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Epigenetic silencing of heat shock protein 70 through DNA hypermethylation in pseudoexfoliation syndrome and glaucoma

Abstract

This study is intended to investigate the epigenetic regulation of the most conserved molecular chaperone, HSP70 and its potential role in the pathophysiology of pseudoexfoliation syndrome (PEXS) and glaucoma (PEXG), a protein aggregopathy, contributing significantly to world blindness. Expression levels of HSP70 were significantly decreased in the lens capsule (LC) of PEXS but not in PEXG compared with that in control. Bisulfite sequencing of the LC of the study subjects revealed that the CpG islands (CGIs) located in the exonic region but not in the promoter region of HSP70 displayed hypermethylation only in PEXS individuals. There was a corresponding increase in DNA methyltransferase 3A (DNMT3A) expression in only PEXS individuals suggesting de novo methylation in this stage of the disease condition. On the other hand, peripheral blood of both PEXS and PEXG cases showed hypermethylation in the exonic region when compared with non-PEX controls displaying tissue-specific effects. Further, functional analyses of CGI spanning the exon revealed a decreased gene expression in the presence of methylated in comparison with unmethylated reporter gene vectors. Treatment of human lens epithelial B-3 (HLE B-3) cells with DNMT inhibitor restored the expression of HSP70 following depletion in methylation level at exonic CpG sites. In conclusion, a decreased HSP70 expression correlates with hypermethylation of a CGI of HSP70 in PEXS individuals. The present findings enhance our current understanding of the mechanism underlying HSP70 repression, contributing to the pathogenesis of PEX.

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References

  1. Ritch R, Schlötzer-Schrehardt U. Exfoliation syndrome. Surv Ophthalmol. 2001;45:265–315.

    Article  CAS  Google Scholar 

  2. Ritch R. Exfoliation syndrome and occludable angles. Trans Am Ophthalmol Soc. 1994;92:845–944.

    CAS  PubMed  PubMed Central  Google Scholar 

  3. Heijl A, Bengtsson B, Hyman L, Leske MC. Natural history of open-angle glaucoma. Ophthalmology. 2009;116:2271–6.

    Article  Google Scholar 

  4. Schlotzer-Schrehardt U, Naumann GOH. Trabecular meshwork in pseudoexfoliation syndrome with and without open-angle glaucoma: a morphometric, ultrastructural study. Investig Ophthalmol Vis Sci. 1995;36:1750–64.

    CAS  Google Scholar 

  5. Ehrlich R, Harris A, Lopez CR, Kheradiya NS. Pseudoexfoliation and blood flow abnormalities. Curr J Glaucoma Pract. 2008;2:18–25.

  6. Takai Y, Tanito M, Ohira A. Multiplex cytokine analysis of aqueous humor in eyes with primary open-angle glaucoma, exfoliation glaucoma, and cataract. Investig Ophthalmol Vis Sci. 2012;53:241–7.

    Article  CAS  Google Scholar 

  7. Helbig H, Schlötzer-Schrehardt U, Noske W, Kellner U, Foerster MH, Naumann GO. Anterior-chamber hypoxia and iris vasculopathy in pseudoexfoliation syndrome. Ger J Ophthalmol. 1994;3:148–53.

    CAS  PubMed  Google Scholar 

  8. Tanito M, Kaidzu S, Takai Y, Ohira A. Status of systemic oxidative stresses in patients with primary open-angle glaucoma and pseudoexfoliation syndrome. PLoS ONE. 2012;7:1–7.

    Article  Google Scholar 

  9. Hayat B, Padhy B, Mohanty PP, Alone DP. Altered unfolded protein response and proteasome impairment in pseudoexfoliation pathogenesis. Exp Eye Res. 2019;181:197–207.

    Article  CAS  Google Scholar 

  10. Schlötzer-Schrehardt U, Naumann GOH. Ocular and systemic pseudoexfoliation syndrome. Am J Ophthalmol. 2006;141:921–37.

  11. Zenkel M, Pöscbl E, Von Der Mark K, Hofmann-Rummelt C, Naumann GOH, Kruse FE, et al. Differential gene expression in pseudoexfoliation syndrome. Investig Ophthalmol Vis Sci. 2005;46:3742–52.

    Article  Google Scholar 

  12. Zenkel M, Kruse FE, Naumann GOH, Schlötzer-Schrehardt U. Impaired cytoprotective mechanisms in eyes with pseudoexfoliation syndrome/glaucoma. Investig Ophthalmol Vis Sci. 2007;48:5558–66.

    Article  Google Scholar 

  13. Bock C, Lengauer T. Computational epigenetics. Bioinformatics. 2008;24:1–10.

    Article  CAS  Google Scholar 

  14. Mathelier A, Fornes O, Arenillas DJ, Chen CY, Denay G, Lee J, et al. JASPAR 2016: a major expansion and update of the open-access database of transcription factor binding profiles. Nucleic Acids Res. 2016;44:D110–5.

    Article  CAS  Google Scholar 

  15. Gardiner-Garden M, Frommer M. CpG Islands in vertebrate genomes. J Mol Biol. 1987;196:261–82.

    Article  CAS  Google Scholar 

  16. Goll MG, Bestor TH. Eukaryotic cytosine methyltransferases. Annu Rev Biochem. 2005;74:481–514.

    Article  CAS  Google Scholar 

  17. Padhy B, Nanda GG, Chowdhury M, Padhi D, Rao A, Alone DP. Role of an extracellular chaperone, clusterin in the pathogenesis of pseudoexfoliation syndrome and pseudoexfoliation glaucoma. Exp Eye Res. 2014;127:69–76.

    Article  CAS  Google Scholar 

  18. Padhy B, Hayat B, Nanda GG, Mohanty PP, Alone DP. Pseudoexfoliation and Alzheimer’s associated CLU risk variant, rs2279590, lies within an enhancer element and regulates CLU, EPHX2 and PTK2B gene expression. Hum Mol Genet. 2017;26:4519–29.

    Article  CAS  Google Scholar 

  19. Ryan MT, Pfanner N. Hsp70 proteins in protein translocation. Adv Protein Chem. 2001;59:223–42.

    Article  CAS  Google Scholar 

  20. Hartl FU, Bracher A, Hayer-Hartl M. Molecular chaperones in protein folding and proteostasis. Nature. 2011;475:324–32.

    Article  CAS  Google Scholar 

  21. Mathur SK, Sistonen L, Brown IR, Murphy SP, Sarge KD, Morimoto RI. Deficient induction of human hsp70 heat shock gene transcription in Y79 retinoblastoma cells despite activation of heat shock factor 1. Proc Natl Acad Sci USA. 1994;91:8695–9.

    Article  CAS  Google Scholar 

  22. Deaton AM, Bird A. CpG islands and the regulation of transcription. Genes Dev. 2011;25:1010–22.

    Article  CAS  Google Scholar 

  23. Illingworth R, Kerr A, DeSousa D, Jørgensen H, Ellis P, Stalker J, et al. A novel CpG island set identifies tissue-specific methylation at developmental gene loci. PLoS Biol. 2008;6:37–51.

    Article  CAS  Google Scholar 

  24. Zhou P, Luo Y, Liu X, Fan L, Lu Y. Down-regulation and CpG island hypermethylation of CRYAA in age-related nuclear cataract. FASEB J. 2012;26:4897–902.

    Article  CAS  Google Scholar 

  25. Palsamy P, Ayaki M, Elanchezhian R, Shinohara T. Promoter demethylation of Keap1 gene in human diabetic cataractous lenses. Biochem Biophys Res Commun. 2012;423:542–8.

    Article  CAS  Google Scholar 

  26. Ye H, Jiang Y, Jing Q, Li D, Maimaiti T, Kasimu D, et al. LOXL1 hypermethylation in pseudoexfoliation syndrome in the uighur population. Investig Ophthalmol Vis Sci. 2015;56:5838–43.

    Article  CAS  Google Scholar 

  27. Okano M, Bell DW, Haber DA, Li E. DNA methyltransferases Dnmt3a and Dnmt3b are essential for de novo methylation and mammalian development. Cell. 1999;99:247–57.

    Article  CAS  Google Scholar 

  28. Venugopal R, Jaiswal AK. Nrf2 and Nrf1 in association with Jun proteins regulate antioxidant response element-mediated expression and coordinated induction of genes encoding detoxifying enzymes. Oncogene. 1998;17:3145–56.

    Article  CAS  Google Scholar 

  29. Izumi H, Ohta R, Nagatani G, Ise T, Nakayama Y, Nomoto M, et al. p300/CBP-associated factor (P/CAF) interacts with nuclear respiratory factor-1 to regulate the UDP-N-acetyl-α-D-galactosamine: polypeptide N-acetylgalactosaminyltransferase-3 gene. Biochem J. 2003;373:713–22.

    Article  CAS  Google Scholar 

  30. Gui Y, Guo G, Huang Y, Hu X, Tang A, Gao S, et al. Frequent mutations of chromatin remodeling genes in transitional cell carcinoma of the bladder. Nat Genet. 2011;43:875–8.

    Article  CAS  Google Scholar 

  31. Zhang Z. Phosphorylation of Kruppel-like factor 5 (KLF5/IKLF) at the CBP interaction region enhances its transactivation function. Nucleic Acids Res. 2003;31:2196–208.

    Article  CAS  Google Scholar 

  32. Wang GL, Semenza GL. General involvement of hypoxia-inducible factor 1 in transcriptional response to hypoxia. Proc Natl Acad Sci USA. 1993;90:4304–8.

    Article  CAS  Google Scholar 

  33. Laurenzana A, Petruccelli LA, Pettersson F, Figueroa ME, Melnick A, Baldwin AS, et al. Inhibition of DNA methyltransferase activates tumor necrosis factor A-induced monocytic differentiation in acute myeloid leukemia cells. Cancer Res. 2009;69:55–64.

    Article  CAS  Google Scholar 

  34. Tabolacci E, Mancano G, Lanni S, Palumbo F, Goracci M, Ferrè F, et al. Genome-wide methylation analysis demonstrates that 5-aza-2-deoxycytidine treatment does not cause random DNA demethylation in fragile X syndrome cells. Epigenetics Chromatin. 2016;9:12. http://epigeneticsandchromatin.biomedcentral.com/articles/10.1186/s13072-016-0060-x.

    Article  Google Scholar 

  35. Juttermann R, Li E, Jaenisch R. Toxicity of 5-aza-2′-deoxycytidine to mammalian cells is mediated primarily by covalent trapping of DNA methyltransferase rather than DNA demethylation. Proc Natl Acad Sci USA. 1994;91:11797–801.

    Article  CAS  Google Scholar 

  36. Jones PA, Taylor SM. Cellular differentiation, cytidine analogs and DNA methylation. Cell. 1980;20:85–93. https://www.sciencedirect.com/science/article/pii/0092867480902378?via%3Dihub.

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Acknowledgements

The authors thank the study participants for their contribution and consent for this study. This work was supported by the intramural grant to DPA from Microbes and Disease Biology Project (Project No.: XII-R&D-NIS-5.04-02), National Institute of Science Education and Research, Department of Atomic Energy (India).

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This work is supported by National Institute of Science Education and Research (NISER) an autonomous organization under Department of Atomic Energy, Government of India.

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Conceived and designed the experiments: DPA and BH; performed the experiments: BH, RSK, and BP; analyzed the data: BH, RSK, DPA, and BP; collection of samples: PPM; wrote and/or proofed the paper: BH, DPA, and RSK.

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Correspondence to Debasmita Pankaj Alone.

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Hayat, B., Kapuganti, R.S., Padhy, B. et al. Epigenetic silencing of heat shock protein 70 through DNA hypermethylation in pseudoexfoliation syndrome and glaucoma. J Hum Genet 65, 517–529 (2020). https://doi.org/10.1038/s10038-020-0736-8

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