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Evolutionary transcriptomics implicates HAND2 in the origins of implantation and regulation of gestation length

The developmental origins and evolutionary histories of cell types, tissues, and organs contribute to the ways in which their dysfunction produces disease. In mammals, the nature, development and evolution of maternal-fetal interactions likely influence diseases of pregnancy. Here we show genes that...

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Autores principales: Marinić, Mirna, Mika, Katelyn, Chigurupati, Sravanthi, Lynch, Vincent J
Formato: Online Artículo Texto
Lenguaje:English
Publicado: eLife Sciences Publications, Ltd 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7943190/
https://www.ncbi.nlm.nih.gov/pubmed/33522483
http://dx.doi.org/10.7554/eLife.61257
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author Marinić, Mirna
Mika, Katelyn
Chigurupati, Sravanthi
Lynch, Vincent J
author_facet Marinić, Mirna
Mika, Katelyn
Chigurupati, Sravanthi
Lynch, Vincent J
author_sort Marinić, Mirna
collection PubMed
description The developmental origins and evolutionary histories of cell types, tissues, and organs contribute to the ways in which their dysfunction produces disease. In mammals, the nature, development and evolution of maternal-fetal interactions likely influence diseases of pregnancy. Here we show genes that evolved expression at the maternal-fetal interface in Eutherian mammals play essential roles in the evolution of pregnancy and are associated with immunological disorders and preterm birth. Among these genes is HAND2, a transcription factor that suppresses estrogen signaling, a Eutherian innovation allowing blastocyst implantation. We found dynamic HAND2 expression in the decidua throughout the menstrual cycle and pregnancy, gradually decreasing to a low at term. HAND2 regulates a distinct set of genes in endometrial stromal fibroblasts including IL15, a cytokine also exhibiting dynamic expression throughout the menstrual cycle and gestation, promoting migration of natural killer cells and extravillous cytotrophoblasts. We demonstrate that HAND2 promoter loops to an enhancer containing SNPs implicated in birth weight and gestation length regulation. Collectively, these data connect HAND2 expression at the maternal-fetal interface with evolution of implantation and gestational regulation, and preterm birth.
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spelling pubmed-79431902021-03-10 Evolutionary transcriptomics implicates HAND2 in the origins of implantation and regulation of gestation length Marinić, Mirna Mika, Katelyn Chigurupati, Sravanthi Lynch, Vincent J eLife Evolutionary Biology The developmental origins and evolutionary histories of cell types, tissues, and organs contribute to the ways in which their dysfunction produces disease. In mammals, the nature, development and evolution of maternal-fetal interactions likely influence diseases of pregnancy. Here we show genes that evolved expression at the maternal-fetal interface in Eutherian mammals play essential roles in the evolution of pregnancy and are associated with immunological disorders and preterm birth. Among these genes is HAND2, a transcription factor that suppresses estrogen signaling, a Eutherian innovation allowing blastocyst implantation. We found dynamic HAND2 expression in the decidua throughout the menstrual cycle and pregnancy, gradually decreasing to a low at term. HAND2 regulates a distinct set of genes in endometrial stromal fibroblasts including IL15, a cytokine also exhibiting dynamic expression throughout the menstrual cycle and gestation, promoting migration of natural killer cells and extravillous cytotrophoblasts. We demonstrate that HAND2 promoter loops to an enhancer containing SNPs implicated in birth weight and gestation length regulation. Collectively, these data connect HAND2 expression at the maternal-fetal interface with evolution of implantation and gestational regulation, and preterm birth. eLife Sciences Publications, Ltd 2021-02-01 /pmc/articles/PMC7943190/ /pubmed/33522483 http://dx.doi.org/10.7554/eLife.61257 Text en © 2021, Marinić et al https://creativecommons.org/licenses/by/4.0/This article is distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use and redistribution provided that the original author and source are credited.
spellingShingle Evolutionary Biology
Marinić, Mirna
Mika, Katelyn
Chigurupati, Sravanthi
Lynch, Vincent J
Evolutionary transcriptomics implicates HAND2 in the origins of implantation and regulation of gestation length
title Evolutionary transcriptomics implicates HAND2 in the origins of implantation and regulation of gestation length
title_full Evolutionary transcriptomics implicates HAND2 in the origins of implantation and regulation of gestation length
title_fullStr Evolutionary transcriptomics implicates HAND2 in the origins of implantation and regulation of gestation length
title_full_unstemmed Evolutionary transcriptomics implicates HAND2 in the origins of implantation and regulation of gestation length
title_short Evolutionary transcriptomics implicates HAND2 in the origins of implantation and regulation of gestation length
title_sort evolutionary transcriptomics implicates hand2 in the origins of implantation and regulation of gestation length
topic Evolutionary Biology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7943190/
https://www.ncbi.nlm.nih.gov/pubmed/33522483
http://dx.doi.org/10.7554/eLife.61257
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AT chigurupatisravanthi evolutionarytranscriptomicsimplicateshand2intheoriginsofimplantationandregulationofgestationlength
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