检索结果(检索关键词为:IDENTIFICATION;结果共26条)
  • Xia, Xue; Peng, Chang-Wu; Ye, Qing-Tong; Bing, Xiao-Li; Hong, Xiao-Yue
    INSECT SCIENCE 2023年第30卷第2期 DOI:10.1111/1744-7917.13103
    关键词: TETRANYCHUS-URTICAE; PROTEIN; GENE; IDENTIFICATION; RESISTANCE; DROSOPHILA; MUTATIONS; EVOLUTION; SEQUENCES; SERVER
    摘要: Ras opposite (Rop) is known to play an essential role in regulating vesicle trafficking, including synaptic transmission and general secretion. The fundamental roles of Rop have been confirmed by the observation that null mutations in many organisms generate lethal phenotypes during embryogenesis. However, the effects of Rop during the postembryonic stages, especially in non-model organisms, remain largely unknown. Here, we provide new data that enhance our understanding of Rop's roles in the adults of multiple species of Tetranychus spider mites (Acari: Tetranychidae), a class of notorious agricultural pests. Our in silico and experimental evidence demonstrated that Rop is under purifying selection and is highly conserved in Tetranychus spp. RNA interference experiments showed that Rop is required for maintaining normal fecundity but has no significant effect on survival. We further demonstrate that knockdown of Rop darkens the body color of spider mites and blocks the excretion of fecal pellets, which is likely to be related to an abnormality in the excretion of food waste in the digestive system. Overall, our findings clarify novel functions of a vesicle trafficking-related gene in the adult stage of multiple Tetranychus species and highlight the need to evaluate the roles of essential genes in various organisms.

  • Kou, Zongqing; Luo, Xingyu; Jiang, Yuguo; Chen, Bihui; Song, Yu; Wang, Yaohui; Xu, Jun; Tomberlin, Jeffery K.; Huang, Yongping
    INSECT SCIENCE 2023年第30卷第4期 DOI:10.1111/1744-7917.13147
    关键词: GERM-LINE TRANSFORMATION; HYPERACTIVE PIGGYBAC TRANSPOSASE; DROSOPHILA-MELANOGASTER; MALARIA VECTOR; SILKWORM; GENOME; RNA; IDENTIFICATION; MUTAGENESIS; EXPRESSION
    摘要: The black soldier fly (BSF), Hermetia illucens, is a promising insect for mitigating solid waste problems as its larvae are able to bioconvert organic waste into valuable biomass. We recently reported a high-quality genome assembly of the BSF; analysis of this genome sequence will further the understanding of insect biology and identify genes that can be manipulated to improve efficiency of bioconversion. To enable genetic manipulation of the BSF, we have established the first transgenic methods for this economically important insect. We cloned and identified the ubiquitous actin5C promoter (Hiactin5C-p3k) and 3 endogenous U6 promoters (HiU6:1, HiU6:2, and HiU6:3). The Hiactin5C promoter was used to drive expression of a hyperactive variant of the piggyBac transposase, which exhibited up to 6-fold improvement in transformation rate when compared to the wild-type transposase. Furthermore, we evaluated the 3 HiU6 promoters using this transgenic system. HiU6:1 and HiU6:2 promoters provided the highest knockdown efficiency with RNAi and are thus promising candidates for future Clustered Regularly Interspaced Short Palindromic Repeats (CRISPR) development. Overall, our findings provide valuable genetic engineering toolkits for basic research and genetic manipulation of the BSF.

  • Jiang, Qin-Hong; Li, Ting; Liu, Yan; Zhou, Zi-Yi; Yang, Yang; Wei, Ying; Yin, Mei-Zhen; Shen, Jie; Yan, Shuo
    INSECT SCIENCE 2023年第30卷第3期 DOI:10.1111/1744-7917.13136
    关键词: BEMISIA-TABACI; NANOCARRIER; GENE; MITOGEN; DEATH; NANOTECHNOLOGY; IDENTIFICATION; ENCAPSULATION; POPULATION; PROSPECTS
    摘要: Nano-delivery systems have been applied to deliver various synthetic/botanical pesticides to increase the efficiency of pesticide use and reduce the volumes of pesticides applied. Previous studies have supported the hypothesis that the nanocarriers can help expand the insecticidal target of pesticides to include non-target pests. However, the potential mechanism underlying this interesting phenomenon remains unclear. Herein, a widely applied star polycation (SPc) nanocarrier was synthesized to construct a thiamethoxam (TMX) nano-delivery system. The SPc-based delivery system could promote the translocation of exogenous substances across the membrane of Sf9 cells, increase the cytotoxicity of TMX against Sf9 cells by nearly 20%, and expand the insecticidal target of TMX to include Spodoptera frugiperda (the fall armyworm), with a 27.5% mortality increase at a concentration of 0.25 mg/mL. Moreover, the RNA-seq analysis demonstrated that the SPc could upregulate various transport-related genes, such as Rab, SORT1, CYTH, and PIKfyve, for the enhanced cellular uptake of TMX. Furthermore, enhanced cell death in larvae treated with the TMX-SPc complex was observed through changes in the expression levels of death-related genes, such as Casp7, BIRC5, MSK1, and PGAM5. The SPc-based nano-delivery system improved the cellular uptake of TMX and expanded its insecticidal target by adjusting the expression levels of death-related genes. The current study mainly identified the transport and cell death genes related to nanocarrier-based insecticidal target expansion, which is beneficial for understanding the bioactivity enhancement of the nano-delivery system.

  • Tang, Yu; Chen, Huaqing; Lin, Zhinan; Zhang, Lei; Upadhyay, Archana; Liao, Chenghong; Merkler, David J.; Han, Qian
    INSECT SCIENCE 2023年第30卷第2期 DOI:10.1111/1744-7917.13100
    关键词: YELLOW-FEVER MOSQUITO; SEQUENCE; DUPLICATION; ACYLTRANSFERASE; IDENTIFICATION; SELECTION; ALIGNMENT; SOFTWARE
    摘要: Arylalkylamine N-acetyltransferase (aaNAT), considered a potential new insecticide target, catalyzes the acetylation of arylalkylamine substrates such as serotonin and dopamine and, hence, mediates diverse functions in insects. However, the origin of insect aaNATs (iaaNATs) and the evolutionary process that generates multiple aaNATs in mosquitoes remain largely unknown. Here, we have analyzed the genomes of 33 species to explore and expand our understanding of the molecular evolution of this gene family in detail. We show that aaNAT orthologs are present in Bacteria, Cephalochordata, Chondrichthyes, Cnidaria, Crustacea, Mammalia, Placozoa, and Teleoste, as well as those from a number of insects, but are absent in some species of Annelida, Echinozoa, and Mollusca as well as Arachnida. Particularly, more than 10 aaNATs were detected in the Culicinae subfamily of mosquitoes. Molecular evolutionary analysis of aaNAT/aaNAT-like genes in mosquitoes reveals that tandem duplication events led to gene expansion in the Culicinae subfamily of mosquitoes more than 190 million years ago. Further selection analysis demonstrates that mosquito aaNATs evolved under strongly positive pressures that generated functional diversity following gene duplication events. Overall, this study may provide novel insights into the molecular evolution of the aaNAT family in mosquitoes.

  • Wang, Xiong; Ma, Guangyu; Ren, Feifei; Awais, Mian Muhammad; Sun, Jingchen
    INSECT SCIENCE 2023年第30卷第6期 DOI:10.1111/1744-7917.13200
    关键词: ACID-BINDING-PROTEIN; TRANS-RETINOIC ACID; GENE-EXPRESSION; I EXPRESSION; FATTY-ACIDS; LIVER; IDENTIFICATION
    摘要: Fatty acid binding proteins (FABPs) play an important role as endogenous cytoprotectants. However, studies on FABPs in invertebrates are scarce. Previously, we discovered Bombyx mori fatty acid binding protein 1 (BmFABP1) through co-immunoprecipitation. Here, we cloned and identified BmFABP1 from BmN cells. The results of immunofluorescence indicated that BmFABP1 was localized in the cytoplasm. The tissue expression profile of silkworms showed that BmFABP1 was expressed in all tissues except hemocytes. The expression level of BmFABP1 gradually decreases in BmN cells and B. mori larvae after infection with B. mori nucleopolyhedrovirus (BmNPV). Upregulation of BmFABP1 expression through overexpression or WY14643 treatment significantly inhibited the replication of BmNPV, while downregulation of BmFABP1 expression by RNA interference promoted the replication of BmNPV. The same results were obtained in experiments on silkworm larvae. These results suggest that BmNPV induces BmFABP1 downregulation to promote its proliferation and that BmFABP1 has a potential anti-BmNPV role. This is the first report on the antiviral effect of BmFABP1 in silkworms and provides new insights into the study of the FABP protein family. Also, it is important to study BmNPV resistance in silkworms to breed transgenic silkworms with BmNPV resistance.