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A new role for the oncogenic high-mobility group A2 transcription factor in myogenesis of embryonic stem cells

Abstract

The high mobility group type A-2 (HMGA2) transcription factor is involved in proliferation and differentiation, mainly during embryogenesis. Its activated form (HMGA2/T) presents oncogenic activities both in vivo and in vitro. However, its precise role during embryogenesis is unknown. We investigated its role during the commitment of mouse embryonic stem (ES) cells by constructing cell lines expressing either wild type (wt) or HMGA2/T forms of the gene. Following differentiation, control and wt HMGA2 ES cells did not display myotubes; whereas HMGA2/T ES cell lines massively formed contractile myotubes. Furthermore, as opposed to control cells, HMGA2/T ES cells highly expressed the muscle myosin heavy chain (MHC) marker. Interestingly, in experimental conditions inhibitory for myogenesis, we observed a strong expression of MyoD and myogenin in HMGA2/T cells. By contrast, commitment into adipocyte, neuron, and cardiomyocyte lineages was not affected. Teratocarcinomas induced by HMGA2/T ES cell lines presented numerous skeletal muscle-differentiated tissues that were not observed in wt HMGA2 or control tumours. Finally, rapamycin, an inhibitor of the mTOR kinase, downregulated endogenous HMGA-2 expression and inhibited myogenesis. This effect was prevented by overexpression of exogenous HMGA-2. Our results reveal a novel function of HMGA-2 in skeletal muscle differentiation.

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References

  • Anand A and Chada K . (2000). Nat. Genet., 24, 377–380.

  • Anisimov SV, Tarasov KV, Riordon D, Wobus AM and Boheler KR . (2002). Mech. Dev., 117, 25–74.

  • Ashar HR, Fejzo MS, Tkachenko A, Zhou X, Fletcher JA, Weremowicz S, Morton CC and Chada K . (1995). Cell, 82, 57–65.

  • Baldassarre G, Fedele M, Battista S, Vecchione A, Klein-Szanto AJ, Santoro M, Waldmann TA, Azimi N, Croce CM and Fusco A . (2001). Proc. Natl. Acad. Sci. USA, 98, 7970–7975. Epub Jun 26, 2001.

  • Battista S, Fidanza V, Fedele M, Klein-Szanto AJ, Outwater E, Brunner H, Santoro M, Croce CM and Fusco A . (1999). Cancer Res., 59, 4793–4797.

  • Bost F, Caron L, Marchetti I, Dani C, Le Marchand-Brustel Y and Binetruy B . (2002). Biochem. J., 361, 621–627.

  • Chieffi P, Battista S, Barchi M, Di Agostino S, Pierantoni GM, Fedele M, Chiariotti L, Tramontano D and Fusco A . (2002). Oncogene, 21, 3644–3650.

  • Colmenares C and Stavnezer E . (1989). Cell, 59, 293–303.

  • Fedele M, Berlingieri MT, Scala S, Chiariotti L, Viglietto G, Rippel V, Bullerdiek J, Santoro M and Fusco A . (1998). Oncogene, 17, 413–418.

  • Gao X, Zhang Y, Arrazola P, Hino O, Kobayashi T, Yeung RS, Ru B and Pan D . (2002). Nat. Cell. Biol., 4, 699–704.

  • Hirning-Folz U, Wilda M, Rippe V, Bullerdiek J and Hameister H . (1998). Genes Chromosomes Cancer, 23, 350–357.

  • Hunter DS, Klotzbucher M, Kugoh H, Cai SL, Mullen JP, Manfioletti G, Fuhrman U and Walker CL . (2002). Cancer Res., 62, 3766–3772.

  • Molkentin JD and Olson EN . (1996). Curr. Opin. Genet. Dev., 6, 445–453.

  • Niwa H, Yamamura K and Miyazaki J . (1991). Gene, 108, 193–199.

  • Noro B, Licheri B, Sgarra R, Rustighi A, Tessari MA, Chau KY, Ono SJ, Giancotti V and Manfioletti G . (2003). Biochemistry, 42, 4569–4577.

  • Pende M, Um SH, Mieulet V, Sticker M, Goss VL, Mestan J, Mueller M, Fumagalli S, Kozma SC and Thomas G . (2004). Mol. Cell. Biol., 24, 3112–3124.

  • Reeves R and Beckerbauer L . (2001). Biochim. Biophys. Acta, 1519, 13–29.

  • Reeves R and Nissen M . (1999). Methods Enzymol., 304, 155–188.

  • Tallini G, Vanni R, Manfioletti G, Kazmierczak B, Faa G, Pauwels P, Bullerdiek J, Giancotti V, Van Den Berghe H and Dal Cin P . (2000). Lab. Invest., 80, 359–369.

  • Vernochet C, Milstone DS, Iehle C, Belmonte N, Phillips B, Wdziekonski B, Villageois P, Amri EZ, O'Donnell PE, Mortensen RM, Ailhaud G and Dani C . (2002). FEBS Lett., 510, 94–98.

  • Wobus AM . (2001). Mol. Aspects Med., 22, 149–164.

  • Zhou X, Benson KF, Ashar HR and Chada K . (1995). Nature, 376, 771–774.

  • Zhou X, Benson KF, Przybysz K, Liu J, Hou Y, Cherath L and Chada K . (1996). Nucleic Acids Res., 24, 4071–4077.

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Acknowledgements

We thank Y Le Marchand-Brustel, J Vukmirica and JF Tanti for critical reading of the manuscript and Dr Niwa for the gift of CAG plasmid. This work was supported by Fondation Bettencourt-Schueller, ARC (Grants no. 4525 and 7720) and AFM (Grant no. 9986). LC was supported by fellowships from INSERM/Région Provence Alpes Côte d'Azur and the Ligue Nationale Contre le Cancer.

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Correspondence to Bernard Binétruy.

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Caron, L., Bost, F., Prot, M. et al. A new role for the oncogenic high-mobility group A2 transcription factor in myogenesis of embryonic stem cells. Oncogene 24, 6281–6291 (2005). https://doi.org/10.1038/sj.onc.1208781

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