飞蝗载脂蛋白对卵巢发育和脂质沉积的影响

doi:10.3864/j.issn.0578-1752.2024.04.007

Abstract

Abstract:

【Background】Lipids are one of the important nutrients required by organisms, which play important physiological functions, including diapause, flight, embryonic development and energy regulation in insects. Apolipophorins (apoLps) are the main components of insect lipophorin particles, which are involved in the transport of lipids among different tissues.【Objective】The objective of this study is to investigate the function of apolipophorins (LmapoLp-II/I and LmapoLp-III) by RNA interference (RNAi) in ovarian lipid transport in Locusta migratoria, and to provide a new molecular target for pest control.【Method】RNAi was performed to silence two apolipophorin genes (LmapoLp-II/I and LmapoLp-III) at 1 day post adult eclosion (1 PAE), respectively. dsGFP was used as control, 15 μg dsRNA was injected into each insect. The ovaries at 4, 6 and 8 PAE were dissected and observed after dsRNA injection. The silencing efficiency of LmapoLps in the ovaries at 8 PAE was analyzed by reverse-transcription quantitative PCR (RT-qPCR), and EF1α was used as internal reference gene. Lipidomics technique was used to determine and analyze the differences of lipid metabolites in the ovaries between dsGFP- and dsLmapoLp-II/I-treated groups. The approach combining the fold change, the P value and the VIP value of the OPLS-DA model was adopted to screen for differential abundance of lipids. The contents of neutral lipids and total triglycerides were determined by Bodipy staining and triglyceride assay kit.【Result】After injection of dsLmapoLp-II/I and dsLmapoLp-III, the expression level of target genes could be significantly silenced by 80.84% and 92.89%, respectively. RNAi-mediated silencing of LmapoLp-II/I led to a retarded ovarian development, with significantly decreased neutral lipid content and triglyceride content, while the ovaries of L. migratoria injected with dsLmapoLp-III were the same as those in the control group, which could develop normally and gradually grow larger, with the color gradually changing from white to yellow. After LmapoLp-II/I silencing, a total of 1 166 up-regulated metabolites and 1 384 down-regulated metabolites were detected by lipidomics analysis, of which 20 triglycerides were significantly down-regulated.【Conclusion】LmapoLp-II/I is a major apolipophorin gene that affects ovarian development and is involved in the accumulation and transport of ovarian lipids. These research results not only enrich the research content of lipid metabolism in insects, but also help to find new targets for pest control.

Key words: Locusta migratoria, apolipophorin, RNA interference (RNAi), ovary, lipid transport

ZHAO YiYan, GUO HongFang, LIU WeiMin, ZHAO XiaoMing, ZHANG JianZhen. Effects of Apolipophorin on Ovarian Development and Lipid Deposition in Locusta migratoria[J].Scientia Agricultura Sinica, 2024, 57(4): 711-720.

0
/ / Recommend

Add to citation manager EndNote|Reference Manager|ProCite|BibTeX|RefWorks

URL: https://www.chinaagrisci.com/EN/10.3864/j.issn.0578-1752.2024.04.007

https://www.chinaagrisci.com/EN/Y2024/V57/I4/711

Figures/Tables 5

Table 1

Fig. 1

Fig. 2

Fig. 3

Fig. 4

References 52

[1]	石旺鹏, 谭树乾. 蝗虫生物防治发展现状及趋势. 中国生物防治学报, 2019, 35(3): 307-324. doi: 10.16409/j.cnki.2095-039x.2019.03.020
	SHI W P, TAN S Q. Current status and trend on grasshopper and locust biological control. Chinese Journal of Biological Control, 2019, 35(3): 307-324. (in Chinese) doi: 10.16409/j.cnki.2095-039x.2019.03.020
[2]	张建珍, 柴林, 史学凯, 高璐, 范云鹤. RNA干扰技术与害虫防治. 山西大学学报(自然科学版), 2021, 44(5): 980-987.
	ZHANG J Z, CHAI L, SHI X K, GAO L, FAN Y H. RNA interference technology and pest control. Journal of Shanxi University (Natural Science Edition), 2021, 44(5): 980-987. (in Chinese)
[3]	魏琪, 苏建亚. 昆虫糖脂代谢研究进展. 昆虫学报, 2016, 59(8): 906-916. doi: 10.16380/j.kcxb.2016.08.013
	WEI Q, SU J Y. Research advances in carbohydrate and lipid metabolism in insects. Acta Entomologica Sinica, 2016, 59(8): 906-916. (in Chinese) doi: 10.16380/j.kcxb.2016.08.013
[4]	PARVY J P, NAPAL L, RUBIN T, POIDEVIN M, PERRIN L, WICKER-THOMAS C, MONTAGNE J. Drosophila melanogaster acetyl-CoA-carboxylase sustains a fatty acid-dependent remote signal to waterproof the respiratory system. PLoS Genetics, 2012, 8(8): e1002925. doi: 10.1371/journal.pgen.1002925
[5]	YU Z T, ZHANG X Y, WANG Y W, MOUSSIAN B, ZHU K Y, LI S, MA E B, ZHANG J Z. LmCYP4G102: An oenocyte-specific cytochrome P450 gene required for cuticular waterproofing in the migratory locust, Locusta migratoria. Scientific Reports, 2016, 6: 29980.
[6]	WU L X, ZHANG Z F, YU Z T, YU R R, MA E B, FAN Y L, LIU T X, FEYEREISEN R, ZHU K Y, ZHANG J Z. Both LmCYP4G genes function in decreasing cuticular penetration of insecticides in Locusta migratoria. Pest Management Science, 2020, 76(11): 3541-3550. doi: 10.1002/ps.v76.11
[7]	ZHAO X M, YANG Y, NIU N, ZHAO Y Y, LIU W M, MA E B, MOUSSIAN B, ZHANG J Z. The fatty acid elongase gene LmELO7 is required for hydrocarbon biosynthesis and cuticle permeability in the migratory locust, Locusta migratoria. Journal of Insect Physiology, 2020, 123: 104052.
[8]	YANG Y, ZHAO X M, NIU N, ZHAO Y Y, LIU W M, MOUSSIAN B, ZHANG J Z. Two fatty acid synthase genes from the integument contribute to cuticular hydrocarbon biosynthesis and cuticle permeability in Locusta migratoria. Insect Molecular Biology, 2020, 29(6): 555-568. doi: 10.1111/imb.v29.6
[9]	LI D T, DAI Y T, CHEN X, WANG X Q, LI Z D, MOUSSIAN B, ZHANG C X. Ten fatty acyl-CoA reductase family genes were essential for the survival of the destructive rice pest, Nilaparvata lugens. Pest Management Science, 2020, 76(7): 2304-2315.
[10]	BALABANIDOU V, KAMPOURAKI A, MACLEAN M, BLOMQUIST G J, TITTIGER C, JUAREZ M P, MIJAILOVSKY S J, CHALEPAKIS G, ANTHOUSI A, LYND A, ANTOINE S, HEMINGWAY J, RANSON H, LYCETT G J, VONTAS J. Cytochrome P 450 associated with insecticide resistance catalyzes cuticular hydrocarbon production in Anopheles gambiae. Proceedings of the National Academy of Sciences of the United States of America, 2016, 113(33): 9268-9273.
[11]	LIU J Q, LI W X, ZHENG J J, TIAN Q N, HUANG J F, DAI S X. Gain and loss events in the evolution of the apolipoprotein family in vertebrata. BMC Evolutionary Biology, 2019, 19(1): 209. doi: 10.1186/s12862-019-1519-8
[12]	MAHLEY R W, INNERARITY T L, RALL S C, WEISGRABER K H. Plasma lipoproteins apolipoprotein structure and function. Journal of Lipid Research, 1984, 25(12): 1277-1294. doi: 10.1016/S0022-2275(20)34443-6
[13]	SU X, PENG D Q. The exchangeable apolipoproteins in lipid metabolism and obesity. Clinica Chimica Acta, 2020, 503: 128-135. doi: S0009-8981(20)30025-5 pmid: 31981585
[14]	RYAN R O, VAN DER HORST D J. Lipid transport biochemistry and its role in energy production. Annual Review of Entomology, 2000, 45: 233-260. pmid: 10761577
[15]	WEERS P M, VAN MARREWIJK W J, BEENAKKERS A M, VAN DER HORST D J. Biosynthesis of locust lipophorin. Apolipophorins I and II originate from a common precursor. The Journal of Biological Chemistry, 1993, 268(6): 4300-4303. doi: 10.1016/S0021-9258(18)53609-7
[16]	SMOLENAARS M M, KASPERAITIS M A, RICHARDSON P E, RODENBURG K W, VAN DER HORST D J. Biosynthesis and secretion of insect lipoprotein: Involvement of furin in cleavage of the apoB homolog, apolipophorin-II/I. Journal of Lipid Research, 2005, 46(3): 412-421. doi: 10.1194/jlr.M400374-JLR200 pmid: 15604521
[17]	VAN DER HORST D J, RODENBURG K W. Lipoprotein assembly and function in an evolutionary perspective. Biomolecular Concepts, 2010, 1(2): 165-183. doi: 10.1515/bmc.2010.012 pmid: 25961995
[18]	WEERS P M, RYAN R O. Apolipophorin III: Role model apolipoprotein. Insect Biochemistry and Molecular Biology, 2006, 36(4): 231-240. pmid: 16551537
[19]	COLE K D, FERNANDO-WARNAKULASURIYA G P, BOGUSKI M S, FREEMAN M, GORDON J I, CLARK W A, LAW J H, WELLS M A. Primary structure and comparative sequence analysis of an insect apolipoprotein. Apolipophorin-III from Manduca sexta. The Journal of Biological Chemistry, 1987, 262(24): 11794-11800. doi: 10.1016/S0021-9258(18)60882-8
[20]	WEN D H, LUO H, LI T N, WU C F, ZHANG J H, WANG X L, ZHANG R. Cloning and characterization of an insect apolipoprotein (apolipophorin-II/I) involved in the host immune response of Antheraea pernyi. Developmental & Comparative Immunology, 2017, 77: 221-228.
[21]	SUNDERMEYER K, HENDRICKS J K, PRASAD S V, WELLS M A. The precursor protein of the structural apolipoproteins of lipophorin: cDNA and deduced amino acid sequence. Insect Biochemistry and Molecular Biology, 1996, 26(8/9): 735-738. doi: 10.1016/S0965-1748(96)00060-4
[22]	KANOST M R, BOGUSKI M S, FREEMAN M, GORDON J I, WYATT G R, WELLS M A. Primary structure of apolipophorin-III from the migratory locust, Locusta migratoria. Potential amphipathic structures and molecular evolution of an insect apolipoprotein. The Journal of Biological Chemistry, 1988, 263(22): 10568-10573.
[23]	VAN HEUSDEN M C, THOMPSON F, DENNIS J. Biosynthesis of Aedes aegypti lipophorin and gene expression of its apolipoproteins. Insect Biochemistry and Molecular Biology, 1998, 28(10): 733-738. doi: 10.1016/S0965-1748(98)00068-X
[24]	PALM W, SAMPAIO J L, BRANKATSCHK M, CARVALHO M, MAHMOUD A, SHEVCHENKO A, EATON S. Lipoproteins in Drosophila melanogaster-Assembly, function, and influence on tissue lipid composition. PLoS Genetics, 2012, 8(7): e1002828. doi: 10.1371/journal.pgen.1002828
[25]	TSUCHIDA K, WELLS M. Digestion, absorption, transport and storage of fat during the last larval stadium of Manduca sexta. Changes in the role of lipophorin in the delivery of dietary lipid to the fat body. Insect Biochemistry, 1988, 18(3): 263-268. doi: 10.1016/0020-1790(88)90090-X
[26]	KONUMA T, TSUKAMOTO Y, NAGASAWA H, NAGATA S. Imbalanced hemolymph lipid levels affect feeding motivation in the two-spotted cricket, Gryllus bimaculatus. PLoS ONE, 2016, 11(5): e0154841. doi: 10.1371/journal.pone.0154841
[27]	BOGERD J, BABIN P J, KOOIMAN F P, ANDRÉ M, BALLAGNY C, VAN MARREWIJK W J, VAN DER HORST D J. Molecular characterization and gene expression in the eye of the apolipophorin II/I precursor from Locusta migratoria. Journal of Comparative Neurology, 2000, 427(4): 546-558.
[28]	ZHAO Y, LIU W, ZHAO X, YU Z, GUO H, YANG Y, ZHANG J, MOUSSIAN B, ZHANG J. Apolipophorin-II/I contributes to cuticular hydrocarbon transport and cuticle barrier construction in Locusta migratoria. Frontiers in Physiology, 2020, 11: 790. doi: 10.3389/fphys.2020.00790
[29]	BENOIT J B, YANG G, KRAUSE T B, PATRICK K R, AKSOY S, ATTARDO G M. Lipophorin acts as a shuttle of lipids to the milk gland during tsetse fly pregnancy. Journal of Insect Physiology, 2011, 57(11): 1553-1561. doi: 10.1016/j.jinsphys.2011.08.009 pmid: 21875592
[30]	VAN DER HORST D J, RODENBURG K W. Locust flight activity as a model for hormonal regulation of lipid mobilization and transport. Journal of Insect Physiology, 2010, 56(8): 844-853. doi: 10.1016/j.jinsphys.2010.02.015 pmid: 20206629
[31]	ZDYBICKA-BARABAS A, CYTRYŃSKA M. Apolipophorins and insects immune response. Invertebrate Survival Journal, 2013, 10(1): 58-68.
[32]	DHAWAN R, GUPTA K, KAJLA M, KAKANI P, CHOUDHURY T P, KUMAR S, KUMAR V, GUPTA L. Apolipophorin-III acts as a positive regulator of Plasmodium development in Anopheles stephensi. Frontiers in Physiology, 2017, 8: 185.
[33]	KIM B Y, JIN B R. Apolipophorin III from honeybees (Apis cerana) exhibits antibacterial activity. Comparative Biochemistry and Physiology Part B: Biochemistry and Molecular Biology, 2015, 182: 6-13. doi: 10.1016/j.cbpb.2014.11.010
[34]	NIERE M, MEISSLITZER C, DETTLOFF M, WEISE C, ZIEGLER M, WIESNER A. Insect immune activation by recombinant Galleria mellonella apolipophorin III. Biochimica et Biophysica Acta, 1999, 1433(1/2): 16-26.
[35]	NOH J Y, PATNAIK B B, TINDWA H, SEO G W, KIM D H, PATNAIK H H, JO Y H, LEE Y S, LEE B L, KIM N J, HAN Y S. Genomic organization, sequence characterization and expression analysis of Tenebrio molitor apolipophorin-III in response to an intracellular pathogen, Listeria monocytogenes. Gene, 2014, 534(2): 204-217.
[36]	PALUSINSKA-SZYSZ M, ZDYBICKA-BARABAS A, RESZCZYNSKA E, LUCHOWSKI R, KANIA M, GISCH N, WALDOW F, MAK P, DANIKIEWICZ W, GRUSZECKI W I, CYTRYNSKA M. The lipid composition of Legionella dumoffii membrane modulates the interaction with Galleria mellonella apolipophorin III. Biochimica et Biophysica Acta, 2016, 1861(7): 617-629.
[37]	WEN D H, WANG X L, SHANG L, HUANG Y, LI T N, WU C F, ZHANG R, ZHANG J H. Involvement of a versatile pattern recognition receptor, apolipophorin-III in prophenoloxidase activation and antibacterial defense of the Chinese oak silkworm, Antheraea pernyi. Developmental & Comparative Immunology, 2016, 65: 124-131.
[38]	WIJERATNE T U, WEERS P M M. Lipid-bound apoLp-III is less effective in binding to lipopolysaccharides and phosphatidylglycerol vesicles compared to the lipid-free protein. Molecular and Cellular Biochemistry, 2019, 458(1/2): 61-70. doi: 10.1007/s11010-019-03530-x
[39]	YU H Z, WANG J, ZHANG S Z, TOUFEEQ S, LI B, LI Z, YANG L A, HU P, XU J P. Molecular characterisation of Apolipophorin-III gene in Samia cynthia ricini and its roles in response to bacterial infection. Journal of Invertebrate Pathology, 2018, 159: 61-70. doi: 10.1016/j.jip.2018.10.009
[40]	LIVAK K J, SCHMITTGEN T D. Analysis of relative gene expression data using real-time quantitative PCR and the 2^-ΔΔCt method. Methods, 2001, 25(4): 402-408. doi: 10.1006/meth.2001.1262
[41]	LEYRIA J, FRUTTERO L L, AGUIRRE S A, CANAVOSO L E. Ovarian nutritional resources during the reproductive cycle of the hematophagous Dipetalogaster maxima (Hemiptera: Reduviidae): Focus on lipid metabolism. Archives of Insect Biochemistry and Physiology, 2014, 87(3): 148-163. doi: 10.1002/arch.v87.3
[42]	ATELLA G C, GONDIM K C, MACHADO E A, MEDEIROS M N, SILVA-NETO M A, MASUDA H. Oogenesis and egg development in triatomines: A biochemical approach. Anais da Academia Brasileira de Ciencias, 2005, 77(3): 405-430. doi: 10.1590/S0001-37652005000300005
[43]	SANTOS R, ROSAS-OLIVEIRA R, SARAIVA F B, MAJEROWICZ D, GONDIM K C. Lipid accumulation and utilization by oocytes and eggs of Rhodnius prolixus. Archives of Insect Biochemistry and Physiology, 2011, 77(1): 1-16. doi: 10.1002/arch.v77.1
[44]	RUBIN E M, KRAUSS R M, SPANGLER E A, VERSTUYFT J G, CLIFT S M. Inhibition of early atherogenesis in transgenic mice by human apolipoprotein AI. Nature, 1991, 353(6341): 265-267.
[45]	ROSES A D. Apolipoprotein E alleles as risk factors in Alzheimer’s disease. Annual Review of Medicine, 1996, 47: 387-400. doi: 10.1146/med.1996.47.issue-1
[46]	MASUCCI-MAGOULAS L, GOLDBERG I J, BISGAIER C L, SERAJUDDIN H, FRANCONE O L, BRESLOW J L, TALL A R. A mouse model with features of familial combined hyperlipidemia. Science, 1997, 275(5298): 391-394. doi: 10.1126/science.275.5298.391
[47]	SHACHTER N S. Apolipoproteins C-I and C-III as important modulators of lipoprotein metabolism. Current Opinion in Lipidology, 2001, 12(3): 297-304. doi: 10.1097/00041433-200106000-00009
[48]	HANADA Y, SEKIMIZU K, KAITO C. Silkworm apolipophorin protein inhibits Staphylococcus aureus virulence. The Journal of Biological Chemistry, 2011, 286(45): 39360-39369. doi: 10.1074/jbc.M111.278416
[49]	KAWOOYA J K, LAW J H. Role of lipophorin in lipid transport to the insect egg. The Journal of Biological Chemistry, 1988, 263(18): 8748-8753.
[50]	CANAVOSO L E, JOUNI Z E, KARNAS K J, PENNINGTON J E, WELLS M A. Fat metabolism in insects. Annual Review of Nutrition, 2001, 21: 23-46. pmid: 11375428
[51]	COELHO H S, ATELLA G C, MOREIRA M F, GONDIM K C, MASUDA H. Lipophorin density variation during oogenesis on Rhodnius prolixus. Archives of Insect Biochemistry and Physiology, 1997, 35(3): 301-313. doi: 10.1002/(ISSN)1520-6327
[52]	ATELLA G C, SILVA-NETO M A C, GOLODNE D M, AREFIN S, SHAHABUDDIN M. Anopheles gambiae lipophorin: Characterization and role in lipid transport to developing oocyte. Insect Biochemistry and Molecular Biology, 2006, 36(5): 375-386.

Metrics

Viewed

Full text

Abstract

Cited

Shared

Discussed

Comments

Recommended 0

No Suggested Reading articles found!

用途 Application	引物名称 Primer name	引物序列 Primer sequence (5′-3′)	产物长度 Product size (bp)
dsRNA合成 dsRNA synthesis	dsLmapoLp-II/I-F	taatacgactcactatagggCTCCAAGCAGAAGGTCGTG	460
	dsLmapoLp-II/I-R	taatacgactcactatagggCAGGCTGAGATGAGAATGT	460
	dsLmapoLp-III-F	taatacgactcactatagggGCTGAATCACACCATCGTCA	420
	dsLmapoLp-III-R	taatacgactcactatagggTGGATGGAGTTCTGCAGGTT	420
	dsGFP-F	taatacgactcactatagggGTGGAGAGGGTGAAGG	571
	dsGFP-R	taatacgactcactatagggGGGCAGATTGTGTGGAC	571
RT-qPCR分析 RT-qPCR analysis	LmapoLp-II/I-F	AGCGATTTCATCCGGTGGC	103
	LmapoLp-II/I-R	GGTGTATGTCTGTCCCTTTT	103
	LmapoLp-III-F	ACGCTGCTCGCAGTCCTC	83
	LmapoLp-III-R	ACCGCCTCCGCGATGTT	83
	EF1α-F	AGCCCAGGAGATGGGTAAAG	155
	EF1α-R	CTCTGTGGCCTGGAGCATC	155

Effects of Apolipophorin on Ovarian Development and Lipid Deposition in Locusta migratoria

RichHTML

PDF

Abstract

Cite this article

share this article

Figures/Tables 5

References 52

Related Articles 15

Metrics

Comments

Recommended 0

[1]	CHEH ErHu, YUAN GuoQing, CHEN Yan, CHEN MengQiu, SUN ShengYuan, TANG PeiAn. Mitochondrial Protein-Coding Genes Nad5, Nad6 and Atp6 are Involved in Phosphine Resistance of Cryptolestes ferrugineus [J]. Scientia Agricultura Sinica, 2024, 57(9): 1722-1733.
[2]	LUO LiDan, CHEN JiaMing, AN Qi, LIU Lei, SUN QinZhe, LIU Huan, WANG SenShan, SONG LiWen. Effects of Extreme High Temperature on Trehalose Content and Trehalose Transporter Gene in Tetranychus truncatus [J]. Scientia Agricultura Sinica, 2024, 57(6): 1091-1101.
[3]	YUAN GuoQing, CHEN ErHu, TANG PeiAn. The Mechanisms of Mitochondrial Protein-Coding Genes ND6 and ATP6 in Regulating Cold Tolerance of Cryptolestes ferrugineus [J]. Scientia Agricultura Sinica, 2024, 57(22): 4483-4494.
[4]	LI ChuXin, SONG ChenHu, ZHOU JinHuan, LI JiaXin, WANG XinLiang, TIAN XuBin, SONG Zhen. Research on Prevention and Control Technology of Citrus Yellow Vein Clearing Virus Based on VIGS [J]. Scientia Agricultura Sinica, 2024, 57(22): 4473-4482.
[5]	WANG Ni, SHI ZheYi, YOU YuanZheng, ZHANG Chao, ZHOU WenWu, ZHOU Ying, ZHU ZengRong. Effects of miRNA on Gene Expression of Sphingolipids Metabolism and Small RNA Analysis of Silencing NlSPT1 and NlSMase4 in Nilaparvata lugens [J]. Scientia Agricultura Sinica, 2024, 57(20): 4022-4034.
[6]	CHEH ErHu, SHEN DanRong, DU WenWei, MENG HongJie, TANG PeiAn. Cuticle Protein Genes are Involved in Phosphine Resistance of Cryptolestes ferrugineus [J]. Scientia Agricultura Sinica, 2023, 56(9): 1696-1707.
[7]	SHAO HongYang, MENG Xiang, ZHANG Tao, CHEN Min. Analysis of Cytochrome P450 Genes in Response to Quercetin and Function of CYP6ZB2 in Hyphantria cunea [J]. Scientia Agricultura Sinica, 2023, 56(7): 1322-1332.
[8]	ZHANG Rui,ZHANG XueYao,ZHAO XiaoMing,MA EnBo,ZHANG JianZhen. Antibody Preparation and Subcellular Localization of LmKnk3-5′ in Locusta migratoria [J]. Scientia Agricultura Sinica, 2022, 55(2): 329-338.
[9]	LI LiYing,HE YingTing,ZHONG YuYi,ZHOU XiaoFeng,ZHANG Hao,YUAN XiaoLong,LI JiaQi,CHEN ZanMou. CTNNB1 Regulates the Function of Porcine Ovarian Granulosa Cells [J]. Scientia Agricultura Sinica, 2022, 55(15): 3050-3061.
[10]	GUAN RuoBing,LI HaiChao,MIAO XueXia. Commercialization Status and Existing Problems of RNA Biopesticides [J]. Scientia Agricultura Sinica, 2022, 55(15): 2949-2960.
[11]	YIN Fei,LI ZhenYu,SAMINA Shabbir,LIN QingSheng. Expression and Function Analysis of Cytochrome P450 Genes in Plutella xylostella with Different Chlorantraniliprole Resistance [J]. Scientia Agricultura Sinica, 2022, 55(13): 2562-2571.
[12]	WU Wei,XU HuiLi,WANG ZhengLiang,YU XiaoPing. Cloning and Function Analysis of a Serine Protease Inhibitor Gene Nlserpin2 in Nilaparvata lugens [J]. Scientia Agricultura Sinica, 2022, 55(12): 2338-2346.
[13]	CHEN ErHu,MENG HongJie,CHEN Yan,TANG PeiAn. Cuticle Protein Genes TcCP14.6 and TcLCPA3A are Involved in Phosphine Resistance of Tribolium castaneum [J]. Scientia Agricultura Sinica, 2022, 55(11): 2150-2160.
[14]	ZHANG Jing,ZHANG JiYue,YUE YongQi,ZHAO Dan,FAN YiLing,MA Yan,XIONG Yan,XIONG XianRong,ZI XiangDong,LI Jian,YANG LiXue. LKB1 Regulates Steroids Synthesis Related Genes Expression in Bovine Granulosa Cells [J]. Scientia Agricultura Sinica, 2022, 55(10): 2057-2066.
[15]	Xiang XU,Yi XIE,LiYun SONG,LiLi SHEN,Ying LI,Yong WANG,MingHong LIU,DongYang LIU,XiaoYan WANG,CunXiao ZHAO,FengLong WANG,JinGuang YANG. Screening and Large-Scale Preparation of dsRNA for Highly Targeted Degradation of Tobacco Mosaic Virus (TMV) Nucleic Acids [J]. Scientia Agricultura Sinica, 2021, 54(6): 1143-1153.