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The Master Male Sex Determinant Gdf6Y of the Turquoise Killifish Arose Through Allelic Neofunctionalization

Abstract

Although sex determination is a fundamental process in vertebrate development, it is very plastic. Diverse genes became major sex determinants in teleost fishes. Deciphering how individual sex-determining genes orchestrate sex determination can reveal new actors in sexual development. Here, we demonstrate that the Y-chromosomal copy of the TGF-β family member gdf6 (gdf6Y) in Nothobranchius furzeri, an emerging model organism in aging research, gained the function of the male sex determinant through allelic diversification while retaining the skeletal developmental function shared with the X-chromosomal gdf6 allele (gdf6X). Concerning sex determination, gdf6Y is expressed by somatic supporting cells of the developing testes. There it induces the male sex in a germ cell-independent manner in contrast to sex determination in zebrafish and the medaka. Looking for downstream effectors of Gdf6Y, we identified besides TGF-β signaling modulators, especially the inhibitor of DNA binding genes id1/2/3, the mRNA decay activator zfp36l2 as a new GDF6 signaling target.

Citing Articles

The master male sex determinant Gdf6Y of the turquoise killifish arose through allelic neofunctionalization.

Richter A, Morl H, Thielemann M, Kleemann M, Geissen R, Schwarz R Nat Commun. 2025; 16(1):540.

PMID: 39788971 PMC: 11718055. DOI: 10.1038/s41467-025-55899-7.

References
1.
Ball C, Rodriguez K, Stumpo D, Ribeiro-Neto F, Korach K, Blackshear P . The RNA-binding protein, ZFP36L2, influences ovulation and oocyte maturation. PLoS One. 2014; 9(5):e97324. PMC: 4022657. DOI: 10.1371/journal.pone.0097324. View

2.
Adolfi M, Herpin A, Schartl M . The replaceable master of sex determination: bottom-up hypothesis revisited. Philos Trans R Soc Lond B Biol Sci. 2021; 376(1832):20200090. PMC: 8273498. DOI: 10.1098/rstb.2020.0090. View

3.
Love M, Huber W, Anders S . Moderated estimation of fold change and dispersion for RNA-seq data with DESeq2. Genome Biol. 2014; 15(12):550. PMC: 4302049. DOI: 10.1186/s13059-014-0550-8. View

4.
Labun K, Montague T, Krause M, Torres Cleuren Y, Tjeldnes H, Valen E . CHOPCHOP v3: expanding the CRISPR web toolbox beyond genome editing. Nucleic Acids Res. 2019; 47(W1):W171-W174. PMC: 6602426. DOI: 10.1093/nar/gkz365. View

5.
Leinonen R, Sugawara H, Shumway M . The sequence read archive. Nucleic Acids Res. 2010; 39(Database issue):D19-21. PMC: 3013647. DOI: 10.1093/nar/gkq1019. View