Abstract

In crustaceans, the regulation of sex differentiation is mediated by insulin-like androgenic hormone (IAG) and crustacean female sex hormone (CFSH). CFSH is reported to inhibit IAG gene (Sp-IAG) expression in the mud crab Scylla paramamosain, but the regulatory mechanism is not well understood. A 2674 bp 5′ flanking Sp-IAG contains many potential transcription factor binding sites. In this study, analysis of serially deleted 5′ flanking Sp-IAG and site-directed mutation (SDM) of transcription factor binding sites of the same gene showed that the promoter activity of reporter vectors with Sox-5-binding site, signal transducers and activators of transcription (STAT)-binding site and activator protein 1 (AP-1)-binding site were significantly higher than that of vectors without these regions, suggesting that they were involved in transcriptional regulation of Sp-IAG expression. The expression analysis of these transcription factor showed that there was no difference in the level of mRNA in Sox-5 and AP-1 in androgenic gland treated with recombinant CFSH, but expression of Sp-STAT was significantly reduced, suggesting that CFSH regulates the expression of Sp-STAT, inhibiting its function to regulate Sp-IAG. Further experiment revealed that RNAi mediated Sp-STAT gene knockdown reduced the expression of Sp-IAG. These results suggested that Sp-CFSH regulates Sp-IAG by inhibiting STAT. This is a pioneering finding on the transcriptional mechanism of IAG gene in crustaceans.

Highlights

  • Dimorphic traits are widespread in various species, and rely on changes initiated and maintained by key reproductive hormones [1,2]

  • Results the mechanism of insulin-like androgenic hormone (IAG) inhibition by crustacean female sex hormone (CFSH). This process was explored in S. paramamosain by analyzing transcriptional mechanism of IAG and expression of transcription factors in androgenic gland (AG) treated with CFSH in vitro

  • EGFP were detected in HEK293FT cells transfected with pEGFP-N1 (A), pEGFP-pSpIAG (B), and pEGFP-1 (C). pEGFP-N1 and pEGFP-1 were used as positive control and negative control, respectively

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Summary

Introduction

Dimorphic traits are widespread in various species, and rely on changes initiated and maintained by key reproductive hormones [1,2]. Sex differentiation is largely controlled by the androgenic gland (AG) [3]. CDNA for androgenic gland hormone (AGH) from terrestrial isopod Armadillidium vulgare was isolated and characterized [5]. Removing AG or silencing the gene for AGH, as well as AG implantation or injection of AG extracts has been shown to affect primary and secondary sex characteristics in various crustacean species, including A. vulgare, the red-claw crayfish Cherax quadricarinatus and the giant freshwater prawn Macrobrachium rosenbergii [6,7,8,9,10,11]. In M. rosenbergii, removal of the AG caused sex reversal in juvenile males, while silencing Mr-AGH resulted in hypertrophy of AG and arrested testicular spermatogenesis [12,13]

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