Held Madison, Castillo-Madeen Helen, Vigh-Conrad Katinka A, Aston Kenneth I, Conrad Donald F
Division of Genetics, Oregon National Primate Research Center, Oregon Health and Science University, Beaverton, Oregon.
Andrology and IVF Laboratory, Department of Surgery (Urology), University of Utah, Salt Lake City, Utah.
Fertil Steril. 2025 Jun;123(6):970-979. doi: 10.1016/j.fertnstert.2025.03.024. Epub 2025 Mar 31.
Genetic and genomic analysis continues to drive important insights into male reproductive tract (MRT) development. Here, we briefly review normal MRT development, highlighting recent discoveries of cell types and cellular processes delivered by single-cell sequencing. We report a systematic review of phenotype terms and genes linked to MRT development, identifying 35 terms from the Human Phenotype Ontology associated with 269 unique genes. A parallel review of mouse data revealed differences in the phenotype terms available and the number and identity of genes linked to MRT defects, indicating opportunities for harmonization of knowledge. We used a published single-cell atlas of the developing testis to characterize the regulation of MRT genes across cell types and stages of fetal testis development. Single-cell RNA sequencing data support the conclusion that Leydig cells and Sertoli cells are the primary testicular cell types expressing MRT genes. Furthermore, we find post-conception weeks 6, 8, and 16 to be the key points of upregulation of testicular MRT genes. New advances, especially in imaging and spatially resolved molecular measurements, provide exciting prospects for MRT research and diagnosis, and we expect rapid progress in the coming years. Continued investigation in this space is essential to understand the genetic basis of MRT development and how MRT defects are related to medical outcomes in adult life.
遗传和基因组分析不断推动对男性生殖道(MRT)发育的重要见解。在此,我们简要回顾正常MRT发育,重点介绍单细胞测序在细胞类型和细胞过程方面的最新发现。我们报告了对与MRT发育相关的表型术语和基因的系统综述,从人类表型本体中确定了35个术语,这些术语与269个独特基因相关。对小鼠数据的平行综述揭示了可用表型术语以及与MRT缺陷相关的基因数量和身份的差异,这表明知识协调存在机会。我们使用已发表的发育中睾丸的单细胞图谱来描述MRT基因在胎儿睾丸发育的不同细胞类型和阶段的调控情况。单细胞RNA测序数据支持以下结论:睾丸间质细胞和支持细胞是表达MRT基因的主要睾丸细胞类型。此外,我们发现受孕后第6、8和16周是睾丸MRT基因上调的关键点。新进展,尤其是在成像和空间分辨分子测量方面,为MRT研究和诊断提供了令人兴奋的前景,我们预计未来几年会有快速进展。在这个领域持续进行研究对于理解MRT发育的遗传基础以及MRT缺陷如何与成年后的医学结果相关至关重要。