Please use this identifier to cite or link to this item:
Type: Thesis
Title: The role of the hexosamine biosynthesis pathway and β-O-linked glycosylation in determining oocyte developmental competence.
Author: Frank, Laura Alice
Issue Date: 2012
School/Discipline: School of Paediatrics and Reproductive Health
Abstract: Maternal diabetes and conditions such as obesity in which blood glucose levels are elevated are associated with reduced fertility and poor pregnancy outcomes. Many studies have examined the effects of hyperglycaemia on the early embryo and fetus; however, it is becoming increasingly evident that the peri-conceptual environment surrounding the oocyte has a significant impact on developmental competence and the long-term health of offspring. In this thesis, I aimed to investigate the role of the hexosamine biosynthesis pathway (HBP) in oocyte developmental competence. The HBP is a glucose-metabolising pathway which can also be upregulated by glucosamine, a potent hyperglycaemic mimetic which enters the HBP downstream of the rate-limiting enzyme. The HBP produces uridine diphosphate-N acetylglucosamine, which can be used for the β-O-linked glycosylation (O-GlcNAcylation) of proteins, regulating their function in a similar manner to phosphorylation. Firstly I established the effect of hyper- and hypo-glycaemic conditions during in vitro maturation (IVM) of mouse cumulus-oocyte complexes (COCs) on a range of measures associated with oocyte developmental competence, including cumulus expansion, meiotic maturation, cleavage and blastocyst development rates. A low (1 mM) glucose concentration achieved optimal oocyte competence, and glucose supplementation during only the first hour of IVM was necessary and sufficient to support oocyte maturation and embryo development to the blastocyst stage. Glucosamine was able to substitute for glucose during this first hour. In the absence of glucose throughout IVM, glucosamine was not able to increase developmental competence, and at higher concentrations (2.5 and 5 mM) had a detrimental effect on these outcomes. These experiments underscored the importance of the other glucose metabolic pathways, during COC maturation, and supported the concept that excess flux through the HBP has detrimental consequences. Using Western blots and immunohistochemistry, it was shown that both glucosamine and high glucose levels induced an increase in total O-GlcNAcylation in COCs, which was reduced in the presence of an inhibitor of the β-O-linked glycosyltransferase enzyme. Several specific proteins were identified using mass spectrometry as potential targets of O-GlcNAcylation in COCs, including heat-shock protein 90 (HSP90, both α and β isoforms). While glucosamine treatment of COCs significantly decreased blastocyst development rate, inhibiting HSP90 with 17-allylamino-17-demethoxygeldanamycin during IVM in the presence of glucosamine recovered blastocyst rates to control levels. This effect was not due to an increase in overall HSP90 levels, since inhibiting HSP90 in control COCs did not affect blastocyst rate. These results suggest O-GlcNacylated HSP90 has an aberrant function in the COC. This study is the first to examine in detail O-GlcNAcylation levels in the COC, and their correlation to oocyte developmental competence. HSP90 was identified as a potential target of O-GlcNAcylation in the COC, and subsequently shown to mediate oocyte developmental competence. This research is significant because of the increasing numbers of women wishing to become pregnant who have high blood glucose levels due to diabetes, obesity or poor diet. I have generated critically needed knowledge towards understanding how these lifestyle factors affect fertility and identifying possible avenues for new therapies.
Advisor: Thompson, Jeremy Gilbert E.
Sutton-McDowall, Melanie
Gilchrist, Robert Bruce
Russell, Darryl
Lane, Michelle Therese
Dissertation Note: Thesis (Ph.D.) -- University of Adelaide, School of Paediatrics and Reproductive Health, 2012
Keywords: glucose; glucosamine; cumulus-oocyte complex; hexosamine biosynthesis pathway; β-O-linked glycosylation
Provenance: This electronic version is made publicly available by the University of Adelaide in accordance with its open access policy for student theses. Copyright in this thesis remains with the author. This thesis may incorporate third party material which has been used by the author pursuant to Fair Dealing exceptions. If you are the owner of any included third party copyright material you wish to be removed from this electronic version, please complete the take down form located at:
Appears in Collections:Research Theses

Files in This Item:
File Description SizeFormat 
01front.pdf468.98 kBAdobe PDFView/Open
02whole.pdf3.58 MBAdobe PDFView/Open
PermissionsLibrary staff access only233.39 kBAdobe PDFView/Open
RestrictedLibrary staff access only3.87 MBAdobe PDFView/Open

Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.