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Elevated methylation of the vault RNA2-1 promoter in maternal blood is associated with preterm birth
BACKGROUND: Preterm birth, defined as parturition before 37 completed weeks of gestation, is associated with an increased risk of neonatal complications and death, as well as poor health and disease later in life. Epigenetics could contribute to the mechanism underlying preterm birth. RESULTS: Genom...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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BioMed Central
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8272312/ https://www.ncbi.nlm.nih.gov/pubmed/34246240 http://dx.doi.org/10.1186/s12864-021-07865-y |
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author | You, Young-Ah Kwon, Eun Jin Hwang, Han-Sung Choi, Suk-Joo Choi, Sae Kyung Kim, Young Ju |
author_facet | You, Young-Ah Kwon, Eun Jin Hwang, Han-Sung Choi, Suk-Joo Choi, Sae Kyung Kim, Young Ju |
author_sort | You, Young-Ah |
collection | PubMed |
description | BACKGROUND: Preterm birth, defined as parturition before 37 completed weeks of gestation, is associated with an increased risk of neonatal complications and death, as well as poor health and disease later in life. Epigenetics could contribute to the mechanism underlying preterm birth. RESULTS: Genome-wide DNA methylation analysis of whole blood cells from 10 women (5 term and 5 preterm deliveries) was performed using an Illumina Infinium HumanMethylation450 BeadChips array. We identified 1,581 differentially methylated CpG sites in promoter regions between term and preterm birth. Although the differences were not significant after correcting for multiple tests, seven CpGs on the genomically imprinted vault RNA2-1 (VTRNA2-1; also known as non-coding RNA, nc886 or miR-886) showed the largest differences (range: 26–39 %). Pyrosequencing verification was performed with blood samples from pregnant women recruited additionally (39 term and 43 preterm deliveries). In total, 28 (34.1 %) samples showed hypomethylation of the VTRNA2-1 promoter (< 13 % methylation), while 54 (65.9 %) samples showed elevated methylation levels between 30 and 60 %. Elevated methylation of VTRNA2-1 promoter was associated with an increased risk of preterm birth after adjusting for maternal age, season of delivery, parity and white blood cell count. The mRNA expression of VTRNA2-1 was 0.51-fold lower in women with preterm deliveries (n = 20) compared with women with term deliveries (n = 20). CONCLUSIONS: VTRNA2-1 is a noncoding transcript to environmentally responsive epialleles. Our results suggest that elevated methylation of the VTRNA2-1 promoter may result in increased risk of PTB caused by the pro-inflammatory cytokines. Further studies are needed to confirm the association of VTRNA2-1 methylation with preterm birth in a large population, and to elucidate the underlying mechanism. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12864-021-07865-y. |
format | Online Article Text |
id | pubmed-8272312 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-82723122021-07-12 Elevated methylation of the vault RNA2-1 promoter in maternal blood is associated with preterm birth You, Young-Ah Kwon, Eun Jin Hwang, Han-Sung Choi, Suk-Joo Choi, Sae Kyung Kim, Young Ju BMC Genomics Research Article BACKGROUND: Preterm birth, defined as parturition before 37 completed weeks of gestation, is associated with an increased risk of neonatal complications and death, as well as poor health and disease later in life. Epigenetics could contribute to the mechanism underlying preterm birth. RESULTS: Genome-wide DNA methylation analysis of whole blood cells from 10 women (5 term and 5 preterm deliveries) was performed using an Illumina Infinium HumanMethylation450 BeadChips array. We identified 1,581 differentially methylated CpG sites in promoter regions between term and preterm birth. Although the differences were not significant after correcting for multiple tests, seven CpGs on the genomically imprinted vault RNA2-1 (VTRNA2-1; also known as non-coding RNA, nc886 or miR-886) showed the largest differences (range: 26–39 %). Pyrosequencing verification was performed with blood samples from pregnant women recruited additionally (39 term and 43 preterm deliveries). In total, 28 (34.1 %) samples showed hypomethylation of the VTRNA2-1 promoter (< 13 % methylation), while 54 (65.9 %) samples showed elevated methylation levels between 30 and 60 %. Elevated methylation of VTRNA2-1 promoter was associated with an increased risk of preterm birth after adjusting for maternal age, season of delivery, parity and white blood cell count. The mRNA expression of VTRNA2-1 was 0.51-fold lower in women with preterm deliveries (n = 20) compared with women with term deliveries (n = 20). CONCLUSIONS: VTRNA2-1 is a noncoding transcript to environmentally responsive epialleles. Our results suggest that elevated methylation of the VTRNA2-1 promoter may result in increased risk of PTB caused by the pro-inflammatory cytokines. Further studies are needed to confirm the association of VTRNA2-1 methylation with preterm birth in a large population, and to elucidate the underlying mechanism. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12864-021-07865-y. BioMed Central 2021-07-10 /pmc/articles/PMC8272312/ /pubmed/34246240 http://dx.doi.org/10.1186/s12864-021-07865-y Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
spellingShingle | Research Article You, Young-Ah Kwon, Eun Jin Hwang, Han-Sung Choi, Suk-Joo Choi, Sae Kyung Kim, Young Ju Elevated methylation of the vault RNA2-1 promoter in maternal blood is associated with preterm birth |
title | Elevated methylation of the vault RNA2-1 promoter in maternal blood is associated with preterm birth |
title_full | Elevated methylation of the vault RNA2-1 promoter in maternal blood is associated with preterm birth |
title_fullStr | Elevated methylation of the vault RNA2-1 promoter in maternal blood is associated with preterm birth |
title_full_unstemmed | Elevated methylation of the vault RNA2-1 promoter in maternal blood is associated with preterm birth |
title_short | Elevated methylation of the vault RNA2-1 promoter in maternal blood is associated with preterm birth |
title_sort | elevated methylation of the vault rna2-1 promoter in maternal blood is associated with preterm birth |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8272312/ https://www.ncbi.nlm.nih.gov/pubmed/34246240 http://dx.doi.org/10.1186/s12864-021-07865-y |
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