Connecting DCX, COMT and FMR1 in social behavior and cognitive impairment

Abstract Genetic variants of DCX, COMT and FMR1 have been linked to neurodevelopmental disorders related to intellectual disability and social behavior. In this systematic review we examine the roles of the DCX, COMT and FMR1 genes in the context of hippocampal neurogenesis with respect to these dis...

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Main Authors: Anna Delprato, Emily Xiao, Devika Manoj
Format: Article
Language:English
Published: BMC 2022-05-01
Series:Behavioral and Brain Functions
Subjects:
Online Access:https://doi.org/10.1186/s12993-022-00191-7
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author Anna Delprato
Emily Xiao
Devika Manoj
author_facet Anna Delprato
Emily Xiao
Devika Manoj
author_sort Anna Delprato
collection DOAJ
description Abstract Genetic variants of DCX, COMT and FMR1 have been linked to neurodevelopmental disorders related to intellectual disability and social behavior. In this systematic review we examine the roles of the DCX, COMT and FMR1 genes in the context of hippocampal neurogenesis with respect to these disorders with the aim of identifying important hubs and signaling pathways that may bridge these conditions. Taken together our findings indicate that factors connecting DCX, COMT, and FMR1 in intellectual disability and social behavior may converge at Wnt signaling, neuron migration, and axon and dendrite morphogenesis. Data derived from genomic research has identified a multitude of genes that are linked to brain disorders and developmental differences. Information about where and how these genes function and cooperate is lagging behind. The approach used here may help to shed light on the biological underpinnings in which key genes interface and may prove useful for the testing of specific hypotheses.
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spelling doaj.art-998ca5456a0e4830ae935f5cba3c907c2022-12-22T03:25:54ZengBMCBehavioral and Brain Functions1744-90812022-05-0118111110.1186/s12993-022-00191-7Connecting DCX, COMT and FMR1 in social behavior and cognitive impairmentAnna Delprato0Emily Xiao1Devika Manoj2Department of Research and Education, BioScience ProjectDepartment of Research and Education, BioScience ProjectDepartment of Research and Education, BioScience ProjectAbstract Genetic variants of DCX, COMT and FMR1 have been linked to neurodevelopmental disorders related to intellectual disability and social behavior. In this systematic review we examine the roles of the DCX, COMT and FMR1 genes in the context of hippocampal neurogenesis with respect to these disorders with the aim of identifying important hubs and signaling pathways that may bridge these conditions. Taken together our findings indicate that factors connecting DCX, COMT, and FMR1 in intellectual disability and social behavior may converge at Wnt signaling, neuron migration, and axon and dendrite morphogenesis. Data derived from genomic research has identified a multitude of genes that are linked to brain disorders and developmental differences. Information about where and how these genes function and cooperate is lagging behind. The approach used here may help to shed light on the biological underpinnings in which key genes interface and may prove useful for the testing of specific hypotheses.https://doi.org/10.1186/s12993-022-00191-7Intellectual disabilitySocial behaviorNeurogenesisHippocampusWnt signalingCOMT
spellingShingle Anna Delprato
Emily Xiao
Devika Manoj
Connecting DCX, COMT and FMR1 in social behavior and cognitive impairment
Behavioral and Brain Functions
Intellectual disability
Social behavior
Neurogenesis
Hippocampus
Wnt signaling
COMT
title Connecting DCX, COMT and FMR1 in social behavior and cognitive impairment
title_full Connecting DCX, COMT and FMR1 in social behavior and cognitive impairment
title_fullStr Connecting DCX, COMT and FMR1 in social behavior and cognitive impairment
title_full_unstemmed Connecting DCX, COMT and FMR1 in social behavior and cognitive impairment
title_short Connecting DCX, COMT and FMR1 in social behavior and cognitive impairment
title_sort connecting dcx comt and fmr1 in social behavior and cognitive impairment
topic Intellectual disability
Social behavior
Neurogenesis
Hippocampus
Wnt signaling
COMT
url https://doi.org/10.1186/s12993-022-00191-7
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