Ukita Yumiko, Suzuki Ryoka, Miyoshi Keita, Saito Kuniaki, Okumura Misako, Chihara Takahiro
Program of Biomedical Science, Graduate School of Integrated Sciences for Life, Hiroshima University, Higashi-Hiroshima, Hiroshima, Japan.
Department of Chromosome Science, National Institute of Genetics, Research Organization of Information and Systems (ROIS), Shizuoka, Japan.
Genes Cells. 2025 Jul;30(4):e70028. doi: 10.1111/gtc.70028.
Drosophila melanogaster has provided numerous insights into the olfactory system, primarily relying on a series of transgenic Gal4 drivers. The combined use of Gal4/UAS and a second binary expression system, such as the QF/QUAS system, provides the opportunity to manipulate the two distinct cell populations, thereby accelerating the elucidation of the olfactory neural mechanisms. However, resources apart from the Gal4/UAS system have been poorly developed. In this study, we generated a series of odorant receptor (Or)-QF2 knock-in driver (Or-QF2) lines for 23 Ors using the CRISPR/Cas9 knock-in method. In these lines, the QF2 protein is cotranslated with each Or product. The expression pattern of the Or-QF2 drivers mostly corresponded to that of the Or-Gal4 drivers. In addition, the Or42a-QF2 driver identified the additional expression pattern of Or42a, which is consistent with the data of single-nucleus RNA sequencing and is attributed to the Or-QF2 drivers' ability to reflect the endogenous expression of the Or genes. Thus, these Or-QF2 drivers can be used as valuable genetic tools for olfactory research in Drosophila.
黑腹果蝇为嗅觉系统提供了诸多见解,主要依赖于一系列转基因Gal4驱动子。Gal4/UAS与第二个二元表达系统(如QF/QUAS系统)的联合使用,为操纵两个不同的细胞群体提供了机会,从而加速了对嗅觉神经机制的阐明。然而,除了Gal4/UAS系统之外的资源开发得很差。在本研究中,我们使用CRISPR/Cas9敲入方法为23种气味受体(Or)生成了一系列气味受体-QF2敲入驱动子(Or-QF2)品系。在这些品系中,QF2蛋白与每种Or产物共翻译。Or-QF2驱动子的表达模式大多与Or-Gal4驱动子的表达模式相对应。此外,Or42a-QF2驱动子确定了Or42a的额外表达模式,这与单核RNA测序的数据一致,并且归因于Or-QF2驱动子反映Or基因内源性表达的能力。因此,这些Or-QF2驱动子可用作果蝇嗅觉研究中有价值的遗传工具。