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Epitranscriptomic profiling in human placenta: N6‐methyladenosine modification at the 5′‐untranslated region is related to fetal growth and preeclampsia
Intracellular mRNA levels are not always proportional to their respective protein levels, especially in the placenta. This discrepancy may be attributed to various factors including post‐transcriptional regulation, such as mRNA methylation (N6‐methyladenosine: m(6)A). Here, we conducted a comprehens...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7027905/ https://www.ncbi.nlm.nih.gov/pubmed/31914637 http://dx.doi.org/10.1096/fj.201900619RR |
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author | Taniguchi, Kosuke Kawai, Tomoko Kitawaki, Jo Tomikawa, Junko Nakabayashi, Kazuhiko Okamura, Kohji Sago, Haruhiko Hata, Kenichiro |
author_facet | Taniguchi, Kosuke Kawai, Tomoko Kitawaki, Jo Tomikawa, Junko Nakabayashi, Kazuhiko Okamura, Kohji Sago, Haruhiko Hata, Kenichiro |
author_sort | Taniguchi, Kosuke |
collection | PubMed |
description | Intracellular mRNA levels are not always proportional to their respective protein levels, especially in the placenta. This discrepancy may be attributed to various factors including post‐transcriptional regulation, such as mRNA methylation (N6‐methyladenosine: m(6)A). Here, we conducted a comprehensive m(6)A analysis of human placental tissue from neonates with various birth weights to clarify the involvement of m(6)A in placental biology. The augmented m(6)A levels at the 5′‐untranslated region (UTR) in mRNAs of small‐for‐date placenta samples were dominant compared to reduction of m(6)A levels, whereas a decrease in m(6)A in the vicinity of stop codons was common in heavy‐for‐date placenta samples. Notably, most of these genes showed similar expression levels between the different birth weight categories. In particular, preeclampsia placenta samples showed consistently upregulated SMPD1 protein levels and increased m(6)A at 5′‐UTR but did not show increased mRNA levels. Mutagenesis of adenosines at 5′‐UTR of SMPD1 mRNAs actually decreased protein levels in luciferase assay. Collectively, our findings suggest that m(6)A both at the 5′‐UTR and in the vicinity of stop codon in placental mRNA may play important roles in fetal growth and disease. |
format | Online Article Text |
id | pubmed-7027905 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-70279052020-02-24 Epitranscriptomic profiling in human placenta: N6‐methyladenosine modification at the 5′‐untranslated region is related to fetal growth and preeclampsia Taniguchi, Kosuke Kawai, Tomoko Kitawaki, Jo Tomikawa, Junko Nakabayashi, Kazuhiko Okamura, Kohji Sago, Haruhiko Hata, Kenichiro FASEB J Research Articles Intracellular mRNA levels are not always proportional to their respective protein levels, especially in the placenta. This discrepancy may be attributed to various factors including post‐transcriptional regulation, such as mRNA methylation (N6‐methyladenosine: m(6)A). Here, we conducted a comprehensive m(6)A analysis of human placental tissue from neonates with various birth weights to clarify the involvement of m(6)A in placental biology. The augmented m(6)A levels at the 5′‐untranslated region (UTR) in mRNAs of small‐for‐date placenta samples were dominant compared to reduction of m(6)A levels, whereas a decrease in m(6)A in the vicinity of stop codons was common in heavy‐for‐date placenta samples. Notably, most of these genes showed similar expression levels between the different birth weight categories. In particular, preeclampsia placenta samples showed consistently upregulated SMPD1 protein levels and increased m(6)A at 5′‐UTR but did not show increased mRNA levels. Mutagenesis of adenosines at 5′‐UTR of SMPD1 mRNAs actually decreased protein levels in luciferase assay. Collectively, our findings suggest that m(6)A both at the 5′‐UTR and in the vicinity of stop codon in placental mRNA may play important roles in fetal growth and disease. John Wiley and Sons Inc. 2019-11-25 2020-01 /pmc/articles/PMC7027905/ /pubmed/31914637 http://dx.doi.org/10.1096/fj.201900619RR Text en © 2019 The Authors. The FASEB Journal published by Wiley Periodicals, Inc. on behalf of Federation of American Societies for Experimental Biology This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited and is not used for commercial purposes. |
spellingShingle | Research Articles Taniguchi, Kosuke Kawai, Tomoko Kitawaki, Jo Tomikawa, Junko Nakabayashi, Kazuhiko Okamura, Kohji Sago, Haruhiko Hata, Kenichiro Epitranscriptomic profiling in human placenta: N6‐methyladenosine modification at the 5′‐untranslated region is related to fetal growth and preeclampsia |
title | Epitranscriptomic profiling in human placenta: N6‐methyladenosine modification at the 5′‐untranslated region is related to fetal growth and preeclampsia |
title_full | Epitranscriptomic profiling in human placenta: N6‐methyladenosine modification at the 5′‐untranslated region is related to fetal growth and preeclampsia |
title_fullStr | Epitranscriptomic profiling in human placenta: N6‐methyladenosine modification at the 5′‐untranslated region is related to fetal growth and preeclampsia |
title_full_unstemmed | Epitranscriptomic profiling in human placenta: N6‐methyladenosine modification at the 5′‐untranslated region is related to fetal growth and preeclampsia |
title_short | Epitranscriptomic profiling in human placenta: N6‐methyladenosine modification at the 5′‐untranslated region is related to fetal growth and preeclampsia |
title_sort | epitranscriptomic profiling in human placenta: n6‐methyladenosine modification at the 5′‐untranslated region is related to fetal growth and preeclampsia |
topic | Research Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7027905/ https://www.ncbi.nlm.nih.gov/pubmed/31914637 http://dx.doi.org/10.1096/fj.201900619RR |
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