Sakai Hiroki, Sakaguchi Honami, Aoki Fugaku, Suzuki Masataka G
Department of Integrated Biosciences, Graduate School of Frontier Sciences, The University of Tokyo, Kashiwa, Japan.
Department of Integrated Biosciences, Graduate School of Frontier Sciences, The University of Tokyo, Kashiwa, Japan.
Mech Dev. 2015 Aug;137:45-52. doi: 10.1016/j.mod.2015.03.002. Epub 2015 Mar 28.
The sexual fate of B. mori is determined genetically; ZW, female and ZZ, male. Recently, we successfully identified a strong candidate gene at the top of the sex determination cascade in B. mori. This gene was termed Feminizer (Fem) and revealed to be a source of Fem-piRNA. Further, we found that B. mori doublesex (Bmdsx) splicing was markedly altered to produce the male-type isoform when a Fem-piRNA inhibitor was injected into ZW embryos. Moreover, knockdown of Masculinizer (Masc), a Fem-piRNA target gene, altered to produce the female-type isoform of Bmdsx in male embryos. However, it remains unclear as to whether Masc directly regulates the sex-specific expression of Bmdsx. In previous studies, we determined that the male-specific isoform of the Bombyx homolog of IGF-II mRNA-binding protein (Imp(M)) was involved in the male-specific splicing of Bmdsx. In an attempt to clarify the genetic relationship between Fem, Masc, Imp(M), and Bmdsx, knockdown experiments were performed. Knockdown of Fem shifted into male-type Bmdsx, Imp(M) and Masc in female embryos. Knockdown of Masc led to the production of the female-type Bmdsx and a dramatic reduction in Imp(M) expression in male embryos. Knockdown of Imp(M) shifted Bmdsx splice mode from the male-type into the female-type. Our results suggest that: (1) Fem reduces Masc expression, (2) Masc dramatically induces Imp(M) expression, and (3) Imp(M) shifting Bmdsx splice mode from the female-type into the male-type. Based on these findings, we propose a possible genetic cascade regulating sex determination in B. mori.
家蚕的性别命运由基因决定;ZW为雌性,ZZ为雄性。最近,我们成功地在家蚕性别决定级联反应的顶端鉴定出一个强有力的候选基因。该基因被命名为“雌性化因子”(Fem),并被发现是Fem-piRNA的来源。此外,我们发现,当将Fem-piRNA抑制剂注入ZW胚胎时,家蚕双性基因(Bmdsx)的剪接会发生显著改变,从而产生雄性类型的异构体。此外,敲低Fem-piRNA靶基因“雄性化因子”(Masc),会使雄性胚胎中Bmdsx产生雌性类型的异构体。然而,Masc是否直接调节Bmdsx的性别特异性表达仍不清楚。在之前的研究中,我们确定胰岛素样生长因子-II mRNA结合蛋白(Imp(M))的家蚕同源物的雄性特异性异构体参与了Bmdsx的雄性特异性剪接。为了阐明Fem、Masc、Imp(M)和Bmdsx之间的遗传关系,我们进行了敲低实验。敲低Fem会使雌性胚胎中的Bmdsx、Imp(M)和Masc转变为雄性类型。敲低Masc会导致雄性胚胎中产生雌性类型的Bmdsx,并且Imp(M)的表达显著降低。敲低Imp(M)会使Bmdsx的剪接模式从雄性类型转变为雌性类型。我们的结果表明:(1)Fem降低Masc的表达,(2)Masc显著诱导Imp(M)的表达,(3)Imp(M)将Bmdsx的剪接模式从雌性类型转变为雄性类型。基于这些发现,我们提出了一种可能的调节家蚕性别决定的遗传级联反应。