piggyBac-based transgenic RNAi of serine protease 2 results in male sterility in Hyphantria cunea
文献类型: 外文期刊
作者: Li, Xiaowei 1 ; Liu, Qun 2 ; Bi, Honglun 2 ; Wang, Yaohui 2 ; Xu, Xia 3 ; Sun, Wei 1 ; Zhang, Ze 1 ; Huang, Yongping 2 ;
作者机构: 1.Chongqing Univ, Sch Life Sci, Lab Evolutionary & Funct Genom, Chongqing 401331, Peoples R China
2.Inst Plant Physiol & Ecol, CAS Ctr Excellence Mol Plant Sci, CAS Key Lab Insect Dev & Evolutionary Biol, Shanghai 200030, Peoples R China
3.Zhejiang Acad Agr Sci, Inst Sericulture & Tea Res, Hangzhou 310021, Peoples R China
4.Univ Chinese Acad Sci, CAS Ctr Excellence Biot Interact, Beijing 100049, Peoples R China
关键词: Hyphantria cunea; ser2; Male sterility; piggyBac; CRISPR; Cas9
期刊名称:INSECT BIOCHEMISTRY AND MOLECULAR BIOLOGY ( 影响因子:4.421; 五年影响因子:4.774 )
ISSN: 0965-1748
年卷期: 2022 年 143 卷
页码:
收录情况: SCI
摘要: Fall webworm, Hyphantria cunea, is a global invasive forest pest that causes serious damage to the economy and ecosystem of agriculture and forestry. Due to the extent of the problem and the difficulty of conventional chemical control, new technologies must be pursued, such as genetic-based inheritable insect sterile technology (gSIT), which exhibits promise for pest control. In the present study, we established a piggyBac-based transgenic system in fall webworm and generated a dominant male-sterile strain by targeting the seminal fluid protein serine protease 2 (Hcser2), displaying an outstanding trait of gSIT. First, an RNA polymerase type III (Pol III) promoter, the HcU62 small nuclear RNA (snRNA) gene promoter, was identified and characterized through direct injection of RNAi plasmids in vivo. Quantitative real-time PCR revealed that HcU62 had the greatest knockdown efficiency of the Hcyellow gene among five short hairpin RNA (shRNA) plasmids tested, designated HcU61-HcU65. Second, subsequent application of piggyBac-based transgenic RNAi (HcU62: shHcyellow, Ysh2) significantly reduced the expression level of the Hcyellow gene, resulting in a stable yellow observable phenotype from the larval to pupal stages in Ysh2 transgenic mutants. Finally, an HcU62-driven transgenic RNAi strain targeting the Hcser2 gene was obtained, resulting in a dominant male-sterile phenotype. Significantly, this process did not affect the growth, development, mating behavior or egg laying of the mutants, and the dominant sterile trait could be inherited in the next generation through female Hcser2 mutants. Furthermore, CRISPR/Cas9-mediated disruption of the Hcser2 gene further confirmed the dominant sterile phenotype, supporting it as a generalized target for genetic control of H. cunea. This study reports the first piggyBac-mediated transgenic system in H. cunea, providing a promising genetic method for controlling this pest by targeting Hcser2 gene.
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