RGD Reference Report - Retinal dehydrogenase-2 is inhibited by compounds that induce congenital diaphragmatic hernias in rodents. - Rat Genome Database
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Retinal dehydrogenase-2 is inhibited by compounds that induce congenital diaphragmatic hernias in rodents.

Authors: Mey, J  Babiuk, RP  Clugston, R  Zhang, W  Greer, JJ 
Citation: Mey J, etal., Am J Pathol. 2003 Feb;162(2):673-9.
RGD ID: 1576367
Pubmed: (View Article at PubMed) PMID:12547725
DOI: Full-text: DOI:10.1016/S0002-9440(10)63861-8

Currently, the etiology of the serious developmental anomaly congenital diaphragmatic hernia (CDH) is unknown. We have used an animal model of CDH to address this issue. We characterized four separate teratogens that produced diaphragmatic defects in embryonic rats that are similar to those in infants with CDH. We then tested the hypothesis that all these agents share the common mechanism of perturbing the retinoid-signaling pathway. Specifically, inhibition of retinal dehydrogenase-2 (RALDH2), a key enzyme necessary for the production of retinoic acid and that is expressed in the developing diaphragm, was assayed by measuring retinoic acid production in cytosolic extracts from an oligodendrocyte cell line. The following compounds all induce posterolateral defects in the rat diaphragm; nitrofen, 4-biphenyl carboxylic acid, bisdiamine, and SB-210661. Importantly, we demonstrate that they all share the common mechanism of inhibiting RALDH2. These data provide an important component of mounting evidence suggesting that the retinoid system warrants consideration in future studies of the etiology of CDH.

Annotation

Gene Ontology Annotations    

Biological Process

Cellular Component
cytosol  (IDA)

Molecular Function

Molecular Pathway Annotations    
Objects Annotated

Genes (Rattus norvegicus)
Aldh1a2  (aldehyde dehydrogenase 1 family, member A2)

Genes (Mus musculus)
Aldh1a2  (aldehyde dehydrogenase family 1, subfamily A2)

Genes (Homo sapiens)
ALDH1A2  (aldehyde dehydrogenase 1 family member A2)


Additional Information