The Zebrafish moonshine Gene Encodes Transcriptional Intermediary Factor 1γ, an Essential Regulator of Hematopoiesis

Hematopoiesis is precisely orchestrated by lineage-specific DNA-binding proteins that regulate transcription in concert with coactivators and corepressors. Mutations in the zebrafish moonshine (mon) gene specifically disrupt both embryonic and adult hematopoiesis, resulting in severe red blood cell aplasia. We report that mon encodes the zebrafish ortholog of mammalian transcriptional intermediary factor 1γ (TIF1γ) (or TRIM33), a member of the TIF1 family of coactivators and corepressors. During development, hematopoietic progenitor cells in mon mutants fail to express normal levels of hematopoietic transcription factors, including gata1, and undergo apoptosis. Three different mon mutant alleles each encode premature stop codons, and enforced expression of wild-type tif1γ mRNA rescues embryonic hematopoiesis in homozygous mon mutants. Surprisingly, a high level of zygotic tif1γ mRNA expression delineates ventral mesoderm during hematopoietic stem cell and progenitor formation prior to gata1 expression. Transplantation studies reveal that tif1γ functions in a cell-autonomous manner during the differentiation of erythroid precursors. Studies in murine erythroid cell lines demonstrate that Tif1γ protein is localized within novel nuclear foci, and expression decreases during erythroid cell maturation. Our results establish a major role for this transcriptional intermediary factor in the differentiation of hematopoietic cells in vertebrates.

[1]  Leonard I Zon,et al.  Transplantation and in vivo imaging of multilineage engraftment in zebrafish bloodless mutants , 2003, Nature Immunology.

[2]  R. Urrutia KRAB-containing zinc-finger repressor proteins , 2003, Genome Biology.

[3]  M. Harbers,et al.  The Bromodomain Mediates Transcriptional Intermediary Factor 1α-Nucleosome Interactions* , 2002, The Journal of Biological Chemistry.

[4]  L. Zon,et al.  SUMO-1 protease-1 regulates gene transcription through PML. , 2002, Molecular cell.

[5]  Pierre Chambon,et al.  Cell differentiation induces TIF1beta association with centromeric heterochromatin via an HP1 interaction. , 2002, Journal of cell science.

[6]  F. Rauscher,et al.  Hetero-oligomerization among the TIF family of RBCC/TRIM domain-containing nuclear cofactors: a potential mechanism for regulating the switch between coactivation and corepression. , 2002, Journal of molecular biology.

[7]  B. Weinstein,et al.  A nonsense mutation in zebrafish gata1 causes the bloodless phenotype in vlad tepes , 2002, Proceedings of the National Academy of Sciences of the United States of America.

[8]  Stuart H. Orkin,et al.  Hematopoiesis and stem cells: plasticity versus developmental heterogeneity , 2002, Nature Immunology.

[9]  D. Ransom,et al.  Non-cell autonomous requirement for the bloodless gene in primitive hematopoiesis of zebrafish. , 2002, Development.

[10]  Leonard I. Zon,et al.  Organogenesis--Heart and Blood Formation from the Zebrafish Point of View , 2002, Science.

[11]  B. Paw,et al.  Myelopoiesis in the zebrafish, Danio rerio. , 2001, Blood.

[12]  J. Palis,et al.  Yolk-sac hematopoiesis: the first blood cells of mouse and man. , 2001, Experimental hematology.

[13]  Alessandro Guffanti,et al.  The tripartite motif family identifies cell compartments , 2001, The EMBO journal.

[14]  P. Kingsley,et al.  Subtractive hybridization reveals tissue‐specific expression of ahnak during embryonic development , 2001, Development, growth & differentiation.

[15]  P. Chambon,et al.  Conserved interaction between distinct Krüppel-associated box domains and the transcriptional intermediary factor 1 beta. , 2001, Proceedings of the National Academy of Sciences of the United States of America.

[16]  J. McPherson,et al.  The syntenic relationship of the zebrafish and human genomes. , 2000, Genome research.

[17]  P. Chambon,et al.  Mice lacking the transcriptional corepressor TIF1beta are defective in early postimplantation development. , 2000, Development.

[18]  Pier Paolo Pandolfi,et al.  The transcriptional role of PML and the nuclear body , 2000, Nature Cell Biology.

[19]  P. Pandolfi,et al.  Role of SUMO-1-modified PML in nuclear body formation. , 2000, Blood.

[20]  P. Pandolfi,et al.  A RA-dependent, tumour-growth suppressive transcription complex is the target of the PML-RARα and T18 oncoproteins , 1999, Nature Genetics.

[21]  R. Losson,et al.  Expression of the transcriptional intermediary factor TIF1α during mouse development and in the reproductive organs , 1999, Mechanisms of Development.

[22]  P. Chambon,et al.  TIF1γ, a novel member of the transcriptional intermediary factor 1 family , 1999, Oncogene.

[23]  A. Brownlie,et al.  Positional cloning of the zebrafish sauternes gene: a model for congenital sideroblastic anaemia , 1998, Nature Genetics.

[24]  A. Amores,et al.  The cloche and spadetail genes differentially affect hematopoiesis and vasculogenesis. , 1998, Developmental biology.

[25]  M. Ekker,et al.  A microsatellite genetic linkage map for zebrafish (Danio rerio) , 1998, Nature Genetics.

[26]  M. Farrell,et al.  GATA-1 expression pattern can be recapitulated in living transgenic zebrafish using GFP reporter gene. , 1997, Development.

[27]  S. Orkin,et al.  Erythroid-cell-specific properties of transcription factor GATA-1 revealed by phenotypic rescue of a gene-targeted cell line , 1997, Molecular and cellular biology.

[28]  D. Stainier,et al.  The zebrafish gene cloche acts upstream of a flk-1 homologue to regulate endothelial cell differentiation. , 1997, Development.

[29]  M. Vidal,et al.  A novel member of the RING finger family, KRIP-1, associates with the KRAB-A transcriptional repressor domain of zinc finger proteins. , 1996, Proceedings of the National Academy of Sciences of the United States of America.

[30]  D A Kane,et al.  Characterization of zebrafish mutants with defects in embryonic hematopoiesis. , 1996, Development.

[31]  A. Schier,et al.  Hematopoietic mutations in the zebrafish. , 1996, Development.

[32]  Y Fujiwara,et al.  Arrested development of embryonic red cell precursors in mouse embryos lacking transcription factor GATA-1. , 1996, Proceedings of the National Academy of Sciences of the United States of America.

[33]  D. Speicher,et al.  KAP-1, a novel corepressor for the highly conserved KRAB repression domain. , 1996, Genes & development.

[34]  D. Ransom,et al.  Intraembryonic hematopoietic cell migration during vertebrate development. , 1995, Proceedings of the National Academy of Sciences of the United States of America.

[35]  P. Chambon,et al.  The N‐terminal part of TIF1, a putative mediator of the ligand‐dependent activation function (AF‐2) of nuclear receptors, is fused to B‐raf in the oncogenic protein T18. , 1995, The EMBO journal.

[36]  L. Zon,et al.  Ontogeny of hematopoiesis: examining the emergence of hematopoietic cells in the vertebrate embryo. , 2003, Current topics in developmental biology.

[37]  D. Ransom,et al.  Mapping zebrafish mutations by AFLP. , 1999, Methods in cell biology.

[38]  P. Chambon,et al.  TIF1gamma, a novel member of the transcriptional intermediary factor 1 family. , 1999, Oncogene.

[39]  Y. Kunz,et al.  ONTOGENESIS OF HAEMATOPOIETIC SITES IN BRACHYDANIO RERIO (HAMILTON‐BUCHANAN) (TELEOSTEI) * , 1977, Development, growth & differentiation.