Itokawa Kentaro, Komagata Osamu, Kasai Shinji, Ogawa Kohei, Tomita Takashi
Department of Medical Entomology, National Institute of Infectious Diseases, 1-23-1 Toyama, Shinjuku-ku, Tokyo 162-8640, Japan.
Japan Agency for Medical Research and Development (AMED), 20F Yomiuri Shimbun Bldg. 1-7-1 Otemachi, Chiyoda-ku, Tokyo 100-0004 Japan.
Sci Rep. 2016 Apr 20;6:24652. doi: 10.1038/srep24652.
Recently-emerging genome editing technologies have enabled targeted gene knockout experiments even in non-model insect species. For studies on insecticide resistance, genome editing technologies offer some advantages over the conventional reverse genetic technique, RNA interference, for testing causal relationships between genes of detoxifying enzymes and resistance phenotypes. There were relatively abundant evidences indicating that the overexpression of a cytochrome P450 gene CYP9M10 confers strong pyrethroid resistance in larvae of the southern house mosquito Culex quinquefasciatus. However, reverse genetic verification has not yet been obtained because of the technical difficulty of microinjection into larvae. Here, we tested two genome editing technologies, transcription activator-like effector nucleases (TALEN)s and clustered regularly interspaced short palindromic repeats (CRISPR/Cas9), to disrupt CYP9M10 in a resistant strain of C. quinquefasciatus. Additionally, we developed a novel, effective approach to construct a TALE using the chemical cleavage of phosphorothioate inter-nucleotide linkages in the level 1 assembly. Both TALEN and CRISPR/Cas9 induced frame-shifting mutations in one or all copies of CYP9M10 in a pyrethroid-resistant strain. A line fixed with a completely disrupted CYP9M10 haplotype showed more than 100-fold reduction in pyrethroid resistance in the larval stage.
最近出现的基因组编辑技术甚至能够在非模式昆虫物种中进行靶向基因敲除实验。对于杀虫剂抗性研究而言,与传统的反向遗传学技术RNA干扰相比,基因组编辑技术在测试解毒酶基因与抗性表型之间的因果关系方面具有一些优势。有相对丰富的证据表明,细胞色素P450基因CYP9M10的过表达赋予了南方家蚊致倦库蚊幼虫对拟除虫菊酯的强抗性。然而,由于向幼虫显微注射的技术难度,尚未获得反向遗传学验证。在此,我们测试了两种基因组编辑技术,即转录激活样效应物核酸酶(TALEN)和成簇规律间隔短回文重复序列(CRISPR/Cas9),以破坏致倦库蚊抗性品系中的CYP9M10。此外,我们开发了一种新颖、有效的方法,利用硫代磷酸酯核苷酸间连接在一级组装中的化学切割来构建TALE。TALEN和CRISPR/Cas9均在拟除虫菊酯抗性品系的CYP9M10的一个或所有拷贝中诱导了移码突变。一个固定有完全破坏的CYP9M10单倍型的品系在幼虫阶段对拟除虫菊酯的抗性降低了100倍以上。