DNA hypomethylation and aberrant expression of the human endogenous retrovirus ERVWE1/syncytin-1 in seminomas

. 2017 Mar 17 ; 14 (1) : 20. [epub] 20170317

Jazyk angličtina Země Anglie, Velká Británie Médium electronic

Typ dokumentu časopisecké články, práce podpořená grantem

Perzistentní odkaz   https://www.medvik.cz/link/pmid28302141
Odkazy

PubMed 28302141
PubMed Central PMC5356313
DOI 10.1186/s12977-017-0342-9
PII: 10.1186/s12977-017-0342-9
Knihovny.cz E-zdroje

BACKGROUND: Syncytin-1 and 2, human fusogenic glycoproteins encoded by the env genes of the endogenous retroviral loci ERVWE1 and ERVFRDE1, respectively, contribute to the differentiation of multinucleated syncytiotrophoblast in chorionic villi. In non-trophoblastic cells, however, the expression of syncytins has to be suppressed to avoid potential pathogenic effects. Previously, we have shown that the transcriptional suppression of ERVWE1 promoter is controlled epigenetically by DNA methylation and chromatin modifications. In this study, we describe the aberrant expression of syncytin-1 in biopsies of testicular germ cell tumors. RESULTS: We found efficient expression and splicing of syncytin-1 in seminomas and mixed germ cell tumors with seminoma component. Although another fusogenic gene, syncytin-2 was also derepressed in seminomas, its expression was significantly lower than that of syncytin-1. Neither the transcription factor GCM1 nor the increased copy number of ERVWE1 were sufficient for this aberrant expression of syncytin-1 in seminomas. In accordance with our recent finding of the highly increased expression of TET1 dioxygenase in most seminomas, the ERVWE1 promoter was significantly hypomethylated in comparison with the matched controls. In contrast, 5-hydroxymethylcytosine levels were not detectable at the ERVWE1 promoter. We further describe that another endogenous retroviral element adjacent to ERVWE1 remains transcriptionally suppressed and two additional HERV-W family members are only slightly upregulated in seminomas. CONCLUSIONS: We conclude that DNA demethylation of the ERVWE1 promoter in seminomas is a prerequisite for syncytin-1 derepression. We propose the spliced syncytin-1 expression as a marker of seminoma and suggest that aberrant expression of endogenous retroviruses might be a correlate of the hypomethylated genome of seminomas.

Zobrazit více v PubMed

Blaise S, de Parseval N, Benit L, Heidmann T. Genomewide screening for fusogenic human endogenous retrovirus envelopes identifies syncytin 2, a gene conserved on primate evolution. Proc Natl Acad Sci USA. 2003;100(22):13013–13018. doi: 10.1073/pnas.2132646100. PubMed DOI PMC

Frendo JL, Olivier D, Cheynet V, Blond JL, Bouton O, Vidaud M, et al. Direct involvement of HERV-W Env glycoprotein in human trophoblast cell fusion and differentiation. Mol Cell Biol. 2003;23(10):3566–3574. doi: 10.1128/MCB.23.10.3566-3574.2003. PubMed DOI PMC

Mi S, Lee X, Li X, Veldman GM, Finnerty H, Racie L, et al. Syncytin is a captive retroviral envelope protein involved in human placental morphogenesis. Nature. 2000;403(6771):785–789. doi: 10.1038/35001608. PubMed DOI

Moller AMJ, Delaisse J-M, Soe K. Osteoclast fusion: time-lapse reveals involvement of CD47 and syncytin-1 at different stages of nuclearity. J Cell Physiol. 2016;232(6):1396–1140. doi: 10.1002/jcp.25633. PubMed DOI PMC

Lavillette D, Marin M, Ruggieri A, Mallet F, Cosset FL, Kabat D. The envelope glycoprotein of human endogenous retrovirus type W uses a divergent family of amino acid transporters/cell surface receptors. J Virol. 2002;76(13):6442–6452. doi: 10.1128/JVI.76.13.6442-6452.2002. PubMed DOI PMC

Marin M, Lavillette D, Kelly SM, Kabat D. N-linked glycosylation and sequence changes in a critical negative control region of the ASCT1 and ASCT2 neutral amino acid transporters determine their retroviral receptor functions. J Virol. 2003;77(5):2936–2945. doi: 10.1128/JVI.77.5.2936-2945.2003. PubMed DOI PMC

Grandi N, Cadeddu M, Blomberg J, Tramontano E. Contribution of type W human endogenous retroviruses to the human genome: characterization of HERV-W proviral insertions and processed pseudogenes. Retrovirology. 2016;13(1):67. doi: 10.1186/s12977-016-0301-x. PubMed DOI PMC

Pavlicek A, Paces J, Elleder D, Hejnar J. Processed pseudogenes of human endogenous retroviruses generated by LINEs: their integration, stability, and distribution. Genome Res. 2002;12(3):391–399. doi: 10.1101/gr.216902. PubMed DOI PMC

Prudhomme S, Oriol G, Mallet F. A retroviral promoter and a cellular enhancer define a bipartite element which controls env ERVWE1 placental expression. J Virol. 2004;78(22):12157–12168. doi: 10.1128/JVI.78.22.12157-12168.2004. PubMed DOI PMC

Yu C, Shen K, Lin M, Chen P, Lin C, Chang GD, et al. GCMa regulates the syncytin-mediated trophoblastic fusion. J Biol Chem. 2002;277(51):50062–50068. doi: 10.1074/jbc.M209316200. PubMed DOI

Gimenez J, Montgiraud C, Oriol G, Pichon JP, Ruel K, Tsatsaris V, et al. Comparative methylation of ERVWE1/syncytin-1 and other human endogenous retrovirus LTRs in placenta tissues. DNA Res. 2009;16(4):195–211. doi: 10.1093/dnares/dsp011. PubMed DOI PMC

Matouskova M, Blazkova J, Pajer P, Pavlicek A, Hejnar J. CpG methylation suppresses transcriptional activity of human syncytin-1 in non-placental tissues. Exp Cell Res. 2006;312(7):1011–1020. doi: 10.1016/j.yexcr.2005.12.010. PubMed DOI

Trejbalova K, Blazkova J, Matouskova M, Kucerova D, Pecnova L, Vernerova Z, et al. Epigenetic regulation of transcription and splicing of syncytins, fusogenic glycoproteins of retroviral origin. Nucleic Acids Res. 2011;39(20):8728–8739. doi: 10.1093/nar/gkr562. PubMed DOI PMC

Gimenez J, Montgiraud C, Pichon JP, Bonnaud B, Arsac M, Ruel K, et al. Custom human endogenous retroviruses dedicated microarray identifies self-induced HERV-W family elements reactivated in testicular cancer upon methylation control. Nucleic Acids Res. 2010;38(7):2229–2246. doi: 10.1093/nar/gkp1214. PubMed DOI PMC

Vargas A, Moreau J, Landry S, LeBellego F, Toufaily C, Rassart E, et al. Syncytin-2 plays an important role in the fusion of human trophoblast cells. J Mol Biol. 2009;392(2):301–318. doi: 10.1016/j.jmb.2009.07.025. PubMed DOI

Liang CY, Wang LJ, Chen CP, Chen LF, Chen YH, Chen HW. GCM1 regulation of the expression of syncytin 2 and its cognate receptor MFSD2A in human placenta. Biol Reprod. 2010;83(3):387–395. doi: 10.1095/biolreprod.110.083915. PubMed DOI

Strissel PL, Ruebner M, Thiel F, Wachter D, Ekici AB, Wolf F, et al. Reactivation of codogenic endogenous retroviral (ERV) envelope genes in human endometrial carcinoma and prestages: emergence of new molecular targets. Oncotarget. 2012;3(10):1204–1219. doi: 10.18632/oncotarget.679. PubMed DOI PMC

Strick R, Ackermann S, Langbein M, Swiatek J, Schubert SW, Hashemolhosseini S, et al. Proliferation and cell-cell fusion of endometrial carcinoma are induced by the human endogenous retroviral syncytin-1 and regulated by TGF-beta. J Mol Med. 2007;85(1):23–38. doi: 10.1007/s00109-006-0104-y. PubMed DOI

Moch H, Cubilla AL, Humphrey PA, Reuter VE, Ulbright TM. The 2016 WHO classification of tumours of the urinary system and male genital organs-part A: renal, penile, and testicular tumours. Eur Urol. 2016;70(1):93–105. doi: 10.1016/j.eururo.2016.02.029. PubMed DOI

Almstrup K, Nielsen JE, Mlynarska O, Jansen MT, Jorgensen A, Skakkebaek NE, et al. Carcinoma in situ testis displays permissive chromatin modifications similar to immature foetal germ cells. Br J Cancer. 2010;103(8):1269–1276. doi: 10.1038/sj.bjc.6605880. PubMed DOI PMC

Kristensen DG, Nielsen JE, Jorgensen A, Skakkebaek NE, Rajpert-De Meyts E, Almstrup K. Evidence that active demethylation mechanisms maintain the genome of carcinoma in situ cells hypomethylated in the adult testis. Br J Cancer. 2014;110(3):668–678. doi: 10.1038/bjc.2013.727. PubMed DOI PMC

Looijenga LH, Gillis AJ, van Gurp RJ, Verkerk AJ, Oosterhuis JW. X inactivation in human testicular tumors. XIST expression and androgen receptor methylation status. Am J Pathol. 1997;151(2):581–590. PubMed PMC

Netto GJ, Nakai Y, Nakayama M, Jadallah S, Toubaji A, Nonomura N, et al. Global DNA hypomethylation in intratubular germ cell neoplasia and seminoma, but not in nonseminomatous male germ cell tumors. Mod Pathol. 2008;21(11):1337–1344. doi: 10.1038/modpathol.2008.127. PubMed DOI PMC

Peltomaki P. DNA methylation changes in human testicular cancer. Biochim Biophys Acta. 1991;1096(3):187–196. doi: 10.1016/0925-4439(91)90004-S. PubMed DOI

Smiraglia DJ, Szymanska J, Kraggerud SM, Lothe RA, Peltomaki P, Plass C. Distinct epigenetic phenotypes in seminomatous and nonseminomatous testicular germ cell tumors. Oncogene. 2002;21(24):3909–3916. doi: 10.1038/sj.onc.1205488. PubMed DOI

Wermann H, Stoop H, Gillis AJ, Honecker F, van Gurp RJ, Ammerpohl O, et al. Global DNA methylation in fetal human germ cells and germ cell tumours: association with differentiation and cisplatin resistance. J Pathol. 2010;221(4):433–442. PubMed

Gkountela S, Zhang KX, Shafiq TA, Liao WW, Hargan-Calvopina J, Chen PY, et al. DNA demethylation dynamics in the human prenatal germline. Cell. 2015;161(6):1425–1436. doi: 10.1016/j.cell.2015.05.012. PubMed DOI PMC

Guo F, Yan L, Guo H, Li L, Hu B, Zhao Y, et al. The transcriptome and DNA methylome landscapes of human primordial germ cells. Cell. 2015;161(6):1437–1452. doi: 10.1016/j.cell.2015.05.015. PubMed DOI

Tang WW, Dietmann S, Irie N, Leitch HG, Floros VI, Bradshaw CR, et al. A unique gene regulatory network resets the human germline epigenome for development. Cell. 2015;161(6):1453–1467. doi: 10.1016/j.cell.2015.04.053. PubMed DOI PMC

Benesova M, Trejbalova K, Kucerova D, Vernerova Z, Hron T, Szabo A, et al. Overexpression of TET dioxygenases in seminomas associates with low levels of DNA methylation and hydroxymethylation. Mol Carcinog. 2017 PubMed PMC

Ito S, D’Alessio AC, Taranova OV, Hong K, Sowers LC, Zhang Y. Role of tet proteins in 5mC to 5hmC conversion, ES-cell self-renewal and inner cell mass specification. Nature. 2010;466(7310):1129–1133. doi: 10.1038/nature09303. PubMed DOI PMC

He YF, Li BZ, Li Z, Liu P, Wang Y, Tang Q, et al. Tet-mediated formation of 5-carboxylcytosine and its excision by TDG in mammalian DNA. Science. 2011;333(6047):1303–1307. doi: 10.1126/science.1210944. PubMed DOI PMC

Ito S, Shen L, Dai Q, Wu SC, Collins LB, Swenberg JA, et al. Tet proteins can convert 5-methylcytosine to 5-formylcytosine and 5-carboxylcytosine. Science. 2011;333(6047):1300–1303. doi: 10.1126/science.1210597. PubMed DOI PMC

Yamaguchi S, Shen L, Liu Y, Sendler D, Zhang Y. Role of Tet1 in erasure of genomic imprinting. Nature. 2013;504(7480):460–464. doi: 10.1038/nature12805. PubMed DOI PMC

Kagiwada S, Kurimoto K, Hirota T, Yamaji M, Saitou M. Replication-coupled passive DNA demethylation for the erasure of genome imprints in mice. EMBO J. 2013;32(3):340–353. doi: 10.1038/emboj.2012.331. PubMed DOI PMC

Rengstl B, Newrzela S, Heinrich T, Weiser C, Thalheimer FB, Schmid F, et al. Incomplete cytokinesis and re-fusion of small mononucleated Hodgkin cells lead to giant multinucleated Reed-Sternberg cells. Proc Natl Acad Sci USA. 2013;110(51):20729–20734. doi: 10.1073/pnas.1312509110. PubMed DOI PMC

Strissel PL, Ellmann S, Loprich E, Thiel F, Fasching PA, Stiegler E, et al. Early aberrant insulin-like growth factor signaling in the progression to endometrial carcinoma is augmented by tamoxifen. Int J Cancer. 2008;123(12):2871–2879. doi: 10.1002/ijc.23900. PubMed DOI

Kassiotis G. Endogenous retroviruses and the development of cancer. J Immunol. 2014;192(4):1343–1349. doi: 10.4049/jimmunol.1302972. PubMed DOI PMC

Muroi Y, Sakurai T, Hanashi A, Kubota K, Nagaoka K, Imakawa K. CD9 regulates transcription factor GCM1 and ERVWE1 expression through the cAMP/protein kinase A signaling pathway. Reproduction. 2009;138(6):945–951. doi: 10.1530/REP-09-0082. PubMed DOI

von Hochstetter AR, Sigg C, Saremaslani P, Hedinger C. The significance of giant cells in human testicular seminomas. Virchows Arch A. 1985;407(3):309–322. doi: 10.1007/BF00710656. PubMed DOI

Butcher DN, Gregory WM, Gunter PA, Masters JR, Parkinson MC. The biological and clinical significance of HCG-containing cells in seminoma. Br J Cancer. 1985;51(4):473–478. doi: 10.1038/bjc.1985.68. PubMed DOI PMC

Trejbalova K, Kovarova D, Blazkova J, Machala L, Jilich D, Weber J, et al. Development of 5 LTR DNA methylation of latent HIV-1 provirus in cell line models and in long-term-infected individuals. Clin Epigenetics. 2016;8:19. doi: 10.1186/s13148-016-0185-6. PubMed DOI PMC

Bestor TH, Tycko B. Creation of genomic methylation patterns. Nat Genet. 1996;12(4):363–367. doi: 10.1038/ng0496-363. PubMed DOI

Roulois D, Yau HL, Singhania R, Wang YD, Danesh A, Shen SY, et al. DNA-demethylating agents target colorectal cancer cells by inducing viral mimicry by endogenous transcripts. Cell. 2015;162(5):961–973. doi: 10.1016/j.cell.2015.07.056. PubMed DOI PMC

Chiappinelli KB, Strissel PL, Desrichard A, Li HL, Henke C, Akman B, et al. Inhibiting DNA methylation causes an interferon response in cancer via dsRNA including endogenous retroviruses. Cell. 2015;162(5):974–986. doi: 10.1016/j.cell.2015.07.011. PubMed DOI PMC

Stengel S, Fiebig U, Kurth R, Denner J. Regulation of human endogenous retrovirus-K expression in melanomas by CpG methylation. Gene Chromosome Cancer. 2010;49(5):401–411. doi: 10.1002/gcc.20751. PubMed DOI

Santoni FA, Guerra J, Luban J. HERV-H RNA is abundant in human embryonic stem cells and a precise marker for pluripotency. Retrovirology. 2012;9:111. doi: 10.1186/1742-4690-9-111. PubMed DOI PMC

Friedli M, Turelli P, Kapopoulou A, Rauwel B, Castro-Diaz N, Rowe HM, et al. Loss of transcriptional control over endogenous retroelements during reprogramming to pluripotency. Genome Res. 2014;24(8):1251–1259. doi: 10.1101/gr.172809.114. PubMed DOI PMC

Fuchs NV, Loewer S, Daley GQ, Izsvak Z, Lower J, Lower R. Human endogenous retrovirus K (HML-2) RNA and protein expression is a marker for human embryonic and induced pluripotent stem cells. Retrovirology. 2013;10:115. doi: 10.1186/1742-4690-10-115. PubMed DOI PMC

Najít záznam

Citační ukazatele

Nahrávání dat ...

Možnosti archivace

Nahrávání dat ...