High Temperature Causes Masculinization of Genetically Female Medaka by Elevation of Cortisol

被引:155
作者
Hayashi, Yuki [1 ]
Kobira, Hiroshi [1 ]
Yamaguchi, Toshiya [1 ]
Shiraishi, Eri [1 ]
Yazawa, Takashi [2 ]
Hirai, Toshiaki [3 ]
Kamei, Yasuhiro [4 ]
Kitano, Takeshi [1 ]
机构
[1] Kumamoto Univ, Dept Biol Sci, Grad Sch Sci & Technol, Kumamoto 8608555, Japan
[2] Univ Fukui, Dept Biochem, Fac Med Sci, Fukui 910, Japan
[3] Teikyo Univ Sci, Dept Biosci, Yamanashi, Japan
[4] Natl Inst Basic Biol, NIBB Core Res Facil, Spectrog & Bioimaging Facil, Okazaki, Aichi 444, Japan
关键词
DEPENDENT SEX DETERMINATION; RAT GRANULOSA-CELLS; ORYZIAS-LATIPES; GERM-CELLS; FUNCTIONAL-CHARACTERIZATION; PARALICHTHYS-OLIVACEUS; OVARIAN-FOLLICLES; JAPANESE FLOUNDER; AROMATASE GENE; RAINBOW-TROUT;
D O I
10.1002/mrd.21203
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
In poikilothermic vertebrates, sex determination is sometimes influenced by environmental factors such as temperature. However, little is known about the molecular mechanisms underlying environmental sex determination. The medaka (Oryzias latipes) is a teleost fish with an XX/XY sex determination system. Recently, it was reported that XX medaka can be sex-reversed into phenotypic males by high water temperature (HT; 32-34 degrees C) treatment during the sex differentiation period. Here we report that cortisol caused female-to-male sex reversal and that metyrapone (an inhibitor of cortisol synthesis) inhibited HT-induced masculinization of XX medaka. HT treatment caused elevation of whole-body levels of cortisol, while metyrapone suppressed the elevation by HT treatment during sexual differentiation. Moreover, cortisol and 33 degrees C treatments inhibited female-type proliferation of germ cells as well as expression of follicle-stimulating hormone receptor (fshr) mRNA in XX medaka during sexual differentiation. These results strongly suggest that HT induces masculinization of XX medaka by elevation of cortisol level, which, in turn, causes suppression of germ cell proliferation and of fshr mRNA expression.
引用
收藏
页码:679 / 686
页数:8
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