Regulation of Histone Acetylation in the Nucleus by Sphingosine-1-Phosphate

Author:

Hait Nitai C.1,Allegood Jeremy1,Maceyka Michael1,Strub Graham M.1,Harikumar Kuzhuvelil B.1,Singh Sandeep K.1,Luo Cheng23,Marmorstein Ronen2,Kordula Tomasz1,Milstien Sheldon4,Spiegel Sarah1

Affiliation:

1. Department of Biochemistry and Molecular Biology and the Massey Cancer Center, Virginia Commonwealth University School of Medicine, Richmond, VA 23298, USA.

2. The Wistar Institute and Department of Chemistry, University of Pennsylvania, Philadelphia, PA 19104, USA.

3. State Key Laboratory of Drug Research, Shanghai Institute of Materia Medica, Chinese Academy of Sciences, Shanghai 201203, P. R. China.

4. National Institute of Mental Health, National Institutes of Health, Bethesda, MD 20892, USA.

Abstract

Epigenetic Signals The lipid sphingosine-1-phosphate (S1P) is a signaling molecule that binds to receptors on the cell surface to initiate biochemical changes that control a range of biological processes from growth and survival to immune reactions. Hait et al. (p. 1254 ) report that S1P can also function by direct binding to the nuclear enzymes, histone deacetylases (HDACs) 1 and 2. The enzyme that generates S1P, sphingosine kinase 2 (ShpK2) is present in the nucleus in complexes with HDAC1 and HDAC2. Generation of S1P and its binding to HDACs inhibited deacetylation of histone. Such histone modification is an epigenetic mechanism that controls gene transcription. Thus, generation of S1P in the nucleus appears to be a signaling mechanism by which cells can control gene expression in response to various stimuli.

Publisher

American Association for the Advancement of Science (AAAS)

Subject

Multidisciplinary

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