作物学报 ›› 2011, Vol. 37 ›› Issue (07): 1196-1204.doi: 10.3724/SP.J.1006.2011.01196
尹明智,官梅,肖钢,李栒,官春云*
YIN Ming-Zhi,GUAN Mei,XIAO Gang,LI Xun,GUAN Chun-Yun*
摘要: DOF (DNA binding with one finger)转录因子是植物特有的转录因子家族,含有一个独特的富含Cys残基的单锌指DNA结合区域,在植物生长发育中参与多种生物学过程。本研究根据拟南芥AtDof1.7基因(GenBank登录号为AT1G51700)序列设计含有不同酶切位点的特异性扩增引物,以拟南芥总DNA为模板,扩增AtDof1.7基因片段,将AtDof1.7基因正向反向分别插入表达载体的相应位置,构建成AtDof1.7基因的RNA干扰载体pADOF1。利用改良的floral-dip方法将干扰载体pADOF1成功转入野生型拟南芥,经草甘膦抗性筛选和PCR检测获得5株阳性转基因植株。利用RT-PCR技术和气相色谱法分别分析了AtDof1.7基因的表达和种子脂肪酸组成,结果表明5株转基因植株中AtDof1.7基因的表达量不同程度低于野生型植株,种子油酸含量明显上升,亚麻酸含量明显下降,说明AtDof1.7转录因子与拟南芥种子脂肪酸代谢途径有一定的关系,为进一步研究其在脂肪酸代谢过程中的调控作用以及在油菜中研究该类转录因子的功能奠定了基础。
[1]Ashrafi K, Chang F Y, Watts J L, Fraser A G, Kamath R S, Ahringer J, Ruvkun G. Genome-wide RNAi analysis of Caenorhabditis elegans fat regulatory genes. Nature, 2003, 421: 268-272 [2]Chuang C F, Meyerowitz E M. Specific and heritable genetic interference by double-stranded RNA in Arabidopsis thaliana. Proc Natl Acad Sci USA, 2000, 97: 4985-4990 [3]Prasanth S G, Prasanth K V, Stillman B. Orc6 involved in DNA replication, chromosome segregation, and cytokinesis. Science, 2002, 297: 1026-1031 [4]Yanagisawa S. A novel DNA binding domain that may form a single zinc finger motif. Nucl Acid Res, 1995, 23: 3403-3410 [5]Yanagisawa S. The Dof family of plant transcription factor. Trends Plant Sci, 2002, 7: 555-560 [6]Lijavetzky D, Carbonero P, Vicente-Carbajosa J. Genome-wide comparative phylogenetic analysis of the rice and Arabidopsis Dof gene families. BMC Evol Biol, 2003, 3:17 [7]Shigyo M, Tabei N, Yoneyama T, Yanagisawa S. Evolutionary processes during the formation of the plant-specific Dof transcription factor family. Plant Cell Physiol, 2007, 48: 179-185 [8]Tsujimoto-Inui Y, Naito Y, Sakurai N, Suzuki H, Sasaki R, Takahashi H, Ohtsuki N, Nakano T, Yanagisawa S, Shibata D, Uchimiya H, Shinshi H, Suzuki K. Functional genomics of the DOF transcription factor family genes in suspension-cultured cells of Arabidopsis thaliana. Plan Biotechnol, 2009, 26: 15-28 [9]Mena M, Vicente-Carbajosa J, Schmidt R J, Pilar Carbonero. An endosperm-specific dof protein from barley, highly conserved in wheat, binds to and activates transcription from the prolamin-box of a native B-hordein promoter in barley endosperm. Plant J, 1998, 16: 53-62 [10]Vicente-Carbajosa J, Moose S P, Parsons R L, Schmidt K J. A maize zinc-finger protein binds the prolamin box in zein gene promoters and interact with the basic leucine zipper transcriptional activator opaque2. Proc Natl Acad Sci USA, 1997, 94: 7685-7690 [11]Mena M, Cejudo F J, Isabel-Lamoneda I, Pilar Carbonero. A role for the DOF transcription factor BPBF in the regulation of gibberellin-responsive genes in barley aleurone. Plant Physiol, 2002, 130: 111-119 [12]Isabel-LaMoneda I, Díaz I, Martínez M, Mena M, Pilar Carbonero. SAD: a new DOF protein from barley that activates transcription of a cathepsin B-like thiol protease gene in the aleurone of germinating seeds. Plant J, 2003, 33: 329-340 [13]Imaizumi T, Schultz T F, Harmon F G, Ho L A, Kay S A. FKF1 F-Box protein mediates cyclic degradation of a repressor of CONSTANS in Arabidopsis. Science, 2005, 309: 293-297 [14]Wang H W, Zhang B, Hao Y J, Huang J, Tian A G, Liao Y, Zhang J S, Chen S Y. The soybean Dof-type transcription factor genes, GmDof4 and GmDof11, enhance lipid content in the seeds of transgenic Arabidopsis plants. Plant J, 2007, 52: 716-729 [15]Yanagisawa S, Sheen J. Involvement of maize Dof zinc finger proteins in tissue-specific and light-regulated gene expression. Plant Cell, 1998, 10:75-89 [16]Yanagisawa S. Dof1 and Dof2 transcription factors are associated with expression of multiple genes involved in carbon metabolism in maize. Plant J, 2000, 21: 281-288 [17]Yanagisawa S, Akiyama A, Kisaka H, Uchimiya H, Miwa T. Metabolic engineering with Dof1 transcription factor in plants: improved nitrogen assimilation and growth under low-nitrogen conditions. Proc Natl Acad Sci USA, 2004, 101: 7833-7838 [18]Pan L-F(潘丽峰). Improvement of Tobacco Nitrogen Utilization Rate by Increasing Expression of Dof1. MS Dissertation of Kunming University of Science and Technology, 2007 (in Chinese with English abstract) [19]Chen J-Q(陈锦清), Lang C-X(郎春秀), Hu Z-H(胡张华), Liu Z-H(刘智宏), Huang R-Z(黄锐之). Antisense PEP gene regulates to ratio of protein and lipid content in Brassica napus seeds. J Agric Biotechnol (农业生物技术学报), 1999, 7(4): 316-320 (in Chinese with English abstract) [20]Martinez-Trujillo M, Limones-Briones V, Cabrera-Ponce J L, Herrera-Estrella L. Improving transformation efficiency of Arabidopsis thaliana by modifying the floral-dip method. Plant Mol Biol Rep, 2004, 22: 63-70 [21]Du P-F(杜培粉), Wu L-T(伍林涛), Yao Y-T(姚远颋), Yin F(尹峰), Ruan Y(阮颖), Liu C-L(刘春林). Construction of the RNAi vector of AtTPSO3 Gene and Arabidopsis transformation. Mol Plant Breed (分子植物育种), 2009, 7(3): 451-455 (in Chinese with English abstract) [22]Li M(李明), Jiang S-L(姜世玲), Wang Y-Q(王幼群), Liu G-Q(刘国琴). Post-transcriptional silencing signal of gene can be fast two-way transfer in grafted Arabidopsis. Sci Bull (科学通报), 2006, 52: 142-147 (in Chinese) [23]Stoutjesdijk P A, Singh S P, Hurlstone C J, Waterhouse P A, Green A G. hpRNA-mediated targeting of the Arabidopsis FAD2 gene gives highly efficient and stable silencing. Plant Physiol, 2002, 129: 1723-1731 [24]Wesley S V, Helliwell C A, Smith N A, Wang M B, Rouse D T, Liu Q, Gooding P S, Singh S P, Abbott D, Stoutjesdijk P K, Robinson S P, Gleave A P, Green A G, Waterhouse P M. Construct design for efficient, effective and high-throughput gene silencing in plants. Plant J, 2001, 27: 581-590 [25]Fourmann M, Barret P, Renard M, Pelletier G, Delourme R, Brunel D. The two genes homologous to Arabidopsis Fae1 co-segregate with the two loci governing erucic acid content in Brassica napus. Theor Appl Gene, 1998, 96: 852-858 [26]Gupta A, Mukhopadhyay A, Arumugam N, Sodhi Y S, Pental D, Pradhan A K. Molecular tagging of erucic acid trait in oilseed mustard (Brassica juncea) by QTL mapping and single nucleotide polymorphisms in Fae1 gene. Theor Appl Genet, 2004, 108: 743-749 [27]Burns M J, Barnes S R, Bowman J G, Clarke M H E, Werner C P, Kearsey M J. QTL analysis of an intervarietal set of substitution lines in Brassica napus: Seed oil content and fatty acid composition. Heredity, 2003, 90: 39-48 [28]Liu X-P(刘雪平), Tu J-X(涂金星), Liu Z-W(刘志文), Chen B-Y(陈宝元), Fu T-D(傅廷栋). Construction of a molecular marker linkage map and its use for QTL analysis of erucic acid content in Brassica napus L. Acta Agron Sin (作物学报), 2005, 31 (3): 275-282 (in Chinese with English abstract) [29]Hu X Y, Sullivan-Gilbert M, Gupta M, Thompson S A. Mapping of the loci controlling oleic and linolenic acid contents and development of fad2 and fad3 allele-specific markers in canola (Brassica napus L.). Theor Appl Genet, 2006, 113: 497-507 [30]Scheffler J A, Sharpe A G, Schmidt H, Sperling P, Parkin I A P, Lühs W, Lydiate D J, Heinz E. Desaturase multigene families of Brassica napus arose through genome duplication. Theor Appl Genet, 1997, 94: 583-591 [31]Barret P, Delourme R, Renard M, Domergue F, Lessire R, Delseny M, Roscoe T J. A rapeseed FAE1 gene is linked to the E1 locus associated with variation in the content of erucic acid. Theor Appl Genet, 1998, 96: 177-186 [32]Tanhuanpaa P, Vilkki J, Vihinen M. Mapping and cloning of FAD2 gene to develop allele-specific PCR for oleic acid in spring turnip rape (Brassica rapa ssp.oleifera). Mol Breed, 1998, 4: 543-550 [33]Stoutjesdijkl P A, Hurlestone C, Singh S P, Green A G. High-oleic acid Australian Brassica napus and B. juncea varieties produced by co-suppression of endogenous D12-desaturases. Biochem Soc Transact, 2000, 28: 938-940 [34]Peng Q, Hu Y, Wei R, Zhang Y, Guan C Y, Ruan Y, Liu C L. Simultaneous silencing of FAD2 and FAE1 genes affects both oleic acid and erucic acid contents in Brassica napus seeds. Plant Cell Rep, 2010, 29: 317-325 [35]Schwartzbeck J L, Jung S, Abbott A G, Mosley E, Lewis S, Pries G L, Powell G L. Endoplasmic oleoyl-PC desaturase references the second double bond. Phytochemistry, 2001, 57: 643-652 [36]Maher L, Burton W, Salisbury P, Debonte L, Deng X M. High oleic, low linolenic (HOLL) specialty canola development in Australia. The 12th International Rapeseed Congress, 2007. pp 22-24 [37]Carré P, Evrard J, Judde A, Labalette F, Mazette S. Technological performances of low linolenic / high oleic rapeseed oils for food and non-food application. The 12th International Rapeseed Congress, 2007. pp 152-159 [38]Tu J-X(涂金星), Zhang D-X(张冬晓), Zhang Y(张毅), Fu T-D(傅廷栋). Discussion on some standards of variety registration and breeding goals of Brassica napus in China. Chin J Oil Crop Sci (中国油料作物学报), 2007, 29(3): 350-352 (in Chinese with English abstract) |
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