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Cloning and the expression pattern of Sp?tzle gene during embryonic development and bacterial challenge in Artemia sinica
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  • 作者:Lu-ping Zheng (12)
    Lin Hou (2) houlin01@126.com
    Miao Yu (2)
    Xiang Li (2)
    Xiang-yang Zou (3) zouxiangyang@126.com
  • 关键词:Artemia sinica – Innate immunity – Sp?tzle – Embryonic development
  • 刊名:Molecular Biology Reports
  • 出版年:2012
  • 出版时间:May 2012
  • 年:2012
  • 卷:39
  • 期:5
  • 页码:6035-6042
  • 全文大小:374.3 KB
  • 参考文献:1. Kambris Z, Brun S, Jang IH, Nam HJ, Romeo Y, Takahashi K, Lee WJ, Ueda R, Lemaitre B (2006) Drosophila immunity: a large-scale in vivo RNAi screen identifies five serine proteases required for Toll activation. Curr Biol 16:808–813
    2. Morisato D, Anderson K (1995) Signaling pathways that establish the dorsal-ventral pattern of the Drosophila embryo. Annu Rev Genet 29:371–399
    3. Weber AN, Tauszig-Delamasure S, Hoffmann JA, Lelievre E, Gascan H, Ray KP, Morse MA, Imler JL, Gay NJ (2003) Binding of the Drosophila cytokine Spatzle to Toll is direct and establishes signaling. Nat Immunol 4:794–800
    4. De Lotto Y, Smith C, De Lotto R (2001) Multiple isoforms of the Drosophila Spatzle protein are encoded by alternatively spliced maternal mRNAs in the precellular blastoderm embryo. Mol Gen Genet 264:643–652
    5. Hoffmann A, Funkner A, Neumann P, Juhnke S, Walther M, Schierhorn A, Weininger U, Balbach J, Reuter G, Stubbs MT (2008) Biophysical characterization of refolded Drosophila Spatzle, a cystine-knot protein, reveals distinct properties of three isoforms. J Biol Chem 283:32598–32609
    6. De Lotto Y, De Lotto R (1998) Proteolytic processing of the Drosophila Spatzle protein by easter generates a dimeric NGF-like molecule with ventralising activity. Mech Dev 72:141–148
    7. Weber AN, Gangloff M, Moncrieffe MC, Hyvert Y, Imler JL, Gay NJ (2007) Role of the Spatzle pro-domain in the generation of an active toll receptor ligand. J Biol Chem 282:13522–13531
    8. Brown GD, Gordon S (2003) Fungal beta-glucans and mammalian immunity. Immunity 19:311–315
    9. Christophides GK, Zdobnov E, Barillas-Mury C et al (2002) Immunity-related genes and gene families in Anopheles gambiae. Science 298(5591):159–165
    10. Hultmark D (2003) Drosophila immunity: paths and patterns. Curr Opin Immunol 15(1):12–19
    11. Janeway CA, Medzhitov R (2002) Innate immune recognition. Annu Rev Immunol 20:197–216
    12. Matskevich AA, Quintin J, Ferrandon D (2010) The Drosophila PRR GNBP3 assembles effector complexes involved in antifungal defenses independently of its Toll-pathway activation function. Eur J Immunol 40(5):1244–1254
    13. Shia AK, Glittenberg M, Thompson G, Weber AN, Reichhart JM, Ligoxygakis P (2009) Toll-dependent antimicrobial responses in Drosophila larval fat body require Sp?tzle secreted by haemocytes. J Cell Sci 122:4505–4515
    14. Dissing M, Giordano H, De Lotto R (2001) Autoproteolusis and feedback in a protease cascade directing Drosophlia dorsal-ventral cell fate. EMBO J 20:2387–2393
    15. Schneider DS, Jin Y, Morisato D, Anderson KV (1994) A processed form of the Sp?tzle protein defines dorsal-ventral polarity in the Drosophila embryo. Development 120(5):1243–1250
    16. Shin SW, Bian G, Raikhel AS (2006) A Toll Receptor and a cytokine, Toll5A and Spz1C, are involved in Toll antifungal immune signaling in the mosquito Aedes aegypti. J Biol Chem 281(51):39388–39395
    17. Jiang H, Kanost MR (2000) The clip-domain family of serine proteinases in arthropods. Insect Biochem Mol Biol 30:95–105
    18. LeMosy EK, Tan YQ, Hashimoto C (2001) Activation of a protease cascade involved in patterning the Drosophila embryo. Proc Natl Acad Sci 98:5055–5060
    19. Gangloff M, Murali A, Xiong J, Arnot CJ, Weber AN, Sandercock AM, Robinson CV, Sarisky R, Holzenburg A, Kao C, Gay NJ (2008) Structural insight into the mechanism of activation of the Toll receptor by the dimeric ligand Spatzle. J Biol Chem 283:14629–14635
    20. Hu X, Yagi Y, Tanji T, Zhou S, Ip YT (2004) Multimerization and interaction of Toll and Spatzle in Drosophila. Proc Natl Acad Sci 101:9369–9374
    21. An C, Jiang H, Kanost MR (2010) Proteolytic activation and function of the cytokine Sp?tzle in the innate immune response of a lepidopteran insect, Manduca sexta. FEBS J 277:148–162
    22. Shi XZ, Zhang RR, Jia YP, Zhao XF, Yu XQ, Wang JX (2009) Identification and molecular characterization of a Sp?tzle-like protein from Chinese shrimp (Fenneropenaeus chinensis). Fish Shellfish Immunol 27:610–617
    23. Wang Y, Cheng T, Rayaprolu S, Zou Z, Xia Q, Xiang Z, Jiang H (2007) Proteolytic activation of pro-Sp?tzle is required for the induced transcription of antimicrobial peptide genes in lepidopteran insects. Dev Comp Immunol 31:1002–1012
    24. Hou L, Jiang LJ, Sun WJ, Zhang RF, Wang JQ, Zhao XT, An JL (2006) Establishment and improvement of real-time fluorescence quantitative PCR for actin gene of Artemia sinica. J Liaoning Normal University 29:15–19
    25. Sun PS, Soderlund M, Venzon NC, Ye D, Lu Y (2007) Isolation and characterization of two actins of the Pacific white shrimp, Litopenaeus vannamei. Mar Biol 151:2145–2151
    26. Mizuguchi K, Parker JS, Blundell TL, Gay NJ (1998) Getting knotted: a model for the structure and activation of Spatzle. Trends Biochem Sci 23:239–242
    27. Arnot CJ, Gay NJ, Gangloff M (2010) Molecular mechanism that induces activation of Sp?tzle, the ligand for the Drosophila Toll receptor. J Biol Chem 285(25):19502–19509
    28. Cai Y (1989) A redescription of the brine shrimp (Artemia sinica). Wasmann J Biol 47:105–110
    29. Ferrandon D, Imler JL, Hetru C, Hoffmann JA (2007) The Drosophila systemic immune response: sensing and signalling during bacterial and fungal infections. Nat Rev Immunol 7:862–874
    30. Royet J (2004) Infectious non-self recognition in invertebrates: lessons from Drosophila and other insect models. Mol Immunol 41:1063–1075
    31. Gobert V, Gottar M, Matskevich AA, Rutschmann S, Royet J, Belvin M, Hoffmann JA, Ferrandon D (2003) Dual activation of the Drosophila toll pathway by two pattern recognition receptors. Science 302(5653):2126–2130
    32. Lemaitre B, Reichhart JM, Hoffmann JA (1997) Drosophila host defense: differential display of antimicrobial peptide genes after infection by various classes of microorganisms. Proc Natl Acad Sci 94:14614–14619
    33. Zheng LP, Hou L, Chang AK, Yu M, Ma J, Li X, Zou XY (2011) Expression pattern of a Gram-negative bacteria-binding protein in early embryonic development of Artemia sinica and after bacterial challenge. Dev Comp Immunol 35:35–43
  • 作者单位:1. Research Institute of Integrated Traditional and Western Medicine, Dalian Medical University, Dalian, 116044 China2. College of Life Sciences, Liaoning Normal University, Dalian, 116029 People’s Republic of China3. Department of Biotechnology, Dalian Medical University, Dalian, 116040 China
  • 刊物类别:Biomedical and Life Sciences
  • 刊物主题:Life Sciences
    Animal Anatomy, Morphology and Histology
    Animal Biochemistry
  • 出版者:Springer Netherlands
  • ISSN:1573-4978
文摘
Sp?tzle gene codes for a NGF-like protein, it involves in the embryonic development and innate immune response of insects and other invertebrate. In dorsal ventral axis differentiation, proSp?tzle is activated by serine endoproteases Easter and then binds to the Toll receptor in ventral axis of oocyte which initiates the ventral axis development. Besides, it could also be activated by another protease named Sp?tzle-processing enzyme (SPZ) to mediate Toll pathway which involves in innate immune response in fungal and Gram-positive bacterial infection of invertebrate. In this paper, a full-length cDNA of Sp?tzle was firstly isolated from Artemia sinica which belonged to Sp?tzle-4 family. The expression of Sp?tzle was investigated at various stages during the embryonic development of A. sinica using real-time PCR and immunohistochemistry assays. The result showed that the high expression level of Sp?tzle appeared at 7 and 10 days of the embryo. A gradual increased level of Sp?tzle transcript occurred after being challenged with Gram-positive bacteria. Immunohistochemistry assay showed that Sp?tzle was mainly expressed in the cephalothorax and on the alimentary canal surface during embryonic development. This new Sp?tzle member showed a constitutive and regional expression during the embryonic development of A. sinica. It may play an important role in dorsal–ventral differentiation at the early development stages and in immune response pathway at the pseudoadult and adult stage, as well as during infection.

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