2004
DOI: 10.1016/j.bbrc.2004.07.162
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Sexually dimorphic expression of a teleost homologue of Müllerian inhibiting substance during gonadal sex differentiation in Japanese flounder, Paralichthys olivaceus

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Cited by 122 publications
(77 citation statements)
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“…For instance, in this case, amh was expressed predominantly in the somatic cells of the medullar area of the gonads of putative males, which is devoid of germ cells and where eventually the efferent ducts are formed. This pattern of distribution agrees with reports for Japanese flounder (Yoshinaga et al, 2004), rainbow trout (Baron et al, 2005), zebrafish (Rodríguez-Mari et al, 2005), and Japanese eel (Miura et al, 2002) and suggests that amh plays a similar role, probably related to the formation of the efferent ducts, in these four teleost species.…”
Section: Discussionsupporting
confidence: 90%
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“…For instance, in this case, amh was expressed predominantly in the somatic cells of the medullar area of the gonads of putative males, which is devoid of germ cells and where eventually the efferent ducts are formed. This pattern of distribution agrees with reports for Japanese flounder (Yoshinaga et al, 2004), rainbow trout (Baron et al, 2005), zebrafish (Rodríguez-Mari et al, 2005), and Japanese eel (Miura et al, 2002) and suggests that amh plays a similar role, probably related to the formation of the efferent ducts, in these four teleost species.…”
Section: Discussionsupporting
confidence: 90%
“…On the other hand, most teleost fish do not have Mü llerian ducts but they do possess an amh homologue that usually shows a sexually dimorphic expression profiles during gonadal sex differentiation and/or adulthood. For example in Japanese flounder (Yoshinaga et al 2004), zebrafish (Rodrí-guez-Mari et al, 2005;Wang and Orban, 2007), and rainbow trout (Baron et al, 2005), amh is first expressed at low levels in the undifferentiated gonads of both sexes and then at higher levels in the male gonads compared with those of females during the process of gonadal sex differentiation. A sex-related difference in gene expression during this process was also observed in the amh type II receptor, but not in amh itself in the Japanese medaka (Kluver et al, 2007).…”
Section: Introductionmentioning
confidence: 99%
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“…Immature Sertoli cells around the spermatogonia are the source for Amh in fish testis (Miura et al 2002, Yoshinaga et al 2004, Vizziano et al 2008. One effect of 11-KT (or testosterone in mammals) in a complex regulative network is the down-regulation of Amh (Al-Attar et al 1997, Miura et al 2002, Rey et al 2003.…”
Section: Role Of 11-kt In Stable D-malesmentioning
confidence: 99%
“…Upregulation of amh expression has been observed during TIM in Japanese flounder (Yoshinaga et al 2004, Kitano et al 2007, Yamaguchi & Kitano 2012, Southern flounder (Paralichthys lethostigma; Mankiewicz et al 2013), Nile tilapia (Oreochromis niloticus; Poonlaphdecha et al 2013) and pejerrey (Fernandino et al 2008), and likewise during protogynous sex change in ricefield eel (Monopterus albus) (Hu et al 2015). Acting as a transcription factor, the Amh protein is also known to directly inhibit the cyp19a1a expression in mammals, and an inverse association between amh and cyp19a1a expression is reported in numerous fishes, including Japanese flounder (Kitano et al 2007), pejerrey (Fernandino et al 2008), rainbow trout (Vizziano et al 2008), southern flounder (Mankiewicz et al 2013) and zebrafish (Danio rerio; Rodríguez-Marí et al 2005, Wang & Orban 2007.…”
Section: Upregulation Of Amh Promoting Gonadal Apoptosis and Malenessmentioning
confidence: 99%