PUBLICATION
Photoreceptor Progenitors Depend Upon Coordination of gdf6a, thrβ, and tbx2b to Generate Precise Populations of Cone Photoreceptor Subtypes
- Authors
- DuVal, M.G., Allison, W.T.
- ID
- ZDB-PUB-181230-11
- Date
- 2018
- Source
- Investigative ophthalmology & visual science 59: 6089-6101 (Journal)
- Registered Authors
- Allison, Ted, Duval, Michèle
- Keywords
- none
- MeSH Terms
-
- T-Box Domain Proteins/physiology*
- Photoreceptor Cells, Vertebrate/physiology
- Thyroid Hormone Receptors beta/physiology*
- Stem Cells/physiology*
- Cell Differentiation/physiology*
- Gene Expression Regulation/physiology
- Genotyping Techniques
- Immunohistochemistry
- Retinal Cone Photoreceptor Cells/cytology*
- Zebrafish Proteins/physiology*
- Animals
- Retina/embryology*
- Animals, Genetically Modified
- Growth Differentiation Factor 6/physiology*
- Polymorphism, Restriction Fragment Length
- Zebrafish
- Embryo, Nonmammalian
- Models, Animal
- Gene Silencing
- PubMed
- 30592497 Full text @ Invest. Ophthalmol. Vis. Sci.
Citation
DuVal, M.G., Allison, W.T. (2018) Photoreceptor Progenitors Depend Upon Coordination of gdf6a, thrβ, and tbx2b to Generate Precise Populations of Cone Photoreceptor Subtypes. Investigative ophthalmology & visual science. 59:6089-6101.
Abstract
Purpose Replacing cone photoreceptors, the units of the retina necessary for daytime vision, depends upon the successful production of a full variety of new cones from, for example, stem cells. Using genetic experiments in a model organism with high cone diversity, zebrafish, we map the intersecting effects of cone development factors gdf6a, tbx2b, and thrβ.
Methods We investigated these genes of interest by using genetic combinations of mutants, gene knockdown, and dominant negative gene expression, and then quantified cone subtype outcomes (which normally develop in tightly regulated ratios).
Results Gdf6a mutants have reduced blue cones and, discovered here, reduced red cones. In combined gdf6a/tbx2b disruption, the loss of gdf6a in heterozygous tbx2b mutants reduced UV cones. Intriguingly, when we disrupted thrβ in gdf6a mutants by using a thrβ morpholino, their combined early disruption revealed a lamination phenotype. Disrupting thrβ activity via expression of a dominant negative thrβ (dnthrβ) at either early or late retinal development had differential outcomes on red cones (reduced abundance), versus UV and blue cones (increased abundance). By using dnthrβ in gdf6a mutants, we revealed that disrupting thrβ activity did not change gdf6a mutant cone phenotypes.
Conclusions Gdf6a loss directly affects blue and red cones and indirectly affects UV cones by increasing sensitivity to additional disruption, such as reduced tbx2b, resulting in fewer UV cones. The effects of thrβ change through photoreceptor development, first promoting red cones and restricting UV cones, and later restricting UV and blue cones. The effects of gdf6a on UV, blue, and red cone development overlap with, but likely supersede, those of thrβ.
Genes / Markers
Expression
Phenotype
Mutations / Transgenics
Human Disease / Model
Sequence Targeting Reagents
Fish
Orthology
Engineered Foreign Genes
Mapping