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Profile of miR-23 Expression and Possible Role in Regulation of Glutamic Acid Decarboxylase during Postnatal Retinal Development
by
Fekete, Csaba
, Pöstyéni, Etelka
, Urbán, Péter
, Sétáló, György
, Kovács-Valasek, Andrea
, Czuni, Lilla
, Gabriel, Robert
in
Enzymes
/ Gene expression
/ Hybridization
/ Labeling
/ MicroRNAs
/ Retina
2021
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Profile of miR-23 Expression and Possible Role in Regulation of Glutamic Acid Decarboxylase during Postnatal Retinal Development
by
Fekete, Csaba
, Pöstyéni, Etelka
, Urbán, Péter
, Sétáló, György
, Kovács-Valasek, Andrea
, Czuni, Lilla
, Gabriel, Robert
in
Enzymes
/ Gene expression
/ Hybridization
/ Labeling
/ MicroRNAs
/ Retina
2021
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Profile of miR-23 Expression and Possible Role in Regulation of Glutamic Acid Decarboxylase during Postnatal Retinal Development
by
Fekete, Csaba
, Pöstyéni, Etelka
, Urbán, Péter
, Sétáló, György
, Kovács-Valasek, Andrea
, Czuni, Lilla
, Gabriel, Robert
in
Enzymes
/ Gene expression
/ Hybridization
/ Labeling
/ MicroRNAs
/ Retina
2021
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Profile of miR-23 Expression and Possible Role in Regulation of Glutamic Acid Decarboxylase during Postnatal Retinal Development
Journal Article
Profile of miR-23 Expression and Possible Role in Regulation of Glutamic Acid Decarboxylase during Postnatal Retinal Development
2021
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Overview
As neurotransmitter, GABA is fundamental for physiological processes in the developing retina. Its synthesis enzymes are present during retinal development, although the molecular regulatory mechanisms behind the changes in expression are not entirely understood. In this study, we revealed the expression patterns of glutamic acid decarboxylase 67(GAD67) and its coding gene (GAD1) and its potential miRNA-dependent regulation during the first three postnatal weeks in rat retina. To gain insight into the molecular mechanisms, miRNA-sequencing supported by RT-qPCR and in situ hybridization were carried out. GAD1 expression shows an increasing tendency, peaking at P15. From the in silico-predicted GAD1 targeting miRNAs, only miR-23 showed similar expression patterns, which is a known regulator of GAD1 expression. For further investigation, we made an in situ hybridization investigation where both GAD67 and miR-23 also showed lower expression before P7, with the intensity of expression gradually increasing until P21. Horizontal cells at P7, amacrine cells at P15 and P21, and some cells in the ganglion cell layer at several time points were double labelled with miR-23 and GAD67. Our results highlight the complexity of these regulatory networks and the possible role of miR-23 in the regulation of GABA synthesizing enzyme expression during postnatal retina development.
Publisher
MDPI AG,MDPI
Subject
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