Transcriptome Analysis of the Cerebellum of Mice Fed a Manganese-Deficient Diet

Manganese (Mn), primarily acquired through diet, is required for brain function and development. Epidemiological studies have found an association between both low and high levels of Mn and impaired neurodevelopment in children. Recent genetic studies have revealed that patients with congenital Mn d...

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Main Authors: Young Ah Seo, Eun-Kyung Choi, Luisa Aring, Molly Paschall, Shigeki Iwase
Format: Article
Language:English
Published: Frontiers Media S.A. 2020-12-01
Series:Frontiers in Genetics
Subjects:
Online Access:https://www.frontiersin.org/articles/10.3389/fgene.2020.558725/full
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author Young Ah Seo
Eun-Kyung Choi
Luisa Aring
Molly Paschall
Shigeki Iwase
author_facet Young Ah Seo
Eun-Kyung Choi
Luisa Aring
Molly Paschall
Shigeki Iwase
author_sort Young Ah Seo
collection DOAJ
description Manganese (Mn), primarily acquired through diet, is required for brain function and development. Epidemiological studies have found an association between both low and high levels of Mn and impaired neurodevelopment in children. Recent genetic studies have revealed that patients with congenital Mn deficiency display severe psychomotor disability and cerebral and cerebellar atrophy. Although the impact of Mn on gene expression is beginning to be appreciated, Mn-dependent gene expression remains to be explored in vertebrate animals. The goal of this study was to use a mouse model to define the impact of a low-Mn diet on brain metal levels and gene expression. We interrogated gene expression changes in the Mn-deficient mouse brain at the genome-wide scale by RNA-seq analysis of the cerebellum of mice fed low or normal Mn diets. A total of 137 genes were differentially expressed in Mn-deficient cerebellums compared with Mn-adequate cerebellums (Padj < 0.05). Mn-deficient mice displayed downregulation of key pathways involved with “focal adhesion,” “neuroactive ligand-receptor interaction,” and “cytokine-cytokine receptor interaction” and upregulation of “herpes simplex virus 1 infection,” “spliceosome,” and “FoxO signaling pathway.” Reactome pathway analysis identified upregulation of the splicing-related pathways and transcription-related pathways, as well as downregulation of “metabolism of carbohydrate,” and “extracellular matrix organization,” and “fatty acid metabolism” reactomes. The recurrent identifications of splicing-related pathways suggest that Mn deficiency leads to upregulation of splicing machineries and downregulation of diverse biological pathways.
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spelling doaj.art-386b063897644784bfc24d78f229617c2022-12-21T22:18:17ZengFrontiers Media S.A.Frontiers in Genetics1664-80212020-12-011110.3389/fgene.2020.558725558725Transcriptome Analysis of the Cerebellum of Mice Fed a Manganese-Deficient DietYoung Ah Seo0Eun-Kyung Choi1Luisa Aring2Molly Paschall3Shigeki Iwase4Department of Nutritional Sciences, University of Michigan School of Public Health, Ann Arbor, MI, United StatesDepartment of Nutritional Sciences, University of Michigan School of Public Health, Ann Arbor, MI, United StatesDepartment of Nutritional Sciences, University of Michigan School of Public Health, Ann Arbor, MI, United StatesDepartment of Nutritional Sciences, University of Michigan School of Public Health, Ann Arbor, MI, United StatesDepartment of Human Genetics, Michigan Medicine, University of Michigan, Ann Arbor, MI, United StatesManganese (Mn), primarily acquired through diet, is required for brain function and development. Epidemiological studies have found an association between both low and high levels of Mn and impaired neurodevelopment in children. Recent genetic studies have revealed that patients with congenital Mn deficiency display severe psychomotor disability and cerebral and cerebellar atrophy. Although the impact of Mn on gene expression is beginning to be appreciated, Mn-dependent gene expression remains to be explored in vertebrate animals. The goal of this study was to use a mouse model to define the impact of a low-Mn diet on brain metal levels and gene expression. We interrogated gene expression changes in the Mn-deficient mouse brain at the genome-wide scale by RNA-seq analysis of the cerebellum of mice fed low or normal Mn diets. A total of 137 genes were differentially expressed in Mn-deficient cerebellums compared with Mn-adequate cerebellums (Padj < 0.05). Mn-deficient mice displayed downregulation of key pathways involved with “focal adhesion,” “neuroactive ligand-receptor interaction,” and “cytokine-cytokine receptor interaction” and upregulation of “herpes simplex virus 1 infection,” “spliceosome,” and “FoxO signaling pathway.” Reactome pathway analysis identified upregulation of the splicing-related pathways and transcription-related pathways, as well as downregulation of “metabolism of carbohydrate,” and “extracellular matrix organization,” and “fatty acid metabolism” reactomes. The recurrent identifications of splicing-related pathways suggest that Mn deficiency leads to upregulation of splicing machineries and downregulation of diverse biological pathways.https://www.frontiersin.org/articles/10.3389/fgene.2020.558725/fullmanganesecerebellumtranscriptomeneurodevelopmentspliceosome
spellingShingle Young Ah Seo
Eun-Kyung Choi
Luisa Aring
Molly Paschall
Shigeki Iwase
Transcriptome Analysis of the Cerebellum of Mice Fed a Manganese-Deficient Diet
Frontiers in Genetics
manganese
cerebellum
transcriptome
neurodevelopment
spliceosome
title Transcriptome Analysis of the Cerebellum of Mice Fed a Manganese-Deficient Diet
title_full Transcriptome Analysis of the Cerebellum of Mice Fed a Manganese-Deficient Diet
title_fullStr Transcriptome Analysis of the Cerebellum of Mice Fed a Manganese-Deficient Diet
title_full_unstemmed Transcriptome Analysis of the Cerebellum of Mice Fed a Manganese-Deficient Diet
title_short Transcriptome Analysis of the Cerebellum of Mice Fed a Manganese-Deficient Diet
title_sort transcriptome analysis of the cerebellum of mice fed a manganese deficient diet
topic manganese
cerebellum
transcriptome
neurodevelopment
spliceosome
url https://www.frontiersin.org/articles/10.3389/fgene.2020.558725/full
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