State Key Laboratory of Cellular Stress Biology, Innovation Center for Cell Signal Network, School of Life Sciences, Xiamen University, Xiamen, Fujian 361102, China.
State Key Laboratory of Cellular Stress Biology, Innovation Center for Cell Signal Network, School of Life Sciences, Xiamen University, Xiamen, Fujian 361102, China.
Mol Biochem Parasitol. 2021 Jan;241:111346. doi: 10.1016/j.molbiopara.2020.111346. Epub 2020 Dec 8.
The auxin-inducible degron (AID) system is a robust chemical-genetic method for manipulating endogenous protein level by conditional proteasomal degradation via a small molecule. So far, this system has not been adapted in the P. yoelii, an important and widely used Plasmodium rodent parasite model for malaria biology. Here, using the CRISPR/Cas9 genome editing method, we generated two marker-free transgenic P. yoelii parasite lines (eef1a-Tir1 and soap-Tir1) stably expressing the Oryza sativa gene tir1 under the promoters of eef1a and soap respectively. These two lines develop normally during the parasite life cycle. In these backgrounds, we used the CRISPR/Cas9 method to tag two genes (cdc50c and fbxo1) with the AID motif and interrogate the expression of these two proteins with auxin. The eef1a-Tir1 line allows efficient degradation of the AID-tagged endogenous protein in the asexual schizont and sexual gametocyte stages, while the soap-Tir1 line allows protein degradation in the ookinetes. These two lines will be a useful resource for studying the Plasmodium parasite biology based on the P. yoelii.
生长素诱导的降解结构域(AID)系统是一种通过小分子进行条件性蛋白酶体降解来操纵内源性蛋白质水平的强大的化学遗传学方法。到目前为止,该系统尚未在疟原虫(Plasmodium)中得到应用,疟原虫是一种重要且广泛使用的用于疟疾生物学研究的啮齿动物寄生虫模型。在这里,我们使用 CRISPR/Cas9 基因组编辑方法,生成了两条无标记的转基因 P. yoelii 寄生虫系(eef1a-Tir1 和 soap-Tir1),它们分别在 eef1a 和 soap 启动子的控制下稳定表达水稻基因 tir1。这两条寄生虫系在寄生虫生命周期中正常发育。在这些背景下,我们使用 CRISPR/Cas9 方法标记了两个基因(cdc50c 和 fbxo1),并将 AID 基序与生长素一起用于研究这两个蛋白的表达情况。eef1a-Tir1 系允许在无性裂殖体和有性配子体阶段高效降解 AID 标记的内源性蛋白,而 soap-Tir1 系允许在动合子阶段降解蛋白。这两个系将成为基于 P. yoelii 研究疟原虫寄生虫生物学的有用资源。