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<jats:p>Complex and hybrid <jats:italic>N</jats:italic>-glycans generated by <jats:italic>N</jats:italic>-acetylglucosaminyltransferase I (GlcNAcT-I), encoded by <jats:italic>Mgat1</jats:italic>, affect the functions of glycoproteins. We have previously shown that females with oocyte-specific deletion of a floxed <jats:italic>Mgat1</jats:italic> gene using a zona pellucida protein 3 (ZP3)<jats:italic>Cre</jats:italic> transgene produce fewer pups primarily due to a reduction in ovulation rate. Here, we show that the ovulation rate of mutant females is decreased due to aberrant development of preovulatory follicles. After a superovulatory regime of 48 h pregnant mare's serum (PMSG) and 9 h human chorionic gonadotropin (hCG), mutant ovaries weighed less and contained ∼60% fewer preovulatory follicles and more atretic and abnormal follicles than controls. Unlike controls, a proportion of mutant follicles underwent premature luteinization. In addition, mutant preovulatory oocytes exhibited gross abnormalities with ∼36% being blebbed or zona-free. While 97% of wild-type oocytes had a perivitelline space at the preovulatory stage, ∼54% of mutant oocytes did not. The cumulus mass surrounding mutant oocytes was also smaller with a decreased number of proliferating cells compared with controls, although hyaluronan around mutant oocytes was similar to controls. In addition, cumulus cells surrounding mutant eggs were resistant to removal by either hyaluronidase or incubation with capacitated sperm. Therefore, the absence of complex and hybrid <jats:italic>N</jats:italic>-glycans on oocyte glycoproteins leads to abnormal folliculogenesis resulting in a decreased ovulation rate.</jats:p>

Original publication

DOI

10.1530/rep-07-0469

Type

Journal article

Journal

REPRODUCTION

Publisher

Bioscientifica

Publication Date

02/2009

Volume

137

Pages

321 - 331