|ZFIN ID: ZDB-PUB-171113-12|
Role of gabra2, GABAA receptor alpha-2 subunit, in CNS development.
|Source:||Biochemistry and biophysics reports 3: 190-201 (Journal)|
|Registered Authors:||González Nuñez, Veronica|
|Keywords:||CNS, central nervous system, Central nervous system, Development, Differentiation, GABA, GABA, γ-aminobutyric acid, GABAA, gamma-aminobutyric acid (GABA) A receptor, Gabra2, ISH, in situ hybridisation, KCC2, neuron-specific potassium/chloride cotransporter 2, MHB, mid-hindbrain boundary, ORF, open reading frame, Proliferation, fgf8, fibroblast growth factor 8, gabra2, gamma-aminobutyric acid receptor subunit alpha-2, gad1b, glutamate decarboxylase, hpf, hours post-fertilisation, neuroD, neurogenic differentiation, notch1a, notch homologue 1a, pax2a, paired box gene 2a, pax6a, paired box gene 2a, shh a, sonic hedgehog, wnt1, wingless-type MMTV integration site family, member 1|
|PubMed:||29124181 Full text @ Biochem Biophys Rep|
Gonzalez-Nunez, V. (2015) Role of gabra2, GABAA receptor alpha-2 subunit, in CNS development.. Biochemistry and biophysics reports. 3:190-201.
ABSTRACTgabra2 gene codes for the alpha-2 subunit of the GABAA receptor, one of the ionotropic receptors which has been related to anxiety, depression and other behavioural disorders, including drug dependence and schizophrenia. GABAergic signalling also plays a role during development, by promoting neural stem cell maintenance and renewal. To investigate the role of gabra2 in CNS development, gabra2 deficient zebrafish were generated. The pattern of proliferation during the embryonic development was disrupted in morphant embryos, which also displayed an increase in the number of apoptotic nuclei mainly at the mid- and hindbrain regions. The expression of several genes (notch1, pax2, fgf8 and wnt1) known to contribute to the development of the central nervous system was also affected in gabra2 morpholino-injected embryos, although no changes were found for pax6a and shh a expression. The transcriptional activity of neuroD (a proneural gene involved in early neuronal determination) was down-regulated in gabra2 deficient embryos, and the expression pattern of gad1b (GABA-synthesising enzyme GAD67) was clearly reduced in injected fish. I propose that gabra2 might be interacting with those signalling pathways that regulate proliferation, differentiation and neurogenesis during the embryonic development; thus, gabra2 might be playing a role in the differentiation of the mesencephalon and cerebellum. Given that changes in GABAergic circuits during development have been related to several psychiatric disorders, such as autism and schizophrenia, this work might be helpful to understand the role of neurotransmitter systems during CNS development and to assess the developmental effects of several GABAergic drugs.