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Cytochrome c oxidase activity in T/t6 (balanced lethal) mutant mice.
Biochemical Genetics
|August 1, 1977
Summary
Mitochondrial function, specifically cytochrome c oxidase activity, is impaired in T/t6 mice liver fractions. This suggests the T/t locus on chromosome 17 may influence mitochondrial biogenesis and function.
Area of Science:
- Biochemistry
- Genetics
- Cell Biology
Background:
- Mitochondrial dysfunction is implicated in various diseases.
- The T/t locus on mouse chromosome 17 is known for its role in development and genetics.
Purpose of the Study:
- To investigate mitochondrial enzyme activities in T/t6 mice compared to B6CBAF1 controls.
- To explore the potential role of the T/t locus in mitochondrial function and biogenesis.
Main Methods:
- Analysis of liver fractions (R-1 and R-2) from T/t6 and B6CBAF1 mice.
- Quantification of protein content, mitochondria concentration, and activities of key respiratory-chain enzymes: cytochrome c oxidase, alpha-glycerophosphate dehydrogenase, and succinate-cytochrome c reductase.
Main Results:
- Cytochrome c oxidase activity per mitochondrion was significantly lower in both R-1 and R-2 liver fractions of T/t6 mice (approx. 40% lower in R-1).
- Significant variability in cytochrome c oxidase activity, mitochondria concentration, and body weight was observed among T/t6 mice.
- Alpha-glycerophosphate dehydrogenase activity was frequently elevated in T/t6 mice, particularly in the R-2 fraction.
Conclusions:
- The T/t locus may harbor genes crucial for mitochondrial function and biogenesis.
- Impaired cytochrome c oxidase activity in T/t6 mice suggests a specific mitochondrial defect linked to this genetic locus.