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Int J Mol Sci. 2019 May 8;20(9). pii: E2275. doi: 10.3390/ijms20092275.

Sonic Hedgehog Signaling Is Required for Cyp26 Expression during Embryonic Development.

Author information

1
Department of Oral Biochemistry, Sahlgrenska Academy at the University of Gothenburg, SE-40530 Göteborg, Sweden. maha.el.shahawy@odontologi.gu.se.
2
Department of Oral Biology, Minia University, Minia 51161, Egypt. maha.el.shahawy@odontologi.gu.se.
3
Department of Oral Biochemistry, Sahlgrenska Academy at the University of Gothenburg, SE-40530 Göteborg, Sweden. claes-goran.reibring@gu.se.
4
Department of Oral Biochemistry, Sahlgrenska Academy at the University of Gothenburg, SE-40530 Göteborg, Sweden. kristina.hallberg@odontologi.gu.se.
5
Program in Craniofacial Biology and Department of Orofacial Sciences, University of California San Francisco, San Francisco, CA 94143, USA. cynthianeben@gmail.com.
6
Program in Craniofacial Biology and Department of Orofacial Sciences, University of California San Francisco, San Francisco, CA 94143, USA. Pauline.Marangoni@ucsf.edu.
7
Department of Molecular Genetics and Microbiology, University of Florida College of Medicine, Gainesville, FL 32610, USA. bharfe@UFL.EDU.
8
Program in Craniofacial Biology and Department of Orofacial Sciences, University of California San Francisco, San Francisco, CA 94143, USA. Ophir.Klein@ucsf.edu.
9
Department of Pediatrics and Institute for Human Genetics, University of California San Francisco, San Francisco, CA 94143, USA. Ophir.Klein@ucsf.edu.
10
Department of Oral Biochemistry, Sahlgrenska Academy at the University of Gothenburg, SE-40530 Göteborg, Sweden. linde@odontologi.gu.se.
11
Department of Oral Biochemistry, Sahlgrenska Academy at the University of Gothenburg, SE-40530 Göteborg, Sweden. amel@odontologi.gu.se.

Abstract

Deciphering how signaling pathways interact during development is necessary for understanding the etiopathogenesis of congenital malformations and disease. In several embryonic structures, components of the Hedgehog and retinoic acid pathways, two potent players in development and disease are expressed and operate in the same or adjacent tissues and cells. Yet whether and, if so, how these pathways interact during organogenesis is, to a large extent, unclear. Using genetic and experimental approaches in the mouse, we show that during development of ontogenetically different organs, including the tail, genital tubercle, and secondary palate, Sonic hedgehog (SHH) loss-of-function causes anomalies phenocopying those induced by enhanced retinoic acid signaling and that SHH is required to prevent supraphysiological activation of retinoic signaling through maintenance and reinforcement of expression of the Cyp26 genes. Furthermore, in other tissues and organs, disruptions of the Hedgehog or the retinoic acid pathways during development generate similar phenotypes. These findings reveal that rigidly calibrated Hedgehog and retinoic acid activities are required for normal organogenesis and tissue patterning.

KEYWORDS:

CRE/LoxP; Cyp26 enzymes; congenital anomalies; hedgehog signaling; mouse models; retinoic acid; smoothened; sonic hedgehog

PMID:
31072004
PMCID:
PMC6540044
DOI:
10.3390/ijms20092275
[Indexed for MEDLINE]
Free PMC Article

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