Cellular retinoic acid-binding proteins are essential for hindbrain patterning and signal robustness in zebrafish
- Authors
- Cai, A.Q., Radtke, K., Linville, A., Lander, A.D., Nie, Q., and Schilling, T.F.
- ID
- ZDB-PUB-120529-33
- Date
- 2012
- Source
- Development (Cambridge, England) 139(12): 2150-2155 (Journal)
- Registered Authors
- Schilling, Tom
- Keywords
- Danio rerio, hindbrain, morphogen
- MeSH Terms
-
- Animals
- Body Patterning/drug effects
- Body Patterning/genetics*
- Gene Expression Regulation, Developmental/drug effects
- Homeodomain Proteins/genetics
- Homeodomain Proteins/metabolism
- Mice
- Models, Biological
- Receptors, Retinoic Acid/genetics
- Receptors, Retinoic Acid/metabolism*
- Rhombencephalon/drug effects
- Rhombencephalon/embryology*
- Rhombencephalon/metabolism
- Signal Transduction/drug effects
- Signal Transduction/genetics*
- Tretinoin/pharmacology
- Zebrafish/embryology*
- Zebrafish/genetics*
- Zebrafish Proteins/genetics
- Zebrafish Proteins/metabolism*
- PubMed
- 22619388 Full text @ Development
The vitamin A derivative retinoic acid (RA) is a morphogen that patterns the anterior-posterior axis of the vertebrate hindbrain. Cellular retinoic acid-binding proteins (Crabps) transport RA within cells to both its nuclear receptors (RARs) and degrading enzymes (Cyp26s). However, mice lacking Crabps are viable, suggesting that Crabp functions are redundant with those of other fatty acid-binding proteins. Here we show that Crabps in zebrafish are essential for posterior patterning of the hindbrain and that they provide a key feedback mechanism that makes signaling robust as they are able to compensate for changes in RA production. Of the four zebrafish Crabps, Crabp2a is uniquely RA inducible and depletion or overexpression of Crabp2a makes embryos hypersensitive to exogenous RA. Computational models confirm that Crabp2a improves robustness within a narrow concentration range that optimizes a ‘robustness index’, integrating spatial information along the RA morphogen gradient. Exploration of signaling parameters in our models suggests that the ability of Crabp2a to transport RA to Cyp26 enzymes for degradation is a major factor in promoting robustness. These results demonstrate a previously unrecognized requirement for Crabps in RA signaling and hindbrain development, as well as a novel mechanism for stabilizing morphogen gradients despite genetic or environmental fluctuations in morphogen availability.