bioRxiv Science⌕ Search

bioRxiv · 10.1101/427310

Fine-tuned adaptation of embryo-endometrium pairs at implantation revealed by gene regulatory networks

Abstract

Interactions between embryo and endometrium at implantation are critical for the progression and the issue of pregnancy. These reciprocal actions involve exchange of paracrine signals that govern implantation and placentation. However, it remains unknown how these interactions between the conceptus and the endometrium are coordinated at the level of an individual pregnancy. Under the hypothesis that gene expression of endometrium is dependent on gene expression of extraembryonic tissues, we performed an integrative analysis of transcriptome profiles of paired conceptuses and endometria obtained from pregnancies initiated by artificial insemination. We quantified strong dependence (|r|>0.95, eFDR<0.01) in transcript abundance of genes expressed in the extraembryonic tissues and genes expressed in the endometrium. The profiles of connectivity revealed distinct co-expression patterns of extraembryonic tissues with caruncular and intercaruncular areas of the endometrium. Notably, a subset of highly co-expressed genes between conceptus (n=229) and caruncular areas of the endometrium (n=218, r>0.9999, eFDR<0.001) revealed a blueprint of gene expression specific to each pregnancy. Functional analyses of genes co-expressed between conceptus and endometrium revealed significantly enriched functional modules with critical contribution for implantation and placentation, including \"in utero embryonic development\", \"placenta development\" and \"regulation of transcription\". Functional modules were remarkably specific to caruncular or intercaruncular areas of the endometrium. The quantitative and functional association between genes expressed in conceptus and endometrium emphasize a coordinated communication between these two entities in mammals. To our knowledge, we provide first evidence that implantation in mammalian pregnancy relies on the ability of the conceptus and the endometrium to develop a fine-tuned adaptive response characteristic of each pregnancy.

Source connections

Explore related subjects

Keep this discovery

Explore connections, maps & timelines

BibTeXRIS

Biase, F., Hue, I., Dickinson, S., Jaffrezic, F., Laloe, D., Lewin, H., Sandra, O.. 2018-09-25. Fine-tuned adaptation of embryo-endometrium pairs at implantation revealed by gene regulatory networks. https://doi.org/10.1101/427310

Cite the original work for its findings. Save a collection to share your selection of sources.

KEEP EXPLORING

Related preprints

Optimizing the efficiency of assisted reproduction procedures in the common marmoset (Callithrix jacchus) improved IVF outcomes

The marmoset has emerged as a model species for genetic studies of complex neurodevelopmental conditions because of their brain development, behavior, communication, and compact size. IVF has been used to generate wild-type and transgenic marmoset embryos, but inefficiency of IVF in the marmoset compared to other primates poses challenges for genetic manipulation. To address this limitation, we analyzed the association between variables of age, number of cycles, and progesterone levels for IVF and embryology outcomes. Longitudinal data collected over 2 years indicated that the progesterone levels 24 hours after Cloprostenol sodium (Estrumate) administration, the number of days of ovarian stimulation during an IVF cycle, and the number of oocyte retrievals that an animal had undergone all influenced IVF cycle outcomes. Higher serum progesterone levels at cycle start were negatively correlated with the likelihood of fertilized eggs progressing to the cleavage stage of embryo development. Additionally, a shorter duration of ovarian stimulation (ranging 7 to 14 days of medication) coupled with a GnRH antagonist correlated with an increased percentage of fertilized eggs. We observed a trend that a shorter hormonal stimulation cycle length was associated with a higher percentage of embryos reaching the cleavage stage. The optimization of stimulation cycle protocol and embryology has led to a high percentage of implantation after embryo transfer regardless of whether the embryo was fresh or cryopreserved. These findings suggest that shorter IVF cycles and a progesterone level <10 ng/mL at cycle start were correlated with an increased likelihood of a cleavage stage embryo development.

developmental biology↗

Yap is a key regulator of tracheoesophageal separation during foregut development

Separation of the anterior foregut into the esophagus and trachea involves dynamic cellular movement that requires the coordinated activity of multiple signaling pathways and transcription factors. Disruption of this process can result in esophageal atresia (EA) with or without tracheoesophageal fistula (TEF), manifesting in five major anatomical types (Types A-E). Here, we examine the role of the Hippo pathway effector Yes-associated protein (Yap) in foregut separation. Conditional deletion of Yap in the dorsal and medial portions of the anterior foregut endoderm leads to the formation of Type A EA/TEF, isolated EA. This separation defect only occurs in Sox2-CreER;Yaploxp/loxp but not in Shh-Cre;Yaploxp/loxp mutants. Our findings further reveal that Yap mutants exhibit a reduction in Sox2+ esophageal progenitor cells accompanied by the absence of the middle esophageal segment. Combined deletion of Yap and Taz (transcriptional coactivator with PDZ-binding motif) also results in isolated EA accompanied by severe craniofacial abnormalities. Therefore, loss of Yap causes a distinct Type A EA/TEF, which differs from existing mouse models of EA/TEF that predominantly exhibit the Type C phenotype. Our findings also suggest that epithelial cells at the dorsal-ventral boundary play a critical role in tracheoesophageal separation.

developmental biology↗

Tissue geometry patterns epidermal stem cell fate in murine interfollicular skin

How tissues maintain spatial patterns of stem cell renewal and differentiation despite continuous cellular turnover remains poorly understood. Here, we show that microscopic undulations of the dermal-epidermal junction (DEJ) are associated with distinct stem cell behaviors in the mouse epidermis. Using longitudinal intravital imaging and quantitative analysis of cell morphology and lineage dynamics, we find that local DEJ curvature predicts the subsequent fate of daughter cells up to three days before mother cell division. Cells residing in concave valleys preferentially produce proliferating descendants, whereas convex ridges are associated with increased differentiation. These spatial biases are reflected in the expression of stem- and differentiation-associated markers and accumulate into differences in long-term clonal expansion. Remarkably, DEJ geometry remains stable for weeks, persisting across multiple generations of epidermal cells. Moreover, human epidermal equivalents grown on devitalized dermis recapitulate the preferential retention of basal layer cells in valleys, indicating that living dermal cells are not required for this spatial organization. Our findings suggest that stable tissue architecture can pattern stem cell fate probabilities across generations, contributing to functional stem cell heterogeneity.

developmental biology↗