Heterologous avian system for quantitative analysis of Syncytin-1 interaction with ASCT2 receptor

. 2021 Jun 22 ; 18 (1) : 15. [epub] 20210622

Jazyk angličtina Země Velká Británie, Anglie Médium electronic

Typ dokumentu časopisecké články, práce podpořená grantem

Perzistentní odkaz   https://www.medvik.cz/link/pmid34158079
Odkazy

PubMed 34158079
PubMed Central PMC8220723
DOI 10.1186/s12977-021-00558-0
PII: 10.1186/s12977-021-00558-0
Knihovny.cz E-zdroje

BACKGROUND: Human Syncytin-1 is a placentally-expressed cell surface glycoprotein of retroviral origin. After interaction with ASCT2, its cellular receptor, Syncytin-1 triggers cell-cell fusion and formation of a multinuclear syncytiotrophoblast layer of the placenta. The ASCT2 receptor is a multi-spanning membrane protein containing a protruding extracellular part called region C, which has been suggested to be a retrovirus docking site. Precise identification of the interaction site between ASCT2 and Syncytin-1 is challenging due to the complex structure of ASCT2 protein and the background of endogenous ASCT2 gene in the mammalian genome. Chicken cells lack the endogenous background and, therefore, can be used to set up a system with surrogate expression of the ASCT2 receptor. RESULTS: We have established a retroviral heterologous chicken system for rapid and reliable assessment of ectopic human ASCT2 protein expression. Our dual-fluorescence system proved successful for large-scale screening of mutant ASCT2 proteins. Using this system, we demonstrated that progressive deletion of region C substantially decreased the amount of ASCT2 protein. In addition, we implemented quantitative assays to determine the interaction of ASCT2 with Syncytin-1 at multiple levels, which included binding of the soluble form of Syncytin-1 to ASCT2 on the cell surface and a luciferase-based assay to evaluate cell-cell fusions that were triggered by Syncytin-1. Finally, we restored the envelope function of Syncytin-1 in a replication-competent retrovirus and assessed the infection of chicken cells expressing human ASCT2 by chimeric Syncytin-1-enveloped virus. The results of the quantitative assays showed that deletion of the protruding region C did not abolish the interaction of ASCT2 with Syncytin-1. CONCLUSIONS: We present here a heterologous chicken system for effective assessment of the expression of transmembrane ASCT2 protein and its interaction with Syncytin-1. The system profits from the absence of endogenous ASCT2 background and implements the quantitative assays to determine the ASCT2-Syncytin-1 interaction at several levels. Using this system, we demonstrated that the protruding region C was essential for ASCT2 protein expression, but surprisingly, not for the interaction with Syncytin-1 glycoprotein.

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Blond JL, Lavillette D, Cheynet V, Bouton O, Oriol G, Chapel-Fernandes S, et al. An envelope glycoprotein of the human endogenous retrovirus HERV-W is expressed in the human placenta and fuses cells expressing the type D mammalian retrovirus receptor. J Virol. 2000;74(7):3321–3329. doi: 10.1128/jvi.74.7.3321-3329.2000. 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

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

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;56(8):1837–1850. doi: 10.1002/mc.22638. PubMed DOI PMC

Lin C, Lin M, Chen H. Biochemical characterization of the human placental transcription factor GCMa/1. Biochem Cell Biol. 2005;83(2):188–195. doi: 10.1139/o05-026. PubMed DOI

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

Benesova M, Trejbalova K, Kovarova D, Vernerova Z, Hron T, Kucerova D, et al. DNA hypomethylation and aberrant expression of the human endogenous retrovirus ERVWE1/syncytin-1 in seminomas. Retrovirology. 2017;14(1):20. doi: 10.1186/s12977-017-0342-9. PubMed DOI PMC

Cheynet V, Ruggieri A, Oriol G, Blond JL, Boson B, Vachot L, et al. Synthesis, assembly, and processing of the Env ERVWE1/syncytin human endogenous retroviral envelope. J Virol. 2005;79(9):5585–5593. doi: 10.1128/JVI.79.9.5585-5593.2005. PubMed DOI PMC

Cheynet V, Oriol G, Mallet F. Identification of the hASCT2-binding domain of the Env ERVWE1/syncytin-1 fusogenic glycoprotein. Retrovirology. 2006;3:41. doi: 10.1186/1742-4690-3-41. 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

Guo H, Xu Y, Wang F, Shen Z, Tuo X, Qian H, et al. Clinical associations between ASCT2 and pmTOR in the pathogenesis and prognosis of epithelial ovarian cancer. Oncol Rep. 2018;40(6):3725–3733. doi: 10.3892/or.2018.6729. PubMed DOI

Scalise M, Pochini L, Console L, Losso MA, Indiveri C. The Human SLC1A5 (ASCT2) Amino Acid Transporter: From Function to Structure and Role in Cell Biology. Front Cell Dev Biol. 2018;6:96. doi: 10.3389/fcell.2018.00096. PubMed DOI PMC

Zhang Z, Liu R, Shuai Y, Huang Y, Jin R, Wang X, et al. ASCT2 (SLC1A5)-dependent glutamine uptake is involved in the progression of head and neck squamous cell carcinoma. Br J Cancer. 2020;122(1):82–93. doi: 10.1038/s41416-019-0637-9. PubMed DOI PMC

Gesemann M, Lesslauer A, Maurer CM, Schonthaler HB, Neuhauss SC. Phylogenetic analysis of the vertebrate excitatory/neutral amino acid transporter (SLC1/EAAT) family reveals lineage specific subfamilies. BMC Evol Biol. 2010;10:117. doi: 10.1186/1471-2148-10-117. PubMed DOI PMC

Rasko JE, Battini JL, Gottschalk RJ, Mazo I, Miller AD. The RD114/simian type D retrovirus receptor is a neutral amino acid transporter. Proc Natl Acad Sci USA. 1999;96(5):2129–2134. doi: 10.1073/pnas.96.5.2129. PubMed DOI PMC

Sommerfelt MA, Weiss RA. Receptor interference groups of 20 retroviruses plating on human cells. Virology. 1990;176(1):58–69. doi: 10.1016/0042-6822(90)90230-o. PubMed DOI

Tailor CS, Nouri A, Zhao Y, Takeuchi Y, Kabat D. A sodium-dependent neutral-amino-acid transporter mediates infections of feline and baboon endogenous retroviruses and simian type D retroviruses. J Virol. 1999;73(5):4470–4474. doi: 10.1128/JVI.73.5.4470-4474.1999. PubMed DOI PMC

Sinha A, Johnson WE. Retroviruses of the RDR superinfection interference group: ancient origins and broad host distribution of a promiscuous Env gene. Curr Opin Virol. 2017;25:105–112. doi: 10.1016/j.coviro.2017.07.020. PubMed DOI

Funk M, Cornelis G, Vernochet C, Heidmann O, Dupressoir A, Conley A, et al. Capture of a hyena-specific retroviral envelope gene with placental expression associated in evolution with the unique emergence among carnivorans of hemochorial placentation in hyaenidae. J Virol. 2019 doi: 10.1128/JVI.01811-18. PubMed DOI PMC

Heidmann O, Vernochet C, Dupressoir A, Heidmann T. Identification of an endogenous retroviral envelope gene with fusogenic activity and placenta-specific expression in the rabbit: a new "syncytin" in a third order of mammals. Retrovirology. 2009;6:107. doi: 10.1186/1742-4690-6-107. PubMed DOI PMC

Malicorne S, Vernochet C, Cornelis G, Mulot B, Delsuc F, Heidmann O, et al. Genome-Wide Screening of Retroviral Envelope Genes in the Nine-Banded Armadillo (Dasypus novemcinctus, Xenarthra) Reveals an Unfixed Chimeric Endogenous Betaretrovirus Using the ASCT2 Receptor. J Virol. 2016;90(18):8132–8149. doi: 10.1128/JVI.00483-16. 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

Garaeva AA, Guskov A, Slotboom DJ, Paulino C. A one-gate elevator mechanism for the human neutral amino acid transporter ASCT2. Nat Commun. 2019;10(1):3427. doi: 10.1038/s41467-019-11363-x. PubMed DOI PMC

Garaeva AA, Oostergetel GT, Gati C, Guskov A, Paulino C, Slotboom DJ. Cryo-EM structure of the human neutral amino acid transporter ASCT2. Nat Struct Mol Biol. 2018;25(6):515–521. doi: 10.1038/s41594-018-0076-y. PubMed DOI

Console L, Scalise M, Tarmakova Z, Coe IR, Indiveri C. N-linked glycosylation of human SLC1A5 (ASCT2) transporter is critical for trafficking to membrane. Biochem Biophys Acta. 2015;1853(7):1636–1645. doi: 10.1016/j.bbamcr.2015.03.017. PubMed DOI

Canul-Tec JC, Assal R, Cirri E, Legrand P, Brier S, Chamot-Rooke J, et al. Structure and allosteric inhibition of excitatory amino acid transporter 1. Nature. 2017;544(7651):446–451. doi: 10.1038/nature22064. PubMed DOI PMC

Adkins HB, Brojatsch J, Young JA. Identification and characterization of a shared TNFR-related receptor for subgroup B, D, and E avian leukosis viruses reveal cysteine residues required specifically for subgroup E viral entry. J Virol. 2000;74(8):3572–3578. doi: 10.1128/jvi.74.8.3572-3578.2000. PubMed DOI PMC

Brojatsch J, Naughton J, Rolls MM, Zingler K, Young JA. CAR1, a TNFR-related protein, is a cellular receptor for cytopathic avian leukosis-sarcoma viruses and mediates apoptosis. Cell. 1996;87(5):845–855. doi: 10.1016/s0092-8674(00)81992-3. PubMed DOI

Capon DJ, Chamow SM, Mordenti J, Marsters SA, Gregory T, Mitsuya H, et al. Designing CD4 immunoadhesins for AIDS therapy. Nature. 1989;337(6207):525–531. doi: 10.1038/337525a0. PubMed DOI

Holmen SL, Federspiel MJ. Selection of a subgroup A avian leukosis virus [ALV(A)] envelope resistant to soluble ALV(A) surface glycoprotein. Virology. 2000;273(2):364–373. doi: 10.1006/viro.2000.0424. PubMed DOI

Zingler K, Young JA. Residue Trp-48 of Tva is critical for viral entry but not for high-affinity binding to the SU glycoprotein of subgroup A avian leukosis and sarcoma viruses. J Virol. 1996;70(11):7510–7516. doi: 10.1128/JVI.70.11.7510-7516.1996. PubMed DOI PMC

Cornelis G, Heidmann O, Degrelle SA, Vernochet C, Lavialle C, Letzelter C, et al. Captured retroviral envelope syncytin gene associated with the unique placental structure of higher ruminants. Proc Natl Acad Sci USA. 2013;110(9):E828–E837. doi: 10.1073/pnas.1215787110. PubMed DOI PMC

Redelsperger F, Cornelis G, Vernochet C, Tennant BC, Catzeflis F, Mulot B, et al. Capture of syncytin-Mar1, a fusogenic endogenous retroviral envelope gene involved in placentation in the Rodentia squirrel-related clade. J Virol. 2014;88(14):7915–7928. doi: 10.1128/JVI.00141-14. PubMed DOI PMC

Buchrieser J, Degrelle SA, Couderc T, Nevers Q, Disson O, Manet C, et al. IFITM proteins inhibit placental syncytiotrophoblast formation and promote fetal demise. Science. 2019;365(6449):176–180. doi: 10.1126/science.aaw7733. PubMed DOI

Garcia-Murria MJ, Exposito-Dominguez N, Duart G, Mingarro I, Martinez-Gil L. A bimolecular multicellular complementation system for the detection of syncytium formation: a new methodology for the identification of nipah virus entry inhibitors. Viruses. 2019;11(3):229. doi: 10.3390/v11030229. PubMed DOI PMC

Yamamoto M, Matsuyama S, Li X, Takeda M, Kawaguchi Y, Inoue JI, et al. Identification of nafamostat as a potent inhibitor of middle east respiratory syndrome coronavirus s protein-mediated membrane fusion using the split-protein-based cell-cell fusion assay. Antimicrob Agents Chemother. 2016;60(11):6532–6539. doi: 10.1128/AAC.01043-16. PubMed DOI PMC

Senigl F, Plachy J, Hejnar J. The core element of a CpG island protects avian sarcoma and leukosis virus-derived vectors from transcriptional silencing. J Virol. 2008;82(16):7818–7827. doi: 10.1128/JVI.00419-08. PubMed DOI PMC

Pecenka V, Dvorak M, Travnicek M. Avian nephroblastomas induced by a retrovirus (MAV-2) lacking oncogene. I. Construction of MAV-1 and MAV-2 proviral restriction maps and preparation of specific proviral molecular subclones. Folia Biol (Praha) 1988;34(3):129–146. PubMed

Yan RT, Wang SZ. Production of high-titer RCAS retrovirus. Methods Mol Biol. 2012;884:193–199. doi: 10.1007/978-1-61779-848-1_13. PubMed DOI PMC

Petropoulos CJ, Hughes SH. Replication-competent retrovirus vectors for the transfer and expression of gene cassettes in avian cells. J Virol. 1991;65(7):3728–3737. doi: 10.1128/JVI.65.7.3728-3737.1991. PubMed DOI PMC

Mallet F, Bouton O, Prudhomme S, Cheynet V, Oriol G, Bonnaud B, et al. The endogenous retroviral locus ERVWE1 is a bona fide gene involved in hominoid placental physiology. Proc Natl Acad Sci USA. 2004;101(6):1731–1736. doi: 10.1073/pnas.0305763101. PubMed DOI PMC

Blond JL, Beseme F, Duret L, Bouton O, Bedin F, Perron H, et al. Molecular characterization and placental expression of HERV-W, a new human endogenous retrovirus family. J Virol. 1999;73(2):1175–1185. doi: 10.1128/JVI.73.2.1175-1185.1999. PubMed DOI PMC

Federspiel MJ, Hughes SH. Retroviral gene delivery. Methods Cell Biol. 1997;52:179–214. doi: 10.1016/S0091-679X(08)60379-9. PubMed DOI

Schaefer-Klein J, Givol I, Barsov EV, Whitcomb JM, VanBrocklin M, Foster DN, et al. The EV-O-derived cell line DF-1 supports the efficient replication of avian leukosis-sarcoma viruses and vectors. Virology. 1998;248(2):305–311. doi: 10.1006/viro.1998.9291. PubMed DOI

Plachy J, Kotab J, Divina P, Reinisova M, Senigl F, Hejnar J. Proviruses selected for high and stable expression of transduced genes accumulate in broadly transcribed genome areas. J Virol. 2010;84(9):4204–4211. doi: 10.1128/JVI.02511-09. PubMed DOI PMC

Rainey GJ, Natonson A, Maxfield LF, Coffin JM. Mechanisms of avian retroviral host range extension. J Virol. 2003;77(12):6709–6719. doi: 10.1128/jvi.77.12.6709-6719.2003. PubMed DOI PMC

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