Transmembrane protein 184B (TMEM184B) promotes expression of synaptic gene networks in the mouse hippocampus

Abstract In Alzheimer’s Disease (AD) and other dementias, hippocampal synaptic dysfunction and loss contribute to the progression of memory impairment. Recent analysis of human AD transcriptomes has provided a list of gene candidates that may serve as drivers of disease. One such candidate is the me...

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Main Authors: Elizabeth B. Wright, Erik G. Larsen, Cecilia M. Coloma-Roessle, Hannah R. Hart, Martha R.C. Bhattacharya
Format: Article
Language:English
Published: BMC 2023-09-01
Series:BMC Genomics
Subjects:
Online Access:https://doi.org/10.1186/s12864-023-09676-9
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author Elizabeth B. Wright
Erik G. Larsen
Cecilia M. Coloma-Roessle
Hannah R. Hart
Martha R.C. Bhattacharya
author_facet Elizabeth B. Wright
Erik G. Larsen
Cecilia M. Coloma-Roessle
Hannah R. Hart
Martha R.C. Bhattacharya
author_sort Elizabeth B. Wright
collection DOAJ
description Abstract In Alzheimer’s Disease (AD) and other dementias, hippocampal synaptic dysfunction and loss contribute to the progression of memory impairment. Recent analysis of human AD transcriptomes has provided a list of gene candidates that may serve as drivers of disease. One such candidate is the membrane protein TMEM184B. To evaluate whether TMEM184B contributes to neurological impairment, we asked whether loss of TMEM184B in mice causes gene expression or behavior alterations, focusing on the hippocampus. Because one major risk factor for AD is age, we compared young adult (5-month-old) and aged (15-month-old) wild type and Tmem184b-mutant mice to assess the dual contributions of age and genotype. TMEM184B loss altered expression of pre- and post-synaptic transcripts by 5 months and continued through 15 months, specifically affecting genes involved in synapse assembly and neural development. Wnt-activated enhancer elements were enriched among differentially expressed genes, suggesting an intersection with this pathway. Few differences existed between young adult and aged mutants, suggesting that transcriptional effects of TMEM184B loss are relatively constant. To understand how TMEM184B disruption may impact behaviors, we evaluated memory using the novel object recognition test and anxiety using the elevated plus maze. Young adult Tmem184b-mutant mice show normal object discrimination, suggesting a lack of memory impairment at this age. However, mutant mice showed decreased anxiety, a phenotype seen in some neurodevelopmental disorders. Taken together, our data suggest that TMEM184B is required for proper synaptic gene expression and anxiety-related behavior and is more likely to be linked to neurodevelopmental disorders than to dementia.
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spelling doaj.art-9fc924d2f7b543e4bf8e27a28c8da80b2023-11-19T12:27:24ZengBMCBMC Genomics1471-21642023-09-0124111210.1186/s12864-023-09676-9Transmembrane protein 184B (TMEM184B) promotes expression of synaptic gene networks in the mouse hippocampusElizabeth B. Wright0Erik G. Larsen1Cecilia M. Coloma-Roessle2Hannah R. Hart3Martha R.C. Bhattacharya4Department of NeuroscienceDepartment of NeuroscienceDepartment of NeuroscienceDepartment of NeuroscienceDepartment of NeuroscienceAbstract In Alzheimer’s Disease (AD) and other dementias, hippocampal synaptic dysfunction and loss contribute to the progression of memory impairment. Recent analysis of human AD transcriptomes has provided a list of gene candidates that may serve as drivers of disease. One such candidate is the membrane protein TMEM184B. To evaluate whether TMEM184B contributes to neurological impairment, we asked whether loss of TMEM184B in mice causes gene expression or behavior alterations, focusing on the hippocampus. Because one major risk factor for AD is age, we compared young adult (5-month-old) and aged (15-month-old) wild type and Tmem184b-mutant mice to assess the dual contributions of age and genotype. TMEM184B loss altered expression of pre- and post-synaptic transcripts by 5 months and continued through 15 months, specifically affecting genes involved in synapse assembly and neural development. Wnt-activated enhancer elements were enriched among differentially expressed genes, suggesting an intersection with this pathway. Few differences existed between young adult and aged mutants, suggesting that transcriptional effects of TMEM184B loss are relatively constant. To understand how TMEM184B disruption may impact behaviors, we evaluated memory using the novel object recognition test and anxiety using the elevated plus maze. Young adult Tmem184b-mutant mice show normal object discrimination, suggesting a lack of memory impairment at this age. However, mutant mice showed decreased anxiety, a phenotype seen in some neurodevelopmental disorders. Taken together, our data suggest that TMEM184B is required for proper synaptic gene expression and anxiety-related behavior and is more likely to be linked to neurodevelopmental disorders than to dementia.https://doi.org/10.1186/s12864-023-09676-9TMEM184BHippocampusRNAseqSynapseAlzheimer’s Disease
spellingShingle Elizabeth B. Wright
Erik G. Larsen
Cecilia M. Coloma-Roessle
Hannah R. Hart
Martha R.C. Bhattacharya
Transmembrane protein 184B (TMEM184B) promotes expression of synaptic gene networks in the mouse hippocampus
BMC Genomics
TMEM184B
Hippocampus
RNAseq
Synapse
Alzheimer’s Disease
title Transmembrane protein 184B (TMEM184B) promotes expression of synaptic gene networks in the mouse hippocampus
title_full Transmembrane protein 184B (TMEM184B) promotes expression of synaptic gene networks in the mouse hippocampus
title_fullStr Transmembrane protein 184B (TMEM184B) promotes expression of synaptic gene networks in the mouse hippocampus
title_full_unstemmed Transmembrane protein 184B (TMEM184B) promotes expression of synaptic gene networks in the mouse hippocampus
title_short Transmembrane protein 184B (TMEM184B) promotes expression of synaptic gene networks in the mouse hippocampus
title_sort transmembrane protein 184b tmem184b promotes expression of synaptic gene networks in the mouse hippocampus
topic TMEM184B
Hippocampus
RNAseq
Synapse
Alzheimer’s Disease
url https://doi.org/10.1186/s12864-023-09676-9
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