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家蚕氨肽酶N家族基因在5龄幼虫中肠组织的表达分析 被引量:2

Expression Analysis of Aminopeptidase N Family Genes in Midgut Tissue of the Fifth Instar Bombyx mori Larvae
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摘要 氨肽酶N(aminopeptidase N,APN)是一种偏好水解蛋白质或寡肽N端中性氨基酸的酶,在鳞翅目昆虫中主要分布于中肠上皮细胞的刷状缘囊膜上,是苏云金芽孢杆菌(Bacillus thuringiensis,Bt)伴孢晶体(Cry)毒素的重要受体蛋白。为了研究家蚕APN家族基因的表达特征,运用Real-time PCR技术检测分析该家族基因在不同家蚕品种幼虫中肠组织的表达差异以及同一家蚕品种幼虫中肠组织中该家族基因各个成员的表达丰度。在所有供试家蚕品种的幼虫中肠组织均可检测到APN家族基因的表达,但不同化性家蚕品种间APN基因的表达水平存在显著差异(P<0.05),而相同化性品种间的差异较小(P>0.05);在同一家蚕品种幼虫中肠组织中,APN2、APN4、APN5基因的表达量较高,而APN1及APN3基因的表达量较低。研究结果有助于进一步研究家蚕APN家族基因的作用机制,并为家蚕抗Bt品种的选育提供理论依据。 Aminopeptidase N(APN) is an enzyme that readily hydrolyzes protein or neutral amino acids at the N-terminal of an oligopeptide.It is mainly distributed in the brush border membrane vesicle of midgut epithelial cells of lepidopterous insects and is the important receptor of Bacillus thuringiensis crystal toxins(Cry).To investigate expression patterns of APN family genes,Real-time PCR was employed to analyze the differential expression of APN family genes in larva migut tissue of different silkworm(Bombyx mori) varieties and the expression level of various family members in larva midgut tissue of the same silkworm variety.The results showed that APN family genes were expressed in larva midgut of all tested silkworm varieties.The expression level of APN genes were significantly different between silkworm varieties having different voltinisms(P&lt;0.05).However,there was little difference between silkworm varieties having the same voltinism(P&gt;0.05).The expression levels of APN 2,APN 4 and APN 5 genes were relatively higher in larva midgut tissue of the same silkworm variety,whereas those of APN 1 and APN 3 were relatively lower.The obtained results would facilitate further study on functioning mechanism of silkworm APN family genes,and provide theoretical basis for breeding silkworm strains resistant to Bacillus thuringiensis.
出处 《蚕业科学》 CAS CSCD 北大核心 2013年第4期689-694,共6页 ACTA SERICOLOGICA SINICA
基金 国家重点基础研究发展计划"973"项目(No.2012CB1146-04) 江苏省自然科学基金项目(No.BK2011525) 江苏省教育厅科技项目(No.11KJB180002)
关键词 家蚕 氨肽酶N基因 中肠组织 荧光定量PCR 品种 化性 Bombyx mori Aminopeptidase N gene Midgut tissue Real-time PCR Variety Voltinism
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参考文献19

  • 1Pigott C R,Ellar D J.Role of receptors in Bacillus thuringiensiscrystal toxin activity[J].Microbiol Mol Biol Rev,2007,71(2):255-281.
  • 2Crava C M,Bel Y,Lee S F,et al.Study of the aminopeptidase Ngene family in the lepidopterans Ostrinia nubilalis(Hübner)andBombyx mori(L.):sequences,mapping and expression[J].InsectBiochem Mol Biol,2010,40(7):506-515.
  • 3Griffitts J S,Haslam S M,Yang T,et al.Glycolipids as receptors forBacillus thuringiensis crystal toxin[J].Science,2005,307(5711):922-925.
  • 4Bravo A,Gomez I,Conde J,et al.Oligomerization triggers bindingof a Bacillus thuringiensis Cry1Ab pore-forming toxin to aminopep-tidase N receptor leading to insertion into membrane microdomains[J].Biochim Biophys Acta,2004,1667(1):38-46.
  • 5Schnepf E,Crickmore N,Van Rie J,et al.Bacillus thuringiensisand its pesticidal crystal proteins[J].Microbiol Mol Biol Rev,1998,62(3):775-806.
  • 6Lightwood D J,Ellar D J,Jarrett P.Role of proteolysis in determi-ning potency of Bacillus thuringiensis Cry1Ac delta-endotoxin[J].Appl Environ Microbiol,2000,66(12):5174-5181.
  • 7马文静,韩兰芝,尹新明,曹广春,苏丽娟.鳞翅目昆虫氨肽酶N与Bt毒素的结合及其与Bt抗性的关系[J].环境昆虫学报,2011,33(3):378-387. 被引量:9
  • 8Livak K J,Schmittgen T D.Analysis of relative gene expression da-ta using real time quantitative PCR and the2-△△CT method[J].Methods,2001,25(4):402-408.
  • 9姚勤,刘晓勇,唐旭东,陈克平.家蚕抗核型多角体病毒病分子标记辅助育种[J].分子植物育种,2005,3(4):537-542. 被引量:25
  • 10Angelucci C,Barrett-Wilt G A,Hunt D F,et al.Diversity of amin-opeptidases,derived from four lepidopteran gene duplications,andpolycalins expressed in the midgut of Helicoverpa armigera:identifi-cation of proteins binding theδ-endotoxin,Cry1Ac of Bacillusthuringiensis[J].Insect Biochem Mol Biol,2008,38(7):685-690.

二级参考文献19

  • 1陈克平,林昌麒,姚勤.家蚕对核型多角体病的抗性及遗传规律的研究[J].蚕业科学,1996,22(3):160-164. 被引量:59
  • 2Abe H., Harada T., Kanehara M., Shimada T., O hbayashi F.,and Oshiki T., 1998a, Genetic mapping of RAPD markers linked to the densonucleosis refractoriness gene, nsd-1, in the silkworm, Bombyx mori, Genes. Genet. Syst., 73 (4):237-242
  • 3Abe H., Ohbayashi F., Shimada T., Sugasaki T., Kawai S., and Oshiki T., 1998b, A complete full-length non-LTR retrotransposon, BMC1, on the W chromosome of the silkworm, Bombyx mori, Genes. Genet. Syst., 73(6): 353-35
  • 4Abe H., Ohbayashi F., Shimada T., Sugasaki T., Kawai S., Mita K., and Oshiki T., 2000a, Molecular structure of a novel gypsy-Ty3-like retrotransposon (Kabuki) and nested retrotransposable elements on the W chromosome of the silkwormBombyx mori, Mol. Gen. Genet., 263(6): 916-924
  • 5Abe H., Sugasaki T., Kanehara M., Shimada T., Gomi S.J., Ohbayashi F., and Oshiki T., 2000b, Identification and genetic mapping of RAPD markers linked to the densonucleosis refractoriness gene, nsd-2, in the silkworm, Bombyx mori, Genes. Genet. Syst., 75(2): 93-96
  • 6Chen K.P., Yao Q., Wang Y., and Cheng J.L., 2003, Genetic basis of screening of molecular markers for nuclear polyhedrdsis virus resistance in Bombyx moriL., International Journal of Industrial Entomology, 7(1): 5-10
  • 7Li M.W., Yao Q., and Chen K.P., 2001, Studies on RAPD markers linked the densonucleosis reeractoriness gene, nsd-Z in silkworm, Bombyx mori, Sericologia, 41 (3):409-415
  • 8Parniewski P., and Staczek P., 2002, Molecular mechanisms of TRS instability, Adv. Exp. Med. Biol., 516:1-25
  • 9Powell W., Morgante M., Andre C., Hanafey M., Vogel J.,Tingey S., and Rafalski A., 1996, The comparison of RAPD, RELP, AFLP and SSR (microsatellite) markers for germplasm analysia, Mol. Breed., 2:225-238
  • 10Saiki R.K., Scharf S., Faloona F., Horn G.T., Mullis K.B., and Erlich H.A., 1984, Primer-directed enzymatic amplification of DNA with a thermostable DNA polymerase, Science,239:487-491

共引文献32

同被引文献30

  • 1刘雨芳,王锋,尤民生,汪琼,胡斯琴,刘文海,赵士熙.转基因水稻及其杂交后代对稻纵卷叶螟的田间抗性检测[J].中国农业科学,2005,38(4):725-729. 被引量:22
  • 2翟保平,程家安.2006年水稻两迁害虫研讨会纪要[J].昆虫知识,2006,43(4):585-588. 被引量:104
  • 3张孝羲 耿济国 周威君.我国稻纵卷叶螟迁飞规律的研究[J].南京农学院学报,1981,23(3):43-54.
  • 4陈永年,1985.国外稻纵卷叶螟研究概述.昆虫知识,6:287-289.
  • 5RUSSELL H J,SOUTHERN T R,NASH T E.Role of sulfated glycans in adherence of the microsporidian Encephalitozoon intestinalis to host cells in vitro[J].Infect Immun,2006,73(2):841-848.
  • 6SOUTHERN T R,JOLLY C E,HAYMAN J R.Augmentation of microsporidia adherence and host cell infection by divalent cations[J].FEMS Microbiol Lett,2006,260(2):143-149.
  • 7YANG D L,DANG X Q,PENG P,et al.Nb HSWP11,a microsporidia Nosema bombycis protein,localizing in the spore wall and membranes,reduces spore adherence to host cell BME[J].J Parasitol,2014,100(5):623-632.
  • 8LI Y H,WU Z L,PAN G Q,et al.Identification of a novel spore wall protein(SWP26)from microsporidia Nosema bombycis[J].Int J Parasitol,2009,39(4):391-398.
  • 9SOUTHERN T R,JOLLY C E,LESTER M E,et al.En P1,a microsporidian spore wall protein that enables spores to adhere to and infect host cells in vitro[J].Eukaryot Cell,2007,6(8):1354-1362.
  • 10SZUMOWSKI S C,TROEMEL E R.Microsporidia-host interactions[J].Curr Opin Microbiol,2015,26:10-16.

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