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Genesis. 2017 Mar;55(3). doi: 10.1002/dvg.23021. Epub 2017 Feb 10.

Nkx2.5 regulates endothelin converting enzyme-1 during pharyngeal arch patterning.

Author information

1
Department of Craniofacial Biology, University of Colorado Anschutz Medical Campus, Aurora, Colorado, 80045.
2
Division of Cardiology, Department of Pediatrics, College of Physicians and Surgeons, Columbia University, New York, 10032.
3
Departments of Anatomy and Medical, Biochemistry, and Molecular Genetics, Indiana Medical School, Riley Heart Research Center, Herman B Wells Center for Pediatric Research, Division of Pediatric Cardiology, Indianapolis, 46202.
4
Division of Biological Sciences, University of California, San Diego, La Jolla, California, 92093.

Abstract

In gnathostomes, dorsoventral (D-V) patterning of neural crest cells (NCC) within the pharyngeal arches is crucial for the development of hinged jaws. One of the key signals that mediate this process is Endothelin-1 (EDN1). Loss of EDN1 binding to the Endothelin-A receptor (EDNRA) results in loss of EDNRA signaling and subsequent facial birth defects in humans, mice and zebrafish. A rate-limiting step in this crucial signaling pathway is the conversion of immature EDN1 into a mature active form by Endothelin converting enzyme-1 (ECE1). However, surprisingly little is known about how Ece1 transcription is induced or regulated. We show here that Nkx2.5 is required for proper craniofacial development in zebrafish and acts in part by upregulating ece1 expression. Disruption of nkx2.5 in zebrafish embryos results in defects in both ventral and dorsal pharyngeal arch-derived elements, with changes in ventral arch gene expression consistent with a disruption in Ednra signaling. ece1 mRNA rescues the nkx2.5 morphant phenotype, indicating that Nkx2.5 functions through modulating Ece1 expression or function. These studies illustrate a new function for Nkx2.5 in embryonic development and provide new avenues with which to pursue potential mechanisms underlying human facial disorders.

KEYWORDS:

birth defects; neural crest; patterning; signaling; transcription

PMID:
28109039
PMCID:
PMC5364067
DOI:
10.1002/dvg.23021
[Indexed for MEDLINE]
Free PMC Article

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