| Literature DB >> 25605903 |
Guillaume Cornelis1, Cécile Vernochet2, Quentin Carradec2, Sylvie Souquere2, Baptiste Mulot3, François Catzeflis4, Maria A Nilsson5, Brandon R Menzies6, Marilyn B Renfree6, Gérard Pierron2, Ulrich Zeller7, Odile Heidmann2, Anne Dupressoir2, Thierry Heidmann8.
Abstract
Syncytins are genes of retroviral origin captured by eutherian mammals, with a role in placentation. Here we show that some marsupials-which are the closest living relatives to eutherian mammals, although they diverged from the latter ∼190 Mya-also possess a syncytin gene. The gene identified in the South American marsupial opossum and dubbed syncytin-Opo1 has all of the characteristic features of a bona fide syncytin gene: It is fusogenic in an ex vivo cell-cell fusion assay; it is specifically expressed in the short-lived placenta at the level of the syncytial feto-maternal interface; and it is conserved in a functional state in a series of Monodelphis species. We further identify a nonfusogenic retroviral envelope gene that has been conserved for >80 My of evolution among all marsupials (including the opossum and the Australian tammar wallaby), with evidence for purifying selection and conservation of a canonical immunosuppressive domain, but with only limited expression in the placenta. This unusual captured gene, together with a third class of envelope genes from recently endogenized retroviruses-displaying strong expression in the uterine glands where retroviral particles can be detected-plausibly correspond to the different evolutionary statuses of a captured retroviral envelope gene, with only syncytin-Opo1 being the present-day bona fide syncytin active in the opossum and related species. This study would accordingly recapitulate the natural history of syncytin exaptation and evolution in a single species, and definitely extends the presence of such genes to all major placental mammalian clades.Entities:
Keywords: endogenous retrovirus; envelope protein; fusogenic activity; marsupials; syncytiotrophoblast
Mesh:
Substances:
Year: 2015 PMID: 25605903 PMCID: PMC4321253 DOI: 10.1073/pnas.1417000112
Source DB: PubMed Journal: Proc Natl Acad Sci U S A ISSN: 0027-8424 Impact factor: 11.205