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过量表达内质网小分子热激蛋白增强番茄的衣霉素抗性 被引量:4

Overexpression of Small Heat-Shock Protein of Endoplasmic Reticulum Enhances Resistance of Tomato to Tunicamycin
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摘要 真核细胞内质网腔内未折叠蛋白的过度积累会引起内质网胁迫(ER胁迫),继而激活未折叠蛋白应答(UPR)信号途径,诱导内质网定位的分子伴侣的大量表达(如BiP和calnexin等)。本工作将CaMV35S启动子驱动的内质网小分子热激蛋白基因(ER-sHSP)导入番茄,发现ER-sHSP的过量表达提高了转基因番茄整株对衣霉素的抗性。衣霉素处理使未转基因番茄中BiP和calnexin基因的表达迅速升高,转基因番茄中这两个基因的表达也有增加,但表达强度明显低于未转基因番茄。说明ER-sHSP能够减轻ER胁迫,并可能参与UPR信号转导途径。 The accumulation of unfolded proteins in the endoplasmic reticulum (ER) lumen causes ER stress response in eukaryote cells, activates the unfolded protein response (UPR) and consequently induces the expression of ER-located molecular chaperones (such as BiP, calnexin, etc.). In this study, the full-length small heat-shock protein of endoplasmic reticulum cDNA (ER-sHSP) under the control of CaMV 35S promoter was introduced into tomato by Agrobacterium tumefactions mediated method (Fig. l, Table 1). Overexpression of ER-sHSP enhanced the resistance of the transgenic plant to tunicamycin (Fig.2, Table 2), an inducer of ER stress. Tunicamycin treatment induced an increase in mRNA level of BiP and calnexin in plant cell, but mRNAs of these two genes in transgenic plants were accumulated to a much smaller extent than those in non-transgenic plants (Fig.3). These results indicated that ER-sHSP could alleviate the ER stress and may be involved in the UPR signal transmission pathway.
作者 赵春梅 刘箭
出处 《植物生理与分子生物学学报》 CAS CSCD 北大核心 2006年第4期427-432,共6页 Journal Of Plant Physiology and Molecular Biology
基金 国家自然科学基金项目(No.30270132)资助。~~
关键词 内质网 小分子热激蛋白 未折叠蛋白应答 衣霉素 番茄 endoplasmic reticulum small heat-shock protein unfolded protein response (UPR) tunicamycin, tomato
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  • 1Alvim FC,Carolino SMB,Cascardo JCM,Nunes CC,Martinez CA,Otoni WC,Fontes EPB (2001).Enhanced accumulation of BiP in transgenic plants confers tolerance to water stress.Plant Physiol 126:1042-1054
  • 2Bradford M (1976).A rapid and sensitive method for the quantification of microgram quantities of protein utilizing the principle of protein-dye binding.Anal Biochem 72:248-254
  • 3Chomczynski P,Sacchi N (1987).Single-step method of RNA isolation by acid guanidinium thiocyanate-phenol-chloroform extraction.Anal Biochem 162:156-159
  • 4Cox JS,Walter P (1996).A novel mechanism for regulating activity of a transcription factor that controls the unfolded protein response.Cell 87:391-404
  • 5Forreiter C,Kirschner M,Nover L (1997).Stable transformation of an Arabidopsis cell suspension culture with firefly luciferase providing a cellular system for analysis of chaperone activity in vivo.Plant Cell 9:2171-2181
  • 6Holsters M,de Waele D,Depicker A,Messens E,van Montagu M,Schell J (1978).Transfection and transformation of Agrobacterium tumefaciens.Mol Gen Genet 163:181-187
  • 7Kaufman RJ (1999).Stress signaling from the lumen of the endoplasmic reticulum:coordination of gene transcriptional and translational controls.Genes Dev 13:1211-1233
  • 8Koiwa H,Li F,McCully MG,Mendoza I,Koizumi N,Manabe Y,Nakagawa Y,Zhu JH,Rus A,Pardo JM et al.(2003).The STT3a subunit isoform of the Arabidopsis oligosaccharyltransferase controls adaptive responses to salt/osmotic stress.Plant Cell 15:2273-2284
  • 9Koizumi N,Martínez IM,Kimata Y,Kohno K,Sano H,Chrispeels MJ (2001).Molecular characterization of two Arabidopsis Irel homologs,endoplasmic reticulum-located transmembrane protein kinases.Plant Physiol 127:949-962
  • 10Koizumi N,Ujino T,Sano H,Chrispeels MJ (1999).Overexpression of a gene that encodes the first enzyme in the biosynthesis of asparagine-linked glycans makes plants resistant to tunicamycin and obviates the tunicamycin-induced unfolded protein response.Plant Physiol 121:353-362

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