Pauli D, Oliver B, Mahowald A P
Department of Genetics, Case Western Reserve University, Cleveland, OH 44106.
Development. 1993 Sep;119(1):123-34. doi: 10.1242/dev.119.1.123.
The locus ovarian tumor (otu) is involved in several aspects of oogenesis in Drosophila melanogaster. The possible role of otu in the determination of the sexual identity of germ cells has not been extensively explored. Some otu alleles produce a phenotype known as ovarian tumors: ovarioles are filled with numerous poorly differentiated germ cells. We show that these mutant germ cells have a morphology similar to primary spermatocytes and that they express male germ line-specific reporter genes. This indicates that they are engaged along the male pathway of germ line differentiation. Consistent with this conclusion, we found that the splicing of Sex-lethal (Sxl) pre-mRNAs occurs in the male-specific mode in otu-transformed germ cells. The position of the otu locus in the regulatory cascade of germ line sex determination has been studied by using mutations that constitutively express the feminizing activity of the Sxl gene. The sexual transformation of the germ cells observed with several combinations of otu alleles can be reversed by constitutive expression of Sxl. This shows that otu acts upstream of Sxl in the process of germ line sex determination. Other phenotypes of otu mutations were not rescued by constitutive expression of Sxl, suggesting that several functions of otu are likely to be independent of sex determination. Finally, we show that the gene dosage of otu modifies the phenotype of ovaries heterozygous for the dominant alleles of ovo, another gene involved in germ line sex determination. One dose of otu+ enhances the ovoD ovarian phenotypes, while three doses partially suppress these phenotypes. Synergistic interaction between ovoD1 and otu alleles leads to the occasional transformation of chromosomally female germ cells into early spermatocytes. These interactions are similar to those observed between ovoD and one allele of the sans fille (snf) locus. Altogether, our results imply that the otu locus acts, along with ovo, snf, and Sxl, in a pathway (or parallel pathways) required for proper sex determination of the female germ line.
卵巢肿瘤(otu)基因座参与了黑腹果蝇卵子发生的多个方面。otu在生殖细胞性别身份决定中的可能作用尚未得到广泛研究。一些otu等位基因产生一种被称为卵巢肿瘤的表型:卵巢小管中充满了许多分化不良的生殖细胞。我们发现这些突变的生殖细胞具有与初级精母细胞相似的形态,并且它们表达雄性生殖系特异性报告基因。这表明它们沿着雄性生殖系分化途径发育。与这一结论一致,我们发现性致死(Sxl)前体mRNA的剪接在otu转化的生殖细胞中以雄性特异性模式发生。通过使用组成型表达Sxl基因雌性化活性的突变,研究了otu基因座在生殖细胞性别决定调控级联中的位置。用几种otu等位基因组合观察到的生殖细胞性转化可以通过Sxl的组成型表达来逆转。这表明在生殖细胞性别决定过程中,otu在Sxl的上游起作用。Sxl的组成型表达不能挽救otu突变的其他表型,这表明otu的几种功能可能独立于性别决定。最后,我们表明otu的基因剂量改变了卵巢的表型,该卵巢对于另一个参与生殖细胞性别决定的基因ovo的显性等位基因是杂合的。一份otu +增强了ovoD卵巢表型,而三份则部分抑制了这些表型。ovoD1和otu等位基因之间的协同相互作用导致染色体雌性生殖细胞偶尔转化为早期精母细胞。这些相互作用类似于在ovoD和无女儿(snf)基因座的一个等位基因之间观察到的相互作用。总之,我们的结果表明otu基因座与ovo、snf和Sxl一起,在雌性生殖细胞正确性别决定所需的一条途径(或平行途径)中发挥作用。