An efficient and multiple target transgenic RNAi technique with low toxicity in Drosophila. Issue 1 (December 2018)

• Record Type: Journal Article
• Authors: Qiao, Huan-Huan; Wang, Fang; Xu, Rong-Gang; Sun, Jin; Zhu, Ruibao; Mao, Decai; Ren, Xingjie; Wang, Xia; Jia, Yu; Peng, Ping; Shen, Da; Liu, Lu-Ping; Chang, Zhijie; Wang, Guirong; Li, Shao; Ji, Jun-Yuan; Liu, Qingfei; Ni, Jian-Quan
• Is Part Of: Nature communications. Volume 9:Issue 1(2018)
• Page Start: 1
• Page End: 13
• Publication Date: 2018-12
• Subjects: Biology -- Periodicals; Physical sciences -- Periodicals; 505
• DOI: 10.1038/s41467-018-06537-y
• Languages: English
• ISSNs: 2041-1723

Abstract

Abstract Being relatively simple and practical, Drosophila transgenic RNAi is the technique of top priority choice to quickly study genes with pleiotropic functions. However, drawbacks have emerged over time, such as high level of false positive and negative results. To overcome these shortcomings and increase efficiency, specificity and versatility, we develop a next generation transgenic RNAi system. With this system, the leaky expression of the basal promoter is significantly reduced, as well as the heterozygous ratio of transgenic RNAi flies. In addition, it has been first achieved to precisely and efficiently modulate highly expressed genes. Furthermore, we increase versatility which can simultaneously knock down multiple genes in one step. A case illustration is provided of how this system can be used to study the synthetic developmental effect of histone acetyltransferases. Finally, we have generated a collection of transgenic RNAi lines for those genes that are highly homologous to human disease genes. Drosophila transgenic RNAi can have drawbacks such as false positives and negative results. Here the authors develop a next generation RNAi system with reduced leakiness of expression and simultaneous knockdown.