Department of Molecular Biosciences, University of Kansas, Lawrence, Kansas, United States of America.
PLoS One. 2010 Nov 12;5(11):e15448. doi: 10.1371/journal.pone.0015448.
The Drosophila melanogaster gurken gene encodes a TGF alpha-like signaling molecule that is secreted from the oocyte during two distinct stages of oogenesis to define the coordinate axes of the follicle cell epithelium that surrounds the oocyte and its 15 anterior nurse cells. Because the gurken receptor is expressed throughout the epithelium, axial patterning requires region-specific secretion of Gurken protein, which in turn requires subcellular localization of gurken transcripts. The first stage of Gurken signaling induces anteroposterior pattern in the epithelium and requires the transport of gurken transcripts from nurse cells into the oocyte. The second stage of Gurken signaling induces dorsovental polarity in the epithelium and requires localization of gurken transcripts to the oocyte's anterodorsal corner. Previous studies, relying predominantly on real-time imaging of injected transcripts, indicated that anterodorsal localization involves transport of gurken transcripts to the oocyte's anterior cortex followed by transport to the anterodorsal corner, and anchoring. Such studies further indicated that a single RNA sequence element, the GLS, mediates both transport steps by facilitating association of gurken transcripts with a cytoplasmic dynein motor complex. Finally, it was proposed that the GLS somehow steers the motor complex toward that subset of microtubules that are nucleated around the oocyte nucleus, permitting directed transport to the anterodorsal corner. Here, we re-investigate the role of the GLS using a transgenic fly assay system that includes use of the endogenous gurken promoter and biological rescue as well as RNA localization assays. In contrast to previous reports, our studies indicate that the GLS is sufficient for anterior localization only. Our data support a model in which anterodorsal localization is brought about by repeated rounds of anterior transport, accompanied by specific trapping at the anterodorsal cortex. Our data further indicate that trapping at the anterodorsal corner requires at least one as-yet-unidentified gurken RLE.
果蝇 gurken 基因编码一种 TGF alpha 样信号分子,该分子在卵子发生的两个不同阶段从卵母细胞中分泌出来,以定义围绕卵母细胞及其 15 个前护卵细胞的滤泡细胞上皮的协调轴。由于 gurken 受体在整个上皮细胞中表达,轴突模式需要 gurken 蛋白的区域特异性分泌,而 gurken 转录本的亚细胞定位又需要 gurken 转录本的亚细胞定位。Gurken 信号的第一阶段在上皮细胞中诱导前后模式,并需要将 gurken 转录本从护卵细胞运输到卵母细胞中。Gurken 信号的第二阶段在上皮细胞中诱导背腹极性,并需要将 gurken 转录本定位到卵母细胞的前背角。以前的研究主要依赖于注射转录本的实时成像,表明前背定位涉及 gurken 转录本向卵母细胞的前皮质的运输,然后向前背角的运输,以及锚定。这些研究进一步表明,单个 RNA 序列元件 GLS 通过促进 gurken 转录本与细胞质动力蛋白复合物的结合,介导这两个运输步骤。最后,有人提出 GLS 以某种方式引导动力复合物朝向围绕卵母细胞核形成的微管子集,从而允许定向运输到前背角。在这里,我们使用包括使用内源性 gurken 启动子和生物拯救以及 RNA 定位测定的转基因果蝇测定系统重新研究 GLS 的作用。与以前的报告相反,我们的研究表明,GLS 仅足以进行前定位。我们的数据支持这样一种模型,即前背定位是通过前向运输的反复循环引起的,同时在前背皮质处进行特异性捕获。我们的数据进一步表明,在前背角的捕获需要至少一个尚未确定的 gurken RLE。