# Sexually dimorphic gene expression responses of bovine embryos to the maternal microenvironment on day 13 of gestation

**Authors:** Dessie Salilew-Wondim, Ernst Tholen, Christine Große-Brinkhaus, Eva Held-Hoelker, Dennis Miskel, Franca Rings, Karl Schellander, Urban Besenfelder, Vitezslav Havlicek, Dawit Tesfaye, Michael Hoelker

PMC · DOI: 10.1186/s12864-025-11570-5 · BMC Genomics · 2025-04-14

## TL;DR

This study shows that male and female bovine embryos respond differently to their mother's environment during early development, with distinct gene expression patterns linked to sex and maternal conditions.

## Contribution

The study identifies novel sexually dimorphic gene expression patterns in bovine embryos at the initiation of elongation in response to maternal reproductive tract environments.

## Key findings

- Male and female embryos developed in lactating cows showed differential expression of genes related to steroid biosynthesis and gastrulation.
- Embryos in heifers exhibited sexually dimorphic gene expression linked to placental development and transmembrane transport.
- A significant proportion of differentially expressed genes were located on the X chromosome, with most upregulated in female embryos.

## Abstract

Various studies have highlighted significant differences in developmental kinetics and sensitivity to developmental conditions between male and female bovine embryos. These differences are thought to be caused in part by the sexually dimorphic expression of genes located on the sex or autosomal chromosomes. However, little is known about the dimorphic gene expression patterns of bovine embryos at the initiation of elongation, which is one of the critical stages of development. Furthermore, to the best of our knowledge, there is little or no data available on the sexually dimorphic gene expression patterns in bovine embryos in relation to maternal environmental conditions during the initiation of elongation. Therefore, the main objective of this study was to investigate the sexually dimorphic gene expression responses of embryos to the maternal environment at the initiation of elongation in embryos developed in lactating dairy cows and nonlactating nulliparous heifers.

Gene expression analysis showed that 159 genes including those involved in steroid biosynthesis and gastrulation were differentially expressed exclusively between male and female embryos developed in cows. Among these, 61 genes including CYP39 A1, CYP2R1 and CYP27B1 were upregulated and 98 genes including HSD17B1, HSD17B10 and aromatase (CYP19 A1) were downregulated in male embryos. Chromosomal analysis showed that 31.2% of the differentially expressed genes (DEGs) including glucose-6-phosphate dehydrogenase (G6PD) were located on the X chromosome, and 96% of those were upregulated in female embryos. Similarly, 254 genes including those involved in female sex differentiation, placenta development, transmembrane transport, and cell adhesion were differentially expressed exclusively between the male and female embryos developed in heifers. Of these, 108 genes including HSD17B11, HSD17B12, and HSD3B1 were upregulated, and 146 genes including SLC16 A9, SLC10 A1, SLC10 A3, SLC16 A5, SLC22 A23, SLC25 A43, SLC35 A2, SLC35 C1, and SLC4 were downregulated in male compared to female embryos. In addition, 17.3% of the DEGs were located on the X chromosome and 75% of the DEGs located on the X chromosome were upregulated in female embryos. On the other hand, 38 genes including SLC30 A10, SLC10 A4, ATP6 AP1, and KDM5 C showed sexually dimorphic expression patterns in day 13 bovine embryos irrespective of the maternal environment. These genes accounted for only 19% and 13% of the genes that showed sexually dimorphic expression in embryos developed in cows and heifers, respectively and the expression difference of these genes in male and female embryos was then likely influenced by the sex of the embryo.

This study revealed that embryos developed in lactating cows showed sexually dimorphic expression of genes involved in various functions including steroid biosynthesis and gastrulation. In contrast, embryos developed in heifers displayed sexually dimorphic expression of genes related to placental development, female sex differentiation, and transmembrane transport. This suggests that the reproductive tract environments of cows and heifers differently affect the sex specific expression of genes in bovine embryos. A higher proportion of genes that showed sexually dimorphic expression in cow embryos were located on the X chromosome, and the majority of these genes were upregulated in female embryos. Overall, this study provides insight into genes that exhibit sexually dimorphic expression patterns in day 13 bovine embryos due to the maternal reproductive tract microenvironment or solely due to the sex of the embryo.

The online version contains supplementary material available at 10.1186/s12864-025-11570-5.

## Linked entities

- **Genes:** CYP39A1 (cytochrome P450 family 39 subfamily A member 1) [NCBI Gene 51302], CYP2R1 (cytochrome P450 family 2 subfamily R member 1) [NCBI Gene 120227], CYP27B1 (cytochrome P450 family 27 subfamily B member 1) [NCBI Gene 1594], HSD17B1 (hydroxysteroid 17-beta dehydrogenase 1) [NCBI Gene 3292], HSD17B10 (hydroxysteroid 17-beta dehydrogenase 10) [NCBI Gene 3028], CYP19A1 (cytochrome P450 family 19 subfamily A member 1) [NCBI Gene 1588], G6PD (glucose-6-phosphate dehydrogenase) [NCBI Gene 2539], HSD17B11 (hydroxysteroid 17-beta dehydrogenase 11) [NCBI Gene 51170], HSD17B12 (hydroxysteroid 17-beta dehydrogenase 12) [NCBI Gene 51144], HSD3B1 (hydroxy-delta-5-steroid dehydrogenase, 3 beta- and steroid delta-isomerase 1) [NCBI Gene 3283], SLC16A9 (solute carrier family 16 member 9) [NCBI Gene 220963], SLC10A1 (solute carrier family 10 member 1) [NCBI Gene 6554], SLC10A3 (solute carrier family 10 member 3) [NCBI Gene 8273], SLC16A5 (solute carrier family 16 member 5) [NCBI Gene 9121], SLC22A23 (solute carrier family 22 member 23) [NCBI Gene 63027], SLC25A43 (solute carrier family 25 member 43) [NCBI Gene 203427], SLC35A2 (solute carrier family 35 member A2) [NCBI Gene 7355], SLC35C1 (solute carrier family 35 member C1) [NCBI Gene 55343], ALE1 (lysophospholipid acyltransferase) [NCBI Gene 854346], SLC30A10 (solute carrier family 30 member 10) [NCBI Gene 55532], SLC10A4 (solute carrier family 10 member 4) [NCBI Gene 201780], ATP6AP1 (ATPase H+ transporting accessory protein 1) [NCBI Gene 537], KDM5C (lysine demethylase 5C) [NCBI Gene 8242]

## Full-text entities

- **Genes:** CYP2R1 (cytochrome P450 family 2 subfamily R member 1) [NCBI Gene 541302], HSD17B12 (hydroxysteroid 17-beta dehydrogenase 12) [NCBI Gene 789567] {aka KAR}, KDM5C (lysine demethylase 5C) [NCBI Gene 281490] {aka JARID1C, SMCX}, HSD3B1 (hydroxy-delta-5-steroid dehydrogenase, 3 beta- and steroid delta-isomerase 1) [NCBI Gene 281824] {aka HSD3B}, SLC10A3 (solute carrier family 10 member 3) [NCBI Gene 504534], CYP39A1 (cytochrome P450 family 39 subfamily A member 1) [NCBI Gene 511195], CYP19A1 (cytochrome P450 family 19 subfamily A member 1) [NCBI Gene 281740] {aka CYP19, CYP19P1}, HSD17B10 (hydroxysteroid 17-beta dehydrogenase 10) [NCBI Gene 281809] {aka HADH2, MHBD}, SLC10A1 (solute carrier family 10 member 1) [NCBI Gene 532890], SLC30A10 (solute carrier family 30 member 10) [NCBI Gene 508385], HSD17B1 (hydroxysteroid 17-beta dehydrogenase 1) [NCBI Gene 353107] {aka EDH17B2}, SLC10A4 (solute carrier family 10 member 4) [NCBI Gene 540151], CYP27B1 (cytochrome P450 family 27 subfamily B member 1) [NCBI Gene 539630], HSD17B11 (hydroxysteroid 17-beta dehydrogenase 11) [NCBI Gene 527592], G6PD (glucose-6-phosphate dehydrogenase) [NCBI Gene 281179], ATP6AP1 (ATPase H+ transporting accessory protein 1) [NCBI Gene 327687] {aka ATP6IP1, Ac45}, SLC16A9 (solute carrier family 16 member 9) [NCBI Gene 539514] {aka MCT9}
- **Species:** Bos taurus (bovine, species) [taxon 9913]

## Full text

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## Figures

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## References

3 references — full list in the complete paper: https://tomesphere.com/paper/PMC11998263/full.md

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Source: https://tomesphere.com/paper/PMC11998263