期刊文献+

AGO1基因对拟南芥叶边缘锯齿状发育的影响 被引量:3

Influences of AGO1 to the development of the Arabidopsis leaves with the serration margin
下载PDF
导出
摘要 在拟南芥和水稻中Argonaute(AGO)蛋白是RNA介导的沉默复合体(RISC)的核心组分,在植物叶极性的分化方面具有重要的调节作用。实验根据AGO1基因序列设计一对特异引物,提取野生型拟南芥RNA作为模板,采用反转录PCR方法扩增出AGO1基因,并插入到克隆载体pGEM-T中。筛选鉴定后将AGO1连接到植物表达载体pBI121上,构建起植物表达载体pBI121-AGO1。并且利用农杆菌介导的方法转化拟南芥,通过抗性筛选,获得转基因植株。然后对转基因植株进行表型分析及AGO1蛋白的RT-PCR检测。通过对转基因拟南芥表达分析发现,与野生型拟南芥相比超表达AGO1蛋白的转基因拟南芥叶片明显呈锯齿状,说明AGO1基因影响拟南芥叶片发育。 In Arabidopsis thanalia and Oryza sativa ,Argonaute (AGO) proteins are the core components of RISC which play important roles in miRNA function, and AGO1 encodes an RNA Slicer that selectively recruits microRNAs and siRNAs. Total RNA was extracted from seedlings of Arabidopsis thanalia to clone the AGO1 gene. The plant expression vector of AGO1 was constructed (pBI121-AG01) and transformed into Arabidopsis by the Agrobacteriurn-mediated method. In our results, we se- lected the T1 transgenic Arabidopsis with AGO1 gene by Kanarnycin resistance and RT-PCR analysis. According to the pheno- type of transgenie plants, we discovered the incised margin of the transgenic Arabidopsis leaves.
出处 《河北科技大学学报》 CAS 2014年第1期51-57,共7页 Journal of Hebei University of Science and Technology
基金 山东省自然科学基金(ZR2012CQ021) 山东省高等学校科技计划项目(J12LE07)
关键词 拟南芥 AG01基因超表达agol突变体 叶片发育 Arabidopsis thanalia AGO1 overexpression ago1 Leaf development
  • 相关文献

参考文献15

  • 1ZILBERMAN D,CAO X F,JACOBSEN S E. ARGONAUTF4 control of locus-specific siRNA accumulation and DNA and histone methylation[J].SCIENCE,2003,(5607):716-719.
  • 2GRISHOK A,PASQUINELLI A E,CONTE D. Genes and mechanisms related to RNA interference regulate expression of the small temporal RNAs that control C.elegans developmental timing[J].CELL,2001,(01):23-24.
  • 3MA J B,YE K,PATEL D J. Structural basis for overhang-specific small interfering RNA recognition by the PAZ domain[J].NATURE,2004,(6989):318-322.
  • 4宋雪梅,燕飞,杜立新.RNA诱导沉默复合体中的生物大分子及其装配[J].遗传,2006,28(6):761-766. 被引量:13
  • 5王鹏,赵旵军,朱国萍.植物RNA沉默的分子机制研究进展[J].生命科学,2008,20(5):784-789. 被引量:2
  • 6PERAGINE A,YOSHIKAWA M,WU G. SGS3 and SGS2/SDE1/RDR6 are required for juvenile development and the production of trans acting siRNAs in Arabidopsis[J].Genes & Development,2004.2368-2379.
  • 7奥斯伯F;布伦特R;金斯顿R;颜子颖;王海林.精编分子生物学实验指南[M]北京:科学出版社,1998.
  • 8CLOUGH S J,BENT A F. Floral dip:A simplified method for agrobacterium-mediated transformation of arabidopsis thaliana[J].Plant Journal,1998,(06):735-743.
  • 9CHENG M,FRY J E,PANG S. Genetic transformation of wheat mediated by agrobacterium tumefaciens[J].Plant Physiology,1997,(03):971-980.
  • 10宋锋,孙敏,罗克明.一种基于PCR技术鉴定单拷贝转基因烟草的方法[J].中国生物工程杂志,2010,30(4):83-88. 被引量:7

二级参考文献126

  • 1燕飞,成卓敏.RNA干扰机制研究进展[J].遗传,2005,27(1):167-172. 被引量:7
  • 2Filipenko E A, Filipenko M L, Deineko E V, et al. Analysis of integration sites of T-DNA insertions in transgenic tobacco plants. Cytology and Genetics, 2007, 41 (4) : 199-203.
  • 3Marjanac G, Karimi M, Naudts M, et al. Gene silencing induced by hairpin or inverted repeated sense transgenes varies among promoters and cell types. New Phytologist, 2009, 184(4) : 851- 864.
  • 4Liu H W, Bao X M. Overexpression of the chitosanase gene in Fusarium solani via Agrobacterium tumefaciens-mediated transformation. Current Microbiology, 2009, 58 (3) : 272-282.
  • 5He X L, Miyasaka S C, Fitch M M, et al. Agrobacterium tumefaciens-mediated transformation of taro ( Colocasia esculenta L. Schott) with a rice chitinase gene for improved tolerance to a fungal pathogen Sclerotium rolfsii. Plant Cell Rep, 2008, 27 ( 5 ) : 903 -909.
  • 6Beltran J, Jaimes H, Echeverry M, et al. Quantitative analysis of transgenes in cassava plants using real-time PCR technology. In Vitro Cellular and Development Biology-Plant, 2009, 45 ( 1 ) : 48- 56.
  • 7Yi C X, Zhang J, Chan K M, et al. Quantitative real-time PCR assay to detect transgene copy number in cotton (Gossypium hirsutum). Anal Chem, 2008, 375(1) : 150-152.
  • 8Kihara T, Zhao C R, Kobayashi T, et al. Simple identification of transgenie Arabidopsis plants carrying a single copy of the integrated gene. Biosei Bioteehnol Biochem, 2006, 70 (7): 1780-1783.
  • 9Luo K M, Duan H, Zhao D F, et al. GM-gene-deletor: fused LoxP-FRT recognition sequences dramatically improve the efficiency of FLP or CRE recombinase on transgene excision from pollen and seed of tobacco plants. Plant Biotech J, 2007, 5 : 263- 374.
  • 10Luo K M, Zheng X L, Chen Y Q, et al. Use of the maize Knottedl gene as a positive selectable marker for Agrobacterium- mediated transformation in tobacco. Plant Cell Rep, 2006, 25: 403409.

共引文献41

同被引文献24

引证文献3

二级引证文献1

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部