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Phenotypes associated with this allele
Allele Symbol
Allele Name
Allele ID
Coprstm1.1Efab
targeted mutation 1.1, Eric Fabbrizio
MGI:5646194
Summary 1 genotype
Jump to Allelic Composition Genetic Background Genotype ID
hm1
Coprstm1.1Efab/Coprstm1.1Efab Not Specified MGI:5792563


Genotype
MGI:5792563
hm1
Allelic
Composition
Coprstm1.1Efab/Coprstm1.1Efab
Genetic
Background
Not Specified
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Coprstm1.1Efab mutation (0 available); any Coprs mutation (10 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
adipose tissue
• after induction of adipogenic differentiation with insulin and triiodothyronine, in vitro adipogenic conversion of mutant embryoid bodies (EBs) is markedly delayed at D4, and lipid droplets are rarely observed at D21, unlike in wild-type EB cultures
• after induction of adipogenic differentiation with insulin and rosiglitazone, in vitro adipogenic conversion of mutant primary embryonic fibroblasts (MEFs) is severely impaired, as determined by O Red Oil staining at D7
• surprisingly, transient overexpression of a human form of Copr5 fails to rescue the capacity of mutant MEFs to differentiate into adipocytes, as shown by O Red Oil staining at D6
• retroperitoneal white adipose tissue (WAT) contains fewer adipocytes than wild-type tissue
• retroperitoneal WAT contains larger adipocytes than wild-type tissue
• altered adipocyte cellularity is due to Dlk-1 upregulation leading to a low pool of precursor cells that is able to differentiate into adipocytes
• retroperitoneal fat weight is moderately but significantly reduced at 16 weeks of age relative to wild-type controls
• however, mean body weight is normal
• the proliferation index of the vascular stromal fraction (a major source of progenitor cells in WAT) is reduced relative to wild-type controls, indicating a low pool of preadipocytes
• however, no difference is noted in mature adipocytes at 8 weeks of age

cellular
• after induction of adipogenic differentiation with insulin and triiodothyronine, in vitro adipogenic conversion of mutant embryoid bodies (EBs) is markedly delayed at D4, and lipid droplets are rarely observed at D21, unlike in wild-type EB cultures
• after induction of adipogenic differentiation with insulin and rosiglitazone, in vitro adipogenic conversion of mutant primary embryonic fibroblasts (MEFs) is severely impaired, as determined by O Red Oil staining at D7
• surprisingly, transient overexpression of a human form of Copr5 fails to rescue the capacity of mutant MEFs to differentiate into adipocytes, as shown by O Red Oil staining at D6

homeostasis/metabolism
N
• mice exhibit no differences in glucose and insulin tolerance tests relative to wild-type controls





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