Modulation of Placental Gene Expression in Small-for-Gestational-Age Infants

Small-for-gestational-age (SGA) infants are fetuses that have not reached their genetically programmed growth potential. Low birth weight predisposes these infants to an increased risk of developing cardiovascular, metabolic and neurodevelopmental conditions in later life. However, our understanding...

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Main Authors: Jessica L. O’Callaghan, Vicki L. Clifton, Peter Prentis, Adam Ewing, Yvette D. Miller, Elise S. Pelzer
Format: Article
Language:English
Published: MDPI AG 2020-01-01
Series:Genes
Subjects:
sga
Online Access:https://www.mdpi.com/2073-4425/11/1/80
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spelling doaj-6423a10f75b34ab4ba8f5f552bf48ef92020-11-25T02:05:53ZengMDPI AGGenes2073-44252020-01-011118010.3390/genes11010080genes11010080Modulation of Placental Gene Expression in Small-for-Gestational-Age InfantsJessica L. O’Callaghan0Vicki L. Clifton1Peter Prentis2Adam Ewing3Yvette D. Miller4Elise S. Pelzer5School of Biomedical Sciences, Faculty of Health, Queensland University of Technology, Brisbane 4001, Queensland, AustraliaMater Medical Research Institute, University of Queensland, Brisbane 4101, Queensland, AustraliaSchool of Earth, Environmental and Biological Sciences, Science and Engineering Faculty, Queensland University of Technology, Brisbane 4001, Queensland, AustraliaMater Medical Research Institute, University of Queensland, Brisbane 4101, Queensland, AustraliaSchool of Public Health and Social Work, Faculty of Health, Queensland University of Technology, Brisbane 4059, Queensland, AustraliaSchool of Biomedical Sciences, Faculty of Health, Queensland University of Technology, Brisbane 4001, Queensland, AustraliaSmall-for-gestational-age (SGA) infants are fetuses that have not reached their genetically programmed growth potential. Low birth weight predisposes these infants to an increased risk of developing cardiovascular, metabolic and neurodevelopmental conditions in later life. However, our understanding of how this pathology occurs is currently incomplete. Previous research has focused on understanding the transcriptome, epigenome and bacterial signatures separately. However, we hypothesise that interactions between moderators of gene expression are critical to understanding fetal growth restriction. Through a review of the current literature, we identify that there is evidence of modulated expression/methylation of the placental genome and the presence of bacterial DNA in the placental tissue of SGA infants. We also identify that despite limited evidence of the interactions between the above results, there are promising suggestions of a relationship between bacterial signatures and placental function. This review aims to summarise the current literature concerning fetal growth from multiple avenues and propose a novel relationship between the placental transcriptome, methylome and bacterial signature that, if characterised, may be able to improve our current understanding of the placental response to stress and the aetiology of growth restriction.https://www.mdpi.com/2073-4425/11/1/80placentasgabacterial signaturesgene regulation
collection DOAJ
language English
format Article
sources DOAJ
author Jessica L. O’Callaghan
Vicki L. Clifton
Peter Prentis
Adam Ewing
Yvette D. Miller
Elise S. Pelzer
spellingShingle Jessica L. O’Callaghan
Vicki L. Clifton
Peter Prentis
Adam Ewing
Yvette D. Miller
Elise S. Pelzer
Modulation of Placental Gene Expression in Small-for-Gestational-Age Infants
Genes
placenta
sga
bacterial signatures
gene regulation
author_facet Jessica L. O’Callaghan
Vicki L. Clifton
Peter Prentis
Adam Ewing
Yvette D. Miller
Elise S. Pelzer
author_sort Jessica L. O’Callaghan
title Modulation of Placental Gene Expression in Small-for-Gestational-Age Infants
title_short Modulation of Placental Gene Expression in Small-for-Gestational-Age Infants
title_full Modulation of Placental Gene Expression in Small-for-Gestational-Age Infants
title_fullStr Modulation of Placental Gene Expression in Small-for-Gestational-Age Infants
title_full_unstemmed Modulation of Placental Gene Expression in Small-for-Gestational-Age Infants
title_sort modulation of placental gene expression in small-for-gestational-age infants
publisher MDPI AG
series Genes
issn 2073-4425
publishDate 2020-01-01
description Small-for-gestational-age (SGA) infants are fetuses that have not reached their genetically programmed growth potential. Low birth weight predisposes these infants to an increased risk of developing cardiovascular, metabolic and neurodevelopmental conditions in later life. However, our understanding of how this pathology occurs is currently incomplete. Previous research has focused on understanding the transcriptome, epigenome and bacterial signatures separately. However, we hypothesise that interactions between moderators of gene expression are critical to understanding fetal growth restriction. Through a review of the current literature, we identify that there is evidence of modulated expression/methylation of the placental genome and the presence of bacterial DNA in the placental tissue of SGA infants. We also identify that despite limited evidence of the interactions between the above results, there are promising suggestions of a relationship between bacterial signatures and placental function. This review aims to summarise the current literature concerning fetal growth from multiple avenues and propose a novel relationship between the placental transcriptome, methylome and bacterial signature that, if characterised, may be able to improve our current understanding of the placental response to stress and the aetiology of growth restriction.
topic placenta
sga
bacterial signatures
gene regulation
url https://www.mdpi.com/2073-4425/11/1/80
work_keys_str_mv AT jessicalocallaghan modulationofplacentalgeneexpressioninsmallforgestationalageinfants
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AT adamewing modulationofplacentalgeneexpressioninsmallforgestationalageinfants
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