The gata1/pu.1 lineage fate paradigm varies between blood populations and is modulated by tif1γ

Lineage fate decisions underpin much of development as well as tissue homeostasis in the adult. A mechanistic paradigm for such decisions is the erythroid versus myeloid fate decision controlled by cross‐antagonism between gata1 and pu.1 transcription factors. In this study, we have systematically tested this paradigm in blood‐producing populations in zebrafish embryos, including the haematopoietic stem cells (HSCs), and found that it takes a different form in each population. In particular, gata1 activity varies from autostimulation to autorepression. In addition, we have added a third member to this regulatory kernel, tif1γ (transcription intermediate factor‐1γ). We show that tif1γ modulates the erythroid versus myeloid fate outcomes from HSCs by differentially controlling the levels of gata1 and pu.1. By contrast, tif1γ positively regulates both gata1 and pu.1 in primitive erythroid and prodefinitive erythromyeloid progenitors. We therefore conclude that the gata1/pu.1 paradigm for lineage decisions takes different forms in different cellular contexts and is modulated by tif1γ.

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

[2]  M. Gering,et al.  Hedgehog signaling is required for adult blood stem cell formation in zebrafish embryos. , 2005, Developmental cell.

[3]  Donald A Kane,et al.  Fate mapping embryonic blood in zebrafish: multi- and unipotential lineages are segregated at gastrulation. , 2009, Developmental cell.

[4]  A. Gronenborn,et al.  A palindromic regulatory site within vertebrate GATA-1 promoters requires both zinc fingers of the GATA-1 DNA-binding domain for high-affinity interaction , 1996, Molecular and cellular biology.

[5]  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.

[6]  L. Zon,et al.  Loss of gata1 but not gata2 converts erythropoiesis to myelopoiesis in zebrafish embryos. , 2005, Developmental cell.

[7]  A. Look,et al.  Interplay of pu.1 and gata1 determines myelo-erythroid progenitor cell fate in zebrafish. , 2005, Developmental cell.

[8]  T. Enver,et al.  Forcing cells to change lineages , 2009, Nature.

[9]  N. Speck,et al.  Definitive hematopoietic stem cells first develop within the major arterial regions of the mouse embryo , 2000, The EMBO journal.

[10]  Zilong Wen,et al.  Migratory path of definitive hematopoietic stem/progenitor cells during zebrafish development. , 2007, Blood.

[11]  D. Traver,et al.  CD41+ cmyb+ precursors colonize the zebrafish pronephros by a novel migration route to initiate adult hematopoiesis , 2008, Development.

[12]  L. Zon,et al.  TIF1γ Controls Erythroid Cell Fate by Regulating Transcription Elongation , 2010, Cell.

[13]  A. Medvinsky,et al.  Definitive Hematopoiesis Is Autonomously Initiated by the AGM Region , 1996, Cell.

[14]  N. Rekhtman,et al.  Direct interaction of hematopoietic transcription factors PU.1 and GATA-1: functional antagonism in erythroid cells. , 1999, Genes & development.

[15]  A. Strasser,et al.  Functional characterization of the Bcl-2 gene family in the zebrafish , 2006, Cell Death and Differentiation.

[16]  K. Ottersbach,et al.  Hematopoietic stem cells localize to the endothelial cell layer in the midgestation mouse aorta. , 2002, Immunity.

[17]  T. Graf,et al.  GATA-1 reprograms avian myelomonocytic cell lines into eosinophils, thromboblasts, and erythroblasts. , 1995, Genes & development.

[18]  R. Sood,et al.  Definitive hematopoietic stem/progenitor cells manifest distinct differentiation output in the zebrafish VDA and PBI , 2009, Development.

[19]  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.

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

[21]  Patrick Rodriguez,et al.  Novel binding partners of Ldb1 are required for haematopoietic development. , 2007, Development.

[22]  S. Orkin,et al.  An upstream, DNase I hypersensitive region of the hematopoietic-expressed transcription factor GATA-1 gene confers developmental specificity in transgenic mice. , 1997, Proceedings of the National Academy of Sciences of the United States of America.

[23]  M. J. den Broeder,et al.  The Zebrafish Mutants dre, uki, and lep Encode Negative Regulators of the Hedgehog Signaling Pathway , 2005, PLoS genetics.

[24]  S. Orkin,et al.  Transcriptional regulation of erythropoiesis: an affair involving multiple partners , 2002, Oncogene.

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

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

[27]  E. Querfurth,et al.  GATA-1 interacts with the myeloid PU.1 transcription factor and represses PU.1-dependent transcription. , 2000, Blood.

[28]  D. Stainier,et al.  Hematopoietic stem cells derive directly from aortic endothelium during development , 2009, Nature.

[29]  B. Paw,et al.  Analysis of thrombocyte development in CD41-GFP transgenic zebrafish. , 2005, Blood.

[30]  L. Zon,et al.  Forced GATA-1 expression in the murine myeloid cell line M1: induction of c-Mpl expression and megakaryocytic/erythroid differentiation. , 1998, Blood.

[31]  S. Orkin,et al.  Targeted Deletion of a High-Affinity GATA-binding Site in the GATA-1 Promoter Leads to Selective Loss of the Eosinophil Lineage In Vivo , 2002, The Journal of experimental medicine.

[32]  D. Reines Faculty Opinions recommendation of TIF1gamma controls erythroid cell fate by regulating transcription elongation. , 2010 .

[33]  D. Traver,et al.  Definitive hematopoiesis initiates through a committed erythromyeloid progenitor in the zebrafish embryo , 2007, Development.

[34]  K. Kissa,et al.  Tracing hematopoietic precursor migration to successive hematopoietic organs during zebrafish development. , 2006, Immunity.

[35]  D. Tenen,et al.  Negative cross-talk between hematopoietic regulators: GATA proteins repress PU.1. , 1999, Proceedings of the National Academy of Sciences of the United States of America.

[36]  Elaine Dzierzak,et al.  Of lineage and legacy: the development of mammalian hematopoietic stem cells , 2008, Nature Immunology.

[37]  S. Orkin,et al.  The journey of developing hematopoietic stem cells , 2006, Development.

[38]  K. Kissa,et al.  Live imaging of emerging hematopoietic stem cells and early thymus colonization. , 2008, Blood.

[39]  T. Graf Differentiation plasticity of hematopoietic cells. , 2002, Blood.

[40]  K. Kissa,et al.  Blood stem cells emerge from aortic endothelium by a novel type of cell transition , 2010, Nature.

[41]  K. Kissa,et al.  Origins and unconventional behavior of neutrophils in developing zebrafish. , 2008, Blood.

[42]  T. Krunkosky,et al.  Identification of phagocytic cells, NK-like cytotoxic cell activity and the production of cellular exudates in the coelomic cavity of adult zebrafish. , 2009, Developmental and comparative immunology.

[43]  A. Jegga,et al.  PU.1 Positively Regulates GATA-1 Expression in Mast Cells , 2010, The Journal of Immunology.

[44]  B. Thisse,et al.  Ontogeny and behaviour of early macrophages in the zebrafish embryo. , 1999, Development.

[45]  Yi-Lin Yan,et al.  Double fluorescent in situ hybridization to zebrafish embryos. , 1996, Trends in genetics : TIG.

[46]  A. Brownlie,et al.  Characterization of embryonic globin genes of the zebrafish. , 2003, Developmental biology.

[47]  Carsten Peterson,et al.  Computational Modeling of the Hematopoietic Erythroid-Myeloid Switch Reveals Insights into Cooperativity, Priming, and Irreversibility , 2009, PLoS Comput. Biol..

[48]  T. Graf,et al.  PU.1 induces myeloid lineage commitment in multipotent hematopoietic progenitors. , 1998, Genes & development.

[49]  D. Ransom,et al.  The Zebrafish moonshine Gene Encodes Transcriptional Intermediary Factor 1γ, an Essential Regulator of Hematopoiesis , 2004, PLoS biology.