Identification of Phonology-Related Genes and Functional Characterization of Broca's and Wernicke's Regions in Language and Learning Disorders.

Broca’s area Wernicke’s area development gene expression phonology

Journal

Frontiers in neuroscience
ISSN: 1662-4548
Titre abrégé: Front Neurosci
Pays: Switzerland
ID NLM: 101478481

Informations de publication

Date de publication:
2021
Historique:
received: 15 03 2021
accepted: 04 08 2021
entrez: 20 9 2021
pubmed: 21 9 2021
medline: 21 9 2021
Statut: epublish

Résumé

Impaired phonological processing is a leading symptom of multifactorial language and learning disorders suggesting a common biological basis. Here we evaluated studies of dyslexia, dyscalculia, specific language impairment (SLI), and the logopenic variant of primary progressive aphasia (lvPPA) seeking for shared risk genes in Broca's and Wernicke's regions, being key for phonological processing within the complex language network. The identified "phonology-related genes" from literature were functionally characterized using Atlas-based expression mapping (JuGEx) and gene set enrichment. Out of 643 publications from the last decade until now, we extracted 21 candidate genes of which 13 overlapped with dyslexia and SLI, six with dyslexia and dyscalculia, and two with dyslexia, dyscalculia, and SLI. No overlap was observed between the childhood disorders and the late-onset lvPPA often showing symptoms of learning disorders earlier in life. Multiple genes were enriched in Gene Ontology terms of the topics learning (

Identifiants

pubmed: 34539327
doi: 10.3389/fnins.2021.680762
pmc: PMC8446646
doi:

Types de publication

Journal Article

Langues

eng

Pagination

680762

Informations de copyright

Copyright © 2021 Unger, Heim, Hilger, Bludau, Pieperhoff, Cichon, Amunts and Mühleisen.

Déclaration de conflit d'intérêts

The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.

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Auteurs

Nina Unger (N)

Cécile and Oskar Vogt Institute for Brain Research, Medical Faculty, University Hospital Düsseldorf, Heinrich Heine University Düsseldorf, Düsseldorf, Germany.
Institute of Neuroscience and Medicine (INM-1), Research Centre Jülich, Jülich, Germany.
Department of Neurology, Medical Faculty, RWTH Aachen University, Aachen, Germany.

Stefan Heim (S)

Institute of Neuroscience and Medicine (INM-1), Research Centre Jülich, Jülich, Germany.
Department of Psychiatry, Psychotherapy and Psychosomatics, Medical Faculty, RWTH Aachen University, Aachen, Germany.
JARA-Brain, Jülich-Aachen Research Alliance, Jülich, Germany.

Dominique I Hilger (DI)

Institute of Neuroscience and Medicine (INM-1), Research Centre Jülich, Jülich, Germany.

Sebastian Bludau (S)

Institute of Neuroscience and Medicine (INM-1), Research Centre Jülich, Jülich, Germany.

Peter Pieperhoff (P)

Institute of Neuroscience and Medicine (INM-1), Research Centre Jülich, Jülich, Germany.

Sven Cichon (S)

Institute of Neuroscience and Medicine (INM-1), Research Centre Jülich, Jülich, Germany.
Department of Biomedicine, University of Basel, Basel, Switzerland.
Institute of Medical Genetics and Pathology, University Hospital Basel, Basel, Switzerland.

Katrin Amunts (K)

Cécile and Oskar Vogt Institute for Brain Research, Medical Faculty, University Hospital Düsseldorf, Heinrich Heine University Düsseldorf, Düsseldorf, Germany.
Institute of Neuroscience and Medicine (INM-1), Research Centre Jülich, Jülich, Germany.
JARA-Brain, Jülich-Aachen Research Alliance, Jülich, Germany.

Thomas W Mühleisen (TW)

Cécile and Oskar Vogt Institute for Brain Research, Medical Faculty, University Hospital Düsseldorf, Heinrich Heine University Düsseldorf, Düsseldorf, Germany.
Institute of Neuroscience and Medicine (INM-1), Research Centre Jülich, Jülich, Germany.
Department of Biomedicine, University of Basel, Basel, Switzerland.

Classifications MeSH