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Differential Etv2 threshold requirement for endothelial and erythropoietic development

delete2022-05-01
delete10
delete
OA
AI
T
Tanvi Sinha
K
Kelly Lammerts van Bueren
D
Diane E. Dickel
I
Ivana Zlatanova
R
Reuben Thomas
C
Carlos O. Lizama
S
Shan-Mei Xu
A
Ann C. Zovein
K
Kohta Ikegami
I
Ivan P. Moskowitz
K
Katherine S. Pollard
L
L Pennacchio
B
Brian L. Black *
DOI:10.1016/j.celrep.2022.110881delete
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Abstract

Abstract

En 中文
Endothelial and erythropoietic lineages arise from a common developmental progenitor. Etv2 is a master transcriptional regulator required for the development of both lineages. However, the mechanisms through which Etv2 initiates the gene-regulatory networks (GRNs) for endothelial and erythropoietic specification and how the two GRNs diverge downstream of Etv2 remain incompletely understood. Here, by analyzing a hypomorphic Etv2 mutant, we demonstrate different threshold requirements for initiation of the downstream GRNs for endothelial and erythropoietic development. We show that Etv2 functions directly in a coherent feedforward transcriptional network for vascular endothelial development, and a low level of Etv2 expression is sufficient to induce and sustain the endothelial GRN. In contrast, Etv2 induces the erythropoietic GRN indirectly via activation of Tal1, which requires a significantly higher threshold of Etv2 to initiate and sustain erythropoietic development. These results provide important mechanistic insight into the divergence of the endothelial and erythropoietic lineages.
Keywords:
ETS TRANSCRIPTION FACTORS
MOUSE EMBRYOS LACKING
GENE-EXPRESSION
HEMOGENIC ENDOTHELIUM
AMNIOTIC CELLS
BLOOD
LINEAGE
MICE
STEM
RNA
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Journal

Cell Reports cover
Cell Reports
IF:
6.9
Papers:
1.7W
Citations:
10.2W

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U
university of california san francisco
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U
University of California Berkeley
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U
united states department of energy (doe)
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University of California System cover
University of California System
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J
joint genome institute - jgi
Scholars:
429
Papers: 289
Citations: 0
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