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ZFIN ID: ZDB-PUB-130903-33
Zebrafish guanylate cyclase type 3 signaling in cone photoreceptors
Fries, R., Scholten, A., Säftel, W., and Koch, K.W.
Date: 2013
Source: PLoS One   8(8): e69656 (Journal)
Registered Authors:
Keywords: Retina, Zebrafish, Larvae, Immunohistochemistry techniques, Antibodies, Morpholino, Eyes, Photoreceptors
MeSH Terms:
  • Animals
  • Guanylate Cyclase/metabolism*
  • Guanylate Cyclase-Activating Proteins/metabolism
  • Protein Isoforms/metabolism
  • Retinal Cone Photoreceptor Cells/metabolism*
  • Signal Transduction
  • Zebrafish
  • Zebrafish Proteins/metabolism*
PubMed: 23940527 Full text @ PLoS One

The zebrafish guanylate cyclase type 3 (zGC3) is specifically expressed in cone cells. A specifc antibody directed against zGC3 revealed expression at the protein level at 3.5 dpf in outer and inner retinal layers, which increased in intensity between 3.5 and 7 dpf. This expression pattern differed from sections of the adult retina showing strong immunostaining in outer segments of double cones and short single cones, less intense immunoreactivity in long single cones, but no staining in the inner retina. Although transcription and protein expression levels of zGC3 are similar to that of the cyclase regulator guanylate cyclase-activating protein 3 (zGCAP3), we surprisingly found that zGCAP3 is present in a 28-fold molar excess over zGC3 in zebrafish retinae. Further, zGCAP3 was an efficient regulator of guanylate cyclases activity in native zebrafish retinal membrane preparations. Therefore, we investigated the physiological function of zGCAP3 by two different behavioral assays. Using the morpholino antisense technique, we knocked down expression of zGCAP3 and recorded the optokinetic and optomotor responses of morphants, control morphants, and wild type fish at 5–6 dpf. No significant differences in behavioral responses among wild type, morphants and control morphants were found, indicating that a loss of zGCAP3 has no consequences in primary visual processing in the larval retina despite its prominent expression pattern. Its physiological function is therefore compensated by other zGCAP isoforms.