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Phenotypes associated with this allele
Allele Symbol
Allele Name
Allele ID
Pdpk1tm1Jcbr
targeted mutation 1, Jens C Bruning
MGI:3790718
Summary 2 genotypes
Jump to Allelic Composition Genetic Background Genotype ID
cn1
Pdpk1tm1Jcbr/Pdpk1tm1Jcbr
Tg(Pomc1-cre)16Lowl/0
involves: C57BL/6 * FVB/N MGI:3804310
cn2
Gt(ROSA)26Sortm1(CAG-Foxo1*)Jcbr/Gt(ROSA)26Sor+
Pdpk1tm1Jcbr/Pdpk1tm1Jcbr
Tg(Pomc1-cre)16Lowl/0
involves: C57BL/6 * FVB/N MGI:3804312


Genotype
MGI:3804310
cn1
Allelic
Composition
Pdpk1tm1Jcbr/Pdpk1tm1Jcbr
Tg(Pomc1-cre)16Lowl/0
Genetic
Background
involves: C57BL/6 * FVB/N
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Pdpk1tm1Jcbr mutation (0 available); any Pdpk1 mutation (138 available)
Tg(Pomc1-cre)16Lowl mutation (1 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
growth/size/body
• males and females fed either a normal chow diet or a high-fat chow diet display slightly but significantly increased body weight, although over time, weight normalizes
• corticosterone replacement in mutants increases food intake and body weight

homeostasis/metabolism
• reduction in plasma corticosterone concentrations is seen as early as 3 weeks of age, with levels continuing to decrease over time
• mutants show an impairment in stress-induced corticosterone production
• injection of ACTH analog does not increase plasma corticosterone to the level of control mice, consistent with adrenal insufficiency
• corticosterone replacement in mutants increases food intake and body weight
• initially, mutants exhibit an elevation in serum leptin levels at 8 weeks of age, however by 18 weeks of age, they show lower serum leptin levels than controls but have an unchanged body weight
• glucose-stimulated insulin secretion is lower than in controls
• analysis of glucose-stimulated insulin secretion shows that although insulin secretion is lower, their blood glucose concentration is also lower than in controls
• initial elevation in serum glucose levels at 8 weeks of age
• old mutants perform better than controls during glucose tolerance tests
• old mutants show significantly increased insulin sensitivity during insulin tolerance tests than controls

endocrine/exocrine glands
• decrease in melanotroph numbers in the intermediate lobe of the pituitary, but do not see an obvious change in fur color or skin pigmentation
• glucose-stimulated insulin secretion is lower than in controls

adipose tissue
• at 18 weeks of age, mutants show reduced epigonadal fat-pad mass

behavior/neurological
• significant hyperphagia at 8 weeks of age but not at 10 weeks of age
• corticosterone replacement in mutants increases food intake and body weight

nervous system
• decrease in melanotroph numbers in the intermediate lobe of the pituitary, but do not see an obvious change in fur color or skin pigmentation




Genotype
MGI:3804312
cn2
Allelic
Composition
Gt(ROSA)26Sortm1(CAG-Foxo1*)Jcbr/Gt(ROSA)26Sor+
Pdpk1tm1Jcbr/Pdpk1tm1Jcbr
Tg(Pomc1-cre)16Lowl/0
Genetic
Background
involves: C57BL/6 * FVB/N
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Gt(ROSA)26Sortm1(CAG-Foxo1*)Jcbr mutation (0 available); any Gt(ROSA)26Sor mutation (993 available)
Pdpk1tm1Jcbr mutation (0 available); any Pdpk1 mutation (138 available)
Tg(Pomc1-cre)16Lowl mutation (1 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
homeostasis/metabolism
N
• expression of the mutant foxo1 restores body weight, food consumption and blood glucose levels to normal
• mutants have reduced basal and stress-induced corticosterone levels, similar to double Pdk1tm1Jcbr Tg(Pomc1-cre)16Lowl mutants

endocrine/exocrine glands
• same reduction in corticotrophs as seen in double Pdk1tm1Jcbr Tg(Pomc1-cre)16Lowl mutants

nervous system
• same reduction in corticotrophs as seen in double Pdk1tm1Jcbr Tg(Pomc1-cre)16Lowl mutants





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last database update
11/12/2024
MGI 6.24
The Jackson Laboratory