Journal
JOURNAL OF EXPERIMENTAL BIOLOGY
Volume 224, Issue 2, Pages -Publisher
COMPANY BIOLOGISTS LTD
DOI: 10.1242/jeb.238634
Keywords
Skeletal muscle; Sarcolipin; Ca2+-handling proteins; Mitochondrial metabolism; Mouse strain
Categories
Funding
- Science and Engineering Research Board, Department of Science and Technology, India [ECR/2016/001247]
- Department of Biotechnology, Ministry of Science and Technology, India [BT/RLF/Reentry/41/2014, BT/PR28935/MED/30/2035/2018]
- National Institutes of Health [R01-HL 088555, R01 DK098240-01]
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Comparing SLN expression and key proteins involved in Ca2+ handling and mitochondrial metabolism between FVB/N and C57BU6J mouse strains showed that SLN expression is lower in FVB/N mice. Additionally, Ca2+ transporters and electron transport chain proteins in the mitochondria were also less abundant in FVB/N mice, indicating potential differences in energy metabolism. Researchers should consider these variations when interpreting data from studies using different mouse strains in the future.
Genetically engineered mouse models have been used to determine the role of sarcolipin (SLN) in muscle. However, a few studies had difficulty in detecting SLN in FBV/N mice and questioned its relevance to muscle metabolism. It is known that genetic alteration of proteins in different inbred mice strains produces dissimilar functional outcomes. Therefore, here we compared the expression of SLN and key proteins involved in Ca2+ handling and mitochondrial metabolism between FVB/N and C57BU6J mouse strains. Data suggest that SLN expression is less abundant in the skeletal muscles of FVB/N mice than in the C57BL/6J strain. The expression of Ca2+ transporters in the mitochondrial membranes was also lower in FVB/N than in C57BL/6J mice. Similarly, electron transport chain proteins in the mitochondria were less abundant in FVB/N mice, which may contribute to differences in energy metabolism. Future studies using different mouse strains should take these differences into account when interpreting their data.
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