Key result
Increased binding of Sp3 to GC-rich elements in the βMyHC promoter is a critical event in the down-regulation of βMyHC gene expression under non-weight-bearing conditions.
Population
Adult skeletal muscle (plantaris muscle), Drosophila SL-2 cells, and mouse C2C12 myotubes
Design
Preclinical
Authors
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Does not inform clinical management of disuse atrophy; leaves open Sp3 as a mechanistic target for future human studies.
Sp3 proteins competitively inhibit Sp1 to down-regulate beta myosin heavy chain gene expression during skeletal muscle inactivity.
Tsika et al. (2004) studied Skeletal muscle inactivity. Non-weight-bearing (NWB) conditions vs. Control weight-bearing conditions was evaluated on βMyHC gene expression and Sp protein binding. Increased binding of Sp3 to GC-rich elements in the βMyHC promoter is a critical event in the down-regulation of βMyHC gene expression under non-weight-bearing conditions.
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