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siRNA对鸡胚成纤维细胞中GAPDH基因表达的抑制作用 被引量:4

siRNA inhibit GAPDH gene expression in chicken embryonic fibroblast cells
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摘要 RNA干扰(RNA interference,RNAi)是通过短双链RNA(small interference RNA,siRNA)介导的特异性抑制相应基因表达的新技术。作为研究基因功能的有效手段,该技术已在线虫、果蝇、斑马鱼和鼠等动物中进行了应用。本研究利用体外转录合成的短双链干扰RNA(siRNA),针对鸡的管家基因3-磷酸甘油醛脱氢酶基因(glyceraldehyde-3-phosphate dehydrogenase,GAPDH),在鸡胚成纤维细胞中对其表达进行干扰。结果显示siGAPDH能有效阻断GAPDH基因在鸡胚成纤维细胞中的表达,而不相关的siRNA则对该基因的表达没有影响,证明在鸡细胞中也存在RNA干扰现象,为利用RNAi技术对鸡的基因功能研究奠定了一定基础。 RNA interference (RNAi) is a new methodology to inhibit gene expression specifically by small interference RNA triggering. As an efficient approach, it has been widely used to study gene function on Caenorhabditis elegans. Drosophila, zebrafish and mouse. Here, we inhibit the expression of GAPDH gene in chicken embryonic fibroblast cells by used siRNA that was synthesized through transcription in vitro. The result shows that the siRNA can inhibit the expression of GAPDH gene efficiently but the siIRR can not. Its means there is RNAi mechanism in chicken embryonic fibroblast cells. This experiment will be helpful to the researching gene function of chicken by used RNA interference.
出处 《东北农业大学学报》 CAS CSCD 2005年第2期199-203,共5页 Journal of Northeast Agricultural University
基金 国家"973"计划资助项目(2003CB514129)
关键词 RNAI 鸡胚成纤维细胞:GAPDH RNAi chicken embryonic fibroblast cell GAPDH
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参考文献30

  • 1马峻,周红林,苏雷,季维智.外源性双链RNA对小鼠卵母细胞basonuclin基因表达的影响[J].中国科学(C辑),2002,32(3):248-255. 被引量:5
  • 2袁婺洲,Bodmer R,朱传炳,王跃群,李永清,吴秀山.利用RNAi技术研究果蝇心脏发育基因的功能[J].Acta Genetica Sinica,2002,29(1):34-38. 被引量:30
  • 3Fire A, Xu S, Montgomery M K, et al. Potent and specific genetic interference by double-standed RNA in Caenorhabditis elegans [J]. Nature, 1998, 391: 806-811.
  • 4Hannon G J. RNA interference [J]. Nature. 2002, 418:244-251.
  • 5Sharp PA. RNA intereference-2001 [J]. Genes Dev, 2001, 15(5): 485-490.
  • 6Phillip D Zamore. Ancient pathways programmed by small RNAs [J]. Science, 2002, 296:1265-1269.
  • 7Ronald H, Plasterk A. RNA silencing: the genome's immune system [J]. Science, 2002, 296: 1263-1263.
  • 8Andrew G F, Ravi S. Kamath, et al. Functional genomic analysis of C elegans chromosome Ⅰ by systematic RNA interference [J]. Nature, 2000, 408(6810): 325-330.
  • 9Gonczy P, Echeverri C. Functional genomic analysis of cell division in C elegans using RNAi of genes on chromosome Ⅲ [J].Nature, 2000, 408(6810): 331-336.
  • 10FlorenceWianny, Magdalena Zernicka-Goetz. Specific interference with gene function by double-stranded RNA in early mouse development [J]. Nature Cell Biology, 2000, 2: 70-75.

二级参考文献50

  • 1[12]Wu X, Park M, Golden K et al. The wingless signaling pathway is directly involved in Drosophila development. Developmental Biology, 1996, 177:104~116.
  • 2[13]Kennerdell J R, Carthew R W. Use of deRNA-Mediated Genetic Interference to Demonstrate that frizzled and frizzled 2 Act in the wingless Pathway. Cell, 1998, 96:1017~1026.
  • 3[14]Brand A H, Perrimon N. Targeted gene expression as a means of altering cell fates and generating dominant phenotypes. Development, 1993, 118:401~415.
  • 4[15]Rorth P, Szabo K, Bailey A et al. Systematic gain-of-function genetic in Drosophila. Development, 1998, 125:1049~1057.
  • 5[1]Fire A, Xu A Q, Montgomery M K, Kostas S A, Driver S E, Mello C C. Potent and specific genetic interference by double-stranded RNA in Caenorhabditis elegans . Nature, 1998, 391:806~811.
  • 6[2]Fire A. RNA-triggered gene silencing. TIG, 1999, 15(9):358~363.
  • 7[3]Hammond S M, Bernstein E, Beach D, Hannon G J. An RNA-directed nuclease mediates post-transcriptional gene silencing in Drosophila cells. Nature, 2000, 404: 293~296.
  • 8[4]Svoboda P, Stein P, Hayashi H, Schultz R M. Selective reduction of dormant maternal mRNAs in mouse oocytes by RNA interference. Development, 2000, 127:4147~4156.
  • 9[5]Kennerdell J R, Carthew R W. Heritable gene silencing in Drosophila using double-stranded RNA. Natural Biotechnology, 2000,17:896~898.
  • 10[6]Misquitta L, Paterson B M. Targeted disruption of gene function in Drosophila by RNA interference (RNAi): Arole for nautilus in embryonic somatic muscles formation. Proc. Natl. Acad. Sci. USA, 1999, 96:1451~1456.

共引文献31

同被引文献53

  • 1张立,张元兴,华平,俞俊棠.鸡胚细胞的培养[J].华东理工大学学报(自然科学版),1994,20(3):331-336. 被引量:5
  • 2王云,叶向群,吴亦亮,桂慕燕,左正宏.四种启动子调控RFP报告基因在家蚕细胞(Bm-e-HNU5)内的瞬时表达[J].昆虫学报,2006,49(2):167-171. 被引量:6
  • 3刘伟,高玉龙,高宏雷,王笑梅,许修宏.鸡胚成纤维细胞cDNA表达文库的构建[J].微生物学报,2007,47(3):413-417. 被引量:4
  • 4Tehurikov N A,Zavilgelsky G B, Manukhov 1 V, et al. Gene- specific silencing by expression of parallel complementary RNA in Escherichia coli [J].J Biol Chem, 2000,275 : 26523-26529.
  • 5Youngner J S. Monolayer tissue culture. I. Preparation and stalldardization of suspensions of trypsin dispersed monkey kidney cells[J]. Proc Soc Exp Biol, 1954,85 : 202-207.
  • 6弗雷谢尼RI.动物细胞培养技术指南[M].4版.章静波,徐存拴,陈实平,等,译.北京:科学出版社,2004:192-195.
  • 7Brandt M, Yao K, Liu M,et al. Molecular determinants of virulence, cell tropism, and pathogenic phenotype of infectious bursal disease virus[J].J Virol, 2001, 75(24): 11974-11982.
  • 8Liu W, Gao Y I., Gao H L,et al. Construction of chicken embryo fibroblasts eDNA expression library[J]. Wei Sheng Wu Xue Bao,2007,47(3) :413-417.
  • 9Ravindra P V, Tiwari A K, Sharma B, et al. HN protein of Newcastle disease virus causes apoptosis in chicken embryo fibroblast cells[J]. Archives of Virol,2008,153(4):749-754.
  • 10Sharma A, Sharma V D, Umapati V, et al. Partial purification and cytotoxic effects of Salmonella proteinous moieties on chick embryo fibroblasts[J].Indian J Exp Biol, 2006,44 (8) 666-670.

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