Otake Hiroyuki, Shinomiya Ai, Matsuda Masaru, Hamaguchi Satoshi, Sakaizumi Mitsuru
Graduate School of Science and Technology, Department of Environmental Science, Faculty of Science, Niigata University, Japan.
Genetics. 2006 Aug;173(4):2083-90. doi: 10.1534/genetics.106.058941. Epub 2006 May 15.
The medaka, Oryzias latipes, has an XX/XY sex-determination mechanism. A Y-linked DM domain gene, DMY, has been isolated by positional cloning as a sex-determining gene in this species. Previously, we found 23 XY sex-reversed females from 11 localities by examining the genotypic sex of wild-caught medaka. Genetic analyses revealed that all these females had Y-linked gene mutations. Here, we aimed to clarify the cause of this sex reversal. To achieve this, we screened for mutations in the amino acid coding sequence of DMY and examined DMY expression at 0 days after hatching (dah) using densitometric semiquantitative RT-PCR. We found that the mutants could be classified into two groups. One contained mutations in the amino acid coding sequence of DMY, while the other had reduced DMY expression at 0 dah although the DMY coding sequence was normal. For the latter, histological analyses indicated that YwOurYwOur (YwOur, Y chromosome derived from an Oura XY female) individuals with the lowest DMY expression among the tested mutants were expected to develop into females at 0 dah. These results suggest that early testis development requires DMY expression above a threshold level. Mutants with reduced DMY expression may prove valuable for identifying DMY regulatory elements.
青鳉(Oryzias latipes)具有XX/XY性别决定机制。通过定位克隆已分离出一个Y连锁的DM结构域基因DMY,作为该物种的性别决定基因。此前,我们通过检查野生捕获青鳉的基因型性别,从11个地点发现了23只XY性反转雌性个体。遗传分析表明,所有这些雌性个体都有Y连锁基因突变。在此,我们旨在阐明这种性反转的原因。为实现这一目标,我们筛选了DMY氨基酸编码序列中的突变,并使用光密度半定量RT-PCR检测了孵化后0天(dah)时的DMY表达。我们发现这些突变体可分为两组。一组在DMY氨基酸编码序列中有突变,而另一组虽然DMY编码序列正常,但在0 dah时DMY表达降低。对于后者,组织学分析表明,在所测试的突变体中,DMY表达最低的YwOurYwOur(YwOur,源自Oura XY雌性的Y染色体)个体预计在0 dah时发育为雌性。这些结果表明,早期睾丸发育需要DMY表达高于阈值水平。DMY表达降低的突变体可能对鉴定DMY调控元件具有重要价值。