Institute of Molecular Systems Biology, ETH Zürich, Zürich, Switzerland.
PLoS One. 2020 Feb 14;15(2):e0228995. doi: 10.1371/journal.pone.0228995. eCollection 2020.
Genetically encoded pH indicators (GEpHI) have emerged as important tools for investigating intracellular pH (pHi) dynamics in Drosophila. However, most of the indicators are based on the Gal4/UAS binary expression system. Here, we report the generation of a ubiquitously-expressed GEpHI. The fusion protein of super ecliptic pHluorin and FusionRed was cloned under the tubulin promoter (tpHusion) to drive it independently of the Gal4/UAS system. The function of tpHusion was validated in various tissues from different developmental stages of Drosophila. Differences in pHi were also indicated correctly in fixed tissues. Finally, we describe the use of tpHusion for comparative analysis of pHi in manipulated clones and the surrounding cells in epithelial tissues. Our findings establish tpHusion as a robust tool for studying pHi in Drosophila.
基因编码的 pH 指示剂(GEpHI)已成为研究果蝇细胞内 pH(pHi)动力学的重要工具。然而,大多数指示剂都是基于 Gal4/UAS 二元表达系统。在这里,我们报告了一种普遍表达的 GEpHI 的产生。超荧光素酶和 FusionRed 的融合蛋白在微管蛋白启动子(tpHusion)的控制下被克隆,使其独立于 Gal4/UAS 系统。tpHusion 的功能在果蝇不同发育阶段的不同组织中得到了验证。在固定组织中也正确地显示了 pH 值的差异。最后,我们描述了 tpHusion 在比较分析上皮组织中处理过的克隆和周围细胞的 pH 值方面的应用。我们的研究结果确立了 tpHusion 作为研究果蝇 pHi 的有力工具。