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Dissecting the dynamic cellular transcriptional atlas of adult teleost testis development throughout the annual reproductive cycle. | LitMetric

AI Article Synopsis

  • The study focuses on the testis development in adult black rockfish throughout the annual cycle, utilizing single-cell transcriptome sequencing to analyze cellular changes.
  • It outlines the continuous developmental pathway of spermatogenic cells, emphasizing the gene expression dynamics related to spermatogonia proliferation and differentiation.
  • Furthermore, it highlights the complex interactions between various testicular cells, which may aid in understanding spermatogenesis and contribute to the preservation of endangered species.

Article Abstract

Teleost testis development during the annual cycle involves dramatic changes in cellular compositions and molecular events. In this study, the testicular cells derived from adult black rockfish at distinct stages - regressed, regenerating and differentiating - were meticulously dissected via single-cell transcriptome sequencing. A continuous developmental trajectory of spermatogenic cells, from spermatogonia to spermatids, was delineated, elucidating the molecular events involved in spermatogenesis. Subsequently, the dynamic regulation of gene expression associated with spermatogonia proliferation and differentiation was observed across spermatogonia subgroups and developmental stages. A bioenergetic transition from glycolysis to mitochondrial respiration of spermatogonia during the annual developmental cycle was demonstrated, and a deeper level of heterogeneity and molecular characteristics was revealed by re-clustering analysis. Additionally, the developmental trajectory of Sertoli cells was delineated, alongside the divergence of Leydig cells and macrophages. Moreover, the interaction network between testicular micro-environment somatic cells and spermatogenic cells was established. Overall, our study provides detailed information on both germ and somatic cells within teleost testes during the annual reproductive cycle, which lays the foundation for spermatogenesis regulation and germplasm preservation of endangered species.

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Source
http://dx.doi.org/10.1242/dev.202296DOI Listing

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