Identification of β-Dystrobrevin as a Direct Target of miR-143: Involvement in Early Stages of Neural Differentiation.

Duchenne Muscular Dystrophy, a genetic disorder that results in a gradual breakdown of muscle, is associated to mild to severe cognitive impairment in about one-third of dystrophic patients. The brain dysfunction is independent of the muscular pathology, occurs early, and is most likely due to defec...

Full description

Bibliographic Details
Main Authors: Maria Teresa Quaranta, Isabella Spinello, Rosa Paolillo, Gianfranco Macchia, Alessandra Boe, Marina Ceccarini, Catherine Labbaye, Pompeo Macioce
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2016-01-01
Series:PLoS ONE
Online Access:https://journals.plos.org/plosone/article/file?id=10.1371/journal.pone.0156325&type=printable
_version_ 1826584068982046720
author Maria Teresa Quaranta
Isabella Spinello
Rosa Paolillo
Gianfranco Macchia
Alessandra Boe
Marina Ceccarini
Catherine Labbaye
Pompeo Macioce
author_facet Maria Teresa Quaranta
Isabella Spinello
Rosa Paolillo
Gianfranco Macchia
Alessandra Boe
Marina Ceccarini
Catherine Labbaye
Pompeo Macioce
author_sort Maria Teresa Quaranta
collection DOAJ
description Duchenne Muscular Dystrophy, a genetic disorder that results in a gradual breakdown of muscle, is associated to mild to severe cognitive impairment in about one-third of dystrophic patients. The brain dysfunction is independent of the muscular pathology, occurs early, and is most likely due to defects in the assembly of the Dystrophin-associated Protein Complex (DPC) during embryogenesis. We have recently described the interaction of the DPC component β-dystrobrevin with members of complexes that regulate chromatin dynamics, and suggested that β-dystrobrevin may play a role in the initiation of neuronal differentiation. Since oxygen concentrations and miRNAs appear as well to be involved in the cellular processes related to neuronal development, we have studied how these factors act on β-dystrobrevin and investigated the possibility of their functional interplay using the NTera-2 cell line, a well-established model for studying neurogenesis. We followed the pattern of expression and regulation of β-dystrobrevin during the early stages of neuronal differentiation induced by exposure to retinoic acid (RA) under hypoxia as compared with normoxia, and found that β-dystrobrevin expression is regulated during RA-induced differentiation of NTera-2 cells. We also found that β-dystrobrevin pattern is delayed under hypoxic conditions, together with a delay in the differentiation and an increase in the proliferation rate of cells. We identified miRNA-143 as a direct regulator of β-dystrobrevin expression, demonstrated that β-dystrobrevin is expressed in the nucleus and showed that, in line with our previous in vitro results, β-dystrobrevin is a repressor of synapsin I in live cells. Altogether the newly identified regulatory pathway miR-143/β-dystrobrevin/synapsin I provides novel insights into the functions of β-dystrobrevin and opens up new perspectives for elucidating the molecular mechanisms underlying the neuronal involvement in muscular dystrophy.
first_indexed 2024-12-23T06:21:49Z
format Article
id doaj.art-e9a8e329189344a1a1e5e85851dff4a1
institution Directory Open Access Journal
issn 1932-6203
language English
last_indexed 2025-03-14T15:31:53Z
publishDate 2016-01-01
publisher Public Library of Science (PLoS)
record_format Article
series PLoS ONE
spelling doaj.art-e9a8e329189344a1a1e5e85851dff4a12025-02-25T05:35:55ZengPublic Library of Science (PLoS)PLoS ONE1932-62032016-01-01115e015632510.1371/journal.pone.0156325Identification of β-Dystrobrevin as a Direct Target of miR-143: Involvement in Early Stages of Neural Differentiation.Maria Teresa QuarantaIsabella SpinelloRosa PaolilloGianfranco MacchiaAlessandra BoeMarina CeccariniCatherine LabbayePompeo MacioceDuchenne Muscular Dystrophy, a genetic disorder that results in a gradual breakdown of muscle, is associated to mild to severe cognitive impairment in about one-third of dystrophic patients. The brain dysfunction is independent of the muscular pathology, occurs early, and is most likely due to defects in the assembly of the Dystrophin-associated Protein Complex (DPC) during embryogenesis. We have recently described the interaction of the DPC component β-dystrobrevin with members of complexes that regulate chromatin dynamics, and suggested that β-dystrobrevin may play a role in the initiation of neuronal differentiation. Since oxygen concentrations and miRNAs appear as well to be involved in the cellular processes related to neuronal development, we have studied how these factors act on β-dystrobrevin and investigated the possibility of their functional interplay using the NTera-2 cell line, a well-established model for studying neurogenesis. We followed the pattern of expression and regulation of β-dystrobrevin during the early stages of neuronal differentiation induced by exposure to retinoic acid (RA) under hypoxia as compared with normoxia, and found that β-dystrobrevin expression is regulated during RA-induced differentiation of NTera-2 cells. We also found that β-dystrobrevin pattern is delayed under hypoxic conditions, together with a delay in the differentiation and an increase in the proliferation rate of cells. We identified miRNA-143 as a direct regulator of β-dystrobrevin expression, demonstrated that β-dystrobrevin is expressed in the nucleus and showed that, in line with our previous in vitro results, β-dystrobrevin is a repressor of synapsin I in live cells. Altogether the newly identified regulatory pathway miR-143/β-dystrobrevin/synapsin I provides novel insights into the functions of β-dystrobrevin and opens up new perspectives for elucidating the molecular mechanisms underlying the neuronal involvement in muscular dystrophy.https://journals.plos.org/plosone/article/file?id=10.1371/journal.pone.0156325&type=printable
spellingShingle Maria Teresa Quaranta
Isabella Spinello
Rosa Paolillo
Gianfranco Macchia
Alessandra Boe
Marina Ceccarini
Catherine Labbaye
Pompeo Macioce
Identification of β-Dystrobrevin as a Direct Target of miR-143: Involvement in Early Stages of Neural Differentiation.
PLoS ONE
title Identification of β-Dystrobrevin as a Direct Target of miR-143: Involvement in Early Stages of Neural Differentiation.
title_full Identification of β-Dystrobrevin as a Direct Target of miR-143: Involvement in Early Stages of Neural Differentiation.
title_fullStr Identification of β-Dystrobrevin as a Direct Target of miR-143: Involvement in Early Stages of Neural Differentiation.
title_full_unstemmed Identification of β-Dystrobrevin as a Direct Target of miR-143: Involvement in Early Stages of Neural Differentiation.
title_short Identification of β-Dystrobrevin as a Direct Target of miR-143: Involvement in Early Stages of Neural Differentiation.
title_sort identification of β dystrobrevin as a direct target of mir 143 involvement in early stages of neural differentiation
url https://journals.plos.org/plosone/article/file?id=10.1371/journal.pone.0156325&type=printable
work_keys_str_mv AT mariateresaquaranta identificationofbdystrobrevinasadirecttargetofmir143involvementinearlystagesofneuraldifferentiation
AT isabellaspinello identificationofbdystrobrevinasadirecttargetofmir143involvementinearlystagesofneuraldifferentiation
AT rosapaolillo identificationofbdystrobrevinasadirecttargetofmir143involvementinearlystagesofneuraldifferentiation
AT gianfrancomacchia identificationofbdystrobrevinasadirecttargetofmir143involvementinearlystagesofneuraldifferentiation
AT alessandraboe identificationofbdystrobrevinasadirecttargetofmir143involvementinearlystagesofneuraldifferentiation
AT marinaceccarini identificationofbdystrobrevinasadirecttargetofmir143involvementinearlystagesofneuraldifferentiation
AT catherinelabbaye identificationofbdystrobrevinasadirecttargetofmir143involvementinearlystagesofneuraldifferentiation
AT pompeomacioce identificationofbdystrobrevinasadirecttargetofmir143involvementinearlystagesofneuraldifferentiation