PUBLICATION

Single cell transcriptomes of zebrafish germline reveal progenitor types and feminization by Foxl2l

Authors
Hsu, C.W., Hao, H., Yang, C.H., Wang, Y.W., Li, K.C., Chung, B.C.
ID
ZDB-PUB-250612-1
Date
2025
Source
eLIFE   14: (Journal)
Registered Authors
Chung, Bon-chu
Keywords
developmental biology, zebrafish
Datasets
GEO:GSE173718
MeSH Terms
  • Forkhead Box Protein L2*/genetics
  • Forkhead Box Protein L2*/metabolism
  • Forkhead Transcription Factors*/genetics
  • Forkhead Transcription Factors*/metabolism
  • Stem Cells*/metabolism
  • Germ Cells*/metabolism
  • Gene Expression Regulation, Developmental
  • Zebrafish Proteins*/genetics
  • Zebrafish Proteins*/metabolism
  • Transcriptome*
  • Zebrafish*/genetics
  • Animals
  • Male
  • Sex Differentiation*/genetics
  • Single-Cell Analysis
  • Female
PubMed
40497446 Full text @ Elife
Abstract
Zebrafish is an important organism for genetic studies, but its early germ cell types and the mechanism of sex differentiation have not been fully characterized. Here, we profiled single-cell transcriptomes and charted a developmental trajectory going from germline stem cells, through early, committed, and late progenitors, to pre-meiotic and meiotic cells. We showed that transcription factor Foxl2l expressed in the progenitor directed progenitor differentiation toward oocytes. CRISPR-Cas9-mediated mutation of foxl2l produced 100% male fish with normal fertility. Another single-cell profiling of foxl2l-/- germ cells revealed the arrest of germ cell development at the stage of progenitor commitment. Concomitantly, nanos2 transcript (germline stem cell marker) was elevated together with an increase of nanos2+ germ cells in foxl2l mutants, indicating the acquisition of a novel stem cell state. Thus, we have identified developmental stages of germ cells in juvenile zebrafish and demonstrated that zebrafish Foxl2l drives progenitor germ cells toward feminization and prevents them from expressing nanos2.
Genes / Markers
Figures
Show all Figures
Expression
Phenotype
Mutations / Transgenics
Human Disease / Model
Sequence Targeting Reagents
Fish
Antibodies
Orthology
Engineered Foreign Genes
Mapping