» Articles » PMID: 11081517

Signal-dependent Nuclear Export of a Histone Deacetylase Regulates Muscle Differentiation

Overview
Journal Nature
Specialty Science
Date 2000 Nov 18
PMID 11081517
Citations 460
Authors
Affiliations
Soon will be listed here.
Abstract

Members of the myocyte enhancer factor-2 (MEF2) family of transcription factors associate with myogenic basic helix-loop-helix transcription factors such as MyoD to activate skeletal myogenesis. MEF2 proteins also interact with the class II histone deacetylases HDAC4 and HDAC5, resulting in repression of MEF2-dependent genes. Execution of the muscle differentiation program requires release of MEF2 from repression by HDACs, which are expressed constitutively in myoblasts and myotubes. Here we show that HDAC5 shuttles from the nucleus to the cytoplasm when myoblasts are triggered to differentiate. Calcium/calmodulin-dependent protein kinase (CaMK) signalling, which stimulates myogenesis and prevents formation of MEF2-HDAC complexes, also induces nuclear export of HDAC4 and HDAC5 by phosphorylation of these transcriptional repressors. An HDAC5 mutant lacking two CaMK phosphorylation sites is resistant to CaMK-mediated nuclear export and acts as a dominant inhibitor of skeletal myogenesis, whereas a cytoplasmic HDAC5 mutant is unable to block efficiently the muscle differentiation program. Our results highlight a mechanism for transcriptional regulation through signal- and differentiation-dependent nuclear export of a chromatin-remodelling enzyme, and suggest that nucleo-cytoplasmic trafficking of HDACs is involved in the control of cellular differentiation.

Citing Articles

Sleep need driven oscillation of glutamate synaptic phenotype.

Vogt K, Kulkarni A, Pandi R, Pandey R, Dehnad M, Konopka G Elife. 2025; 13.

PMID: 39950545 PMC: 11828481. DOI: 10.7554/eLife.98280.


Acetylation of E2F1 at K125 facilitates cell apoptosis under serum stress.

Fang Z, Gong C, Hu Y, Cui T, Lin M, Lin S Transl Oncol. 2024; 52():102259.

PMID: 39731810 PMC: 11743828. DOI: 10.1016/j.tranon.2024.102259.


OGT mediated HDAC5 O-GlcNAcylation promotes osteogenesis by regulating the homeostasis of epigenetic modifications and proteolysis.

Du Y, Gao X, Chen J, Chen X, Liu H, He W J Orthop Translat. 2024; 50:14-29.

PMID: 39659899 PMC: 11626777. DOI: 10.1016/j.jot.2024.10.004.


The role of HDAC3 in inflammation: mechanisms and therapeutic implications.

Watson N, Kuppuswamy S, Ledford W, Sukumari-Ramesh S Front Immunol. 2024; 15:1419685.

PMID: 39050859 PMC: 11266039. DOI: 10.3389/fimmu.2024.1419685.


Post-translational modification-dependent oligomerization switch in regulation of global transcription and DNA damage repair during genotoxic stress.

Talukdar P, Pal S, Biswas D Nat Commun. 2024; 15(1):4128.

PMID: 38750015 PMC: 11096357. DOI: 10.1038/s41467-024-48530-8.


References
1.
Miska E, Karlsson C, Langley E, Nielsen S, Pines J, Kouzarides T . HDAC4 deacetylase associates with and represses the MEF2 transcription factor. EMBO J. 1999; 18(18):5099-107. PMC: 1171580. DOI: 10.1093/emboj/18.18.5099. View

2.
Mellon P, Clegg C, Correll L, McKnight G . Regulation of transcription by cyclic AMP-dependent protein kinase. Proc Natl Acad Sci U S A. 1989; 86(13):4887-91. PMC: 297520. DOI: 10.1073/pnas.86.13.4887. View

3.
Wu H, Naya F, McKinsey T, Mercer B, Shelton J, Chin E . MEF2 responds to multiple calcium-regulated signals in the control of skeletal muscle fiber type. EMBO J. 2000; 19(9):1963-73. PMC: 305686. DOI: 10.1093/emboj/19.9.1963. View

4.
Kato Y, Kravchenko V, Tapping R, Han J, Ulevitch R, Lee J . BMK1/ERK5 regulates serum-induced early gene expression through transcription factor MEF2C. EMBO J. 1998; 16(23):7054-66. PMC: 1170308. DOI: 10.1093/emboj/16.23.7054. View

5.
Grozinger C, Schreiber S . Regulation of histone deacetylase 4 and 5 and transcriptional activity by 14-3-3-dependent cellular localization. Proc Natl Acad Sci U S A. 2000; 97(14):7835-40. PMC: 16631. DOI: 10.1073/pnas.140199597. View