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

Lothar C. Dieterich(ETH Zurich), Sarah Klein(ETH Zurich), Anthony Mathelier(University of British Columbia), Adriana Śliwa-Primorac(ETH Zurich), Qiaoli Ma(ETH Zurich), Young‐Kwon Hong(University of Southern California), Jay W. Shin, Michito Hamada(University of Tsukuba), Marina Lizio, Masayoshi Itoh, Hideya Kawaji, Timo Lassmann(The Kids Research Institute Australia), Carsten O. Daub, Erik Arner, Piero Carninci, Yoshihide Hayashizaki(RIKEN), Alistair R. R. Forrest, Wyeth W. Wasserman(University of British Columbia), Michael Detmar(Board of the Swiss Federal Institutes of Technology)
Cell Reports
November 1, 2015
Cited by 50Open Access
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Abstract

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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