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Phenotypes Associated with This Genotype
Genotype
MGI:6404457
Allelic
Composition
Pccatm1Tmiy/Pccatm1Tmiy
Tg(CAG-PCCA*A138T,-EGFP)#Miab/0
Genetic
Background
involves: 129P2/OlaHsd * FVB/N
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Pccatm1Tmiy mutation (1 available); any Pcca mutation (42 available)
Tg(CAG-PCCA*A138T,-EGFP)#Miab mutation (0 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
cellular
• cardiomyocytes show increased ROS levels
• pups from matings of homozygous Pccatm1Tmiy mice harboring the Tg(CAG-PCCA*A138T,-EGFP)#Maba transgene are much smaller than pups from matings of heterozygous Pccatm1Tmiy mice harboring the Tg(CAG-PCCA*A138T,-EGFP)#Maba transgene; phenotypic data reported below is for mice produced from PccatmTmiy/Pccatm1Tmiy Tg(CAG-PCCA*A138T,-EGFP)#Maba/0 parents

mortality/aging
• marginally decreased survival over 3 months after birth, with more than 75% survival beyond 90 days

growth/size/body
• heart mass is increased in 8 month old mice
• pups are smaller
• pups show delayed growth throughout neonatal development

homeostasis/metabolism
• increase in levels of propionylcarnitine/acetylcarnitine (C3/C2) ratio and methyl citrate beginning at 4 weeks of age, with an 18-fold increase in both on average
• 10 week old mice treated with adenoviral vectors expressing codon-optimized human PCCA show increases in growth and partial correction of C3/C2 and methyl citrate levels, however the effects are transient
• mice treated with AAV8 vectors expressing codon-optimized human PCCA show a rapid drop in C3/C2 and methyl citrate that is maintained for at least 13 weeks; treated 5 week old mice show a stronger effect than 10 week old mice
• plasma ammonia levels are elevated in 8 month old mice
• livers show 2.2% of wild-type propionyl-CoA carboxylase activity

cardiovascular system
• heart mass is increased in 8 month old mice
• 58% of mice show depressed cardiac function due to a decrease in ejection fraction
• failure of hearts to complete the systolic cycle, with an increase in left ventricular volume at the end of systole indicating impaired cardiac contractility
• however, no evidence of cardiac hypertrophy development and cardiomyocyte surface and cell capacitance are normal
• 40% of mice show spontaneous premature ventricular beats
• cardiomyocytes show depressed cell shortening and slower cell contraction velocity
• systolic calcium release in field-stimulated isolated cardiomyocytes is impaired, with lower amplitude of intracellular calcium transients elicited at 2 or 4 Hz
• cardiomyocytes show irregular diastolic calcium release, showing an increase in cytosolic calcium levels at rest
• the frequency of calcium sparks normalized to sarcoplasmic reticulum calcium load is higher in cardiomyocytes
• the percentage of cardiomyocytes presenting proarrhythmogenic calcium release is higher than in controls
• cardiomyocytes show impaired sarcoplasmic reticulum calcium load
• sarcoplasmic reticulum (SR)-calcium uptake is impaired in cardiomyocytes, with slower decay time of intracellular transients and lower values of Tau/peak intracellular transients ratio

muscle
• 58% of mice show depressed cardiac function due to a decrease in ejection fraction
• failure of hearts to complete the systolic cycle, with an increase in left ventricular volume at the end of systole indicating impaired cardiac contractility
• however, no evidence of cardiac hypertrophy development and cardiomyocyte surface and cell capacitance are normal

Mouse Models of Human Disease
DO ID OMIM ID(s) Ref(s)
propionic acidemia DOID:14701 OMIM:606054
J:282292 , J:286218


Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
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last database update
12/10/2024
MGI 6.24
The Jackson Laboratory