4.8 Article

DeepCAGE Transcriptomics Reveal an Important Role of the Transcription Factor MAFB in the Lymphatic Endothelium

Journal

CELL REPORTS
Volume 13, Issue 7, Pages 1493-1504

Publisher

CELL PRESS
DOI: 10.1016/j.celrep.2015.10.002

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Funding

  1. Swiss National Science Foundation [310030B_147087]
  2. European Research Council Grant LYVICAM
  3. Oncosuisse
  4. Krebsliga Zurich
  5. Leducq Foundation Transatlantic Network of Excellence Grant Lymph Vessels in Obesity and Cardiovascular Disease [11CVD03]
  6. Genome Canada Large-Scale Applied Research Grant [174CDE]
  7. BC Children's Hospital Foundation
  8. Child and Family Research Institute, Vancouver, Canada
  9. MEXT
  10. MEXT, Japan

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VEGF-C/VEGFR-3 signaling plays a central role in lymphatic development, regulating the budding of lymphatic progenitor cells from embryonic veins and maintaining the expression of PROX1 during later developmental stages. However, how VEGFR-3 activation translates into target gene expression is still not completely understood. We used cap analysis of gene expression (CAGE) RNA sequencing to characterize the transcriptional changes invoked by VEGF-C in LECs and to identify the transcription factors (TFs) involved. We found that MAFB, a TF involved in differentiation of various cell types, is rapidly induced and activated by VEGF-C. MAFB induced expression of PROX1 as well as other TFs and markers of differentiated LECs, indicating a role in the maintenance of the mature LEC phenotype. Correspondingly, E14.5 Mafb(-/-) embryos showed impaired lymphatic patterning in the skin. This suggests that MAFB is an important TF involved in lymphangiogenesis.

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