Expression analyses of PLEKHG2, a Rho family-specific guanine nucleotide exchange factor, during mouse brain development.
Antibody
Brain development
Mouse tissues
PLEKHG2
RhoGEF
Journal
Medical molecular morphology
ISSN: 1860-1499
Titre abrégé: Med Mol Morphol
Pays: Japan
ID NLM: 101239023
Informations de publication
Date de publication:
Jun 2021
Jun 2021
Historique:
received:
25
10
2020
accepted:
03
12
2020
pubmed:
26
1
2021
medline:
16
12
2021
entrez:
25
1
2021
Statut:
ppublish
Résumé
Abnormalities of PLEKHG2 gene, encoding a Rho family-specific guanine nucleotide exchange factor, are involved in microcephaly with intellectual disability. However, not only the role of PLEKHG2 in the developmental process but also its expression profile is unknown. In this study, we prepared a specific antibody against PLEKHG2 and carried out expression analyses with mouse tissues. In western blotting, PLEKHG2 exhibited a tissue-dependent expression profile in adult mouse and was expressed in a developmental stage-dependent manner in brain. Then, in immunohistochemical analyses, while PLEKHG2 was observed in the cortical plate and ventricular zone surface of the cerebral cortex at embryonic day 14, it came to be distributed throughout the cerebral cortex in layer II/III and V during corticogenesis. PLEKHG2 was also detected mainly in the nucleus of neurons in the hippocampal CA regions and dentate gyrus at P7. Notably, the nuclear accumulation disappeared at P30 and PLEKHG2 came to be located at the axons and/or dendrites at this time point. Moreover, in vitro immunofluorescence revealed that PLEKHG2 was at least partially localized at both excitatory and inhibitory synapses in primary cultured hippocampal neurons. These results suggest roles of PLEKHG2 in the development of the central nervous tissue and synaptic function.
Identifiants
pubmed: 33492483
doi: 10.1007/s00795-020-00275-1
pii: 10.1007/s00795-020-00275-1
doi:
Substances chimiques
Clg protein, mouse
0
Guanine Nucleotide Exchange Factors
0
Plekhg2 protein, mouse
0
Types de publication
Journal Article
Langues
eng
Sous-ensembles de citation
IM
Pagination
146-155Subventions
Organisme : Japan Society for the Promotion of Science
ID : 23590124
Organisme : Japan Agency for Medical Research and Development
ID : 15ek0109040h0002
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