"Maturational" globin switching in primary primitive erythroid cells.

Mammals have 2 distinct erythroid lineages. The primitive erythroid lineage originates in the yolk sac and generates a cohort of large erythroblasts that terminally differentiate in the bloodstream. The definitive erythroid lineage generates smaller enucleated erythrocytes that become the predominant cell in fetal and postnatal circulation. These lineages also have distinct globin expression patterns. Our studies in primary murine primitive erythroid cells indicate that betaH1 is the predominant beta-globin transcript in the early yolk sac. Thus, unlike the human, murine beta-globin genes are not up-regulated in the order of their chromosomal arrangement. As primitive erythroblasts mature from proerythroblasts to reticulocytes, they undergo a betaH1- to epsilony-globin switch, up-regulate adult beta1- and beta2-globins, and down-regulate zeta-globin. These changes in transcript levels correlate with changes in RNA polymerase II density at their promoters and transcribed regions. Furthermore, the epsilony- and betaH1-globin genes in primitive erythroblasts reside within a single large hyperacetylated domain. These data suggest that this "maturational" betaH1- to epsilony-globin switch is dynamically regulated at the transcriptional level. Globin switching during ontogeny is due not only to the sequential appearance of primitive and definitive lineages but also to changes in globin expression as primitive erythroblasts mature in the bloodstream.

[1]  J. Lingrel,et al.  KLF2 is essential for primitive erythropoiesis and regulates the human and murine embryonic beta-like globin genes in vivo. , 2005, Blood.

[2]  G. Stamatoyannopoulos Control of globin gene expression during development and erythroid differentiation. , 2005, Experimental hematology.

[3]  J. E. Russell,et al.  Effect of ζ-globin substitution on the O2-transport properties of Hb S in vitro and in vivo , 2004 .

[4]  Jeffrey Malik,et al.  Yolk sac-derived primitive erythroblasts enucleate during mammalian embryogenesis. , 2004, Blood.

[5]  A. Dean,et al.  Developmental stage differences in chromatin subdomains of the β-globin locus , 2004 .

[6]  A. Dean,et al.  Developmental stage differences in chromatin subdomains of the beta-globin locus. , 2004, Proceedings of the National Academy of Sciences of the United States of America.

[7]  J. E. Russell,et al.  Effect of zeta-globin substitution on the O2-transport properties of Hb S in vitro and in vivo. , 2004, Biochemical and biophysical research communications.

[8]  M. Groudine,et al.  A Complex Chromatin Landscape Revealed by Patterns of Nuclease Sensitivity and Histone Modification within the Mouse β-Globin Locus , 2003, Molecular and Cellular Biology.

[9]  Jessica Halow,et al.  The beta -globin locus control region (LCR) functions primarily by enhancing the transition from transcription initiation to elongation. , 2003, Genes & development.

[10]  Jeffrey Malik,et al.  Circulation is established in a stepwise pattern in the mammalian embryo. , 2003, Blood.

[11]  Jo Vandesompele,et al.  RTPrimerDB: the Real-Time PCR primer and probe database , 2003, Nucleic Acids Res..

[12]  E. Bresnick,et al.  Developmentally dynamic histone acetylation pattern of a tissue-specific chromatin domain. , 2000, Proceedings of the National Academy of Sciences of the United States of America.

[13]  Myles Brown,et al.  Cofactor Dynamics and Sufficiency in Estrogen Receptor–Regulated Transcription , 2000, Cell.

[14]  G. Stamatoyannopoulos,et al.  FKLF-2: a novel Krüppel-like transcriptional factor that activates globin and other erythroid lineage genes. , 2000, Blood.

[15]  M. Groudine,et al.  β-globin Gene Switching and DNase I Sensitivity of the Endogenous β-globin Locus in Mice Do Not Require the Locus Control Region , 2000 .

[16]  M. Groudine,et al.  Beta-globin gene switching and DNase I sensitivity of the endogenous beta-globin locus in mice do not require the locus control region. , 2000, Molecular cell.

[17]  J. Palis,et al.  Development of erythroid and myeloid progenitors in the yolk sac and embryo proper of the mouse. , 1999, Development.

[18]  G. Stamatoyannopoulos,et al.  FKLF, a Novel Krüppel-Like Factor That Activates Human Embryonic and Fetal β-Like Globin Genes , 1999, Molecular and Cellular Biology.

[19]  F. Grosveld,et al.  Mechanisms of developmental control of transcription in the murine alpha- and beta-globin loci. , 1999, Genes & development.

[20]  P. Leder,et al.  Summary In situ hybridization reveals co-expression of embryonic and adult globin genes in the earliest murine erythrocyte progenitors , 1999 .

[21]  R. Hardison,et al.  Hemoglobins from bacteria to man: evolution of different patterns of gene expression. , 1998, The Journal of experimental biology.

[22]  J. Palis,et al.  Initiation of murine embryonic erythropoiesis: a spatial analysis. , 1997, Blood.

[23]  P. Kingsley,et al.  Differential gene expression during early murine yolk sac development , 1995, Molecular reproduction and development.

[24]  P. Leder,et al.  In situ hybridization reveals co-expression of embryonic and adult alpha globin genes in the earliest murine erythrocyte progenitors. , 1992, Development.

[25]  G. Stamatoyannopoulos Human hemoglobin switching. , 1991, Science.

[26]  S. Orkin,et al.  Regulated expression of globin chains and the erythroid transcription factor GATA-1 during erythropoiesis in the developing mouse , 1990, Molecular and cellular biology.

[27]  E. Lazarides,et al.  Vimentin downregulation is an inherent feature of murine erythropoiesis and occurs independently of lineage. , 1990, Development.

[28]  M. Monk Mammalian Development: A Practical Approach , 1988, Development.

[29]  D. Chui,et al.  Hemoglobin switching during murine embryonic development: evidence for two populations of embryonic erythropoietic progenitor cells. , 1986, Blood.

[30]  C. Hutchison,et al.  The mouse beta h1 gene codes for the z chain of embryonic hemoglobin. , 1984, The Journal of biological chemistry.

[31]  C. Hutchison,et al.  Two mouse early embryonic beta-globin gene sequences. Evolution of the nonadult beta-globins. , 1984, The Journal of biological chemistry.

[32]  C. Hutchison,et al.  Two Mouse Early Embryonic &Globin Gene Sequences , 1984 .

[33]  G. Stamatoyannopoulos,et al.  Cellular regulation of hemoglobin switching: evidence for inverse relationship between fetal hemoglobin synthesis and degree of maturity of human erythroid cells. , 1979, Proceedings of the National Academy of Sciences of the United States of America.

[34]  J. Gauldie,et al.  Hemoglobin ontogeny during normal mouse fetal development. , 1979, Proceedings of the National Academy of Sciences of the United States of America.

[35]  H. Vogel,et al.  On the kinetics of erythroid cell differentiation in fetal mice. I. Microspectrophotometric determination of the hemoglobin content in erythroid cells during gestation , 1973, Journal of cellular physiology.

[36]  V. Ingram Embryonic Red Blood Cell Formation , 1972, Nature.

[37]  G. Ackerman,et al.  A phase and electron microscopic study of vasculogenesis and erythropoiesis in the yolk sac of the mouse , 1971, The Anatomical record.

[38]  A. de la Chapelle,et al.  Differentiation of mammalian somatic cells: DNA and hemoglobin synthesis in fetal mouse yolk sac erythroid cells. , 1969, Proceedings of the National Academy of Sciences of the United States of America.