TY - JOUR
T1 - A CRISPR screen identifies genes controlling Etv2 threshold expression in murine hemangiogenic fate commitment
AU - Zhao, Haiyong
AU - Choi, Kyunghee
N1 - Funding Information:
We thank the lab members for constructive criticism and helpful discussion. We thank Karen Krchma for help with mouse work, Rong Zhang for help with CRISPR lentivirus library preparation, and Gordon Keller for T/EGFP ES cells. We thank Masa Ema for Flk1GFP/GFP ES cells. We thank the Genome Technology Access Center at Washington University School of Medicine for deep sequencing service. This work was supported by NIH Grants R01HL63736 and R01HL55337 (K.C.).
Publisher Copyright:
© 2017 The Author(s).
PY - 2017/12/1
Y1 - 2017/12/1
N2 - The ETS transcription factor Etv2 is necessary and sufficient for the generation of hematopoietic and endothelial cells. However, upstream regulators of Etv2 in hemangiogenesis, generation of hematopoietic and endothelial cells, have not been clearly addressed. Here we track the developmental route of hemangiogenic progenitors from mouse embryonic stem cells, perform genome-wide CRISPR screening, and transcriptome analysis of en route cell populations by utilizing Brachyury, Etv2, or Scl reporter embryonic stem cell lines to further understand the mechanisms that control hemangiogenesis. We identify the forkhead transcription factor Foxh1, in part through Eomes, to be critical for the formation of FLK1+ mesoderm, from which the hemangiogenic fate is specified. Importantly, hemangiogenic fate is specified not simply by the onset of Etv2 expression, but by a threshold-dependent mechanism, in which VEGF-FLK1 signaling plays an instructive role by promoting Etv2 threshold expression. These studies reveal comprehensive cellular and molecular pathways governing the hemangiogenic cell lineage development.
AB - The ETS transcription factor Etv2 is necessary and sufficient for the generation of hematopoietic and endothelial cells. However, upstream regulators of Etv2 in hemangiogenesis, generation of hematopoietic and endothelial cells, have not been clearly addressed. Here we track the developmental route of hemangiogenic progenitors from mouse embryonic stem cells, perform genome-wide CRISPR screening, and transcriptome analysis of en route cell populations by utilizing Brachyury, Etv2, or Scl reporter embryonic stem cell lines to further understand the mechanisms that control hemangiogenesis. We identify the forkhead transcription factor Foxh1, in part through Eomes, to be critical for the formation of FLK1+ mesoderm, from which the hemangiogenic fate is specified. Importantly, hemangiogenic fate is specified not simply by the onset of Etv2 expression, but by a threshold-dependent mechanism, in which VEGF-FLK1 signaling plays an instructive role by promoting Etv2 threshold expression. These studies reveal comprehensive cellular and molecular pathways governing the hemangiogenic cell lineage development.
UR - http://www.scopus.com/inward/record.url?scp=85029469167&partnerID=8YFLogxK
U2 - 10.1038/s41467-017-00667-5
DO - 10.1038/s41467-017-00667-5
M3 - Article
C2 - 28912455
AN - SCOPUS:85029469167
VL - 8
JO - Nature Communications
JF - Nature Communications
SN - 2041-1723
IS - 1
M1 - 541
ER -