Cargando…
Sex Differences in the Human Placenta MicroRNA Transcriptome
Maternal and fetal pregnancy outcomes vary based on fetal sex likely due to differences in placental function, reflected by sex differences in RNA expression. RNA transcripts are subject to fine-tuning control by post-transcriptional regulation including miRNAs binding to target RNAs and altering ge...
Autores principales: | , , , , , , , , , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2021
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8090262/ http://dx.doi.org/10.1210/jendso/bvab048.1531 |
_version_ | 1783687240836186112 |
---|---|
author | Flowers, Amy E Gonzalez, Tania L Eisman, Laura E Joshi, Nikhil Wu, Di Zhang, Yizhou Santiskulvong, Chintda Tang, Jie Buttle, Rae Sauro, Erica Clark, Ekaterina L Jefferies, Caroline Chan, Jessica Lin, Yayu Williams, John Pisarska, Margareta Danuta |
author_facet | Flowers, Amy E Gonzalez, Tania L Eisman, Laura E Joshi, Nikhil Wu, Di Zhang, Yizhou Santiskulvong, Chintda Tang, Jie Buttle, Rae Sauro, Erica Clark, Ekaterina L Jefferies, Caroline Chan, Jessica Lin, Yayu Williams, John Pisarska, Margareta Danuta |
author_sort | Flowers, Amy E |
collection | PubMed |
description | Maternal and fetal pregnancy outcomes vary based on fetal sex likely due to differences in placental function, reflected by sex differences in RNA expression. RNA transcripts are subject to fine-tuning control by post-transcriptional regulation including miRNAs binding to target RNAs and altering gene expression. Here we identify sexually dimorphic miRNA expression throughout gestation in the human placenta. Next-generation sequencing was used to identify human placenta miRNA expression profiles in first and third trimester uncomplicated pregnancies using discarded tissue obtained after chorionic villous sampling (n=113) and placenta (n=47). Differential expression analysis and mRNA target analysis were also examined. Sequencing identified 2,503 unique mature miRNAs expressed in each trimester. Of these, 13 significantly sexually dimorphic (FDR<0.05) miRNAs were identified in the first trimester and 4 significantly sexually dimorphic miRNAs were identified in the third trimester, including one miRNA, hsa-miR-361-5p, expressed across gestation. All of these sexually dimorphic miRNAs were significantly upregulated in females compared to males. Pathways analysis with predicted targets suggests sex differences in cancer and inflammation-related pathways in the first trimester and inflammation and growth-related pathways in the third trimester. Differential expression analysis on sex-segregated data identified 613 miRNAs upregulated in female placentas and 636 miRNAs upregulated in male placentas across gestation (FDR<0.05). In conclusion, fetal sex affects placental miRNA expression profiles and differentially expressed miRNAs may affect relevant downstream pathways, which may account for differences in pregnancy outcomes due to fetal sex. This work provides an expression atlas to direct functional studies investigating placental sex differences. |
format | Online Article Text |
id | pubmed-8090262 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-80902622021-05-06 Sex Differences in the Human Placenta MicroRNA Transcriptome Flowers, Amy E Gonzalez, Tania L Eisman, Laura E Joshi, Nikhil Wu, Di Zhang, Yizhou Santiskulvong, Chintda Tang, Jie Buttle, Rae Sauro, Erica Clark, Ekaterina L Jefferies, Caroline Chan, Jessica Lin, Yayu Williams, John Pisarska, Margareta Danuta J Endocr Soc Reproductive Endocrinology Maternal and fetal pregnancy outcomes vary based on fetal sex likely due to differences in placental function, reflected by sex differences in RNA expression. RNA transcripts are subject to fine-tuning control by post-transcriptional regulation including miRNAs binding to target RNAs and altering gene expression. Here we identify sexually dimorphic miRNA expression throughout gestation in the human placenta. Next-generation sequencing was used to identify human placenta miRNA expression profiles in first and third trimester uncomplicated pregnancies using discarded tissue obtained after chorionic villous sampling (n=113) and placenta (n=47). Differential expression analysis and mRNA target analysis were also examined. Sequencing identified 2,503 unique mature miRNAs expressed in each trimester. Of these, 13 significantly sexually dimorphic (FDR<0.05) miRNAs were identified in the first trimester and 4 significantly sexually dimorphic miRNAs were identified in the third trimester, including one miRNA, hsa-miR-361-5p, expressed across gestation. All of these sexually dimorphic miRNAs were significantly upregulated in females compared to males. Pathways analysis with predicted targets suggests sex differences in cancer and inflammation-related pathways in the first trimester and inflammation and growth-related pathways in the third trimester. Differential expression analysis on sex-segregated data identified 613 miRNAs upregulated in female placentas and 636 miRNAs upregulated in male placentas across gestation (FDR<0.05). In conclusion, fetal sex affects placental miRNA expression profiles and differentially expressed miRNAs may affect relevant downstream pathways, which may account for differences in pregnancy outcomes due to fetal sex. This work provides an expression atlas to direct functional studies investigating placental sex differences. Oxford University Press 2021-05-03 /pmc/articles/PMC8090262/ http://dx.doi.org/10.1210/jendso/bvab048.1531 Text en © The Author(s) 2021. Published by Oxford University Press on behalf of the Endocrine Society. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs licence (http://creativecommons.org/licenses/by-nc-nd/4.0/ (https://creativecommons.org/licenses/by-nc-nd/4.0/) ), which permits non-commercial reproduction and distribution of the work, in any medium, provided the original work is not altered or transformed in any way, and that the work is properly cited. For commercial re-use, please contact journals.permissions@oup.com |
spellingShingle | Reproductive Endocrinology Flowers, Amy E Gonzalez, Tania L Eisman, Laura E Joshi, Nikhil Wu, Di Zhang, Yizhou Santiskulvong, Chintda Tang, Jie Buttle, Rae Sauro, Erica Clark, Ekaterina L Jefferies, Caroline Chan, Jessica Lin, Yayu Williams, John Pisarska, Margareta Danuta Sex Differences in the Human Placenta MicroRNA Transcriptome |
title | Sex Differences in the Human Placenta MicroRNA Transcriptome |
title_full | Sex Differences in the Human Placenta MicroRNA Transcriptome |
title_fullStr | Sex Differences in the Human Placenta MicroRNA Transcriptome |
title_full_unstemmed | Sex Differences in the Human Placenta MicroRNA Transcriptome |
title_short | Sex Differences in the Human Placenta MicroRNA Transcriptome |
title_sort | sex differences in the human placenta microrna transcriptome |
topic | Reproductive Endocrinology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8090262/ http://dx.doi.org/10.1210/jendso/bvab048.1531 |
work_keys_str_mv | AT flowersamye sexdifferencesinthehumanplacentamicrornatranscriptome AT gonzaleztanial sexdifferencesinthehumanplacentamicrornatranscriptome AT eismanlaurae sexdifferencesinthehumanplacentamicrornatranscriptome AT joshinikhil sexdifferencesinthehumanplacentamicrornatranscriptome AT wudi sexdifferencesinthehumanplacentamicrornatranscriptome AT zhangyizhou sexdifferencesinthehumanplacentamicrornatranscriptome AT santiskulvongchintda sexdifferencesinthehumanplacentamicrornatranscriptome AT tangjie sexdifferencesinthehumanplacentamicrornatranscriptome AT buttlerae sexdifferencesinthehumanplacentamicrornatranscriptome AT sauroerica sexdifferencesinthehumanplacentamicrornatranscriptome AT clarkekaterinal sexdifferencesinthehumanplacentamicrornatranscriptome AT jefferiescaroline sexdifferencesinthehumanplacentamicrornatranscriptome AT chanjessica sexdifferencesinthehumanplacentamicrornatranscriptome AT linyayu sexdifferencesinthehumanplacentamicrornatranscriptome AT williamsjohn sexdifferencesinthehumanplacentamicrornatranscriptome AT pisarskamargaretadanuta sexdifferencesinthehumanplacentamicrornatranscriptome |