Evolutionary transcriptomics implicates HAND2 in the origins of implantation and regulation of gestation length.
Mirna MarinićKatelyn MikaSravanthi ChigurupatiVincent J LynchPublished in: eLife (2021)
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.
Keyphrases
- gestational age
- preterm birth
- birth weight
- poor prognosis
- low birth weight
- genome wide
- transcription factor
- binding protein
- pregnancy outcomes
- weight gain
- gene expression
- preterm infants
- long non coding rna
- stem cells
- genome wide identification
- bone marrow
- natural killer cells
- bioinformatics analysis
- big data
- deep learning
- mesenchymal stem cells