A conserved role of αA-crystallin in the development of the zebrafish embryonic lens.
Journal Article (Journal Article)
αA- and αB-crystallins are small heat shock proteins that bind thermodynamically destabilized proteins thereby inhibiting their aggregation. Highly expressed in the mammalian lens, the α-crystallins have been postulated to play a critical role in the maintenance of lens optical properties by sequestering age-damaged proteins prone to aggregation as well as through a multitude of roles in lens epithelial cells. Here, we have examined the role of α-crystallins in the development of the vertebrate zebrafish lens. For this purpose, we have carried out morpholino-mediated knockdown of αA-, αBa- and αBb-crystallin and characterized the gross morphology of the lens. We observed lens abnormalities, including increased reflectance intensity, as a consequence of the interference with expression of these proteins. These abnormalities were less frequent in transgenic zebrafish embryos expressing rat αA-crystallin suggesting a specific role of α-crystallins in embryonic lens development. To extend and confirm these findings, we generated an αA-crystallin knockout zebrafish line. A more consistent and severe lens phenotype was evident in maternal/zygotic αA-crystallin mutants compared to those observed by morpholino knockdown. The penetrance of the lens phenotype was reduced by transgenic expression of rat αA-crystallin and its severity was attenuated by maternal αA-crystallin expression. These findings demonstrate that the role of α-crystallins in lens development is conserved from mammals to zebrafish and set the stage for using the embryonic lens as a model system to test mechanistic aspects of α-crystallin chaperone activity and to develop strategies to fine-tune protein-protein interactions in aging and cataracts.
Full Text
Duke Authors
Cited Authors
- Zou, P; Wu, S-Y; Koteiche, HA; Mishra, S; Levic, DS; Knapik, E; Chen, W; Mchaourab, HS
Published Date
- September 2015
Published In
Volume / Issue
- 138 /
Start / End Page
- 104 - 113
PubMed ID
- 26149094
Pubmed Central ID
- PMC4638411
Electronic International Standard Serial Number (EISSN)
- 1096-0007
Digital Object Identifier (DOI)
- 10.1016/j.exer.2015.07.001
Language
- eng
Conference Location
- England