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Title page for ETD etd-08052016-144905


Type of Document Dissertation
Author Boortz, Kayla Ann
URN etd-08052016-144905
Title Exploring the Function of G6PC2 in Pancreatic Islet Beta Cells
Degree PhD
Department Molecular Physiology and Biophysics
Advisory Committee
Advisor Name Title
Owen McGuinness Committee Chair
David Jacobson Committee Member
Fiona Yull Committee Member
Richard O'Brien Committee Member
Roger Cone Committee Member
Keywords
  • metabolism
  • G6PC2
  • glucose-6-phosphate
  • islet
  • beta cells
Date of Defense 2016-08-03
Availability unrestricted
Abstract
MOLECULAR PHYSIOLOGY & BIOPHYSICS

Exploring the Function of G6PC2 in Pancreatic Islet Beta Cells

Kayla Boortz

Dissertation under the direction of Professor Richard O’Brien, Ph.D.

G6PC2 encodes an islet-specific glucose-6-phosphatase catalytic subunit. Together with glucokinase, G6PC2 forms a substrate cycle that determines the glucose sensitivity of insulin secretion. Genetic and molecular studies show that elevated G6PC2 expression raises fasting blood glucose (FBG) but because chronically elevated FBG is detrimental, increasing type 2 diabetes risk, it is unclear why G6PC2 evolved. Studies have shown that single nucleotide polymorphisms (SNPs) in G6PC2 associate with variation in FBG and body mass index (BMI) in humans. Previously we confirmed these findings in mice and showed that FBG is repressed in G6pc2 knockout (KO) mice relative to wild type (WT) on a mixed or pure C57BL/6J genetic background. I further confirmed that 129SvEv KO mice also have reduced FBG. Moreover, I identified a glucocorticoid response element in the human and 129SvEv G6pc2 promoter that confers glucocorticoid responsiveness and induction of G6PC2 gene expression following treatment with Dexamethasone (Dex), 11-dehydrocorticosterone (11-DHC) or physical restraint in 129SvEv and C57BL/6J mice. Following stress generated by Dex or physical restraint, FBG is repressed in 6 hour fasted 129SvEv and C57BL/6J KO mice, respectively, enhancing the difference in FBG relative to controls. These data suggest that G6PC2 evolved to modulate FBG under conditions of glucocorticoid-related stress thereby conferring a transient, beneficial modulation of the set point for FBG. This thesis also addresses the observation that the common rs560887 G6PC2 SNP is associated with variation in BMI and adiposity. The results described here indicate that the effect of G6pc2 deletion on the response to diet induced obesity is dependent on genetic modifiers. Finally, an indirect analysis of the effects of human G6PC2 SNPs on protein expression and enzyme activity indicates that mutations at catalytically conserved residues may be critical for proper enzyme function and protein expression.

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