Dipartimento Biologia Evoluzionistica Sperimentale, Università di Bologna, Via Selmi 3, Bologna, Italy.
Cell Mol Life Sci. 2010 May;67(10):1699-712. doi: 10.1007/s00018-010-0273-2. Epub 2010 Feb 6.
Polydnavirus-encoded IkappaB-like proteins are similar to insect and mammalian IkappaB, and an immunosuppressive function in the host cells has been inferred to these proteins. Here we show that the expression of one of these IkappaB-like viral genes, the TnBVank1, in the Drosophila germline affects the localization of gurken, bicoid, and oskar mRNAs whose gene products are relevant for proper embryonic patterning. The altered localization of these mRNAs is suggestive of general defects in the intracellular, microtubule-based, trafficking routes. Analysis of microtubule motor proteins components such as the dynein heavy chain and the kinesin heavy chain revealed defects in the polarized microtubule network. Interestingly, the TnBVANK1 viral protein is uniformly distributed over the entire oocyte cortex, and appears to be anchored to the microtubule ends. Our data open up a very interesting issue on novel function(s) played by the ank gene family by interfering with cytoskeleton organization.
多粒包埋型病毒编码的 IkappaB 样蛋白类似于昆虫和哺乳动物的 IkappaB,并且这些蛋白在宿主细胞中被推断具有免疫抑制功能。在这里,我们表明,这些 IkappaB 样病毒基因之一,即 TnBVank1,在果蝇生殖细胞系中的表达会影响 gurken、bicoid 和 oskar mRNA 的定位,这些 mRNA 的产物与胚胎正确的模式形成有关。这些 mRNA 的定位改变表明细胞内微管为基础的运输途径存在普遍缺陷。对微管马达蛋白成分(如动力蛋白重链和驱动蛋白重链)的分析显示,极化微管网络存在缺陷。有趣的是,TnBVANK1 病毒蛋白均匀分布在整个卵母细胞皮层上,并且似乎锚定在微管末端。我们的数据提出了一个非常有趣的问题,即 ank 基因家族通过干扰细胞骨架组织来发挥新的功能。