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α-Actinin 4 and BAT1 interaction with the Cytochrome c promoter upon skeletal muscle differentiation
- Source :
- Current Genetics. 49:125-135
- Publication Year :
- 2005
- Publisher :
- Springer Science and Business Media LLC, 2005.
-
Abstract
- To identify common regulatory features of nuclear genes encoding mitochondrial proteins we searched for regulatory elements in the Cytochrome c promoter during skeletal muscle differentiation in cell culture. A consensus element with the sequence GCTGCCGCAC-(N4-20)-GGSCGYGGG was found in both rat Cyt c and coxIV promoters. This new sequence element with yet undescribed function, but high abundance in promoters of nuclear genes encoding mitochondrial proteins available from the databases, showed a striking change in protein binding in electromobility shift assays when myoblasts were compared to myotubes. Proteins involved in the observed protein-DNA complexes were isolated from myotubes and identified by MALDI-TOF as BAT1, a DEAD-box protein of yet unknown function, heat shock protein HSP84, and alpha-actinin 4, a non-muscle isoform of the structural protein alpha-actinin. alpha-actinin 4 was found to be preferentially localized in the nucleus upon induction of myogenesis, suggesting a signaling function during muscle differentiation. In conclusion, the analyzed sequence motif may be a new candidate for common regulatory elements specific for nuclear encoded mitochondrial genes, and alpha-actinin 4 may be involved in their regulation.
- Subjects :
- Nuclear gene
Myoblasts, Skeletal
Biology
Mitochondrion
Cell Line
DEAD-box RNA Helicases
Mice
Heat shock protein
Genetics
medicine
Animals
Humans
Myocyte
Actinin
Muscle, Skeletal
Promoter Regions, Genetic
Myogenesis
Computational Biology
Cytochromes c
Skeletal muscle
Cell Differentiation
Promoter
General Medicine
Molecular biology
Rats
Cell biology
medicine.anatomical_structure
Mutation
Sequence motif
Subjects
Details
- ISSN :
- 14320983 and 01728083
- Volume :
- 49
- Database :
- OpenAIRE
- Journal :
- Current Genetics
- Accession number :
- edsair.doi.dedup.....9ad2a72ec796813acc93f4bf5c6e8f7d
- Full Text :
- https://doi.org/10.1007/s00294-005-0043-0