The paralogous hematopoietic regulators Lyl1 and Scl are coregulated by Ets and GATA factors, but Lyl1 cannot rescue the early Scl-/- phenotype

Wan Y.I. Chan, George A. Follows, Georges Lacaud, John E. Pimanda, Josette Renee Landry, Sarah Kinston, Kathy Knezevic, Sandra Piltz, Ian J. Donaldson, Laure Gambardella, Fred Sablitzky, Anthony R. Green, Valerie Kouskoff, Berthold Göttgens

Research output: Contribution to journalArticle

61 Citations (Scopus)

Abstract

Transcription factors are key regulators of hematopoietic stem cells (HSCs), yet the molecular mechanisms that control their expression are largely unknown. Previously, we demonstrated that expression of Scl/Tal1, a transcription factor required for the specification of HSCs, is controlled by Ets and GATA factors. Here we characterize the molecular mechanisms controlling expression of Lyl1, a paralog of Scl also required for HSC function. Two closely spaced promoters directed expression to hematopoietic progenitor, megakaryocytic, and endothelial cells in transgenic mice. Conserved binding sites required for promoter activity were bound in vivo by GATA-2 and the Ets factors Fli1, Elf1, Erg, and PU.1. However, despite coregulation of Scl and Lyl1 by the same Ets and GATA factors, Scl expression was initiated prior to Lyl1 in embryonic stem (ES) cell differentiation assays. Moreover, ectopic expression of Scl but not Lyl1 rescued hematopoietic differentiation in Scl-/- ES cells, thus providing a molecular explanation for the vastly different phenotypes of Scl-/- and Lyl1-/- mouse embryos. Furthermore, coregulation of Scl and Lyl1 later during development may explain the mild phenotype of Scl-/- adult HSCs.

LanguageEnglish
Pages1908-1916
Number of pages9
JournalBlood
Volume109
Issue number5
DOIs
Publication statusPublished - 1 Mar 2007
Externally publishedYes

ASJC Scopus subject areas

  • Biochemistry
  • Immunology
  • Hematology
  • Cell Biology

Cite this

Chan, W. Y. I., Follows, G. A., Lacaud, G., Pimanda, J. E., Landry, J. R., Kinston, S., ... Göttgens, B. (2007). The paralogous hematopoietic regulators Lyl1 and Scl are coregulated by Ets and GATA factors, but Lyl1 cannot rescue the early Scl-/- phenotype. Blood, 109(5), 1908-1916. https://doi.org/10.1182/blood-2006-05-023226
Chan, Wan Y.I. ; Follows, George A. ; Lacaud, Georges ; Pimanda, John E. ; Landry, Josette Renee ; Kinston, Sarah ; Knezevic, Kathy ; Piltz, Sandra ; Donaldson, Ian J. ; Gambardella, Laure ; Sablitzky, Fred ; Green, Anthony R. ; Kouskoff, Valerie ; Göttgens, Berthold. / The paralogous hematopoietic regulators Lyl1 and Scl are coregulated by Ets and GATA factors, but Lyl1 cannot rescue the early Scl-/- phenotype. In: Blood. 2007 ; Vol. 109, No. 5. pp. 1908-1916.
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title = "The paralogous hematopoietic regulators Lyl1 and Scl are coregulated by Ets and GATA factors, but Lyl1 cannot rescue the early Scl-/- phenotype",
abstract = "Transcription factors are key regulators of hematopoietic stem cells (HSCs), yet the molecular mechanisms that control their expression are largely unknown. Previously, we demonstrated that expression of Scl/Tal1, a transcription factor required for the specification of HSCs, is controlled by Ets and GATA factors. Here we characterize the molecular mechanisms controlling expression of Lyl1, a paralog of Scl also required for HSC function. Two closely spaced promoters directed expression to hematopoietic progenitor, megakaryocytic, and endothelial cells in transgenic mice. Conserved binding sites required for promoter activity were bound in vivo by GATA-2 and the Ets factors Fli1, Elf1, Erg, and PU.1. However, despite coregulation of Scl and Lyl1 by the same Ets and GATA factors, Scl expression was initiated prior to Lyl1 in embryonic stem (ES) cell differentiation assays. Moreover, ectopic expression of Scl but not Lyl1 rescued hematopoietic differentiation in Scl-/- ES cells, thus providing a molecular explanation for the vastly different phenotypes of Scl-/- and Lyl1-/- mouse embryos. Furthermore, coregulation of Scl and Lyl1 later during development may explain the mild phenotype of Scl-/- adult HSCs.",
author = "Chan, {Wan Y.I.} and Follows, {George A.} and Georges Lacaud and Pimanda, {John E.} and Landry, {Josette Renee} and Sarah Kinston and Kathy Knezevic and Sandra Piltz and Donaldson, {Ian J.} and Laure Gambardella and Fred Sablitzky and Green, {Anthony R.} and Valerie Kouskoff and Berthold G{\"o}ttgens",
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Chan, WYI, Follows, GA, Lacaud, G, Pimanda, JE, Landry, JR, Kinston, S, Knezevic, K, Piltz, S, Donaldson, IJ, Gambardella, L, Sablitzky, F, Green, AR, Kouskoff, V & Göttgens, B 2007, 'The paralogous hematopoietic regulators Lyl1 and Scl are coregulated by Ets and GATA factors, but Lyl1 cannot rescue the early Scl-/- phenotype', Blood, vol. 109, no. 5, pp. 1908-1916. https://doi.org/10.1182/blood-2006-05-023226

The paralogous hematopoietic regulators Lyl1 and Scl are coregulated by Ets and GATA factors, but Lyl1 cannot rescue the early Scl-/- phenotype. / Chan, Wan Y.I.; Follows, George A.; Lacaud, Georges; Pimanda, John E.; Landry, Josette Renee; Kinston, Sarah; Knezevic, Kathy; Piltz, Sandra; Donaldson, Ian J.; Gambardella, Laure; Sablitzky, Fred; Green, Anthony R.; Kouskoff, Valerie; Göttgens, Berthold.

In: Blood, Vol. 109, No. 5, 01.03.2007, p. 1908-1916.

Research output: Contribution to journalArticle

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T1 - The paralogous hematopoietic regulators Lyl1 and Scl are coregulated by Ets and GATA factors, but Lyl1 cannot rescue the early Scl-/- phenotype

AU - Chan, Wan Y.I.

AU - Follows, George A.

AU - Lacaud, Georges

AU - Pimanda, John E.

AU - Landry, Josette Renee

AU - Kinston, Sarah

AU - Knezevic, Kathy

AU - Piltz, Sandra

AU - Donaldson, Ian J.

AU - Gambardella, Laure

AU - Sablitzky, Fred

AU - Green, Anthony R.

AU - Kouskoff, Valerie

AU - Göttgens, Berthold

PY - 2007/3/1

Y1 - 2007/3/1

N2 - Transcription factors are key regulators of hematopoietic stem cells (HSCs), yet the molecular mechanisms that control their expression are largely unknown. Previously, we demonstrated that expression of Scl/Tal1, a transcription factor required for the specification of HSCs, is controlled by Ets and GATA factors. Here we characterize the molecular mechanisms controlling expression of Lyl1, a paralog of Scl also required for HSC function. Two closely spaced promoters directed expression to hematopoietic progenitor, megakaryocytic, and endothelial cells in transgenic mice. Conserved binding sites required for promoter activity were bound in vivo by GATA-2 and the Ets factors Fli1, Elf1, Erg, and PU.1. However, despite coregulation of Scl and Lyl1 by the same Ets and GATA factors, Scl expression was initiated prior to Lyl1 in embryonic stem (ES) cell differentiation assays. Moreover, ectopic expression of Scl but not Lyl1 rescued hematopoietic differentiation in Scl-/- ES cells, thus providing a molecular explanation for the vastly different phenotypes of Scl-/- and Lyl1-/- mouse embryos. Furthermore, coregulation of Scl and Lyl1 later during development may explain the mild phenotype of Scl-/- adult HSCs.

AB - Transcription factors are key regulators of hematopoietic stem cells (HSCs), yet the molecular mechanisms that control their expression are largely unknown. Previously, we demonstrated that expression of Scl/Tal1, a transcription factor required for the specification of HSCs, is controlled by Ets and GATA factors. Here we characterize the molecular mechanisms controlling expression of Lyl1, a paralog of Scl also required for HSC function. Two closely spaced promoters directed expression to hematopoietic progenitor, megakaryocytic, and endothelial cells in transgenic mice. Conserved binding sites required for promoter activity were bound in vivo by GATA-2 and the Ets factors Fli1, Elf1, Erg, and PU.1. However, despite coregulation of Scl and Lyl1 by the same Ets and GATA factors, Scl expression was initiated prior to Lyl1 in embryonic stem (ES) cell differentiation assays. Moreover, ectopic expression of Scl but not Lyl1 rescued hematopoietic differentiation in Scl-/- ES cells, thus providing a molecular explanation for the vastly different phenotypes of Scl-/- and Lyl1-/- mouse embryos. Furthermore, coregulation of Scl and Lyl1 later during development may explain the mild phenotype of Scl-/- adult HSCs.

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