基于RNAi技术解析美国白蛾HcAnk1HcAnk2基因功能及对HcNPV的敏感性

彭萌萌, 吴红渠, 张佳雯, 闫丽琼, 曹传旺, 孙丽丽

南京林业大学学报(自然科学版) ›› 2024, Vol. 48 ›› Issue (3) : 181-190.

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南京林业大学学报(自然科学版) ›› 2024, Vol. 48 ›› Issue (3) : 181-190. DOI: 10.12302/j.issn.1000-2006.202203049
研究论文

基于RNAi技术解析美国白蛾HcAnk1HcAnk2基因功能及对HcNPV的敏感性

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HcAnk1 and HcAnk2 genes function and HcNPV susceptibility of Hyphantria cunea based on RNAi

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摘要

【目的】 锚定蛋白是连接细胞骨架与质膜的衔接蛋白家族。但昆虫中关于锚定蛋白基因功能研究甚少。笔者克隆美国白蛾(Hyphantria cunea)锚定蛋白基因,阐明该基因在其各发育期和组织中的表达特征及对美国白蛾核型多角体病毒(Hyphantria cunea nucleopolyhedrosisvirus, HcNPV)的敏感性,为进一步开发HcNPV增效剂提供理论依据。【方法】 通过转录组文库筛选出Ankyrin1(HcAnk1)和Ankyrin2(HcAnk2)基因,利用生物信息学分析基因特性,采用qRT-PCR检测不同发育阶段、不同组织以及不同HcNPV浓度胁迫下HcAnks的表达量,通过RNAi技术研究HcAnks基因沉默后美国白蛾对HcNPV的敏感性。【结果】 HcAnk1HcAnk2基因开放阅读框依次为1 392和1 866 bp,分别编码463和621个氨基酸,蛋白质分子质量分别为59.18和69.19 ku,理论等电点分别为5.74 和 8.66;进化树分析显示HcAnk1与粉纹夜蛾(Trichoplusia ni)亲缘关系最近而聚为一类。HcAnks在各个发育阶段均有表达,卵期表达量最高,6龄表达量最低;HcAnks分别在中肠和后肠中表达量最高;在卵巢和精巢中未检测到HcAnk1,而HcAnk2主要在中肠和精巢中表达。在不同浓度HcNPV胁迫下,HcAnks转录水平表现为低浓度诱导,高浓度抑制。沉默HcAnks美国白蛾4龄幼虫的相对生长率(RGR)和食物转化效率(ECD)显著降低。此外,沉默HcAnks的美国白蛾4龄幼虫对HcNPV敏感性显著增加。【结论】 HcAnks在抵抗HcNPV侵染过程中发挥重要作用,HcAnks可作为HcNPV增效剂,用于美国白蛾无公害防治。

Abstract

【Objective】 Ankyrin is a family of adaptor proteins that connect the cytoskeleton to the plasma membrane. However, the functions of insect ankyrin are poorly understood. In this study, the Ankyrin genes of Hyphantria cunea were cloned and their expression characteristics were determined in different developmental stages and tissues of H. cunea. The mortality rate of H. cunea was measured under the stress of exposure to nucleopolyhedrosis virus, which provided a theoretical basis for further developing synergists for NPV-based control strategies. 【Method】 The Ankyrin1 (HcAnk1) and Ankyrin2 (HcAnk2) genes were screened by a transcriptome library, and the characteristics of the two Ankyrin genes were determined using bioinformatics. Using qRT-PCR, the expression of HcAnk1 and HcAnk2 genes were determined at different developmental stages and in different tissues, and under different HcNPV concentrations. The survival rate of H. cunea larvae under HcNPV stress was investigated after the gene silencing of HcAnk1 and HcAnk2 using an RNAi technique. 【Result】 The open reading frames of the HcAnk1 and HcAnk2 genes were 1392 and 1866 bp, encoding 463 and 621 amino acids, respectively. The molecular weights of the HcAnk1 and HcAnk2 proteins were 59.18 and 69.19 ku, respectively, and the theoretical isoelectric points were 5.74 and 8.66, respectively. A phylogenetic analysis showed that HcAnk1 was closely related to Trichoplusia ni and was clustered into one group. HcAnk1 and HcAnk2 were expressed at all developmental stages, with the highest expression in the egg stage and the lowest expression in the sixth instar larva. The highest expression of HcAnk1 and HcAnk2 was observed in the midgut and hindgut, respectively, but HcAnk1 was not detected in the ovary or testis, while HcAnk2 was mainly expressed in the midgut and testis. In tests with different levels of HcNPV stress, the transcription levels of HcAnk1 and HcAnk2 were induced at low concentrations and inhibited at high concentrations. The relative growth rate and food conversion efficiency (ECD) were significantly decreased after silencing HcAnks in H. cunea larvae. Additionally, the H. cunea with HcAnks silencing were significantly less resistant to HcNPV. 【Conclusion】 HcAnk1 and HcAnk2 play an important role in the resistance to HcNPV. HcAnk1 and HcAnk2 can be used as HcNPV synergists for the pollution-free control of H. cunea.

关键词

美国白蛾 / 锚定蛋白 / 美国白蛾核型多角体病毒 / RNAi

Key words

Hyphantria cunea / Ankyrins / Hyphantria cunea nucleopolyhedrovirus / RNAi

引用本文

导出引用
彭萌萌, 吴红渠, 张佳雯, . 基于RNAi技术解析美国白蛾HcAnk1HcAnk2基因功能及对HcNPV的敏感性[J]. 南京林业大学学报(自然科学版). 2024, 48(3): 181-190 https://doi.org/10.12302/j.issn.1000-2006.202203049
PENG Mengmeng, WU Hongqu, ZHANG Jiawen, et al. HcAnk1 and HcAnk2 genes function and HcNPV susceptibility of Hyphantria cunea based on RNAi[J]. JOURNAL OF NANJING FORESTRY UNIVERSITY. 2024, 48(3): 181-190 https://doi.org/10.12302/j.issn.1000-2006.202203049
中图分类号: S763.3   

参考文献

[1]
BENNETT P B. Anchors aweigh!:ion channels,cytoskeletal proteins,and cellular excitability[J]. Circ Res, 2000, 86(4):367-368.DOI: 10.1161/01.res.86.4.367.
[2]
HRYNIEWICZ-JANKOWSKA A, CZOGALLA A, BOK E, et al. Ankyrins,multifunctional proteins involved in many cellular pathways[J]. Folia Histochem Cytobiol, 2002, 40(3):239-249.
[3]
BOULEY M, TIAN M Z, PAISLEY K, et al. The L1-type cell adhesion molecule neuroglian influences the stability of neural ankyrin in the Drosophila embryo but not its axonal localization[J]. J Neurosci, 2000, 20(12):4515-4523.DOI: 10.1523/JNEUROSCI.20-12-04515.2000.
[4]
HORTSCH M, PAISLEY K L, TIAN M Z, et al. The axonal localization of large Drosophila Ankyrin2 protein isoforms is essential for neuronal functionality[J]. Mol Cell Neurosci, 2002, 20(1):43-55.DOI: 10.1006/mcne.2002.1113.
[5]
RUBTSOV A M, LOPINA O D. Ankyrins[J]. FEBS Lett, 2000, 482(1/2):1-5.DOI: 10.1016/s0014-5793(00)01924-4.
[6]
BENNETT V, BAINES A J. Spectrin and Ankyrin-based pathways:metazoan inventions for integrating cells into tissues[J]. Physiol Rev, 2001, 81(3):1353-1392.DOI: 10.1152/physrev.2001.81.3.1353.
[7]
CAI X J, ZHANG Y H. Molecular evolution of the ankyrin gene family[J]. Mol Biol Evol, 2006, 23(3):550-558.DOI: 10.1093/molbev/msj056.
[8]
OTSUKA A J, FRANCO R, YANG B, et al. An ankyrin-related gene (unc-44) is necessary for proper axonal guidance in Caenorhabditis elegans[J]. J Cell Biol, 1995, 129(4):1081-1092.DOI: 10.1083/jcb.129.4.1081.
[9]
DUBREUIL R R, YU J. Ankyrin and beta-spectrin accumulate independently of alpha-spectrin in Drosophila[J]. Proc Natl Acad Sci USA, 1994, 91(22):10285-10289.DOI: 10.1073/pnas.91.22.10285.
[10]
PIELAGE J, FETTER R D, DAVIS G W. A postsynaptic spectrin scaffold defines active zone size,spacing,and efficacy at the Drosophila neuromuscular junction[J]. J Cell Biol, 2006, 175(3):491-503.DOI: 10.1083/jcb.200607036.
[11]
SPURRIER J, SHUKLA A K, BUCKLEY T, et al. Expression of a fragment of Ankyrin2 disrupts the structure of the axon initial segment and causes axonal degeneration in Drosophila[J]. Mol Neurobiol, 2019, 56(8):5689-5700.DOI: 10.1007/s12035-019-1477-6.
[12]
SILVERMAN N, MANIATIS T. NF-kappaB signaling pathways in mammalian and insect innate immunity[J]. Genes Dev, 2001, 15(18):2321-2342.DOI: 10.1101/gad.909001.
[13]
THOETKIATTIKUL H, BECK M H, STRAND M R. Inhibitor kappaB-like proteins from a polydnavirus inhibit NF-kappaB activation and suppress the insect immune response[J]. Proc Natl Acad Sci USA, 2005, 102(32):11426-11431.DOI: 10.1073/pnas.0505240102.
[14]
FALABELLA P, VARRICCHIO P, PROVOST B, et al. Characte-rization of the IkappaB-like gene family in polydnaviruses associated with wasps belonging to different Braconid subfamilies[J]. J Gen Virol, 2007, 88(Pt 1): 92-104.DOI: 10.1099/vir.0.82306-0.
[15]
BITRA K, SUDERMAN R J, STRAND M R. Polydnavirus Ank proteins bind NF-κB homodimers and inhibit processing of Relish[J]. PLoS Pathog, 2012, 8(5):e1002722.DOI: 10.1371/journal.ppat.1002722.
[16]
GUEGUEN G, KALAMARZ M E, RAMROOP J, et al. Polydnaviral ankyrin proteins aid parasitic wasp survival by coordinate and selective inhibition of hematopoietic and immune NF-kappa B signaling in insect hosts[J]. PLoS Pathog, 2013, 9(8):e1003580.DOI: 10.1371/journal.ppat.1003580.
[17]
CHEN Y R, ZHONG S L, FEI Z J, et al. Transcriptome responses of the host Trichoplusia ni to infection by the baculovirus Autographa californica multiple nucleopolyhedrovirus[J]. J Virol, 2014, 88(23):13781-13797.DOI: 10.1128/JVI.02243-14.
[18]
SUN L L, LIU P, SUN S H, et al. Transcriptomic analysis of interactions between Hyphantria cunea larvae and nucleopolyhedro virus[J]. Pest Manag Sci, 2019, 75(4):1024-1033.DOI: 10.1002/ps.5212.
[19]
TAMURA K, STECHER G, PETERSON D, et al. MEGA6:molecular evolutionary genetics analysis version 6.0[J]. Mol Biol Evol, 2013, 30(12):2725-2729.DOI: 10.1093/molbev/mst197.
[20]
PFAFFL M W, HORGAN G W, DEMPFLE L. Relative expression software tool (REST) for group-wise comparison and statistical analysis of relative expression results in real-time PCR[J]. Nucleic Acids Res, 2002, 30(9):e36.DOI: 10.1093/nar/30.9.e36.
[21]
SUN L L, WANG Z Y, WU H Q, et al. Role of ocular albinism type 1 (OA1) GPCR in Asian Gypsy moth development and transcriptional expression of heat-shock protein genes[J]. Pestic Biochem Physiol, 2016, 126:35-41.DOI: 10.1016/j.pestbp.2015.07.004.
[22]
BORK P. Hundreds of Ankyrin-like repeats in functionally diverse proteins:mobile modules that cross phyla horizontally?[J]. Proteins, 1993, 17(4):363-374.DOI: 10.1002/prot.340170405.
[23]
SEDGWICK S G, SMERDON S J. The ankyrin repeat:a diversity of interactions on a common structural framework[J]. Trends Biochem Sci, 1999, 24(8):311-316.DOI: 10.1016/s0968-0004(99)01426-7.
[24]
MOSAVI L K, CAMMETT T J, DESROSIERS D C, et al. The ankyrin repeat as molecular architecture for protein recognition[J]. Protein Sci, 2004, 13(6):1435-1448.DOI: 10.1110/ps.03554604.
[25]
HABYARIMANA F, AL-KHODOR S, KALIA A, et al. Role for the Ankyrin eukaryotic-like genes of Legionella pneumophila in parasitism of protozoan hosts and human macrophages[J]. Environ Microbiol, 2008, 10(6): 1460-1474.DOI: 10.1111/j.1462-2920.2007.01560.x.
[26]
PAN X X, LÜHRMANN A, SATOH A, et al. Ankyrin repeat proteins comprise a diverse family of bacterial type IV effectors[J]. Science, 2008, 320(5883):1651-1654.DOI: 10.1126/science.1158160.
[27]
AXTON J M, SHAMANSKI F L, YOUNG L M, et al. The inhibitor of DNA replication encoded by the Drosophila gene plutonium is a small,ankyrin repeat protein[J]. EMBO J, 1994, 13(2):462-470.DOI: 10.1002/j.1460-2075.1994.tb06281.x.
[28]
ELFRING L K, AXTON J M, FENGER D D, et al. Drosophila PLUTONIUM protein is a specialized cell cycle regulator required at the onset of embryogenesis[J]. Mol Biol Cell, 1997, 8(4):583-593.DOI: 10.1091/mbc.8.4.583.
[29]
ASP M, GIACOMELLO S, LARSSON L, et al. A spatiotemporal organ-wide gene expression and cell atlas of the developing human heart[J]. Cell, 2019, 179(7):1647-1660.e19.DOI: 10.1016/j.cell.2019.11.025.
[30]
KANG H J, KAWASAWA Y I, CHENG F, et al. Spatio-temporal transcriptome of the human brain[J]. Nature, 2011, 478(7370):483-489.DOI: 10.1038/nature10523.
[31]
FERTUZINHOS S, LI M F, KAWASAWA Y I, et al. Laminar and temporal expression dynamics of coding and noncoding RNAs in the mouse neocortex[J]. Cell Rep, 2014, 6(5):938-950.DOI: 10.1016/j.celrep.2014.01.036.
[32]
KAWANO S, BABA M, FUKUSHIMA H, et al. Autism-associated ANK2 regulates embryonic neurodevelopment[J]. Biochem Biophys Res Commun, 2022, 605:45-50.DOI: 10.1016/j.bbrc.2022.03.058.
[33]
ISLAM Z, NAGAMPALLI R S K, FATIMA M T, et al. New paradigm in ankyrin repeats:beyond protein-protein interaction module[J]. Int J Biol Macromol, 2018, 109:1164-1173.DOI: 10.1016/j.ijbiomac.2017.11.101.
[34]
BENNETT V, GILLIGAN D M. The spectrin-based membrane skeleton and micron-scale organization of the plasma membrane[J]. Annu Rev Cell Biol, 1993, 9:27-66.DOI: 10.1146/annurev.cb.09.110193.000331.
[35]
KREIS T, VALE R. Guidebook to the extracellular matrix,anchor,and adhesion proteins[M] Oxford, New York: Sambrook and Tooze Publication at Oxford University Press, 1999:340-392.
[36]
PARK J, KIM K J, CHOI K S, et al. Anaplasma phagocytophilum AnkA binds to granulocyte DNA and nuclear proteins[J]. Cell Microbiol, 2004, 6(8):743-751.DOI: 10.1111/j.1462-5822.2004.00400.x.
[37]
LIN M Q, DEN DULK-RAS A, HOOYKAAS P J J, et al. Anaplasma phagocytophilum AnkA secreted by type IV secretion system is tyrosine phosphorylated by Abl-1 to facilitate infection[J]. Cell Microbiol, 2007, 9(11):2644-2657.DOI: 10.1111/j.1462-5822.2007.00985.x.
[38]
RIKIHISA Y, LIN M Q. Anaplasma phagocytophilum and Ehrlichia chaffeensis type IV secretion and Ank proteins[J]. Curr Opin Microbiol, 2010, 13(1):59-66.DOI: 10.1016/j.mib.2009.12.008.
[39]
STRAND M R. Polydnavirus gene products that interact with the host immune system[M]//Parasitoid Viruses. Amsterdam: Elsevier, 2012:149-161.DOI: 10.1016/b978-0-12-384858-1.00012-6.
[40]
SALVIA R, GROSSI G, AMORESANO A, et al. The multifunctional polydnavirus TnBVANK1 protein:impact on host apoptotic pathway[J]. Sci Rep, 2017, 7(1):11775.DOI: 10.1038/s41598-017-11939-x.
[41]
LOPEZ-ORTIZ C, PEÑA-GARCIA Y, NATARAJAN P, et al. The ankyrin repeat gene family in Capsicum spp:genome-wide survey,characterization and gene expression profile[J]. Sci Rep, 2020, 10(1):4044.DOI: 10.1038/s41598-020-61057-4.

基金

国家自然科学基金面上项目(32171791)
东北林业大学本科生创新项目(202010225031)
黑龙江省优秀青年基金(YQ2021C007)

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