In vivo functions of N-linked glycans on human FSHβ subunit tested in mouse models.
HFSHBWT and HFSHBdgc (encodes a N-glycosylation mutant hFSHβ subunit) mice are generated on an Fshb−/− background.
HFSHB transgenes are targeted to pituitary and specifically expressed in gonadotropes.
HFSHBdgc encoded double N-glycosylation mutant human FSHβ subunit inefficiently assembles with mouse α-subunit.
Double N-glycosylation mutant human FSHβ subunit containing FSH dimer is inefficiently secreted and does not rescue Fshb−/− mice.