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Differentiation

Effects of overexpression of HBP1 upon growth and differentiation of leukemic myeloid cells

Abstract

HMG-box containing protein 1 (HBP1) is a member of the high mobility group (HMG) of chromosomal proteins. Since HBP1 exhibits tumor-suppressor activity in nonmyeloid tissues, we examined the effects of ectopic overexpression of HBP1 upon the growth and differentiation of myeloid cells. We prepared transient and stable transfectants of the myeloblast cell line K562, which overexpress HBP1 mRNA and protein. HBP1 transfectants displayed slower growth in cell culture and reduced colony formation in soft agar, retardation of S-phase progression, reduced expression of cyclin D1 and D3 mRNAs and increased expression of p21 mRNA. HBP1 transfectants also underwent increased apoptosis, as demonstrated by morphology and binding of Annexin V. Fas ligand mRNA levels were increased in HBP1 transfectants, suggesting involvement of the Fas/Fas ligand pathway. HBP1 overexpression enhanced differentiation of K562 cells towards erythroid and megakaryocyte lineages, as evidenced by increased hemoglobin and CD41a expression. Overexpression of HBP1 modulated mRNA levels for myeloid-specific transcription factors C/EBPα, c-Myb, c-Myc, and JunB, as well as lineage-specific transcription factors PU.1, GATA-1, and RUNX1. These findings suggest that in myeloid cells HBP1 may serve as a tumor suppressor and a general differentiation inducer and may synergize with chemical differentiating agents to enhance lineage-specific differentiation.

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References

  1. Lesage F, Hugnot J-P, Amri E-Z, Grimaldi P, Barhanin J, Lazdunski M . Expression cloning in K+ transport defective yeast and distribution of HBP1, a new putative HMG transcriptional regulator. Nucleic Acids Res 1994; 22: 3695–3688.

  2. Landsman D, Bustin M . A signature for the HMG-1 box DNA-binding proteins. Bioessays 1993; 15: 539–546.

    Article  CAS  Google Scholar 

  3. Grosschedl R . Higher-order nucleoprotein complexes in transcription: analogies with site-specific recombination. Curr Opin Cell Biol 1995; 7: 362–370.

    Article  CAS  Google Scholar 

  4. Tjian R, Maniatis T . Transcriptional activation: a complex puzzle with few easy pieces. Cell 1994; 77: 5–8.

    Article  CAS  Google Scholar 

  5. Wolffe AP . Architectural transcription factors. Science 1994; 264: 1100–1101.

    Article  CAS  Google Scholar 

  6. Arie T, Christiansen SK, Yoder OC, Turgeon BG . Efficient cloning of ascomycete mating type genes by PCR amplification of the conserved MAI HMG Box. Fungal Genet Biol 1996; 21: 118–130.

    Article  Google Scholar 

  7. Sugimoto A, Lino Y, Maeda T, Watanabe Y, Yamamoto M . Schizosaccharomyces pombe ste11+ encodes a transcription factor with an HMG motif that is a critical regulator of sexual development. Genes Dev 1991; 5: 1990–1999.

    Article  CAS  Google Scholar 

  8. Van De Wetering M, Oostewegel M, Dooijes D, Clevers H . Identification and cloning of TCF-1, a T lymphocyte-specific transcription factor containing a sequence-specific HMG box. EMBO J 1991; 10: 123–132.

    Article  CAS  Google Scholar 

  9. Alexander-Bridges M, Dugast I, Ercolani L, Giere L, Nasrin N . Multiple insulin-response elements regulate transcription of the GAPDH gene. Adv Enzyme Regul 1992; 32: 149–159.

    Article  CAS  Google Scholar 

  10. Lin KM, Zhao WG, Bhatnagar J, Zhao WD, Lu JP, Simko S et al. Cloning and expression of human HBP1, a high mobility group protein that enhances myeloperoxidase (MPO) promoter activity. Leukemia 2001; 15: 601–612.

    Article  CAS  Google Scholar 

  11. Lavender P, Vandel L, Bannister AJ, Kouzarides T . The HMG-box transcription factor HBP1 is targeted by the pocket proteins and E1A. Oncogene 1997; 14: 2721–2728.

    Article  CAS  Google Scholar 

  12. Tevosian SG, Shih HH, Mendelson KG, Sheppard KA, Paulson KE, Yee AS . HBP1: a HMG box transcriptional repressor that is targeted by the retinoblastoma family. Genes Dev 1997; 11: 383–396.

    Article  CAS  Google Scholar 

  13. Shih HH, Tevosian SG, Yee AS . Regulation of differentiation by HBP1, a target of the retinoblastoma protein. Mol Cell Biol 1998; 18: 4732–4743.

    Article  CAS  Google Scholar 

  14. Gartel AL, Goufman E, Tevosian SG, Shih H, Yee AS, Tyner AL . Activation and repression of p21(WAF1/CIP1) transcription by RB binding proteins. Oncogene 1998; 17: 3463–3469.

    Article  CAS  Google Scholar 

  15. Zhuma T, Tyrrell R, Sekkali B, Skavdis G, Saveliev A, Tolaini M et al. Human HMG box transcription factor HBP1: a role in hCD2 LCR function. EMBO J 1999; 18: 6396–6406.

    Article  CAS  Google Scholar 

  16. Lemercier C, Duncliffe K, Boibessot I, Zhang H, Verdel A, Angelov D et al. Involvement of retinoblastoma protein and HBP1 in histone H1(0) gene expression. Mol Cell Biol 2000; 18: 6627–6637.

    Article  Google Scholar 

  17. Swanson KA, Knoepfler PS, Huang K, Kang RS, Cowley SM, Laherty CD et al. HBP1 and Mad1 repressors bind the sin3 corepressor PAH2 domaine with opposite helical orientations. Nat Struct Mol Biol 2004; 11: 738–746.

    Article  CAS  Google Scholar 

  18. Shih HH, Xiu M, Berasi SP, Sampson EM, Leiter A, Paulson KE et al. HMG box transcriptional repressor HBP1 maintains a proliferation barrier in differentiated liver tissue. Mol Cell Biol 2001; 21: 5723–5732.

    Article  CAS  Google Scholar 

  19. Smith JM, Bowles J, Wilson M, Koopman P . HMG box transcription factor gene HBP1 is expressed in germ cells of the developing mouse testes. Dev Dyn 2004; 230: 366–370.

    Article  CAS  Google Scholar 

  20. Xiu M, Kim J, Sampson E, Huang CY, Davis RJ, Paulson KE et al. The transcriptional repressor HBP1 is a target of the p38 mitogen-activated protein kinase pathway in cell cycle regulation. Mol Cell Biol 2003; 23: 8890–8901.

    Article  CAS  Google Scholar 

  21. Sampson EM, Haque ZK, Ku MC, Tevosian SG, Albanese C, Pestell RG et al. Negative regulation of the Wnt-beta-catenin pathway by the transcriptional repressor HBP1. EMBO J 2001; 20: 4500–4511.

    Article  CAS  Google Scholar 

  22. Berasi SP, Xiu M, Yee AS, Paulson KE . HBP1 repression of the p47phox gene: cell cycle regulation via the NADPH oxidase. Mol Cell Biol 2004; 24: 3011–3024.

    Article  CAS  Google Scholar 

  23. Yee AS, Paulson EK, McDevitt MA, Rieger-Christ K, Summerhayes I, Berasi SP et al. The HBP1 transcriptional repressor and the p38 MAP kinase: unlikely partners in G1 regulation and tumor suppression. Gene 2004; 336: 1–13.

    Article  CAS  Google Scholar 

  24. Bergh G, Ehinger M, Olofsson T, Baldetorp B, Johnsson E, Brycke H et al. Altered expression of the retinoblastoma tumor-suppressor gene in leukemic cell lines inhibits induction of differentiation but not G1-accumulation. Blood 1997; 89: 2938–2950.

    CAS  PubMed  Google Scholar 

  25. Munoz-Alonso MJ, Acosta JC, Richard C, Delgado MD, Sedivy J, Leon J . p21Cip1 and p27Kip1 induce distinct cell cycle effects and differentiation programs in myeloid leukemia cells. J Biol Chem 2005; 280: 18120–18129.

    Article  CAS  Google Scholar 

  26. Labbaye C, Valtieri M, Barberi T, Meccia E, Masella B, Pelosi E et al. Differential expression and functional role of GATA-2, NF-E2, GATA-1 in normal adult hematopoiesis. J Clin Invest 1995; 95: 2346–2358.

    Article  CAS  Google Scholar 

  27. Elagib KE, Racke FK, Mogass M, Khetawat R, Delehanty LL, Goldfarb AN . RUNX1 and GATA-1 coexpression and cooperation in megakaryocytic differentiation. Blood 2003; 101: 4333–4341.

    Article  CAS  Google Scholar 

  28. Keeshan K, Santilli G, Corradini F, Perrotti D, Calabretta B . Transcription activation function of C/EBPalpha is required for induction of granulocytic differentiation. Blood 2003; 102: 1267–1275.

    Article  CAS  Google Scholar 

  29. Yang MY, Liu TC, Chang JG, Lin PM, Lin SF . JunB gene expression is inactivated by methylation in chronic myeloid leukemia. Blood 2003; 101: 3205–3211.

    Article  CAS  Google Scholar 

  30. Bakiri L, Lallemand D, Bossy-Wetzel E, Yaniv M . Cell cycle-dependent variations in c-Jun and JunB phosphorylation: a role in the control of cyclin D1 expression. EMBO J 2000; 19: 2056–2068.

    Article  CAS  Google Scholar 

  31. Rosson D, O'Brien TG . Constitutive c-myb expression in K562 cells inhibits induced erythroid differentiation but not tetradecanoyl phorbol acetate-induced megakaryocytic differentiation. Mol Cell Biol 1995; 15: 772–779.

    Article  CAS  Google Scholar 

  32. Clement M-V, Hirpara JL, Chawdhury S-H, Pervaiz S . Chemopreventive agent Resveratrol, a natural product derived from grapes, triggers CD95 signaling-dependent apoptosis in human tumor cells. Blood 1998; 92: 9996–1002.

  33. Kohmura K, Miyakawa Y, Kawai Y, Ikeda Y, Kizaki M . Different roles of p38 MAPK and ERK in STI571-induced multi-lineage differentiation of K562 cells. J Cell Physiol 2004; 198: 370–376.

    Article  CAS  Google Scholar 

  34. Radomska HS, Huettner CS, Zhang P, Cheng T, Scadden DT, Tenen DG . CCAAT/enhancer binding protein alpha is a regulatory switch sufficient for induction of granulocytic development from bipotential myeloid progenitors. Mol Cell Biol 1998; 18: 4301–4314.

    Article  CAS  Google Scholar 

  35. Koike M, Tasaka T, Spira S, Tsuruoka N, Koeffler HP . Allelotyping of acute myelogenous leukemia: loss of heterozygosity at 7q31.1 (D7S486) and q33-34 (D7S498, D7S505). Leuk Res 1999; 23: 307–310.

    Article  CAS  Google Scholar 

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Acknowledgements

This work was supported by a VA Merit grant to GEA.

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Correspondence to G E Austin.

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Supplementary Information accompanies the paper on the Leukemia website (http://www.nature.com/leu).

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Yao, C., Works, K., Romagnoli, P. et al. Effects of overexpression of HBP1 upon growth and differentiation of leukemic myeloid cells. Leukemia 19, 1958–1968 (2005). https://doi.org/10.1038/sj.leu.2403918

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