A longitudinal single-nucleus transcriptomic atlas of bovine placentation reveals dynamic cellular hierarchies and regulatory programs

BACKGROUND: Elucidating cellular hierarchies and regulatory mechanisms of placental development across gestation is critical for understanding pregnancy maintenance and improving reproductive outcomes in mammals, including cattle. However, a comprehensive, temporally resolved single-cell characterization of the bovine placenta has remained lacking. RESULTS: We construct a longitudinal single-nucleus transcriptomic atlas comprising 311,299 placental cells and nuclei across 13 developmental timepoints (E12, E14, E16, E18, E24, E30, E50, E60, E85, E110, E180, E240, and E280). We identify 13 major cell types and 14 trophoblast subtypes, revealing pronounced cellular heterogeneity and stage-specific transcriptional programs. Regulatory analyses highlight HAND1 and DLX5 as candidate key regulators of maternal recognition of pregnancy. Trajectory inference demonstrates that binucleate cells arise from specific uninucleate cell subpopulations around E24, with differentiation governed by genomic imprinting and metabolic reprogramming. Integration with genome-wide association study data identifies eight early trophoblast subtypes significantly associated with gestation length, along with candidate pathways and risk genes, including CYCS, HMGA1, and VDAC1, under strong evolutionary constraint. Additionally, we find that placental macrophages emerge from E30 in cattle and show significant associations with pregnancy loss in both cattle and humans, sharing conserved risk pathways. CONCLUSIONS: This study provides a comprehensive spatiotemporal single-cell atlas of bovine placental development, defining cellular hierarchies, lineage dynamics, and regulatory networks at the maternal-fetal interface. These findings offer a valuable resource and conceptual framework for understanding pregnancy maintenance and for improving reproductive traits in ruminants.

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Publication Details

Journal
Genome biology
Published
2026-06-27
DOI
https://doi.org/10.1186/s13059-026-04173-0
Primary Topic
Reproductive Physiology in Livestock
Type
article
Field-Weighted Citation Impact
0.00

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article

A longitudinal single-nucleus transcriptomic atlas of bovine placentation reveals dynamic cellular hierarchies and regulatory programs

Hengkuan Li, X Wang, Tao Shi, Yingran Liu et al.
Genome biology
Reproductive Physiology in Livestock
article

A longitudinal single-nucleus transcriptomic atlas of bovine placentation reveals dynamic cellular hierarchies and regulatory programs

Hengkuan Li, X Wang, Tao Shi, Yingran Liu, A Feng Zhang, Yu Jiang, Guanghui Tan, Yi Zhou, J LI, Xiaoru Yan, Yi Zheng, Haoping Wang, Xuesha Cao, Xi Guo
article en

Abstract

BACKGROUND: Elucidating cellular hierarchies and regulatory mechanisms of placental development across gestation is critical for understanding pregnancy maintenance and improving reproductive outcomes in mammals, including cattle. However, a comprehensive, temporally resolved single-cell characterization of the bovine placenta has remained lacking. RESULTS: We construct a longitudinal single-nucleus transcriptomic atlas comprising 311,299 placental cells and nuclei across 13 developmental timepoints (E12, E14, E16, E18, E24, E30, E50, E60, E85, E110, E180, E240, and E280). We identify 13 major cell types and 14 trophoblast subtypes, revealing pronounced cellular heterogeneity and stage-specific transcriptional programs. Regulatory analyses highlight HAND1 and DLX5 as candidate key regulators of maternal recognition of pregnancy. Trajectory inference demonstrates that binucleate cells arise from specific uninucleate cell subpopulations around E24, with differentiation governed by genomic imprinting and metabolic reprogramming. Integration with genome-wide association study data identifies eight early trophoblast subtypes significantly associated with gestation length, along with candidate pathways and risk genes, including CYCS, HMGA1, and VDAC1, under strong evolutionary constraint. Additionally, we find that placental macrophages emerge from E30 in cattle and show significant associations with pregnancy loss in both cattle and humans, sharing conserved risk pathways. CONCLUSIONS: This study provides a comprehensive spatiotemporal single-cell atlas of bovine placental development, defining cellular hierarchies, lineage dynamics, and regulatory networks at the maternal-fetal interface. These findings offer a valuable resource and conceptual framework for understanding pregnancy maintenance and for improving reproductive traits in ruminants.

Genome biology
Jilin University (CN), Westlake University (CN), North West Agriculture and Forestry University (CN), Sanya University (CN), Jilin Agricultural University (CN), Suranaree University of Technology (TH), Northwest A&F University (CN)
National Key Research and Development Program of China
Openalex Percentile: Top 6%
Reproductive Physiology in Livestock
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