Institute of Biochemistry I, University of Regensburg, Universitaetsstrasse 31, D-93053 Regensburg, Germany.
Institute of Zoology, University of Regensburg, Universitaetsstrasse 31, D-93053 Regensburg, Germany.
Nucleic Acids Res. 2019 Mar 18;47(5):2276-2288. doi: 10.1093/nar/gky1284.
In Drosophila, female development is governed by a single RNA-binding protein, Sex-lethal (Sxl), that controls the expression of key factors involved in dosage compensation, germline homeostasis and the establishment of female morphology and behaviour. Sxl expression in female flies is maintained by an auto-regulatory, positive feedback loop with Sxl controlling splicing of its own mRNA. Until now, it remained unclear how males prevent accidental triggering of the Sxl expression cascade and protect themselves against runaway protein production. Here, we identify the protein Sister-of-Sex-lethal (Ssx) as an inhibitor of Sxl auto-regulatory splicing. Sxl and Ssx have a comparable RNA-binding specificity and compete for binding to RNA regulatory elements present in the Sxl transcript. In cultured Drosophila cells, Sxl-induced changes to alternative splicing can be reverted by the expression of Ssx. Moreover, in adult male flies ablation of the ssx gene results in a low level of productive Sxl mRNA splicing and Sxl protein production in isolated, clonal cell populations. In sum, this demonstrates that Ssx safeguards male animals against Sxl protein production to reinforce a stable, male-specific gene expression pattern.
在果蝇中,雌性发育受单个 RNA 结合蛋白 Sex-lethal(Sxl)控制,该蛋白控制着参与剂量补偿、生殖细胞稳态以及雌性形态和行为建立的关键因子的表达。Sxl 在雌性果蝇中的表达通过 Sxl 控制自身 mRNA 剪接的自调节正反馈环来维持。到目前为止,人们仍不清楚雄性如何防止 Sxl 表达级联的意外触发,并防止自身免受失控的蛋白质产生的影响。在这里,我们将蛋白 Sister-of-Sex-lethal(Ssx)鉴定为 Sxl 自动调节剪接的抑制剂。Sxl 和 Ssx 具有可比的 RNA 结合特异性,并竞争结合存在于 Sxl 转录本中的 RNA 调节元件。在培养的果蝇细胞中,Ssx 的表达可以逆转 Sxl 诱导的可变剪接变化。此外,在成年雄性果蝇中,ssx 基因的缺失导致在分离的、克隆细胞群中产生低水平的有功能的 Sxl mRNA 剪接和 Sxl 蛋白产生。总之,这表明 Ssx 保护雄性动物免受 Sxl 蛋白产生的影响,以加强稳定的、雄性特异性的基因表达模式。