Nature CommunicationsDevelopmental BiologyPeer-reviewed journal article
NR2F2 regulation of interstitial to fetal Leydig cell differentiation in the testis: insights into differences of sex development
Martin Andres EstermanniD, Sara A. GrimmiD, Abigail S KitakuleiD, Karina F. RodrigueziD, Paula R. BrowniD, Kathryn S. McClellandiD, Ciro Maurizio AmatoiD, Humphrey Hung‐Chang YaoiD
Abstract
Testicular fetal Leydig cells are a specialized cell type responsible for embryo masculinization. Fetal Leydig cells produce androgens, that induce the differentiation of male reproductive system and sexual characteristics. Deficiencies in Leydig cell differentiation leads to various disorders of sex development and male reproductive defects such as ambiguous genitalia, hypospadias, cryptorchidism, and infertility. Fetal Leydig cells are thought to originate from proliferating progenitor cells in the testis interstitium, marked by genes like Arx, Pdgfra, Tcf21 and Wnt5a. However, the precise mechanisms governing the transition from interstitial cells to fetal Leydig cells remain elusive. Through integrated approaches involving mouse models and single-nucleus multiomic analyses, we discovered that fetal Leydig cells originate from a Nr2f2-positive non-steroidogenic interstitial cell population. Embryonic deletion of Nr2f2 in mouse testes resulted in disorders of sex development, including dysgenic testes, Leydig cell hypoplasia, cryptorchidism, and hypospadias. We found that NR2F2 promotes the progenitor cell fate while suppresses Leydig cell differentiation by directly and indirectly controlling a cohort of transcription factors and downstream genes. Bioinformatic analyses of single-nucleus ATAC-seq and NR2F2 ChIP-seq data revealed putative transcription factors co-regulating the process of interstitial to Leydig cell differentiation. Collectively, our findings not only highlight the critical role of Nr2f2 in orchestrating the transition from interstitial cells to fetal Leydig cells, but also provide molecular insight into the disorders of sex development as a result of Nr2f2 mutations.
- organism: mouse
- assay: ATAC-seq
- research focus: gene regulatory network inference
- approach: statistical model
- Citations
- 21
- FWCI
- 12.34
- Field percentile
- top 1%
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities
- Sperm and Testicular Function
Reproducibility ledger
Nobody has reported trying to reproduce this paper yet. Did you replicate an experiment or run the code? Your report saves the next lab a week.
Sign in to file a reproducibility report.
Related papers
- NR2F2 is required in the embryonic testis for Fetal Leydig Cell development
Aitana Perea-Gómez, Natividad Bellido-Carreras, … Marie‐Christine Chaboissier·eLifePeer-reviewed·Jul 10, 2025
- Evidence for NR2F2/COUP-TFII involvement in human testis development
Somboon Wankanit, Housna Zidoune, … Maëva Elzaïat·bioRxiv·Jan 5, 2024
- Zebrafish Foxl2l suppresses stemness and directs feminization of germline progenitors
Chen-wei Hsu, Hao H. Ho, … Bon‐chu Chung·eLifePeer-reviewed·Jun 11, 2025
- Generation of a Nr2f2-driven inducible Cre mouse to target interstitial cells in the reproductive system
Paula R. Brown, Martin Andres Estermann, … Humphrey Hung‐Chang Yao·Biology of ReproductionPeer-reviewed·Apr 17, 2025
- Specific transcriptomic signatures and dual regulation of steroidogenesis between fetal and adult mouse Leydig cells
Pauline Sararols, Isabelle Stévant, … Serge Nef·Frontiers in Cell and Developmental BiologyPeer-reviewed·Jun 28, 2021
- Fadrozole-mediated sex reversal in the embryonic chicken gonad involves a PAX2 positive undifferentiated supporting cell state
Martin Andres Estermann, Craig A. Smith·Frontiers in Cell and Developmental BiologyPeer-reviewed·Nov 10, 2022