Language
English
Publication Date
1-7-2025
Journal
Circulation
DOI
10.1161/CIRCULATIONAHA.123.067646
PMID
39185559
PMCID
PMC11671299
PubMedCentral® Posted Date
1-7-2026
PubMedCentral® Full Text Version
Author MSS
Abstract
Background: The Hippo pathway effector YAP (Yes-associated protein) plays an essential role in cardiomyocyte proliferation and heart regeneration. In response to physiological changes, YAP moves in and out of the nucleus. The pathophysiological mechanisms regulating YAP subcellular localization after myocardial infarction remain poorly defined.
Methods: We identified YAP acetylation at site K265 by in vitro acetylation followed by mass spectrometry analysis. We used adeno-associated virus to express YAP-containing mutations that either abolished acetylation (YAP-K265R) or mimicked acetylation (YAP-K265Q) and studied how acetylation regulates YAP subcellular localization in mouse hearts. We generated a cell line with YAP-K265R mutation and investigated the protein-protein interactors by YAP immunoprecipitation followed by mass spectrometry, then validated the YAP interaction in neonatal rat ventricular myocytes. We examined colocalization of YAP and TUBA4A (tubulin α 4A) by superresolution imaging. Furthermore, we developed YAP-K265R and αMHC-MerCreMer (MCM); Yap-loxP/K265R mutant mice to examine the pathophysiological role of YAP acetylation in cardiomyocytes during cardiac regeneration.
Results: We found that YAP is acetylated at K265 by CBP (CREB-binding protein)/P300 (E1A-binding protein P300) and is deacetylated by nicotinamide phosphoribosyltransferase/nicotinamide adenine dinucleotide/sirtuins axis in cardiomyocytes. After myocardial infarction, YAP acetylation is increased, which promotes YAP cytoplasmic localization. Compared with controls, mice that were genetically engineered to express a K265R mutation that prevents YAP K265 acetylation showed improved cardiac regenerative ability and increased YAP nuclear localization. Mechanistically, YAP acetylation facilitates its interaction with TUBA4A, a component of the microtubule network that sequesters acetylated YAP in the cytoplasm. After myocardial infarction, the microtubule network increased in cardiomyocytes, resulting in the accumulation of YAP in the cytoplasm.
Conclusions: After myocardial infarction, decreased sirtuin activity enriches YAP acetylation at K265. The growing TUBA4A network sequesters acetylated YAP within the cytoplasm, which is detrimental to cardiac regeneration.
Keywords
Animals, Acetylation, YAP-Signaling Proteins, Adaptor Proteins, Signal Transducing, Myocytes, Cardiac, Regeneration, Cytoplasm, Mice, Microtubules, Myocardial Infarction, Cell Cycle Proteins, Rats, Phosphoproteins, Humans, Transcription Factors, E1A-Associated p300 Protein, Mice, Inbred C57BL, Hippo pathway, NAD+, Sirt1/2, acetylation, myocardial infarction, microtubules
Published Open-Access
yes
Recommended Citation
Liu, Shijie; Deshmukh, Vaibhav; Meng, Fansen; et al., "Microtubules Sequester Acetylated YAP in the Cytoplasm and Inhibit Heart Regeneration" (2025). Faculty, Staff and Students Publications. 6403.
https://digitalcommons.library.tmc.edu/baylor_docs/6403