TY - JOUR
T1 - Murine endogenous retrovirus MuERV-L is the progenitor of the "orphan" epsilon viruslike particles of the early mouse embryo
AU - Ribet, David
AU - Louvet-Vallée, Sophie
AU - Harper, Francis
AU - De Parseval, Nathalie
AU - Dewannieux, Marie
AU - Heidmann, Odile
AU - Pierron, Gérard
AU - Maro, Bernard
AU - Heidmann, Thierry
PY - 2008/2/1
Y1 - 2008/2/1
N2 - Viruslike particles which displayed a peculiar wheellike appearance that distinguished them from A-, B- or C-type particles had previously been described in the early mouse embryo. The maximum expression of these so-called epsilon particles was observed in two-cell-stage embryos, followed by their rapid decline at later stages of development and no particles detected at the zygote one-cell stage. Here, we show that these particles are in fact produced by a newly discovered murine endogenous retrovirus (ERV) belonging to the widespread family of mammalian ERV-L elements and named MuERV-L. Using antibodies that we raised against the Gag protein of these elements, Western blot analysis and in toto immunofluorescence studies of the embryos at various stages disclosed the same developmental expression profile as that observed for epsilon particles. Using expression vectors for cloned, full-length, entirely coding MuERV-L copies and cell transfection, direct identification of the epsilon particles was finally achieved by high-resolution electron microscopy.
AB - Viruslike particles which displayed a peculiar wheellike appearance that distinguished them from A-, B- or C-type particles had previously been described in the early mouse embryo. The maximum expression of these so-called epsilon particles was observed in two-cell-stage embryos, followed by their rapid decline at later stages of development and no particles detected at the zygote one-cell stage. Here, we show that these particles are in fact produced by a newly discovered murine endogenous retrovirus (ERV) belonging to the widespread family of mammalian ERV-L elements and named MuERV-L. Using antibodies that we raised against the Gag protein of these elements, Western blot analysis and in toto immunofluorescence studies of the embryos at various stages disclosed the same developmental expression profile as that observed for epsilon particles. Using expression vectors for cloned, full-length, entirely coding MuERV-L copies and cell transfection, direct identification of the epsilon particles was finally achieved by high-resolution electron microscopy.
UR - http://www.scopus.com/inward/record.url?scp=38349162880&partnerID=8YFLogxK
U2 - 10.1128/JVI.02097-07
DO - 10.1128/JVI.02097-07
M3 - Article
C2 - 18045933
AN - SCOPUS:38349162880
SN - 0022-538X
VL - 82
SP - 1622
EP - 1625
JO - Journal of Virology
JF - Journal of Virology
IS - 3
ER -