Feedback regulation of retinaldehyde reductase <scp>DHRS3</scp> , a critical determinant of retinoic acid homeostasis
Retinoic acid is crucial for vertebrate embryogenesis, influencing anterior-posterior patterning and organogenesis through its interaction with nuclear hormone receptors comprising heterodimers of retinoic acid receptors (RARα, β, or γ) and retinoid X receptors (RXRα, β, or γ). Tissue retinoic acid levels are tightly regulated since both its excess and deficiency are deleterious. Dehydrogenase/reductase 3 (DHRS3) plays a critical role in this regulation by converting retinaldehyde to retinol, preventing excessive retinoic acid formation. Mutations in DHRS3 can result in embryonic lethality and congenital defects. This study shows that mouse Dhrs3 expression is responsive to vitamin A status and is directly regulated by the RAR/RXR complex through cis-regulatory elements. This highlights a negative feedback mechanism that ensures retinoic acid homeostasis.
Authors
- Alexander R. Moise (ORCID: https://orcid.org/0000-0003-2307-6035)
- Parisa Varshosaz
- Catherine O’Connor (ORCID: https://orcid.org/0000-0002-6407-1073)
Institutions
- Laurentian University (CA)
- NOSM University (CA)
Publication Details
- Journal
- FEBS Letters
- Published
- 2024-10-17
- DOI
- https://doi.org/10.1002/1873-3468.15038
- Citations
- 2
- Primary Topic
- Retinoids in leukemia and cellular processes
- Type
- article
- Field-Weighted Citation Impact
- 0.47
Funders
- National Institutes of Health
- Natural Sciences and Engineering Research Council of Canada
- Eunice Kennedy Shriver National Institute of Child Health and Human Development