Identification of candidate genes for developmental colour agnosia in a single unique family.


Journal

PloS one
ISSN: 1932-6203
Titre abrégé: PLoS One
Pays: United States
ID NLM: 101285081

Informations de publication

Date de publication:
2023
Historique:
received: 30 06 2023
accepted: 31 07 2023
medline: 8 9 2023
pubmed: 6 9 2023
entrez: 6 9 2023
Statut: epublish

Résumé

Colour agnosia is a disorder that impairs colour knowledge (naming, recognition) despite intact colour perception. Previously, we have identified the first and only-known family with hereditary developmental colour agnosia. The aim of the current study was to explore genomic regions and candidate genes that potentially cause this trait in this family. For three family members with developmental colour agnosia and three unaffected family members CGH-array analysis and exome sequencing was performed, and linkage analysis was carried out using DominantMapper, resulting in the identification of 19 cosegregating chromosomal regions. Whole exome sequencing resulted in 11 rare coding variants present in all affected family members with developmental colour agnosia and absent in unaffected members. These variants affected genes that have been implicated in neural processes and functions (CACNA2D4, DDX25, GRINA, MYO15A) or that have an indirect link to brain function, development or disease (MAML2, STAU1, TMED3, RABEPK), and a remaining group lacking brain expression or involved in non-neural traits (DEPDC7, OR1J1, OR8D4). Although this is an explorative study, the small set of candidate genes that could serve as a starting point for unravelling mechanisms of higher level cognitive functions and cortical specialization, and disorders therein such as developmental colour agnosia.

Identifiants

pubmed: 37672513
doi: 10.1371/journal.pone.0290013
pii: PONE-D-23-19711
pmc: PMC10482254
doi:

Substances chimiques

Cytoskeletal Proteins 0
RNA-Binding Proteins 0
STAU1 protein, human 0
TMED3 protein, human 0
Vesicular Transport Proteins 0

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

e0290013

Informations de copyright

Copyright: © 2023 Nijboer et al. This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.

Déclaration de conflit d'intérêts

The authors have declared that no competing interests exist.

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Auteurs

Tanja C W Nijboer (TCW)

UMCU Brain Center and Center of Excellence for Rehabilitation Medicine, University Medical Center Utrecht and De Hoogstraat Rehabilitation, Utrecht, The Netherlands.
Department of Experimental Psychology and Helmholtz Institute, Utrecht University, Utrecht, The Netherlands.

Ellen V S Hessel (EVS)

UMCU Brain Center and Center of Excellence for Rehabilitation Medicine, University Medical Center Utrecht and De Hoogstraat Rehabilitation, Utrecht, The Netherlands.
Department of Biomedical Genetics, University Medical Center Utrecht, Utrecht, The Netherlands.

Gijs W van Haaften (GW)

Department of Biomedical Genetics, University Medical Center Utrecht, Utrecht, The Netherlands.

Martine J van Zandvoort (MJ)

Department of Experimental Psychology and Helmholtz Institute, Utrecht University, Utrecht, The Netherlands.

Peter J van der Spek (PJ)

Department of Pathology, Erasmus Medical Center Rotterdam, Rotterdam, the Netherlands.

Christine Troelstra (C)

Department of Pathology, Erasmus Medical Center Rotterdam, Rotterdam, the Netherlands.

Carolien G F de Kovel (CGF)

Department of Biomedical Genetics, University Medical Center Utrecht, Utrecht, The Netherlands.

Bobby P C Koeleman (BPC)

Department of Biomedical Genetics, University Medical Center Utrecht, Utrecht, The Netherlands.

Bert van der Zwaag (B)

Department of Biomedical Genetics, University Medical Center Utrecht, Utrecht, The Netherlands.

Eva H Brilstra (EH)

Department of Biomedical Genetics, University Medical Center Utrecht, Utrecht, The Netherlands.

J Peter H Burbach (JPH)

UMCU Brain Center, Department of Translational Neuroscience, University Medical Center Utrecht, Utrecht, the Netherlands.

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