Zebrafish guanylate cyclase type 3 signaling in cone photoreceptors.

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...

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Main Authors: Ramona Fries, Alexander Scholten, Werner Säftel, Karl-Wilhelm Koch
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2013-01-01
Series:PLoS ONE
Online Access:http://europepmc.org/articles/PMC3734133?pdf=render
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spelling doaj-eea38c9cbde249ecb2157c47d225d7312020-11-25T02:06:24ZengPublic Library of Science (PLoS)PLoS ONE1932-62032013-01-0188e6965610.1371/journal.pone.0069656Zebrafish guanylate cyclase type 3 signaling in cone photoreceptors.Ramona FriesAlexander ScholtenWerner SäftelKarl-Wilhelm KochThe 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.http://europepmc.org/articles/PMC3734133?pdf=render
collection DOAJ
language English
format Article
sources DOAJ
author Ramona Fries
Alexander Scholten
Werner Säftel
Karl-Wilhelm Koch
spellingShingle Ramona Fries
Alexander Scholten
Werner Säftel
Karl-Wilhelm Koch
Zebrafish guanylate cyclase type 3 signaling in cone photoreceptors.
PLoS ONE
author_facet Ramona Fries
Alexander Scholten
Werner Säftel
Karl-Wilhelm Koch
author_sort Ramona Fries
title Zebrafish guanylate cyclase type 3 signaling in cone photoreceptors.
title_short Zebrafish guanylate cyclase type 3 signaling in cone photoreceptors.
title_full Zebrafish guanylate cyclase type 3 signaling in cone photoreceptors.
title_fullStr Zebrafish guanylate cyclase type 3 signaling in cone photoreceptors.
title_full_unstemmed Zebrafish guanylate cyclase type 3 signaling in cone photoreceptors.
title_sort zebrafish guanylate cyclase type 3 signaling in cone photoreceptors.
publisher Public Library of Science (PLoS)
series PLoS ONE
issn 1932-6203
publishDate 2013-01-01
description 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.
url http://europepmc.org/articles/PMC3734133?pdf=render
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