Wnt/β-Catenin-Dependent Transcription in Autism Spectrum Disorders
Autism spectrum disorders (ASD) is a heterogeneous group of neurodevelopmental disorders characterized by synaptic dysfunction and defects in dendritic spine morphology. In the past decade, an extensive list of genes associated with ASD has been identified by genome-wide sequencing initiatives. Seve...
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Frontiers Media S.A.
2021-11-01
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Series: | Frontiers in Molecular Neuroscience |
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Online Access: | https://www.frontiersin.org/articles/10.3389/fnmol.2021.764756/full |
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author | Mario O. Caracci Mario O. Caracci Miguel E. Avila Francisca A. Espinoza-Cavieres Francisca A. Espinoza-Cavieres Héctor R. López Héctor R. López Giorgia D. Ugarte Giorgia D. Ugarte Giancarlo V. De Ferrari Giancarlo V. De Ferrari |
author_facet | Mario O. Caracci Mario O. Caracci Miguel E. Avila Francisca A. Espinoza-Cavieres Francisca A. Espinoza-Cavieres Héctor R. López Héctor R. López Giorgia D. Ugarte Giorgia D. Ugarte Giancarlo V. De Ferrari Giancarlo V. De Ferrari |
author_sort | Mario O. Caracci |
collection | DOAJ |
description | Autism spectrum disorders (ASD) is a heterogeneous group of neurodevelopmental disorders characterized by synaptic dysfunction and defects in dendritic spine morphology. In the past decade, an extensive list of genes associated with ASD has been identified by genome-wide sequencing initiatives. Several of these genes functionally converge in the regulation of the Wnt/β-catenin signaling pathway, a conserved cascade essential for stem cell pluripotency and cell fate decisions during development. Here, we review current information regarding the transcriptional program of Wnt/β-catenin signaling in ASD. First, we discuss that Wnt/β-catenin gain and loss of function studies recapitulate brain developmental abnormalities associated with ASD. Second, transcriptomic approaches using patient-derived induced pluripotent stem cells (iPSC) cells, featuring mutations in high confidence ASD genes, reveal a significant dysregulation in the expression of Wnt signaling components. Finally, we focus on the activity of chromatin-remodeling proteins and transcription factors considered high confidence ASD genes, including CHD8, ARID1B, ADNP, and TBR1, that regulate Wnt/β-catenin-dependent transcriptional activity in multiple cell types, including pyramidal neurons, interneurons and oligodendrocytes, cells which are becoming increasingly relevant in the study of ASD. We conclude that the level of Wnt/β-catenin signaling activation could explain the high phenotypical heterogeneity of ASD and be instrumental in the development of new diagnostics tools and therapies. |
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format | Article |
id | doaj.art-3f6268b8e6b44d5392ac4815be1af1a0 |
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issn | 1662-5099 |
language | English |
last_indexed | 2024-04-11T20:51:50Z |
publishDate | 2021-11-01 |
publisher | Frontiers Media S.A. |
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series | Frontiers in Molecular Neuroscience |
spelling | doaj.art-3f6268b8e6b44d5392ac4815be1af1a02022-12-22T04:03:49ZengFrontiers Media S.A.Frontiers in Molecular Neuroscience1662-50992021-11-011410.3389/fnmol.2021.764756764756Wnt/β-Catenin-Dependent Transcription in Autism Spectrum DisordersMario O. Caracci0Mario O. Caracci1Miguel E. Avila2Francisca A. Espinoza-Cavieres3Francisca A. Espinoza-Cavieres4Héctor R. López5Héctor R. López6Giorgia D. Ugarte7Giorgia D. Ugarte8Giancarlo V. De Ferrari9Giancarlo V. De Ferrari10Faculty of Medicine, Institute of Biomedical Sciences, Universidad Andres Bello, Santiago, ChileFaculty of Life Sciences, Institute of Biomedical Sciences, Universidad Andres Bello, Santiago, ChileFaculty of Veterinary Medicine and Agronomy, Nucleus of Applied Research in Veterinary and Agronomic Sciences (NIAVA), Institute of Natural Sciences, Universidad de Las Américas, Santiago, ChileFaculty of Medicine, Institute of Biomedical Sciences, Universidad Andres Bello, Santiago, ChileFaculty of Life Sciences, Institute of Biomedical Sciences, Universidad Andres Bello, Santiago, ChileFaculty of Medicine, Institute of Biomedical Sciences, Universidad Andres Bello, Santiago, ChileFaculty of Life Sciences, Institute of Biomedical Sciences, Universidad Andres Bello, Santiago, ChileFaculty of Medicine, Institute of Biomedical Sciences, Universidad Andres Bello, Santiago, ChileFaculty of Life Sciences, Institute of Biomedical Sciences, Universidad Andres Bello, Santiago, ChileFaculty of Medicine, Institute of Biomedical Sciences, Universidad Andres Bello, Santiago, ChileFaculty of Life Sciences, Institute of Biomedical Sciences, Universidad Andres Bello, Santiago, ChileAutism spectrum disorders (ASD) is a heterogeneous group of neurodevelopmental disorders characterized by synaptic dysfunction and defects in dendritic spine morphology. In the past decade, an extensive list of genes associated with ASD has been identified by genome-wide sequencing initiatives. Several of these genes functionally converge in the regulation of the Wnt/β-catenin signaling pathway, a conserved cascade essential for stem cell pluripotency and cell fate decisions during development. Here, we review current information regarding the transcriptional program of Wnt/β-catenin signaling in ASD. First, we discuss that Wnt/β-catenin gain and loss of function studies recapitulate brain developmental abnormalities associated with ASD. Second, transcriptomic approaches using patient-derived induced pluripotent stem cells (iPSC) cells, featuring mutations in high confidence ASD genes, reveal a significant dysregulation in the expression of Wnt signaling components. Finally, we focus on the activity of chromatin-remodeling proteins and transcription factors considered high confidence ASD genes, including CHD8, ARID1B, ADNP, and TBR1, that regulate Wnt/β-catenin-dependent transcriptional activity in multiple cell types, including pyramidal neurons, interneurons and oligodendrocytes, cells which are becoming increasingly relevant in the study of ASD. We conclude that the level of Wnt/β-catenin signaling activation could explain the high phenotypical heterogeneity of ASD and be instrumental in the development of new diagnostics tools and therapies.https://www.frontiersin.org/articles/10.3389/fnmol.2021.764756/fullWnt/β-catenin signalingtranscriptionchromatin remodeling proteinssynaptic dysfunctionautism spectrum disorders (ASD) |
spellingShingle | Mario O. Caracci Mario O. Caracci Miguel E. Avila Francisca A. Espinoza-Cavieres Francisca A. Espinoza-Cavieres Héctor R. López Héctor R. López Giorgia D. Ugarte Giorgia D. Ugarte Giancarlo V. De Ferrari Giancarlo V. De Ferrari Wnt/β-Catenin-Dependent Transcription in Autism Spectrum Disorders Frontiers in Molecular Neuroscience Wnt/β-catenin signaling transcription chromatin remodeling proteins synaptic dysfunction autism spectrum disorders (ASD) |
title | Wnt/β-Catenin-Dependent Transcription in Autism Spectrum Disorders |
title_full | Wnt/β-Catenin-Dependent Transcription in Autism Spectrum Disorders |
title_fullStr | Wnt/β-Catenin-Dependent Transcription in Autism Spectrum Disorders |
title_full_unstemmed | Wnt/β-Catenin-Dependent Transcription in Autism Spectrum Disorders |
title_short | Wnt/β-Catenin-Dependent Transcription in Autism Spectrum Disorders |
title_sort | wnt β catenin dependent transcription in autism spectrum disorders |
topic | Wnt/β-catenin signaling transcription chromatin remodeling proteins synaptic dysfunction autism spectrum disorders (ASD) |
url | https://www.frontiersin.org/articles/10.3389/fnmol.2021.764756/full |
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