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1.
Mediators Inflamm ; 2021: 6359652, 2021.
Article in English | MEDLINE | ID: mdl-34924813

ABSTRACT

Ellagic acid (EA) was reported to play protective roles in rheumatoid arthritis (RA). It was found that the level of metastasis-associated gene 1 (MTA1)/histone deacetylase 1 (HDAC1) protein complex was downregulated by polyphenols in several human disorders. Notably, inhibition of MTA1 or HDAC1 has anti-inflammatory effects on RA. Therefore, our study is aimed at investigating whether EA prevents RA progression through regulating the MTA1/HDAC1 complex. Herein, the human fibroblast-like synoviocyte (FLS) cell line MH7A was treated with TNF-α to induce an inflammation model in vitro and then incubated with different concentrations of EA. Western blot analysis showed that EA reduced MTA1 expression in a dose-dependent manner in MH7A cells. Then, TNF-α-treated MH7A cells were incubated with EA alone or together with MTA1 overexpression plasmid (pcDNA-MTA1), and we found that EA inhibited proliferation, inflammation cytokine levels, and oxidative stress marker protein levels and promoted apoptosis in MH7A cells, while MTA1 overexpression abolished these effects. Moreover, coimmunoprecipitation assay verified the interaction between MTA1 and HDAC1. EA downregulated the MTA1/HDAC1 complex in MH7A cells. MTA1 knockdown inhibited proliferation, inflammation, and oxidative stress and promoted apoptosis in MH7A cells, while HDAC1 overexpression reversed these effects. Moreover, chromatin immunoprecipitation assay indicated that EA inhibited HDAC1-mediated Nur77 deacetylation. Rescue experiments demonstrated that Nur77 knockdown reversed the effects of EA on MH7A cell biological behaviors. Additionally, EA treatment attenuated arthritis index, paw swelling, synovial hyperplasia, and inflammation in collagen-induced arthritis (CIA) rats. In conclusion, EA inhibited proliferation, inflammation, and oxidative stress and promoted apoptosis in MH7A cells and alleviated the severity of RA in CIA rats though downregulating MTA1/HDAC1 complex and promoting HDAC1 deacetylation-mediated Nur77 expression.


Subject(s)
Arthritis, Rheumatoid/drug therapy , Ellagic Acid/pharmacology , Histone Deacetylase 1/antagonists & inhibitors , Repressor Proteins/antagonists & inhibitors , Trans-Activators/antagonists & inhibitors , Acetylation , Animals , Apoptosis/drug effects , Cells, Cultured , Histone Deacetylase 1/physiology , Humans , Male , Nuclear Receptor Subfamily 4, Group A, Member 1/physiology , Oxidative Stress/drug effects , Rats , Rats, Wistar , Repressor Proteins/physiology , Trans-Activators/physiology
2.
Nucleic Acids Res ; 49(17): 9783-9798, 2021 09 27.
Article in English | MEDLINE | ID: mdl-34450641

ABSTRACT

The activity of hematopoietic factor GATA-1 is modulated through p300/CBP-mediated acetylation and FOG-1 mediated indirect interaction with HDAC1/2 containing NuRD complex. Although GATA-1 acetylation is implicated in GATA-1 activation, the role of deacetylation is not studied. Here, we found that the FOG-1/NuRD does not deacetylate GATA-1. However, HDAC1/2 can directly bind and deacetylate GATA-1. Two arginine residues within the GATA-1 linker region mediates direct interaction with HDAC1. The arginine to alanine mutation (2RA) blocks GATA-1 deacetylation and fails to induce erythroid differentiation. Gene expression profiling and ChIP-seq analysis further demonstrate the importance of GATA-1 deacetylation for gene activation and chromatin recruitment. GATA-12RA knock-in (KI) mice suffer mild anemia and thrombocytopenia with accumulation of immature erythrocytes and megakaryocytes in bone marrow and spleen. Single cell RNA-seq analysis of Lin- cKit+ (LK) cells further reveal a profound change in cell subpopulations and signature gene expression patterns in HSC, myeloid progenitors, and erythroid/megakaryocyte clusters in KI mice. Thus, GATA-1 deacetylation and its interaction with HDAC1 modulates GATA-1 chromatin binding and transcriptional activity that control erythroid/megakaryocyte commitment and differentiation.


Subject(s)
Chromatin/metabolism , GATA1 Transcription Factor/metabolism , Hematopoiesis/genetics , Histone Deacetylase 1/metabolism , Transcription, Genetic , Anemia/genetics , Animals , Binding Sites , Erythroid Cells/cytology , Erythroid Cells/metabolism , GATA1 Transcription Factor/genetics , GATA1 Transcription Factor/physiology , Gene Expression Regulation , Gene Knock-In Techniques , Histone Deacetylase 1/physiology , Megakaryocytes/cytology , Megakaryocytes/metabolism , Mice , Thrombocytopenia/genetics
3.
IUBMB Life ; 73(5): 784-799, 2021 05.
Article in English | MEDLINE | ID: mdl-33715270

ABSTRACT

The epigenetic abnormality is believed as a major driver for cancer initiation. Histone modification plays a vital role in tumor formation and progression. Particularly, alteration in histone acetylation has been highly associated with gene expression, cell cycle, as well as carcinogenesis. By analyzing glioblastoma (GBM)-related microarray from the GEO database and conducting chromatin immunoprecipitation-sequencing (ChIP-seq), we discovered that solute carrier family 30 member 3 (SLC30A3), a super enhancer (SE)-regulated factor, was significantly reduced in GBM tissues. Furthermore, histone deacetylase 1 (HDAC1), overexpressed in GBM tissues, could inhibit SLC30A3 expression by promoting histone H3K27ac deacetylation modification of the SE region of SLC30A3. Our functional validation revealed that SLC30A3 can inhibit the growth and metastatic spread of GBM cells in vitro and in vivo, and can activate the MAPK signaling pathway to promote apoptosis of GBM cells. Moreover, overexpression of HDAC1 resulted in a significant increase in DNA replication activity, a significant decline in apoptosis and cell cycle arrest in GBM cells. In a word, these findings indicate that combined epigenetic targeting of SLC30A3 by HDAC1 and SE is potentially therapeutically feasible in GBM.


Subject(s)
Brain Neoplasms/pathology , Cation Transport Proteins/genetics , Glioblastoma/pathology , Histone Code , Histone Deacetylase 1/physiology , Neoplasm Proteins/physiology , Acetylation , Adult , Aged , Animals , Apoptosis , Brain Neoplasms/genetics , Cell Cycle Checkpoints , Cell Line, Tumor , Chromatin Immunoprecipitation , DNA, Neoplasm/genetics , Epithelial-Mesenchymal Transition , Female , Glioblastoma/genetics , Heterografts , High-Throughput Nucleotide Sequencing , Histone Deacetylase 1/genetics , Humans , MAP Kinase Signaling System , Male , Mice , Mice, Inbred NOD , Mice, SCID , Middle Aged , Neoplasm Metastasis , Neoplasm Proteins/genetics , Phenotype , Protein Processing, Post-Translational , Young Adult
4.
Cell Death Dis ; 12(1): 5, 2021 01 04.
Article in English | MEDLINE | ID: mdl-33414424

ABSTRACT

Acute pancreatitis (AP), an acute inflammatory process, can be difficult to diagnose. Activating transcription factor 4 (ATF4) has been reported to participate in the pathogenesis of AP. Additionally, histone deacetylases (HDACs) are shown to be closely related to the development of a variety of diseases, including inflammation disease. In our study, we tried to highlight the role of ATF4 in AP through regulation of HDAC1. Firstly, we validated the effect of ATF4 on pancreatic acinar cell proliferation, apoptosis, and inflammation through in vitro experiments on cellular models of caerulein-induced AP. Next, we examined the correlation between ATF4 and HDAC1, and between HDAC1 with neutral endopeptidase (NEP) and kruppel-like factor 4 (KLF4). Finally, the regulatory role of ATF4 in AP was further assessed by determination of pathological conditions, biochemical indicators and inflammation through in vivo experiments on caerulein-induced AP mouse models. After AP induction, highly expressed ATF4 was observed, and silencing ATF4 could promote pancreatic acinar cell proliferation and inhibit apoptosis. ATF4 could bind to the HDAC1 promoter and upregulate its expression in AP. Moreover, HDAC1 could increase KLF4 expression by inhibiting NEP expression. Functionally, silencing ATF4 could suppress AP through regulation of NEP-mediated KLF4 via downregulation of HDAC1. Above all, our study uncovered the promotive role of ATF4 in AP through upregulation of HDAC1.


Subject(s)
Acinar Cells , Activating Transcription Factor 4/metabolism , Histone Deacetylase 1/physiology , Pancreas , Pancreatitis/metabolism , Acinar Cells/metabolism , Acinar Cells/pathology , Animals , Apoptosis , Cell Proliferation , Cells, Cultured , Inflammation , Kruppel-Like Factor 4 , Mice , Mice, Inbred C57BL , Pancreas/metabolism , Pancreas/pathology
5.
Life Sci ; 265: 118760, 2021 Jan 15.
Article in English | MEDLINE | ID: mdl-33212149

ABSTRACT

AIMS: Epigenetic regulation plays an important role in the progression of Alzheimer's disease (AD). Here, we identified differential methylation probes (DMP) and investigated their potential mechanistic roles in AD. MAIN METHODS: DMPs were identified via bioinformatic analysis of GSE66351, which was made up with 106 AD samples and 84 control samples derived from three separate brain regions. Differentially expressed genes (DEGs) were analyzed based on GSE5281 comprising 45 control samples and 58 AD samples. Gene ontology (GO), gene set enrichment analysis (GSEA), and protein-protein interaction (PPI) were used to identify pathways and hub genes. KEY FINDINGS: We found 9007 DMPs in Occipital Cortex glia, 1527 in OC neurons, 100 in Temporal Cortex, and 194 in Frontal Cortex. 74 DEGs were identified in Primary Visual Cortex, 67 of which were downregulated while seven upregulated. 482 were upregulated and 697 downregulated in medial temporal gyrus. In superior frontal gyrus, 687 were upregulated and 85 downregulated. GO and PPI revealed that pathways involving epithelial-cell differentiation, cellular responses to lipids, transcription corepressor activities, apoptotic and organ growth were modulated by histone deacetylase 1 (HDAC1) and associated with AD. Additionally, GSEA illustrated that the transforming growth factor beta signaling pathway was significantly enriched in some brain regions and HDAC1 played an important role in this pathway. SIGNIFICANCE: We found the glial-specific 3'UTR of HDAC1 was hypermethylated and HDAC1 was overexpressed in AD patients. Moreover, we also speculate that HDAC1 triggered signaling pathways linked to many different biological processes and functions via the regulation of histone deacetylation.


Subject(s)
3' Untranslated Regions , Alzheimer Disease/metabolism , Histone Deacetylase 1/metabolism , Neuroglia/metabolism , Signal Transduction , Alzheimer Disease/enzymology , DNA Methylation , Gene Expression Regulation , Histone Deacetylase 1/physiology , Humans , Neuroglia/enzymology , Protein Interaction Maps
6.
J Cell Mol Med ; 24(18): 10876-10888, 2020 09.
Article in English | MEDLINE | ID: mdl-32743904

ABSTRACT

Osteosarcoma (OS) is a malignant bone cancer lacking of effective treatment target when the metastasis occurred. This study investigated the implication of MicroRNA-326 in OS proliferation and metastasis to provide the clue for the treatment of metastatic OS. This study knocked down SP1 in MG63 and 143B cells and then performed Microarray assay to find the expression of miRNAs that were influenced by SP1. MTT, EdU, wound-healing and cell invasion assays were performed to evaluated cell proliferation and invasion. OS metastasis to lung was detected in a nude mice model. ChIP assay and DAPA were applied to determine the regulatory effect of SP1 and histone deacetylase 1 (HDAC) complex on miR-326 expression. Human OS tissues showed lowly expressed miR-326 but highly expressed Sp1 and HDAC. Sp1 recruited HDAC1 to miR-326 gene promoter, which caused the histone deacetylation and subsequent transcriptional inhibition of miR-326 gene. miR-326 deficiency induced the stimulation of SMO/Hedgehog pathway and promoted the proliferation and invasion of 143B and MG63 cells as well as the growth and metastasis in nude mice. SP1/HDAC1 caused the transcriptional inhibition of miR-326 gene by promoting histone deacetylation; miR-326 deficiency conversely stimulated SMO/Hedgehog pathway that was responsible for the proliferation and metastasis of OS.


Subject(s)
Bone Neoplasms/pathology , Histone Deacetylase 1/physiology , MicroRNAs/antagonists & inhibitors , Neoplasm Metastasis/physiopathology , Neoplasm Proteins/physiology , Osteosarcoma/pathology , RNA, Neoplasm/antagonists & inhibitors , Smoothened Receptor/biosynthesis , Sp1 Transcription Factor/physiology , Adolescent , Adult , Animals , Bone Neoplasms/genetics , Cell Division/drug effects , Cell Line, Tumor , Cell Movement/drug effects , Female , Gene Knockdown Techniques , Histone Deacetylase 1/antagonists & inhibitors , Histone Deacetylase 1/genetics , Humans , Male , Matrix Metalloproteinase 9/physiology , Mice , Mice, Nude , MicroRNAs/biosynthesis , MicroRNAs/genetics , Neoplasm Metastasis/genetics , Neoplasm Proteins/biosynthesis , Neoplasm Proteins/genetics , Osteosarcoma/genetics , Osteosarcoma/secondary , RNA Interference , RNA, Messenger/biosynthesis , RNA, Messenger/genetics , RNA, Neoplasm/biosynthesis , RNA, Neoplasm/genetics , RNA, Small Interfering/genetics , RNA, Small Interfering/pharmacology , Smoothened Receptor/genetics , Sp1 Transcription Factor/antagonists & inhibitors , Sp1 Transcription Factor/genetics , Xenograft Model Antitumor Assays , Young Adult , Zinc Finger Protein GLI1/physiology
7.
JCI Insight ; 5(4)2020 02 27.
Article in English | MEDLINE | ID: mdl-32102981

ABSTRACT

Some effector CD4+ T cell subsets display cytotoxic activity, thus breaking the functional dichotomy of CD4+ helper and CD8+ cytotoxic T lymphocytes. However, molecular mechanisms regulating CD4+ cytotoxic T lymphocyte (CD4+ CTL) differentiation are poorly understood. Here we show that levels of histone deacetylases 1 and 2 (HDAC1-HDAC2) are key determinants of CD4+ CTL differentiation. Deletions of both Hdac1 and 1 Hdac2 alleles (HDAC1cKO-HDAC2HET) in CD4+ T cells induced a T helper cytotoxic program that was controlled by IFN-γ-JAK1/2-STAT1 signaling. In vitro, activated HDAC1cKO-HDAC2HET CD4+ T cells acquired cytolytic activity and displayed enrichment of gene signatures characteristic of effector CD8+ T cells and human CD4+ CTLs. In vivo, murine cytomegalovirus-infected HDAC1cKO-HDAC2HET mice displayed a stronger induction of CD4+ CTL features compared with infected WT mice. Finally, murine and human CD4+ T cells treated with short-chain fatty acids, which are commensal-produced metabolites acting as HDAC inhibitors, upregulated CTL genes. Our data demonstrate that HDAC1-HDAC2 restrain CD4+ CTL differentiation. Thus, HDAC1-HDAC2 might be targets for the therapeutic induction of CD4+ CTLs.


Subject(s)
CD4-Positive T-Lymphocytes/cytology , Cell Differentiation/physiology , Histone Deacetylase 1/physiology , Histone Deacetylase 2/physiology , T-Lymphocytes, Cytotoxic/physiology , Animals , CD4-Positive T-Lymphocytes/drug effects , Fatty Acids/pharmacology , Histone Deacetylase 1/genetics , Histone Deacetylase 2/genetics , Humans , Mice , Mice, Knockout , Signal Transduction/physiology , T-Lymphocytes, Cytotoxic/drug effects , Up-Regulation/drug effects , Up-Regulation/physiology
8.
J Clin Invest ; 129(12): 5381-5399, 2019 12 02.
Article in English | MEDLINE | ID: mdl-31487270

ABSTRACT

Oral squamous cell carcinoma (OSCC) frequently invades the maxillary or mandibular bone, and this bone invasion is closely associated with poor prognosis and survival. Here, we show that CCL28 functions as a negative regulator of OSCC bone invasion. CCL28 inhibited invasion and epithelial-mesenchymal transition (EMT), and its inhibition of EMT was characterized by induced E-cadherin expression and reduced nuclear localization of ß-catenin in OSCC cells with detectable RUNX3 expression levels. CCL28 signaling via CCR10 increased retinoic acid receptor-ß (RARß) expression by reducing the interaction between RARα and HDAC1. In addition, CCL28 reduced RANKL production in OSCC and osteoblastic cells and blocked RANKL-induced osteoclastogenesis in osteoclast precursors. Intraperitoneally administered CCL28 inhibited tumor growth and osteolysis in mouse calvaria and tibia inoculated with OSCC cells. RARß expression was also increased in tumor tissues. In patients with OSCC, low CCL28, CCR10, and RARß expression levels were highly correlated with bone invasion. Patients with OSCC who had higher expression of CCL28, CCR10, or RARß had significantly better overall survival. These findings suggest that CCL28, CCR10, and RARß are useful markers for the prediction and treatment of OSCC bone invasion. Furthermore, CCL28 upregulation in OSCC cells or CCL28 treatment can be a therapeutic strategy for OSCC bone invasion.


Subject(s)
Bone and Bones/pathology , Chemokines, CC/pharmacology , Mouth Neoplasms/pathology , Receptors, Retinoic Acid/genetics , Squamous Cell Carcinoma of Head and Neck/pathology , Animals , Cell Line, Tumor , Epithelial-Mesenchymal Transition , Histone Deacetylase 1/physiology , Humans , Male , Mice , Mice, Inbred BALB C , Mice, Inbred ICR , Neoplasm Invasiveness , Osteoclasts/cytology , RANK Ligand/physiology , Receptors, CCR10/physiology , Retinoic Acid Receptor alpha/physiology
9.
FASEB J ; 33(7): 8008-8021, 2019 07.
Article in English | MEDLINE | ID: mdl-30913399

ABSTRACT

Schwann cells are the main supportive cells of the peripheral nerves. Schwann cells suffer inhibition of autophagy under hyperglycemia treatment in diabetic peripheral neuropathy (DPN). However, the exact mechanism is still not fully elucidated. We first observed the decrease of autophagy markers (LC3-II/LC3-I, P62) in the sciatic nerves of diabetic mice vs. normal mice, accompanied with the loss of myelinated nerve fibers and abnormal myelin sheath. In line with this, LC3-II/LC3-I and P62 were also significantly reduced in high glucose-treated rat Schwann cell 96 (RSC96) cells compared with normal glucose-treated cells. Furthermore, we found that trichostatin A [an inhibitor of histone deacetylase (HDAC)] evidently improved LC3-II/LC3-I in high glucose-treated RSC96 cells, without an effect on P62 expression. Again, HDAC1 and HDAC5 were revealed to be increased in RSC96 cells stimulated with high glucose. Inhibition of HDAC1 but not HDAC5 by small hairpin RNA vector enhanced LC3-II/LC3-I in high glucose-cultured RSC96 cells. In addition, LC3-II conversion regulators [autophagy-related protein (Atg)3, Atg5, and Atg7] were detected in high glucose-treated and HDAC1-knockdown RSC96 cells, and Atg3 was proven to be the key target of HDAC1. The presuppression of Atg3 offset the improvement of LC3-II/LC3-I resulting from HDAC1 inhibition in high glucose-treated RSC96 cells. The Janus kinase (JAK)-signal transducer and activator of transcription (STAT) signaling pathway was activated in RSC96 cells treated with high glucose, which was indicated by increased STAT3 phosphorylation. Blocking STAT3 phosphorylation by chemical inhibitor AG490 induced HDAC1 down-regulation followed by increases in Atg3 and LC3-II/LC3-I. Interestingly, we also found that AG490 treatment enhanced P62 expression in high glucose-stimulated RSC96 cells. Taken together, our findings demonstrate that hyperglycemia inhibits LC3-II/LC3-I in an HDAC1-Atg3-dependent manner and decreases P62 expression in an HDAC-independent manner via the JAK-STAT3 signaling pathway in the Schwann cells of DPN.-Du, W., Wang, N., Li, F. Jia, K., An, J., Liu, Y., Wang, Y., Zhu, L., Zhao, S. Hao, J. STAT3 phosphorylation mediates high glucose-impaired cell autophagy in an HDAC1-dependent and -independent manner in Schwann cells of diabetic peripheral neuropathy.


Subject(s)
Autophagy/drug effects , Diabetic Neuropathies/metabolism , Glucose/pharmacology , Histone Deacetylase 1/physiology , Protein Processing, Post-Translational , STAT3 Transcription Factor/metabolism , Schwann Cells/drug effects , Animals , Autophagy-Related Proteins/antagonists & inhibitors , Autophagy-Related Proteins/biosynthesis , Autophagy-Related Proteins/genetics , Biomarkers , Cell Line , Diabetes Mellitus, Experimental/metabolism , Diabetes Mellitus, Experimental/pathology , Diabetic Neuropathies/pathology , Gene Knockdown Techniques , Histone Deacetylase 1/antagonists & inhibitors , Histone Deacetylase 1/genetics , Histone Deacetylases/genetics , Histone Deacetylases/physiology , Hydroxamic Acids/pharmacology , Mice , Microtubule-Associated Proteins/biosynthesis , Microtubule-Associated Proteins/genetics , Myelin Sheath/pathology , Nerve Fibers, Myelinated/pathology , Peptide Synthases/antagonists & inhibitors , Peptide Synthases/biosynthesis , Peptide Synthases/genetics , Phosphorylation , RNA Interference , RNA, Small Interfering/genetics , RNA, Small Interfering/pharmacology , Rats , Schwann Cells/metabolism , Sciatic Nerve/metabolism , Sciatic Nerve/pathology , Tyrphostins/pharmacology , Up-Regulation
10.
Cell Mol Life Sci ; 76(5): 1005-1025, 2019 Mar.
Article in English | MEDLINE | ID: mdl-30599067

ABSTRACT

BACKGROUND: The ADAM10-mediated cleavage of transmembrane proteins regulates cellular processes such as proliferation or migration. Substrate cleavage by ADAM10 has also been implicated in pathological situations such as cancer or Morbus Alzheimer. Therefore, identifying endogenous molecules, which modulate the amount and consequently the activity of ADAM10, might contribute to a deeper understanding of the enzyme's role in both, physiology and pathology. METHOD: To elucidate the underlying cellular mechanism of the TBX2-mediated repression of ADAM10 gene expression, we performed overexpression, RNAi-mediated knockdown and pharmacological inhibition studies in the human neuroblastoma cell line SH-SY5Y. Expression analysis was conducted by e.g. real-time RT-PCR or western blot techniques. To identify the binding region of TBX2 within the ADAM10 promoter, we used luciferase reporter assay on deletion constructs and EMSA/WEMSA experiments. In addition, we analyzed a TBX2 loss-of-function Drosophila model regarding the expression of ADAM10 orthologs by qPCR. Furthermore, we quantified the mRNA level of TBX2 in post-mortem brain tissue of AD patients. RESULTS: Here, we report TBX2 as a transcriptional repressor of ADAM10 gene expression: both, the DNA-binding domain and the repression domain of TBX2 were necessary to effect transcriptional repression of ADAM10 in neuronal SH-SY5Y cells. This regulatory mechanism required HDAC1 as a co-factor of TBX2. Transcriptional repression was mediated by two functional TBX2 binding sites within the core promoter sequence (- 315 to - 286 bp). Analysis of a TBX2 loss-of-function Drosophila model revealed that kuzbanian and kuzbanian-like, orthologs of ADAM10, were derepressed compared to wild type. Vice versa, analysis of cortical brain samples of AD-patients, which showed reduced ADAM10 mRNA levels, revealed a 2.5-fold elevation of TBX2, while TBX3 and TBX21 levels were not affected. CONCLUSION: Our results characterize TBX2 as a repressor of ADAM10 gene expression and suggest that this regulatory interaction is conserved across tissues and species.


Subject(s)
ADAM10 Protein/genetics , Alzheimer Disease/etiology , Gene Expression Regulation , T-Box Domain Proteins/physiology , Amyloid Precursor Protein Secretases/genetics , Animals , Aspartic Acid Endopeptidases/genetics , Binding Sites , Brain/metabolism , Cells, Cultured , Disintegrins/genetics , Drosophila , Drosophila Proteins/genetics , Histone Deacetylase 1/physiology , Humans , Metalloendopeptidases/genetics , Mice , Mice, Inbred C57BL , Neurons/metabolism , Promoter Regions, Genetic , T-Box Domain Proteins/chemistry , Transcription, Genetic
11.
PLoS Genet ; 14(8): e1007578, 2018 08.
Article in English | MEDLINE | ID: mdl-30110327

ABSTRACT

SMYD4 belongs to a family of lysine methyltransferases. We analyzed the role of smyd4 in zebrafish development by generating a smyd4 mutant zebrafish line (smyd4L544Efs*1) using the CRISPR/Cas9 technology. The maternal and zygotic smyd4L544Efs*1 mutants demonstrated severe cardiac malformations, including defects in left-right patterning and looping and hypoplastic ventricles, suggesting that smyd4 was critical for heart development. Importantly, we identified two rare SMYD4 genetic variants in a 208-patient cohort with congenital heart defects. Both biochemical and functional analyses indicated that SMYD4(G345D) was pathogenic. Our data suggested that smyd4 functions as a histone methyltransferase and, by interacting with HDAC1, also serves as a potential modulator for histone acetylation. Transcriptome and bioinformatics analyses of smyd4L544Efs*1 and wild-type developing hearts suggested that smyd4 is a key epigenetic regulator involved in regulating endoplasmic reticulum-mediated protein processing and several important metabolic pathways in developing zebrafish hearts.


Subject(s)
Epigenesis, Genetic , Histone Methyltransferases/physiology , Histone-Lysine N-Methyltransferase/physiology , Zebrafish Proteins/physiology , Zebrafish/genetics , Adolescent , Animals , CRISPR-Cas Systems , Child , Child, Preschool , Cohort Studies , Disease Models, Animal , Embryonic Development/drug effects , Female , Gene Expression Profiling , Gene Expression Regulation, Developmental , Heart/drug effects , Heart/embryology , Heart Defects, Congenital/genetics , Histone Deacetylase 1/genetics , Histone Deacetylase 1/physiology , Histone Methyltransferases/genetics , Histone-Lysine N-Methyltransferase/genetics , Humans , Infant , Male , Mutation, Missense , Protein Conformation , Sequence Analysis, RNA , Transcriptome , Exome Sequencing , Zebrafish/embryology , Zebrafish Proteins/genetics
12.
Nat Commun ; 8(1): 728, 2017 09 28.
Article in English | MEDLINE | ID: mdl-28959017

ABSTRACT

Bilateral symmetry is a striking feature of the vertebrate body plan organization. Vertebral precursors, called somites, provide one of the best illustrations of embryonic symmetry. Maintenance of somitogenesis symmetry requires retinoic acid (RA) and its coactivator Rere/Atrophin2. Here, using a proteomic approach we identify a protein complex, containing Wdr5, Hdac1, Hdac2 and Rere (named WHHERE), which regulates RA signaling and controls embryonic symmetry. We demonstrate that Wdr5, Hdac1, and Hdac2 are required for RA signaling in vitro and in vivo. Mouse mutants for Wdr5 and Hdac1 exhibit asymmetrical somite formation characteristic of RA-deficiency. We also identify the Rere-binding histone methyltransferase Ehmt2/G9a, as a RA coactivator controlling somite symmetry. Upon RA treatment, WHHERE and Ehmt2 become enriched at RA target genes to promote RNA polymerase II recruitment. Our work identifies a protein complex linking key epigenetic regulators acting in the molecular control of embryonic bilateral symmetry.Retinoic acid (RA) regulates the maintenance of somitogenesis symmetry. Here, the authors use a proteomic approach to identify a protein complex of Wdr5, Hdac1, Hdac2 that act together with RA and coactivator Rere/Atrophin2 and a histone methyltransferase Ehmt2 to regulate embryonic symmetry.


Subject(s)
Embryo, Mammalian/metabolism , Embryonic Development , Tretinoin/physiology , Animals , E1A-Associated p300 Protein/genetics , E1A-Associated p300 Protein/metabolism , E1A-Associated p300 Protein/physiology , Embryo, Mammalian/cytology , Epigenesis, Genetic , Histone Deacetylase 1/genetics , Histone Deacetylase 1/metabolism , Histone Deacetylase 1/physiology , Histone Deacetylase 2/genetics , Histone Deacetylase 2/metabolism , Histone Deacetylase 2/physiology , Histone-Lysine N-Methyltransferase/genetics , Histone-Lysine N-Methyltransferase/metabolism , Histone-Lysine N-Methyltransferase/physiology , Histones/chemistry , Histones/metabolism , Intracellular Signaling Peptides and Proteins , Mice , Mice, Transgenic , Nerve Tissue Proteins/genetics , Nerve Tissue Proteins/metabolism , Nerve Tissue Proteins/physiology , Proteins/genetics , Proteins/metabolism , Proteins/physiology , Proteomics , Repressor Proteins/genetics , Repressor Proteins/metabolism , Repressor Proteins/physiology , Signal Transduction , Somites/growth & development , Somites/metabolism , Somites/ultrastructure , Tretinoin/metabolism
13.
Br J Haematol ; 178(5): 728-738, 2017 09.
Article in English | MEDLINE | ID: mdl-28480959

ABSTRACT

PTPN6, a tyrosine phosphatase protein, plays a negative role in cell signal transduction and is negatively correlated with tumour formation and growth. However, epigenetic regulation mechanism of the PTPN6 gene in advanced chronic myeloid leukaemia (CML) remains unclear. This study investigated bone marrow or blood samples from 44 CML patients and 10 healthy volunteers. KCL22 and K562 cells were cultured and treated with demethylation drugs and histone deacetylase inhibitors. Real time quantitative polymerase chain reaction (qPCR), methylation-specific PCR, bisulfite sequencing PCR, Western blotting, co-immunoprecipitation and chromatin immunoprecipitation (ChIP) was performed. PTPN6 was down-regulated in cell lines and patients with advanced phase CML, whereas DNMT1, DNMT3A, MECP2, MBD2 and HDAC1 were up-regulated. Treatment with 5-azacytidine, decitabine, sodium valproate and LBH589 increased PTPN6 expression, but decreased that of DNMT1, DNMT3A, MECP2, MBD2 and HDAC1. Immunoprecipitation and mass spectrometry showed that HDAC1 combined directly with PTPN6. ChIP-seq showed that HDAC1 did not combine with the promoter region of PTPN6, while MAPK, AKT, STAT5, JAK2 and MYC promoter regions all combined with HDAC1. PTPN6 is associated with progression of CML. Low expression level of PTPN6 was associated with DNA methylation and regulated by histone acetylation. HDAC1 participates in the regulation of PTPN6.


Subject(s)
Epigenesis, Genetic , Leukemia, Myelogenous, Chronic, BCR-ABL Positive/genetics , Protein Tyrosine Phosphatase, Non-Receptor Type 6/genetics , Adolescent , Adult , Aged , Antineoplastic Agents/administration & dosage , Antineoplastic Agents/pharmacology , CpG Islands/genetics , DNA Methylation , Dose-Response Relationship, Drug , Female , Gene Expression Regulation, Neoplastic/drug effects , Histone Deacetylase 1/metabolism , Histone Deacetylase 1/physiology , Humans , Leukemia, Myelogenous, Chronic, BCR-ABL Positive/pathology , Male , Middle Aged , Neoplasm Proteins/biosynthesis , Neoplasm Proteins/genetics , Promoter Regions, Genetic , Protein Tyrosine Phosphatase, Non-Receptor Type 6/biosynthesis , RNA, Messenger/genetics , RNA, Neoplasm/genetics , Tumor Cells, Cultured/drug effects , Young Adult
14.
Mol Biol Cell ; 28(2): 346-355, 2017 01 15.
Article in English | MEDLINE | ID: mdl-27903773

ABSTRACT

The Wnt signaling pathway is essential in regulating various cellular processes. Different mechanisms of inhibition for Wnt signaling have been proposed. Besides ß-catenin degradation through the proteasome, nemo-like kinase (NLK) is another molecule that is known to negatively regulate Wnt signaling. However, the mechanism by which NLK mediates the inhibition of Wnt signaling was not known. In the present study, we used primary embryonic fibroblast cells isolated from NLK-deficient mice and showed that these cells proliferate faster and have a shorter cell cycle than wild-type cells. In NLK-knockout cells, we observed sustained interaction between Lef1 and ß-catenin, leading to elevated luciferase reporter of ß-catenin/Lef1-mediated transcriptional activation. The mechanism for the reduced ß-catenin/Lef1 promoter activation was explained by phosphorylation of HDAC1 at serine 421 via NLK. The phosphorylation of HDAC1 was achieved only in the presence of wild-type NLK because a catalytically inactive mutant of NLK was unable to phosphorylate HDAC1 and reduced the luciferase reporter of ß-catenin/Lef1-mediated transcriptional activation. This result suggests that NLK and HDAC1 together negatively regulate Wnt signaling, which is vital in preventing aberrant proliferation of nontransformed primary fibroblast cells.


Subject(s)
Histone Deacetylase 1/metabolism , Mitogen-Activated Protein Kinases/metabolism , Animals , Cell Cycle , Fibroblasts , Histone Deacetylase 1/physiology , Lymphoid Enhancer-Binding Factor 1/metabolism , MAP Kinase Kinase Kinases/metabolism , Mice, Knockout , Mitogen-Activated Protein Kinases/physiology , Phosphorylation , Primary Cell Culture , Protein Serine-Threonine Kinases , Signal Transduction/physiology , Trans-Activators/metabolism , Transcription Factors/metabolism , Transcriptional Activation , Wnt Proteins/metabolism , Wnt Signaling Pathway/genetics , Wnt Signaling Pathway/physiology , beta Catenin/metabolism
15.
Cancer Res ; 77(4): 886-896, 2017 02 15.
Article in English | MEDLINE | ID: mdl-27923833

ABSTRACT

Maspin (SerpinB5) is an epithelial-specific tumor suppressor gene product that displays context-dependent cellular functions. Maspin-deficient mouse models created to date have not definitively established maspin functions critical for cancer suppression. In this study, we generated a mouse strain in which exon 4 of the Maspin gene was deleted, confirming its essential role in development but also enabling a breeding scheme to bypass embryonic lethality. Phenotypic characterization of this viable strain established that maspin deficiency was associated with a reduction in maximum body weight and a variety of context-dependent epithelial abnormalities. Specifically, maspin-deficient mice exhibited pulmonary adenocarcinoma, myoepithelial hyperplasia of the mammary gland, hyperplasia of luminal cells of dorsolateral and anterior prostate, and atrophy of luminal cells of ventral prostate and stratum spinosum of epidermis. These cancer phenotypes were accompanied by increased inflammatory stroma. These mice also displayed the autoimmune disorder alopecia aerate. Overall, our findings defined context-specific tumor suppressor roles for maspin in a clinically relevant model to study maspin functions in cancer and other pathologies. Cancer Res; 77(4); 886-96. ©2017 AACR.


Subject(s)
Embryonic Development , Serpins/physiology , Tumor Suppressor Proteins/physiology , Alopecia Areata/etiology , Animals , Female , Histone Deacetylase 1/physiology , Male , Mammary Glands, Animal/pathology , Mice , Mice, Inbred C57BL , Organ Specificity , Prostate/pathology , Serpins/genetics
16.
Anticancer Res ; 36(6): 2819-26, 2016 Jun.
Article in English | MEDLINE | ID: mdl-27272793

ABSTRACT

BACKGROUND: Loss of FAS expression in ovarian cancer cells has recently been associated with resistance to chemotherapeutic drugs. However, the mechanism for suppression of FAS expression is unknown. MATERIALS AND METHODS: The cell surface and transcript expressions of death receptors in parental chemosensitive (A2780) and their derivative chemoresistant (A2780-AD) ovarian cancer cells were determined by flow cytometry and quantitative real-time polymerase chain reaction, respectively. The epigenetic regulation of FAS promoters in both A2780 and A2780-AD ovarian epithelial cells were determined by chromatin immunoprecipitation assays. CONCLUSION: This study demonstrated that expression of FAS is suppressed in A2780-AD cells compared to parental A2780 ovarian cells. No difference in DNA methylation was observed at FAS promoters between A2780-AD cells compared to parental cells. However, the level of acetylated histone H3 associated with FAS promoter in A2780-AD cells was significantly lower compared to parental cells, and there was a corresponding increase in histone deacetylase 1 (HDAC1) enzyme associated with the FAS promoter in resistant cells. Knockdown of HDAC1 expression, and pharmacological inhibition of HDAC enzymatic activity significantly increased FAS expression in resistant A2780-AD cells. These results suggest that epigenetic changes in histone modifications may contribute to the loss of FAS expression in chemoresistant ovarian cancer cells and that enhancement of FAS expression could increase tumor cell sensitivity to immune cells.


Subject(s)
Histone Deacetylase 1/physiology , Ovarian Neoplasms/drug therapy , fas Receptor/genetics , Acetylation , Cisplatin/pharmacology , DNA Methylation , Drug Resistance, Neoplasm , Female , Humans , Ovarian Neoplasms/genetics , Ovarian Neoplasms/pathology , Promoter Regions, Genetic
17.
Exp Gerontol ; 86: 124-128, 2016 12 15.
Article in English | MEDLINE | ID: mdl-26927903

ABSTRACT

The epigenetic regulation of DNA structure and function is essential for changes in gene expression involved in development, growth, and maintenance of cellular function. Epigenetic changes include histone modifications such as methylation, acetylation, ubiquitination, and phosphorylation. Histone deacetylase (HDAC) proteins have a major role in epigenetic regulation of chromatin structure. HDACs are enzymes that catalyze the removal of acetyl groups from lysine residues within histones, as well as a range of other proteins including transcriptional factors. HDACs are highly conserved proteins divided into two families and based on sequence similarity in four classes. Here we will discuss the roles of Rpd3 in physiology and longevity with emphasis on its role in flies. Rpd3, the Drosophila HDAC1 homolog, is a class I lysine deacetylase and a member of a large family of HDAC proteins. Rpd3 has multiple functions including control of proliferation, development, metabolism, and aging. Pharmacological and dietary HDAC inhibitors have been used as therapeutics in psychiatry, cancer, and neurology.


Subject(s)
Drosophila Proteins/physiology , Histone Deacetylase 1/physiology , Longevity/physiology , Aging/physiology , Animals , Diet , Drosophila/genetics , Drosophila/metabolism , Drosophila/physiology , Drosophila Proteins/deficiency , Drosophila Proteins/genetics , Epigenesis, Genetic/physiology , Histone Deacetylase 1/deficiency , Histone Deacetylase 1/genetics , Histone Deacetylase Inhibitors/pharmacology , Histone Deacetylases/physiology , Sirtuins/physiology
18.
Neurobiol Aging ; 37: 103-116, 2016 Jan.
Article in English | MEDLINE | ID: mdl-26545632

ABSTRACT

With increased histone deacetylase (HDAC) activity and histone hypoacetylation being implicated in neurodegeneration, HDAC inhibitors have been reported to have considerable therapeutic potential. Yet, existing inhibitors lack specificity and may show substantial adverse effect. In this study, we identified a novel HDAC1/2 isoform-specific inhibitor, K560, with protective effects against 1-methyl-4-phenylpyridinium (MPP(+))- and/or 1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine (MPTP)-induced neuronal death in both in vitro and in vivo Parkinson's disease model. K560 attenuated cell death induced by MPP(+) in differentiated SH-SY5Y cells through the sustained expression of an antiapoptotic protein, X-linked inhibitor of apoptosis (XIAP). Inhibition of XIAP expression by locked nucleic acid antisense oligonucleotides abolished the protective effect of K560. Inactivation of mitogen-activated protein kinase cascades, reduced p53 phosphorylation, and down-regulation of p53-upregulated modulator of apoptosis on K560 treatment were also observed. Furthermore, pre- and post-oral administration of K560 to mice prevented MPTP-induced loss of dopaminergic neurons in substantia nigra, suggesting that selective inhibition of HDAC1 and HDAC2 by K560 may pave the way to new strategies for Parkinson's disease treatment.


Subject(s)
Benzamides/therapeutic use , Diketopiperazines/therapeutic use , Enzyme Inhibitors/therapeutic use , Histone Deacetylase 1/antagonists & inhibitors , Histone Deacetylase 2/antagonists & inhibitors , Molecular Targeted Therapy , Neuroprotective Agents/therapeutic use , Parkinson Disease/drug therapy , Acetylation , Administration, Oral , Animals , Benzamides/administration & dosage , Benzamides/pharmacology , Cell Death/drug effects , Cell Death/genetics , Cell Line, Tumor , Diketopiperazines/administration & dosage , Diketopiperazines/pharmacology , Disease Models, Animal , Drug Evaluation, Preclinical , Enzyme Inhibitors/pharmacology , Gene Expression/drug effects , Histone Deacetylase 1/physiology , Histone Deacetylase 2/physiology , Histones/metabolism , Humans , Isoenzymes , Mice , Neuroprotective Agents/pharmacology , Parkinson Disease/etiology , Parkinson Disease/pathology , X-Linked Inhibitor of Apoptosis Protein/genetics , X-Linked Inhibitor of Apoptosis Protein/metabolism
20.
EMBO Rep ; 16(10): 1288-98, 2015 Oct.
Article in English | MEDLINE | ID: mdl-26303947

ABSTRACT

The histone H3K27 demethylase, UTX, is a known component of the H3K4 methyltransferase MLL complex, but its functional association with H3K4 methylation in human cancers remains largely unknown. Here we demonstrate that UTX loss induces epithelial-mesenchymal transition (EMT)-mediated breast cancer stem cell (CSC) properties by increasing the expression of the SNAIL, ZEB1 and ZEB2 EMT transcription factors (EMT-TFs) and of the transcriptional repressor CDH1. UTX facilitates the epigenetic silencing of EMT-TFs by inducing competition between MLL4 and the H3K4 demethylase LSD1. EMT-TF promoters are occupied by c-Myc and MLL4, and UTX recognizes these proteins, interrupting their transcriptional activation function. UTX decreases H3K4me2 and H3 acetylation at these promoters by forming a transcriptional repressive complex with LSD1, HDAC1 and DNMT1. Taken together, our findings indicate that UTX is a prominent tumour suppressor that functions as a negative regulator of EMT-induced CSC-like properties by epigenetically repressing EMT-TFs.


Subject(s)
Epigenetic Repression , Epithelial-Mesenchymal Transition , Histone Demethylases/genetics , Neoplastic Stem Cells/physiology , Nuclear Proteins/genetics , Repressor Proteins/genetics , Breast Neoplasms , Cell Line, Tumor , Epithelial-Mesenchymal Transition/genetics , Female , Gene Expression Regulation, Neoplastic , Histone Deacetylase 1/genetics , Histone Deacetylase 1/physiology , Histone Demethylases/physiology , Humans , Promoter Regions, Genetic , Protein Processing, Post-Translational , Transcription Factors/genetics , Transcription Factors/metabolism
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