Gonocytes in Transition: Establishing the Male Germline Identity.

Authors

Peilin Li, Tatsuya Ohhata, Satoshi Sakai, Hiroyuki Niida, Soichiro Yamanaka

Published in

Advances in experimental medicine and biology. Volume 1517. Pages 3-16.

Abstract

Male germline development is characterized by a unique perinatal phase in which primordial germ cells (PGCs) differentiate into gonocytes (prospermatogonia) and subsequently give rise to spermatogonia. This chapter outlines the cellular, molecular, and epigenetic programs that orchestrate this transition, establishing the foundation of the lifelong spermatogenic lineage. Gonocytes undergo a transient G0/G1 arrest tightly regulated by retinoic acid (RA) metabolism, CDK inhibition, TGF family signaling, and the RNA-binding protein NANOS2, which integrates somatic cues to suppress meiosis and enforce male fate. Concurrently, gonocytes experience genome-wide de novo DNA methylation driven by NSD1-mediated H3K36me2 deposition and the DNMT3A/DNMT3L/DNMT3C machinery, accompanied by piRNA-directed transposon silencing and paternal imprint establishment. These processes collectively reshape the chromatin landscape and stabilize the male germline epigenome. The subsequent gonocyte-to-spermatogonia transition (GST) involves FGF, GDNF, and RA signaling, as well as dynamic histone demethylation, to generate spermatogonial stem cells (SSCs). Aberrant regulation of these pathways can arrest differentiation and predispose germ cells to transformation, as seen in testicular germ cell tumors (TGCTs), whose precursor cells retain gonocyte-like features. We further discuss the interplay between transposon control, imprinting, and chromatin architecture that underpins gonocyte identity. Emerging single-cell and small-input omics approaches are now redefining this transient developmental state, providing new insight into how epigenetic reprogramming and signaling convergence establish the male germline.

PMID:
42455434
Bibliographic data and abstract were imported from PubMed on 15 Jul 2026.

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