s) for this redirected trafficking are unknown. Here, using the polarized Madin-Darby canine kidney (MDCK) cell line, we provide evidence for the molecular basis of the different secretory patterns of LH and CG in vivo. The apical targeting of CG is programmed by a carboxyl-terminal sequence, which encodes a novel sorting signal. It is also apparent that the presence of the O-linked oligosaccharides in the CTP sequence contributes to this apical routing. The CTP, which is absent in LH, redirects CG to the maternal serum and permits the unique arrangement for primate placentation. Our data also show that the MDCK cells can distinguish the different secretory pathways for the gonadotropins and will be a valuable model for elucidating the determinants associated with the unique sorting of these functionally related hormones.The evolution of primates is associated with a fundamental change in the morphogenesis of the placenta (1, 2). Placentation in primates is coupled to the synthesis of glycoprotein hormone chorionic gonadotropin (CG), 1 which is secreted into the maternal serum and stimulates progesterone synthesis from the corpus luteum, thereby allowing early implantation and development of the embryo (3, 4). CG and its pituitary counterpart, lutropin (LH), comprise a family of heterodimeric glycoprotein hormones, including follitropin and thyrotropin, that share a common ␣ subunit, but differ in their hormonespecific  subunits (5). Although the  subunits determine biological specificity of each hormone, there is significant structural similarity between them. This is most evident for the LH and CG subunits, which share 85% amino acid identity in the first 114 amino acids (6). A major difference between the two subunits is the presence in the CG subunit of a 31-amino acid carboxyl-terminal extension (CTP) compared with a shorter 7-amino acid stretch in LH (see "Results").The CG subunit is specific to primates and evolved by a gene duplication event from the LH locus (7); functionally the two are interchangeable. Similar to other mamma...