HORMONAL AND NUTRITIONAL CONTROL OF ENZYME BIOSYNTHESIS
Project Number5R01DK036264-10
Former Number1R01AM034795-01
Contact PI/Project LeaderSUL, HEI SOOK
Awardee OrganizationHARVARD MEDICAL SCHOOL
Description
Abstract Text
Glucose utilization via glycolysis and lipogenesis must be regulated to
meet the changing nutritional state of the animals; glycolysis is low and
fatty acid synthesis is virtually absent during fasting, and fatty acids
and triacylglycerol synthesis for energy storage increase dramatically
during feeding. Secretion of insulin, a major anabolic polypeptide
hormone, is increased during feeding and is involved in this regulation.
In addition, glycolysis and fatty acid synthesis is impaired in diabetic
animals and insulin restores the rates to normal levels. Since diabetes
is among the most common and serious metabolic diseases, understanding
mechanisms of insulin action is of utmost importance.
The goal of this research is to determine the molecular mechanisms by
which insulin increases transcription of two key enzymes of energy
metabolism. Fatty acid synthase (FAS) plays central role in de novo
lipogenesis by catalyzing all the reaction in the conversion of acetyl
CoA and malonyl CoA to palmitate. Phosphofructokinase-1 (PFK) catalyzes
the committed step in glycolysis. We have cloned cDNA and genomic clones
for FAS, liver PFK and other insulin-inducible mRNAs and have shown
transcriptional stimulation of these genes by insulin. The 5'-flanking
regions of FAS and PFK genes contained sequences which confer insulin
activation to linked reporter genes when transfected into 3T3-Ll
adipocytes. A common mechanism may be involved in the insulin induction
of these enzymes. Our goal is to define cis-acting elements and trans-
acting factors for the transcriptional activation of these genes by
insulin. Using in vitro mutagenesis, essential sequences for insulin
regulation will be defined by transfection into adipocytes and by
utilizing transgenic mice. The nuclear factor(s) which interact with
these sequences will be characterized by mobility shift and DNase
footprinting assays. The factor(s) will then be purified and/or cloned
to start studying at the molecular level how insulin stimulates
transcription of these genes. This will lead us in the future to
elucidate a signal transduction pathway of insulin.
National Institute of Diabetes and Digestive and Kidney Diseases
CFDA Code
DUNS Number
047006379
UEI
JDLVAVGYJQ21
Project Start Date
01-March-1985
Project End Date
30-June-1994
Budget Start Date
01-April-1994
Budget End Date
30-June-1994
Project Funding Information for 1994
Total Funding
$54,800
Direct Costs
$37,077
Indirect Costs
$17,723
Year
Funding IC
FY Total Cost by IC
1994
National Institute of Diabetes and Digestive and Kidney Diseases
$54,800
Year
Funding IC
FY Total Cost by IC
Sub Projects
No Sub Projects information available for 5R01DK036264-10
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