Sugimoto Takafumi N, Kayukawa Takumi, Shinoda Tetsuro, Ishikawa Yukio, Tsuchida Tsutomu
Graduate School of Science and Engineering, University of Toyama, Toyama, Toyama 930-8555, Japan.
National Institute of Agrobiological Sciences, Ohwashi 1-2, Tsukuba, Ibaraki 305-8634, Japan.
Insect Biochem Mol Biol. 2015 Nov;66:72-6. doi: 10.1016/j.ibmb.2015.10.001. Epub 2015 Oct 8.
Endosymbiotic bacteria of the genus Wolbachia often manipulate the reproductive system of their hosts to propagate themselves in host populations. Ostrinia scapulalis moths infected with Wolbachia (wSca) produce female-only progeny (sex chromosomes: ZW), whereas females cured of the infection by antibiotic treatment produce male-only progeny (ZZ). The occurrence of female- and male-only progeny has been attributed to the specific death of the opposite sex during embryonic and larval development. In this bidirectional sex-specific lethality, embryos destined to die express a phenotypic sex opposite to their genotypic sex. On the basis of these findings, we suggested that wSca carries a genetic factor that feminizes the male host, the W chromosome of the host has lost its feminizing function, and discordance between the genotypic and phenotypic sexes underlies this sex-specific death. In the present study, we examined whether the failure of dosage compensation was responsible for this sex-specific mortality. Quantitative PCRs showed that Z-linked gene expression levels in embryos destined to die were not properly dosage compensated; they were approximately two-fold higher in the male progeny of wSca-infected females and approximately two-fold lower in the female progeny of infected-and-cured females. These results support our hypothesis that misdirection of dosage compensation underlies the sex-specific death.
沃尔巴克氏体属的内共生细菌常常操纵其宿主的生殖系统,以便在宿主种群中自我繁殖。感染了沃尔巴克氏体(wSca)的二化螟蛾只产生雌性后代(性染色体:ZW),而通过抗生素治疗清除感染的雌性则只产生雄性后代(ZZ)。只产生雌性和雄性后代的现象被归因于胚胎期和幼虫期异性的特异性死亡。在这种双向的性别特异性致死现象中,注定死亡的胚胎表现出与其基因型性别相反的表型性别。基于这些发现,我们推测wSca携带一种使雄性宿主雌性化的遗传因子,宿主的W染色体失去了雌性化功能,基因型性别和表型性别的不一致是这种性别特异性死亡的基础。在本研究中,我们检验了剂量补偿失败是否是这种性别特异性死亡的原因。定量PCR结果显示,注定死亡的胚胎中Z连锁基因的表达水平没有得到适当的剂量补偿;在感染wSca的雌性的雄性后代中,其表达水平大约高两倍,而在感染后又治愈的雌性的雌性后代中,其表达水平大约低两倍。这些结果支持了我们的假设,即剂量补偿的错误导向是性别特异性死亡的基础。