Neuron-enriched phosphatase and actin regulator 3 (Phactr3)/ nuclear scaffold-associated PP1-inhibiting protein (Scapinin) regulates dendritic morphology via its protein phosphatase 1-binding domain.
Animals
Cerebral Cortex
/ cytology
Dendrites
/ metabolism
Female
Male
Mice, Inbred C57BL
Microfilament Proteins
/ chemistry
Mutation
/ genetics
Nuclear Matrix
/ metabolism
Nuclear Matrix-Associated Proteins
/ chemistry
Nuclear Proteins
/ chemistry
Protein Binding
Protein Domains
Protein Phosphatase 1
/ metabolism
RNA, Messenger
/ genetics
Rats, Sprague-Dawley
Subcellular Fractions
/ metabolism
Up-Regulation
/ genetics
Actin
Dendrite
Dendritic spine
Nuclear scaffold-associated PP1-Inhibiting protein
Phosphatase and actin regulator
Protein phosphatase
Journal
Biochemical and biophysical research communications
ISSN: 1090-2104
Titre abrégé: Biochem Biophys Res Commun
Pays: United States
ID NLM: 0372516
Informations de publication
Date de publication:
23 07 2020
23 07 2020
Historique:
received:
15
04
2020
accepted:
01
05
2020
pubmed:
20
5
2020
medline:
14
1
2021
entrez:
20
5
2020
Statut:
ppublish
Résumé
Phosphatase and actin regulator 3/nuclear scaffold-associated protein phosphatase 1-inhibiting protein (Phactr3/Scapinin) is an actin- and protein phosphatase 1 (PP1)-binding protein known to negatively regulate axon elongation. In this study, we examined the expression pattern of Phactr3/Scapinin in several tissues and investigated the effect of Phactr3/Scapinin on dendritic morphology of cortical neurons. Results showed that Phactr3/Scapinin expression was up-regulated in the developing brain and enriched in neurons and in the postsynaptic density fraction, but not in astrocytes. Overexpression of wild type or mutant Phactr3/Scapinin, which lacked actin-binding activity, resulted in increased dendritic complexity and percentage of spines with a mushroom or stubby shape, as well as a decrease in spine density. However, overexpression of mutant Phactr3/Scapinin that lacked PP1-binding activity did not. Taken together, these findings suggest that Phactr3/Scapinin expression is neuronal and might contribute to synaptic formation via distinct actin- and PP1-binding domains involved in dendritic and axonal morphology, respectively.
Identifiants
pubmed: 32423795
pii: S0006-291X(20)30910-4
doi: 10.1016/j.bbrc.2020.05.006
pii:
doi:
Substances chimiques
Microfilament Proteins
0
Nuclear Matrix-Associated Proteins
0
Nuclear Proteins
0
Phactr3 protein, rat
0
RNA, Messenger
0
scapinin protein, mouse
0
Protein Phosphatase 1
EC 3.1.3.16
Types de publication
Journal Article
Research Support, Non-U.S. Gov't
Langues
eng
Sous-ensembles de citation
IM
Pagination
322-329Informations de copyright
Copyright © 2020 Elsevier Inc. All rights reserved.
Déclaration de conflit d'intérêts
Declaration of competing interests The authors have no conflicts of interest to declare.