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A Prox1 enhancer represses haematopoiesis in the lymphatic vasculature

Author

Listed:
  • Jan Kazenwadel

    (University of South Australia and SA Pathology)

  • Parvathy Venugopal

    (University of South Australia and SA Pathology
    SA Pathology)

  • Anna Oszmiana

    (University of South Australia and SA Pathology)

  • John Toubia

    (University of South Australia and SA Pathology
    University of South Australia and SA Pathology)

  • Luis Arriola-Martinez

    (University of South Australia and SA Pathology
    SA Pathology)

  • Virginia Panara

    (Uppsala University
    Uppsala University)

  • Sandra G. Piltz

    (University of Adelaide
    South Australian Health & Medical Research Institute
    University of Adelaide)

  • Chris Brown

    (University of South Australia)

  • Wanshu Ma

    (Northwestern University Feinberg School of Medicine)

  • Andreas W. Schreiber

    (University of South Australia and SA Pathology
    University of South Australia and SA Pathology
    University of Adelaide)

  • Katarzyna Koltowska

    (Uppsala University
    Uppsala University)

  • Samir Taoudi

    (The Walter and Eliza Hall Institute of Medical Research
    University of Melbourne)

  • Paul Q. Thomas

    (University of Adelaide
    South Australian Health & Medical Research Institute
    University of Adelaide)

  • Hamish S. Scott

    (University of South Australia and SA Pathology
    SA Pathology
    University of South Australia and SA Pathology
    University of Adelaide)

  • Natasha L. Harvey

    (University of South Australia and SA Pathology
    University of Adelaide)

Abstract

Transcriptional enhancer elements are responsible for orchestrating the temporal and spatial control over gene expression that is crucial for programming cell identity during development1–3. Here we describe a novel enhancer element that is important for regulating the expression of Prox1 in lymphatic endothelial cells. This evolutionarily conserved enhancer is bound by key lymphatic transcriptional regulators including GATA2, FOXC2, NFATC1 and PROX1. Genome editing of the enhancer to remove five nucleotides encompassing the GATA2-binding site resulted in perinatal death of homozygous mutant mice due to profound lymphatic vascular defects. Lymphatic endothelial cells in enhancer mutant mice exhibited reduced expression of genes characteristic of lymphatic endothelial cell identity and increased expression of genes characteristic of haemogenic endothelium, and acquired the capacity to generate haematopoietic cells. These data not only reveal a transcriptional enhancer element important for regulating Prox1 expression and lymphatic endothelial cell identity but also demonstrate that the lymphatic endothelium has haemogenic capacity, ordinarily repressed by Prox1.

Suggested Citation

  • Jan Kazenwadel & Parvathy Venugopal & Anna Oszmiana & John Toubia & Luis Arriola-Martinez & Virginia Panara & Sandra G. Piltz & Chris Brown & Wanshu Ma & Andreas W. Schreiber & Katarzyna Koltowska & S, 2023. "A Prox1 enhancer represses haematopoiesis in the lymphatic vasculature," Nature, Nature, vol. 614(7947), pages 343-348, February.
  • Handle: RePEc:nat:nature:v:614:y:2023:i:7947:d:10.1038_s41586-022-05650-9
    DOI: 10.1038/s41586-022-05650-9
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