Histone Deacetylases (HDACs): Evolution, Specificity, Role in Transcriptional Complexes, and Pharmacological Actionability
Histone deacetylases (HDACs) are evolutionary conserved enzymes which operate by removing acetyl groups from histones and other protein regulatory factors, with functional consequences on chromatin remodeling and gene expression profiles. We provide here a review on the recent knowledge accrued on t...
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Published in | Genes Vol. 11; no. 5; p. 556 |
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Main Authors | , , , , , , |
Format | Journal Article |
Language | English |
Published |
Switzerland
MDPI AG
15.05.2020
MDPI |
Subjects | |
Online Access | Get full text |
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Abstract | Histone deacetylases (HDACs) are evolutionary conserved enzymes which operate by removing acetyl groups from histones and other protein regulatory factors, with functional consequences on chromatin remodeling and gene expression profiles. We provide here a review on the recent knowledge accrued on the zinc-dependent HDAC protein family across different species, tissues, and human pathologies, specifically focusing on the role of HDAC inhibitors as anti-cancer agents. We will investigate the chemical specificity of different HDACs and discuss their role in the human interactome as members of chromatin-binding and regulatory complexes. |
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AbstractList | Histone deacetylases (HDACs) are evolutionary conserved enzymes which operate by removing acetyl groups from histones and other protein regulatory factors, with functional consequences on chromatin remodeling and gene expression profiles. We provide here a review on the recent knowledge accrued on the zinc-dependent HDAC protein family across different species, tissues, and human pathologies, specifically focusing on the role of HDAC inhibitors as anti-cancer agents. We will investigate the chemical specificity of different HDACs and discuss their role in the human interactome as members of chromatin-binding and regulatory complexes. Histone deacetylases (HDACs) are evolutionary conserved enzymes which operate by removing acetyl groups from histones and other protein regulatory factors, with functional consequences on chromatin remodeling and gene expression profiles. We provide here a review on the recent knowledge accrued on the zinc-dependent HDAC protein family across different species, tissues, and human pathologies, specifically focusing on the role of HDAC inhibitors as anti-cancer agents. We will investigate the chemical specificity of different HDACs and discuss their role in the human interactome as members of chromatin-binding and regulatory complexes.Histone deacetylases (HDACs) are evolutionary conserved enzymes which operate by removing acetyl groups from histones and other protein regulatory factors, with functional consequences on chromatin remodeling and gene expression profiles. We provide here a review on the recent knowledge accrued on the zinc-dependent HDAC protein family across different species, tissues, and human pathologies, specifically focusing on the role of HDAC inhibitors as anti-cancer agents. We will investigate the chemical specificity of different HDACs and discuss their role in the human interactome as members of chromatin-binding and regulatory complexes. |
Author | Milazzo, Giorgio Mercatelli, Daniele Perini, Giovanni Di Muzio, Giulia Giorgi, Federico M. Triboli, Luca De Rosa, Piergiuseppe |
AuthorAffiliation | Department of Pharmacy and Biotechnology, University of Bologna, Via Selmi 3, 41026 Bologna, Italy; giorgio.milazzo@unibo.it (G.M.); danielemercatelli@gmail.com (D.M.); giulia.dimuzio@studio.unibo.it (G.D.M.); luca.triboli@studenti.unitn.it (L.T.); piergiuseppe.derosa2@unibo.it (P.D.R.); giovanni.perini@unibo.it (G.P.) |
AuthorAffiliation_xml | – name: Department of Pharmacy and Biotechnology, University of Bologna, Via Selmi 3, 41026 Bologna, Italy; giorgio.milazzo@unibo.it (G.M.); danielemercatelli@gmail.com (D.M.); giulia.dimuzio@studio.unibo.it (G.D.M.); luca.triboli@studenti.unitn.it (L.T.); piergiuseppe.derosa2@unibo.it (P.D.R.); giovanni.perini@unibo.it (G.P.) |
Author_xml | – sequence: 1 givenname: Giorgio surname: Milazzo fullname: Milazzo, Giorgio – sequence: 2 givenname: Daniele orcidid: 0000-0003-3228-0580 surname: Mercatelli fullname: Mercatelli, Daniele – sequence: 3 givenname: Giulia surname: Di Muzio fullname: Di Muzio, Giulia – sequence: 4 givenname: Luca surname: Triboli fullname: Triboli, Luca – sequence: 5 givenname: Piergiuseppe orcidid: 0000-0002-2632-1473 surname: De Rosa fullname: De Rosa, Piergiuseppe – sequence: 6 givenname: Giovanni surname: Perini fullname: Perini, Giovanni – sequence: 7 givenname: Federico M. orcidid: 0000-0002-7325-9908 surname: Giorgi fullname: Giorgi, Federico M. |
BackLink | https://www.ncbi.nlm.nih.gov/pubmed/32429325$$D View this record in MEDLINE/PubMed |
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Keywords | gene networks phylogenesis epigenomics histone deacetylases HDAC inhibitors cancer chromatin HDACi epigenetics HDAC |
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