| Literature DB >> 31618641 |
Liqing Luo1, Sherry C Martin1, Jascha Parkington1, Samuel M Cadena1, Jiang Zhu1, Chikwendu Ibebunjo1, Serge Summermatter2, Nicole Londraville1, Krystyna Patora-Komisarska2, Leo Widler2, Huili Zhai1, Anne-Ulrike Trendelenburg1, David J Glass1, Jun Shi3.
Abstract
HDAC4, a class IIa histone deacetylase, is upregulated in skeletal muscle in response to denervation-induced atrophy. When HDAC4 is deleted postnatally, mice are partially protected from denervation. Despite the name "histone" deacetylase, HDAC4 demonstrably deacetylates cytosolic and non-histone nuclear proteins. We developed potent and selective class IIa HDAC inhibitors. Using these tools and genetic knockdown, we identified three previously unidentified substrates of HDAC4: myosin heavy chain, peroxisome proliferator-activated receptor gamma co-activator 1alpha (PGC-1α), and heat shock cognate 71 kDa protein (Hsc70). HDAC4 inhibition almost completely prevented denervation-induced loss of myosin heavy chain isoforms and blocked the action of their E3 ligase, MuRF1. PGC-1α directly interacts with class IIa HDACs; selective inhibitors increased PGC-1α protein in muscles. Hsc70 deacetylation by HDAC4 affects its chaperone activity. Through these endogenous HDAC4 substrates, we identified several muscle metabolic pathways that are regulated by class IIa HDACs, opening up new therapeutic options to treat skeletal muscle disorders and potentially other disease where these specific pathways are affected.Entities:
Keywords: HDAC4; Hsc70; PGC-1α; acetylation; atrophy; class IIa HDAC; deacetylation; denervation; dexamethasone; myosin heavy chain; skeletal muscle
Year: 2019 PMID: 31618641 DOI: 10.1016/j.celrep.2019.09.023
Source DB: PubMed Journal: Cell Rep Impact factor: 9.423