PUBLICATION

Cone photoreceptor types in zebrafish are generated by symmetric terminal divisions of dedicated precursors

Authors
Suzuki, S.C., Bleckert, A., Williams, P.R., Takechi, M., Kawamura, S., and Wong, R.O.
ID
ZDB-PUB-130904-45
Date
2013
Source
Proceedings of the National Academy of Sciences of the United States of America   110(37): 15109-14 (Journal)
Registered Authors
Kawamura, Shoji, Wong, Rachel
Keywords
vertebrate cone photoreceptors, cone genesis, zebrafish retina, in vivo time-lapse imaging
MeSH Terms
  • Luminescent Proteins/genetics
  • Stem Cells/cytology
  • Stem Cells/metabolism
  • Cone Opsins/genetics
  • Cone Opsins/metabolism*
  • Zebrafish/genetics
  • Zebrafish/growth & development*
  • Zebrafish/metabolism
  • Retinal Cone Photoreceptor Cells/classification
  • Retinal Cone Photoreceptor Cells/cytology*
  • Retinal Cone Photoreceptor Cells/metabolism
  • Thyroid Hormone Receptors beta/antagonists & inhibitors
  • Thyroid Hormone Receptors beta/genetics
  • Recombinant Proteins/genetics
  • Cell Lineage
  • Promoter Regions, Genetic
  • Molecular Sequence Data
  • Animals, Genetically Modified
  • Gene Expression Regulation, Developmental
  • Zebrafish Proteins/genetics
  • Zebrafish Proteins/metabolism
  • Base Sequence
  • Cell Division
  • Animals
  • Gene Knockdown Techniques
  • Larva/cytology
  • Larva/growth & development
  • Larva/metabolism
  • Cell Differentiation
(all 29)
PubMed
23980162 Full text @ Proc. Natl. Acad. Sci. USA
Abstract

Proper functioning of sensory systems requires the generation of appropriate numbers and proportions of neuronal subtypes that encode distinct information. Perception of color relies on signals from multiple cone photoreceptor types. In cone-dominated retinas, each cone expresses a single opsin type with peak sensitivity to UV, long (L) (red), medium (M) (green), or short (S) (blue) wavelengths. The modes of cell division generating distinct cone types are unknown. We report here a mechanism whereby zebrafish cone photoreceptors of the same type are produced by symmetric division of dedicated precursors. Transgenic fish in which the thyroid hormone receptor β2 (trβ2) promoter drives fluorescent protein expression before L-cone precursors themselves are produced permitted tracking of their division in vivo. Every L cone in a local region resulted from the terminal division of an L-cone precursor, suggesting that such divisions contribute significantly to L-cone production. Analysis of the fate of isolated pairs of cones and time-lapse observations suggest that other cone types can also arise by symmetric terminal divisions. Such divisions of dedicated precursors may help to rapidly attain the final numbers and proportions of cone types (L > M, UV > S) in zebrafish larvae. Loss- and gain-of-function experiments show that L-opsin expression requires trβ2 activity before cone differentiation. Ectopic expression of trβ2 after cone differentiation produces cones with mixed opsins. Temporal differences in the onset of trβ2 expression could explain why some species have mixed, and others have pure, cone types.

Genes / Markers
Figures
Figure Gallery (11 images) / 2
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Expression
Phenotype
No data available
Mutations / Transgenics
Allele Construct Type Affected Genomic Region
a9
    Complex
    fl1TgTransgenic Insertion
      jh1TgTransgenic Insertion
        jh16TgTransgenic Insertion
          mi2001TgTransgenic Insertion
            q20TgTransgenic Insertion
              q21TgTransgenic Insertion
                q22TgTransgenic Insertion
                  q23TgTransgenic Insertion
                    q24TgTransgenic Insertion
                      1 - 10 of 12
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                      Human Disease / Model
                      No data available
                      Sequence Targeting Reagents
                      Target Reagent Reagent Type
                      thrbMO2-thrbMRPHLNO
                      1 - 1 of 1
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                      Fish
                      Antibodies
                      Orthology
                      No data available
                      Engineered Foreign Genes
                      Marker Marker Type Name
                      CFPEFGCFP
                      EGFPEFGEGFP
                      GAL4EFGGAL4
                      GFPEFGGFP
                      TomatoEFGTomato
                      YFPEFGYFP
                      1 - 6 of 6
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                      Mapping
                      No data available