Experimental Hematology
Volume 36, Issue 5 , Pages 559-567 , May 2008

A role for the transcription intermediary factor 2 in zebrafish myelopoiesis

  • Julia Zhuravleva
  • ,
  • Eric Solary
  • ,
  • Johanna Chluba
  • ,
  • Jean-Noël Bastie

      Affiliations

    • Drs. Bastie and Delva contributed to this work equally.
  • ,
  • Laurent Delva

      Affiliations

    • Drs. Bastie and Delva contributed to this work equally.
    • Corresponding Author InformationOffprint requests to: Laurent Delva, Ph.D., Inserm UMR 866, Centre de Recherche Inserm, IFR Santé/STIC, Faculté de Médecine, Université de Bourgogne, 7 Boulevard Jeanne d'Arc, 21000 Dijon, France

Received 5 September 2007 ,Revised 28 December 2007 ,Accepted 31 December 2007.

References 

  1. Strahl BD, Allis CD. The language of covalent histone modifications. Nature. 2000;403:41–45
  2. Turner BM. Cellular memory and the histone code. Cell. 2002;111:285–291
  3. Fischle W, Wang Y, Allis CD. Histone and chromatin cross-talk. Curr Opin Cell Biol. 2003;15:172–183
  4. Carapeti M, Aguiar RC, Goldman JM, Cross NC. A novel fusion between MOZ and the nuclear receptor coactivator TIF2 in acute myeloid leukemia. Blood. 1998;91:3127–3133
  5. Liang J, Prouty L, Williams BJ, Dayton MA, Blanchard KL. Acute mixed lineage leukemia with an inv(8)(p11q13) resulting in fusion of the genes for MOZ and TIF2. Blood. 1998;92:2118–2122
  6. Coulthard S, Chase A, Orchard K, et al. Two cases of inv(8)(p11q13) in AML with erythrophagocytosis: a new cytogenetic variant. Br J Haematol. 1998;124:561–563
  7. Panagopoulos I, Teixeira MR, Micci F, et al. Acute myeloid leukemia with inv(8)(p11q13). Leuk Lymphoma. 2000;39:651–656
  8. Billio A, Steer EJ, Pianezze G, et al. A further case of acute myeloid leukaemia with inv(8)(p11q13) and MOZ-TIF2 fusion. Haematologica. 2002;87:ECR15
  9. Murati A, Adelaide J, Popovici C, et al. A further case of acute myelomonocytic leukemia with inv(8) chromosomal rearrangement and MOZ-NCOA2 gene fusion. Int J Mol Med. 2003;12:423–428
  10. Deguchi K, Ayton PM, Carapeti M, et al. MOZ-TIF2-induced acute myeloid leukemia requires the MOZ nucleosome binding motif and TIF2-mediated recruitment of CBP. Cancer Cell. 2003;3:259–271
  11. Huntly BJP, Shigematsu H, Deguchi K, et al. MOZ-TIF2, but not BCR-ABL, confers properties of leukemic stem cells to committed murine hematopoietic progenitors. Cancer Cell. 2004;6:587–596
  12. Leo C, Chen JD. The SRC family of nuclear receptor coactivators. Gene. 2000;245:1–11
  13. Hong H, Kohli K, Trivedi A, Johnson DL, Stallcup MR. GRIP1, a novel mouse protein that serves as a transcriptional coactivator in yeast for the hormone binding domains of steroid receptors. Proc Natl Acad Sci U S A. 1996;93:4948–4952
  14. Voegel JJ, Heine MJ, Zechel C, Chambon P, Gronemeyer H. TIF2, a 160 kDa transcriptional mediator for the ligand-dependent activation function AF-2 of nuclear receptors. EMBO J. 1996;15:3667–3675
  15. Picard F, Gehin M, Annicotte J, et al. SRC-1 and TIF2 control energy balance between white and brown adipose tissues. Cell. 2002;111:931–941
  16. Xu J, Li Q. Review of the in vivo functions of the p160 steroid receptor coactivator family. Mol Endocrinol. 2003;17:1681–1692
  17. Xu J, Qiu Y, DeMayo FJ, Tsai SY, Tsai MJ, O'Malley BW. Partial Hormone Resistance in Mice with Disruption of the Steroid Receptor Coactivator-1 (SRC-1). Gene. Science. 1998;279:1922–1925
  18. Weiss RE, Xu J, Ning G, Pohlenz J, O'Malley BW, Refetoff S. Mice deficient in the steroid receptor co-activator 1 (SRC-1) are resistant to thyroid hormone. EMBO J. 1999;18:1900–1904
  19. Nishihara E, Yoshida-Komiya H, Chan CS, et al. SRC-1 Null mice exhibit moderate motor dysfunction and delayed development of cerebellar Purkinje cells. J Neurosci. 2003;23:213–222
  20. Qi C, Zhu Y, Pan J, et al. Mouse steroid receptor coactivator-1 is not essential for peroxisome proliferator-activated receptor α-regulated gene expression. Proc Natl Acad Sci U S A. 1999;96:1585–1590
  21. Gehin M, Mark M, Dennefeld C, Dierich A, Gronemeyer H, Chambon P. The function of TIF2/GRIP1 in mouse reproduction is distinct from those of SRC-1 and p/CIP. Mol Cell Biol. 2002;22:5923–5937
  22. Wang Z, Rose DW, Hermanson O, et al. Regulation of somatic growth by the p160 coactivator p/CIP. Proc Natl Acad Sci U S A. 2000;97:13549–13554
  23. Xu J, Liao L, Ning G, Yoshida-Komiya H, Deng C, O'Malley BW. The steroid receptor coactivator SRC-3 (p/CIP/RAC3/AIB1/ACTR/TRAM-1) is required for normal growth, puberty, female reproductive function, and mammary gland development. Proc Natl Acad Sci U S A. 2000;97:6379–6384
  24. Yuan Y, Liao L, Tulis DA, Xu J. Steroid receptor coactivator-3 is required for inhibition of neointima formation by estrogen. Circulation. 2002;105:2653–2659
  25. Solnica-Krezel L. Pattern formation in zebrafish-fruitful liaisons between embryology and genetics. Curr Top Dev Biol. 1999;41:1–35
  26. de Jong JL, Zon LI. Use of the zebrafish system to study primitive and definitive hematopoiesis. Annu Rev Genet. 2005;39:481–501
  27. Berman JN, Kanki JP, Look AT. Zebrafish as a model for myelopoiesis during embryogenesis. Exp Hematol. 2005;33:997–1006
  28. Westerfield M. The Zebrafish Book: A Guide for the Laboratory Use of Zebrafish (Danio rerio). Eugene, OR: University of Oregon Press; 1995;p. 1.1–1.27
  29. Herbomel P, Thisse B, Thisse C. Ontogeny and behaviour of early macrophages in the zebrafish embryo. Development. 1999;126:3735–3745
  30. Thisse B, Heyer V, Lux A, et al. Spatial and temporal expression of the zebrafish genome by large-scale in situ hybridization screening. Methods Cell Biol. 2004;77:505–519
  31. Scott A, Stemple DL. Zebrafish notochordal basement membrane: signaling and structure. Curr Top Dev Biol. 2005;65:229–253
  32. Parsons MJ, Pollard SM, Saude L, et al. Zebrafish mutants identify an essential role for laminins in notochord formation. Development. 2002;129:3137–3146
  33. Robu ME, Larson JD, Nasevicius A, et al. p53 activation by knockdown technologies. PLOS Genet. 2007;3:787–800
  34. Hogan KA, Bautch VL. Blood vessel patterning at the embryonic midline. Curr Top Dev Biol. 2004;62:55–85
  35. Brown LA, Rodaway AR, Schilling TF, et al. Insights into early vasculogenesis revealed by expression of the ETS-domain transcription factor Fli-1 in wild-type and mutant zebrafish embryos. Mech Dev. 2000;90:237–252
  36. Truong AH, Ben-Davis Y. The role of Fli-1 in normal cell function and malignant transformation. Oncogene. 2000;19:6482–6489
  37. Detrich HW, Kieran MW, Chan FY, et al. Intraembryonic hematopoietic cell migration during vertebrate development. Proc Natl Acad Sci U S A. 1995;92:10713–10717
  38. Bennett CM, Kanki JP, Rhodes J, et al. Myelopoiesis in the zebrafish, Danio rerio. Blood. 2001;98:643–651
  39. Lin CS, Park T, Chen ZP, Leavitt J. Human plastin genes: comparative gene structure, chromosome location, and differential expression in normal and neoplastic cells. J Biol Chem. 1993;268:2781–2792
  40. Crowhurst MO, Layton JE, Lieschke GJ. Developmental biology of zebrafish myeloid cells. Int J Dev Biol. 2002;46:483–492

PII: S0301-472X(08)00003-9

doi: 10.1016/j.exphem.2007.12.014

Experimental Hematology
Volume 36, Issue 5 , Pages 559-567 , May 2008