RT Journal Article SR Electronic T1 A pituitary gene network linking vgll3 to regulators of sexual maturation in male Atlantic salmon JF bioRxiv FD Cold Spring Harbor Laboratory SP 2022.06.20.496813 DO 10.1101/2022.06.20.496813 A1 Ehsan Pashay Ahi A1 Marion Sinclair-Waters A1 Iikki Donner A1 Craig R. Primmer YR 2022 UL http://biorxiv.org/content/early/2022/06/21/2022.06.20.496813.abstract AB Age at maturity is a key life history trait and a significant contributor to life history strategy variation. The maturation process is complex and influenced by genetic and environmental factors alike, but specific causes of variation in maturation timing remain elusive. In many species, the increase in the regulatory gonadotropin-releasing hormone 1 (GnRH1) marks the onset of puberty. Atlantic salmon, however, lack the gene encoding GnRH1, suggesting other regulatory factors are involved in the maturation process. Earlier research in Atlantic salmon has found a strong association between alternative alleles of vgll3 and maturation timing, making vgll3 a candidate reproductive axis gene regulator. Recently we reported strong induction of gonadotropin encoding genes (fshb and lhb) in the pituitary of male Atlantic salmon homozygous for the vgll3 allele linked with the early maturation allele (E). The induction of gonadotropins was accompanied by increased expression of their direct upstream regulators, c-jun and sf1 (nr5a1b) in the pituitary. In mammals, the transcriptional activation of c-jun and sf1 is also required for induction of fshb and lhb, however, GnRH1 is responsible for increased transcriptional activity of c-jun and sf1. The absence of gnrh1 in salmon raises the possibility of the involvement of other regulators upstream of these factors. In this study, we investigated such a possibility through a stepwise approach for identifying a gene regulatory network (GRN) containing c-jun and sf1 and using the zebrafish coexpression database and transcription factor motif enrichment analysis. We found a GRN containing c-jun with predicted upstream regulators, e2f1, egr1, foxj1 and klf4, which are also differentially expressed in the pituitary. Finally, we suggest a model for transcriptional regulation of c-jun and sf1in the absence of gnrh1 in the pituitary, which may have broader implications across vertebrates.Competing Interest StatementThe authors have declared no competing interest.