[HTML][HTML] Context-dependent switch in chemo/mechanotransduction via multilevel crosstalk among cytoskeleton-regulated MRTF and TAZ and TGFβ-regulated Smad3

P Speight, M Kofler, K Szászi, A Kapus - Nature communications, 2016 - nature.com
P Speight, M Kofler, K Szászi, A Kapus
Nature communications, 2016nature.com
Myocardin-related transcription factor (MRTF) and TAZ are major mechanosensitive
transcriptional co-activators that link cytoskeleton organization to gene expression. Despite
many similarities in their regulation, their physical and/or functional interactions are
unknown. Here we show that MRTF and TAZ associate partly through a WW domain-
dependent mechanism, and exhibit multilevel crosstalk affecting each other's expression,
transport and transcriptional activity. Specifically, MRTF is essential for TAZ expression; TAZ …
Abstract
Myocardin-related transcription factor (MRTF) and TAZ are major mechanosensitive transcriptional co-activators that link cytoskeleton organization to gene expression. Despite many similarities in their regulation, their physical and/or functional interactions are unknown. Here we show that MRTF and TAZ associate partly through a WW domain-dependent mechanism, and exhibit multilevel crosstalk affecting each other’s expression, transport and transcriptional activity. Specifically, MRTF is essential for TAZ expression; TAZ and MRTF inhibit each other’s cytosolic mobility and stimulus-induced nuclear accumulation; they antagonize each other’s stimulatory effect on the α-smooth muscle actin (SMA) promoter, which harbours nearby cis-elements for both, but synergize on isolated TEAD-elements. Importantly, TAZ confers Smad3 sensitivity to the SMA promoter. Thus, TAZ is a context-dependent switch during mechanical versus mechano/chemical signalling, which inhibits stretch-induced but is indispensable for stretch+TGFβ-induced SMA expression. Crosstalk between these cytoskeleton-regulated factors seems critical for fine-tuning mechanical and mechanochemical transcriptional programmes underlying myofibroblast transition, wound healing and fibrogenesis.
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