| Literature DB >> 29162694 |
Guillaume Cornelis1,2, Mathis Funk1,2, Cécile Vernochet1,2, Francisca Leal3, Oscar Alejandro Tarazona3, Guillaume Meurice4, Odile Heidmann1,2, Anne Dupressoir1,2, Aurélien Miralles5, Martha Patricia Ramirez-Pinilla3, Thierry Heidmann6,2.
Abstract
Syncytins are envelope genes from endogenous retroviruses that have been captured during evolution for a function in placentation. They have been found in all placental mammals in which they have been searched, including marsupials. Placental structures are not restricted to mammals but also emerged in some other vertebrates, most frequently in lizards, such as the viviparous Mabuya Scincidae. Here, we performed high-throughput RNA sequencing of a Mabuya placenta transcriptome and screened for the presence of retroviral env genes with a full-length ORF. We identified one such gene, which we named "syncytin-Mab1," that has all the characteristics expected for a syncytin gene. It encodes a membrane-bound envelope protein with fusogenic activity ex vivo, is expressed at the placental level as revealed by in situ hybridization and immunohistochemistry, and is conserved in all Mabuya species tested, spanning over 25 My of evolution. Its cognate receptor, required for its fusogenic activity, was searched for by a screening assay using the GeneBridge4 human/Chinese hamster radiation hybrid panel and found to be the MPZL1 gene, previously identified in mammals as a signal-transducing transmembrane protein involved in cell migration. Together, these results show that syncytin capture is not restricted to placental mammals, but can also take place in the rare nonmammalian vertebrates in which a viviparous placentotrophic mode of reproduction emerged. It suggests that similar molecular tools have been used for the convergent evolution of placentation in independently evolved and highly distant vertebrates.Entities:
Keywords: endogenous retrovirus; envelope protein; placenta; receptor; syncytin
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Year: 2017 PMID: 29162694 PMCID: PMC5754801 DOI: 10.1073/pnas.1714590114
Source DB: PubMed Journal: Proc Natl Acad Sci U S A ISSN: 0027-8424 Impact factor: 11.205