Yan Dong, Perrimon Norbert
Department of Genetics, Harvard Medical School, Boston, MA 02115;
Department of Genetics, Harvard Medical School, Boston, MA 02115; Howard Hughes Medical Institute, Harvard Medical School, Boston, MA 02115
Proc Natl Acad Sci U S A. 2015 Sep 15;112(37):11606-11. doi: 10.1073/pnas.1515891112. Epub 2015 Aug 31.
Sex-lethal (Sxl) encodes the master regulator of the sex determination pathway in Drosophila and acts by controlling sex identity in both soma and germ line. In females Sxl maintains its own expression by controlling the alternative splicing of its own mRNA. Here, we identify a novel sex determination gene, spenito (nito) that encodes a SPEN family protein. Loss of nito activity results in stem cell tumors in the female germ line as well as female-to-male somatic transformations. We show that Nito is a ubiquitous nuclear protein that controls the alternative splicing of the Sxl mRNA by interacting with Sxl protein and pre-mRNA, suggesting that it is directly involved in Sxl auto-regulation. Given that SPEN family proteins are frequently mutated in cancers, our results suggest that these factors might be implicated in tumorigenesis through splicing regulation.
性别致死基因(Sex-lethal,Sxl)编码果蝇性别决定途径的主要调节因子,并通过控制体细胞和生殖系中的性别特征发挥作用。在雌性果蝇中,Sxl通过控制自身mRNA的可变剪接来维持自身表达。在此,我们鉴定出一个新的性别决定基因——spenito(nito),它编码一种SPEN家族蛋白。nito活性缺失会导致雌性生殖系中的干细胞肿瘤以及雌性向雄性的体细胞转化。我们发现Nito是一种普遍存在的核蛋白,它通过与Sxl蛋白和前体mRNA相互作用来控制Sxl mRNA的可变剪接,这表明它直接参与Sxl的自我调节。鉴于SPEN家族蛋白在癌症中经常发生突变,我们的研究结果表明,这些因子可能通过剪接调节参与肿瘤发生。