The crystal structure of <scene name='69/699997/Hdac8_binding_substrate/3'>HDAC8-substrate complex</scene> shows that aspartate residue <scene name='69/699997/Hdac8_d101/2'>(D101)</scene> is important in the substrate binding <ref>Vannini, A. et al. Substrate binding to histone deacetylases as shown by the crystal structure of the HDAC8–substrate complex. EMBO reports 8, 879–884 (2007).</ref>. The Asp 101 carboxylate moiety makes two consecutive hydrogen bonds with the backbone of the deacetylated peptide substrate. Mutation of Asp 101 to Ala inhibits HDAC8 activity. The Asp residue has been found to be strictly conserved among different HDAC isozymes.
The crystal structure of <scene name='69/699997/Hdac8_binding_substrate/3'>HDAC8-substrate complex</scene> shows that aspartate residue <scene name='69/699997/Hdac8_d101/2'>(D101)</scene> is important in the substrate binding <ref>Vannini, A. et al. Substrate binding to histone deacetylases as shown by the crystal structure of the HDAC8–substrate complex. EMBO reports 8, 879–884 (2007).</ref>. The Asp 101 carboxylate moiety makes two consecutive hydrogen bonds with the backbone of the deacetylated peptide substrate. Mutation of Asp 101 to Ala inhibits HDAC8 activity. The Asp residue has been found to be strictly conserved among different HDAC isozymes.
[[Image:D101.png|400px|left|thumb| '''Fig. 2''' Mutation of Asp 101 to Ala inhibits HDAC8 activity.]]
[[Image:D101.png|400px|left|thumb| '''Fig. 2''' Mutation of Asp 101 to Ala inhibits HDAC8 activity.]]
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Based on the crystallographic studies, a '''mechanism''' of the HDAC8 catalyzed reaction has been proposed.
Based on the crystallographic studies, a '''mechanism''' of the HDAC8 catalyzed reaction has been proposed.
[[Image:HDAC8_mechanism.png|400px|left|thumb| '''Fig. 3''' Catalytic mechanism of HDAC8.]]
[[Image:HDAC8_mechanism.png|400px|left|thumb| '''Fig. 3''' Catalytic mechanism of HDAC8.]]
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Chromatin, in eukaryotes, is a very compact structure mainly due to the electrostatic interaction between DNA and histones[1]. This interaction happens because DNA carries an overall negative charge and the histones carry a positive charge when deacetylated. In order to carry out the basic functions, such as transcription and replication, the chromatin has to be decondensed so that enzymes and transcription factors can access the DNA. The decondensation is mainly carried out by the acetylation of a lysine residue on the histone tail by Histone Acetyl Transferases (HATs). This then neutralizes its positive charge. The removal of the acetyl group is carried out by different enzyme family the histone deacetylases (HDACs).
Fig. 1 Acetylation and deacetylation of the lysine residue by HATs and HDACs, respectively.
HDAC8 contains a nuclear localization signal (NLS) at the center of the catalytic domain, and because of this tag it is found in the nucleus, however, it has been reported that HDAC8 has a cytosolic localization in muscle cells [2]. Global deletion of HDAC8 in mice leads to prenatal death due to instability of the skull [3]. HDACs seem to serve an important function in learning, memory and cognition in humans [4].
Disease
HDAC8 is a part of the class I HDAC isozymes. This class is involved in expression of p21, a cyclin-dependent kinase inhibitor [5]. The p21 proteins main job is to inhibit uncontrolled cell proliferation. A mutation in p53 gene has been reported in many cancer patients [6]. HDAC8 regulates the expression of both the wild type and the mutant form of p53 [6].Inhibition of HDACs provides an anticancer effect [7]. However, a pan-HDAC inhibitor usually shows considerable side effects in a clinical setting. This is probably because multiple HDAC isozymes are involved in several vital cellular processes. Isozyme selective inhibitors are likely to have fewer side effects as compared to a pan-inhibitor. They induce growth inhibition, dedifferentiation, and even cell death in cancer cells [8]. It is widely known that a pan-HDAC inhibitor significantly affects the acetylation status of histones as well as several non-histone proteins, such as HSP90, p53 and others. The therapeutic potential of an HDAC8 selective activator for the treatment of various forms of cancers has recently emerged. In the above case the expression of the tumor suppressor protein (p53) is reportedly suppressed by HDAC8 [6].
In some cases of Cornelia de Lange syndrome (CLdS), the cohesion acetylation cycle is impaired due to mutations in HDAC8[9]. The enzyme activity of all Class I HDACs has been found to be reduced in Chronic Obstructive Pulmonary Disease (COPD) [10]. Therapeutic potential of class I HDAC activators, specifically toward HDAC8, have not been well understood so far. However, there are several human diseases where an HDAC activator could be of great therapeutic benefits. In COPD and CLdS where the HDAC enzyme activity has been reported to be reduced, HDAC activators have a potential to lessen the disease conditions [9].
Structural highlights
HDAC8 was the first among the HDAC isozymes whose crystal structure became available. The image shows the ribbon structure of HDAC8 bound with a canonical hydroxamate inhibitor, SAHA (Suberoylanilide Hydroxamic Acid). HDAC8 contains a single α/β-deacetylase domain consisting of 13 α-helices and an eight-stranded parallel β-sheet. Multiple loops, which emanate from the protein core, play a significant role in maintaining the appropriate geometry of the catalytic pocket. The α/β-fold of the above kind was first observed in a metalloenzyme, Arginase. The active site of HDAC8 contains a tubular cavity leading to catalytic machinery at the end. The catalytic machinery is comprised of a Zn2+ ion penta-coordinated with a square pyramidal geometry. The residues His 180, Asp 267 and Asp 178 occupy the three co-ordination sites, whereas the hydroxamate moiety of SAHA occupies the remaining two sites. In addition, the carbonyl oxygen of the hydroxamate moiety forms a hydrogen bond with Tyr 306. In the absence of any ligand (substrate/inhibitors), two water molecules are bound to the Zn2+ ion. The linker domain of the inhibitor interacts with the residues: Phe 152, Phe 208, His 180, Gly 151, and Met 274, which forms a hydrophobic tunnel. Notably, the above residues involved in the inhibitor/substrate binding, as well as the catalysis, have been found to be conserved during the course of evolution among class I HDACs. Notably, the carbonyl oxygen of the acetyl-lysine substrate forms a hydrogen bond with the hydroxyl moiety of Y306.
Aside from the catalytic Zn2+ ion, the enzyme activity of HDAC8 is dependent on the presence of the monovalent ion, K+/Na+ [60]. The crystal structure of HDAC8 shows the presence of two binding sites for K+/Na+ [58]. The first K+/Na+ binding site (K1) is located in the vicinity of the enzyme catalytic machinery, and it is hexacoordinated (octahedral geometry) with His 180 (carbonyl oxygen of the main chain), Asp 178 (oxygen atom of the main chain and side chain), Leu 200 (carbonyl oxygen of the main chain), and Ser 199 (O). Notably, His 180 and Asp 178 are the common residues coordinated with both the catalytic Zn2+ as well as the K+/Na+ ion. The second binding site for K+/Na+ ion (K2) is located near the surface. It is hexacoordinated (octahedral geometry) with F189, T192, V195, Y225 as well as two water molecule.
The crystal structure of HDAC8-substrate complex shows that aspartate residue (D101) is important in the substrate binding [11]. The Asp 101 carboxylate moiety makes two consecutive hydrogen bonds with the backbone of the deacetylated peptide substrate. Mutation of Asp 101 to Ala inhibits HDAC8 activity. The Asp residue has been found to be strictly conserved among different HDAC isozymes.
Fig. 2 Mutation of Asp 101 to Ala inhibits HDAC8 activity.
Based on the crystallographic studies, a mechanism of the HDAC8 catalyzed reaction has been proposed.
Fig. 3 Catalytic mechanism of HDAC8.
HDAC8 has a some structural features which make it different from other HDACs. It lacks the C-terminal sequence the others use to recruit cofactors [12]. The studies of HDAC8 with different hydroxamate inhibitors: TSA, SAHA and M-334 shows that there is a certain amount of flexibility in its active site pocket. This seems to be due to the presence of the L1 loop (S30-K38)[12].
Conclusion
↑Ramakrishnan, V. Histone Structure and the Organization of the Nucleosome. Annual Review of Biophysics and Biomolecular Structure 26, 83–112 (1997).
↑Waltregny, D. et al. Histone deacetylase HDAC8 associates with smooth muscle alpha-actin and is essential for smooth muscle cell contractility. FASEB J. 19, 966–968 (2005).
↑Haberland, M., Mokalled, M. H., Montgomery, R. L. & Olson, E. N. Epigenetic control of skull morphogenesis by histone deacetylase 8. Genes Dev. 23, 1625–1630 (2009).
↑Gräff, J. & Tsai, L.-H. The Potential of HDAC Inhibitors as Cognitive Enhancers. Annual Review of Pharmacology and Toxicology 53, 311–330 (2013).
↑Blagosklonny, M. V. et al. Histone deacetylase inhibitors all induce p21 but differentially cause tubulin acetylation, mitotic arrest, and cytotoxicity. Mol. Cancer Ther. 1, 937–941 (2002).
↑ 6.06.16.2Yan, W. et al. Histone deacetylase inhibitors suppress mutant p53 transcription via histone deacetylase 8. Oncogene 32, 599–609 (2013).
↑Dokmanovic, M., Clarke, C. & Marks, P. A. Histone Deacetylase Inhibitors: Overview and Perspectives. Mol Cancer Res 5, 981–989 (2007).
↑Bolden, J. E., Peart, M. J. & Johnstone, R. W. Anticancer activities of histone deacetylase inhibitors. Nat Rev Drug Discov 5, 769–784 (2006).
↑ 9.09.1Deardorff, M. A. et al. HDAC8 mutations in Cornelia de Lange syndrome affect the cohesin acetylation cycle. Nature 489, 313–317 (2012).
↑Ito, K. et al. Decreased histone deacetylase activity in chronic obstructive pulmonary disease. N. Engl. J. Med. 352, 1967–1976 (2005).
↑Vannini, A. et al. Substrate binding to histone deacetylases as shown by the crystal structure of the HDAC8–substrate complex. EMBO reports 8, 879–884 (2007).
↑ 12.012.1Somoza, J. R. et al. Structural snapshots of human HDAC8 provide insights into the class I histone deacetylases. Structure 12, 1325–1334 (2004).
