Key Laboratory of Insect Developmental and Evolutionary Biology, Institute of Plant Physiology and Ecology, Shanghai Institutes for Biological Sciences, Chinese Academy of Sciences, Shanghai 200032, China.
College of Life Sciences, Shanghai University, Shanghai 200444, China.
Insect Biochem Mol Biol. 2014 Jan;44:1-11. doi: 10.1016/j.ibmb.2013.10.009. Epub 2013 Nov 12.
Doublesex (dsx) is a downstream key regulator in insect sex determination pathway. In Drosophila, alternative splicing of Dm-dsx gene is sex-specifically regulated by transformer (tra), in which the functional TRA promotes female-specific Dm-dsx. However, the sex determination pathway in Lepidoptera is not well understood; here we focused on alternative splicing of doublesex (dsx) in two agricultural pests, Asian corn borer (Ostrinia furnacalis) and cotton bollworm (Helicoverpa armigera), as well as the silkworm (Bombyx mori). More than a dozen new alternative splicing isoforms of dsx were found in the Lepidopteran females, which exist in all tested developmental stages and differentiated tissues. Alignment of mRNA and protein sequences of doublesex revealed high conservation of this gene in Lepidoptera. Strength analysis of splice sites revealed a weak 5' splice site at intron 3 in Lepidopteran dsx, which was experimentally confirmed. Furthermore, we identified highly conserved RNA sequences in the Lepidopteran dsx, including RNA elements I (14 nt), II (11 nt), III (26 nt), IV (17 nt), 3E-1 (8 nt) and 3E-2 (8 nt). The RNA elements III and IV were previously found in exon 4 of B. mori dsx and bound with Bm-PSI, which suppressed the inclusion of exons 3 & 4 into the male-specific Bm-dsx. Then we identified and analyzed the homologous genes of Bm-psi in the two Lepidopteran pests, which expressed at similar levels and exhibited a unique isoform in the males and females from each Lepidoptera. Importantly, mutagenesis of Bm-dsx mini-genes and their expression in BmN cell line demonstrated that three RNA elements are involved in the female-specific alternative splicing of Bm-dsx. Mutations in the RNA cis-elements 3E-1 and 3E-2 resulted in decreased inclusion of exon 3 into the female-specific dsx mRNA, suggesting that these two elements would be exonic splicing enhancers that facilitate the recognition of the weak 5' splice site at intron 3 of Lepidopteran dsx. We propose that the 5' splice sites at intron 3 are weak, resulting in multiple alternative splicing events in intron 3 of female Lepidoptera dsx. Activation of the 5' splice site requires regulatory cis-elements in exons 3 for female-specific splicing of Lepidoptera dsx.
双性基因(dsx)是昆虫性别决定途径中的一个下游关键调控因子。在果蝇中,Dm-dsx 基因的选择性剪接由转座因子(tra)特异性调控,其中功能性 TRA 促进了雌性特异性的 Dm-dsx。然而,鳞翅目昆虫的性别决定途径尚不清楚;在这里,我们专注于两种农业害虫,亚洲玉米螟(Ostrinia furnacalis)和棉铃虫(Helicoverpa armigera),以及家蚕(Bombyx mori)中 doublesex(dsx)的选择性剪接。在鳞翅目雌性中发现了十几个新的 dsx 选择性剪接异构体,这些异构体存在于所有测试的发育阶段和分化组织中。dsx 基因的 mRNA 和蛋白质序列比对表明该基因在鳞翅目昆虫中高度保守。剪接位点的强度分析表明,在鳞翅目 dsx 的内含子 3 中存在一个较弱的 5'剪接位点,这一结果在实验中得到了证实。此外,我们在鳞翅目 dsx 中鉴定了高度保守的 RNA 序列,包括 RNA 元件 I(14 nt)、II(11 nt)、III(26 nt)、IV(17 nt)、3E-1(8 nt)和 3E-2(8 nt)。RNA 元件 III 和 IV 以前在 B. mori dsx 的外显子 4 中被发现,并与 Bm-PSI 结合,后者抑制了外显子 3 和 4 被包含到雄性特异性的 Bm-dsx 中。然后,我们在两种鳞翅目害虫中鉴定并分析了 Bm-psi 的同源基因,这些基因在每个鳞翅目动物的雄性和雌性中以相似的水平表达,并表现出一种独特的异构体。重要的是,Bm-dsx 迷你基因的突变及其在 BmN 细胞系中的表达表明,三个 RNA 元件参与了 Bm-dsx 的雌性特异性选择性剪接。RNA 顺式元件 3E-1 和 3E-2 的突变导致外显子 3 被包含到雌性特异性 dsx mRNA 中的比例降低,这表明这两个元件可能是外显子剪接增强子,促进了对鳞翅目 dsx 内含子 3 中较弱的 5'剪接位点的识别。我们提出,内含子 3 中的 5'剪接位点较弱,导致雌性鳞翅目 dsx 内含子 3 中发生多种选择性剪接事件。激活 5'剪接位点需要外显子 3 中的调节顺式元件,以实现鳞翅目 dsx 的雌性特异性剪接。