Key result
ABLIM-2 and -3 were identified as novel STARS-interacting proteins that bind F-actin, localize to actin stress fibers, and synergistically enhance STARS-dependent activation of SRF.
ABLIM-2 and -3 are novel actin-binding proteins that interact with STARS and modulate SRF-dependent transcription in muscle cells.
Does not yet inform clinical practice; extends preclinical understanding of STARS-SRF signaling in muscle.
In addition to regulating cell motility, contractility, and cytokinesis, the actin cytoskeleton plays a critical role in the regulation of transcription and gene expression. We have previously identified a novel muscle-specific actin-binding protein, STARS (striated muscle activator of Rho signaling), which directly binds actin and stimulates serum-response factor (SRF)-dependent transcription. To further dissect the STARS/SRF pathway, we performed a yeast two-hybrid screen of a skeletal muscle cDNA library using STARS as bait, and we identified two novel members of the ABLIM protein family, ABLIM-2 and -3, as STARS-interacting proteins. ABLIM-1, which is expressed in retina, brain, and muscle tissue, has been postulated to function as a tumor suppressor. ABLIM-2 and -3 display distinct tissue-specific expression patterns with the highest expression levels in muscle and neuronal tissue. Moreover, these novel ABLIM proteins strongly bind F-actin, are localized to actin stress fibers, and synergistically enhance STARS-dependent activation of SRF. Conversely, knockdown of endogenous ABLIM expression utilizing small interfering RNA significantly blunted SRF-dependent transcription in C2C12 skeletal muscle cells. These findings suggest that the members of the novel ABLIM protein family may serve as a scaffold for signaling modules of the actin cytoskeleton and thereby modulate transcription.
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Barrientos et al. (2006) studied this question. ABLIM-2 and ABLIM-3 identification and siRNA knockdown was evaluated on STARS-interacting proteins and SRF-dependent transcription. ABLIM-2 and -3 were identified as novel STARS-interacting proteins that bind F-actin, localize to actin stress fibers, and synergistically enhance STARS-dependent activation of SRF.
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