利用RNA干扰技术研究拟南芥EARLI1基因功能
详细信息    本馆镜像全文|  推荐本文 |  |   获取CNKI官网全文
摘要
拟南芥(Arabidopsis thaliana)是一种模式植物,属于十字花科(Cruciferae)拟南芥属(Arabidopsis),具有基因组小、生命周期短等特点,近年来已被广泛用于功能基因组学研究领域,并已取得大量的研究成果。EARLI1基因编码一个大小为14.7kDa、定位于细胞壁的蛋白质,是脯氨酸富含蛋白(PRP)家族成员。EARLI1基因已被证明具有抵抗低温胁迫和真菌侵染的功能。本工作的主要目的是通过生理学、组织化学和分子生物学等实验手段,进一步研究和探索EARLI1基因的功能。
     显微观察结果显示,EARLI1与拟南芥叶片细胞的形态建成有关。通过组织化学染色发现EARLI1还参与了花序茎中木质素的合成调控过程。野生型和EARLI1 RNA干扰植株花序茎中的木质素含量平均值分别为9.67%和8.76%。表达分析表明木质素合成的关键酶CCR(肉桂酰辅酶A还原酶)受EARLI1转录水平的影响。
     EARLI1还能够在很大程度上调节拟南芥的开花过程。下调EARLI1表达水平会使开花时间明显提前。野生型和EARLI1 RNA干扰植株开花所需时间平均分别为39.7天和19.4天。二者的主茎长、节间数、莲座叶数统计数据也有明显差异。RT-PCR结果显不EARLI1可能是通过自主途径维持FLC(FLOWERING LOCUS C)的表达,从而延迟开花的。
     用过氧化氢处理Col-FRI-Sf2和RNAi Col-FRI-Sf2植株,并统计萌发率、根伸长量等数据,发现RNA干扰植株比野生型对胁迫条件更加敏感,它的种子萌发率在过氧化氢浓度为5mmol/L时相对于野生型有显著下降,而根伸长量则在0.1mmol/L和0.5mmol/L过氧化氢处理时明显低于野生型。用100mmol/L的过氧化氢处理不同时间,RNA印迹分析结果显示过氧化氢确实能够诱导EARLI1基因表达。
Arabidopsis thaliana is a model plant, it belongs to Cruciferae. In recent years, Arabidopsis has been widely used in fields related to functional genomics owing to its advantages such as small genome and short life cycle, and has made a lot of research achievements. EARLI1 gene encodes a 14.7kDa protein located in cell wall, it is a member of PRP (proline-rich protein) family. EARLI1 has been documented to have multiple functions including resistance to low temperature and fungus infection. The main purpose of this study is to further study the function of EARLI1 gene with physiology, histochemistry, molecular biology or other experimental methods.
     Microscopic observation showed that EARLI1 is associated with the morphogenesis of leaf cells in Arabidopsis. Through the histochemistry study, EARLI1 was found to be involved in regulation of lignin synthesis in inflorescence stems. The mean value of lignin content in inflorescence stems of Col-FRI-Sf2 and RNAi Col-FRI-Sf2 plants were 9.67% and 8.76% respectively. Expression analysis of EARLI1 revealed that CCR, a key enzyme in lignin synthesis, could be affected by EARLI1.
     EARLI1 also can control the flowering process to a large extent in Arabidopsis. RNAi Col-FRI-Sf2 plants of EARLI1 flowered earlier than Col-FRI-Sf2 wild type plants. The average flowering time of Col-FRI-Sf2 and RNAi Col-FRI-Sf2 were 39.7 and 19.4 days, respectively. There are significant differences in main stem length, internode number and rosette leaf number between Col-FRI-Sf2 and RNAi Col-FRI-Sf2 plants. The results of RT-PCR showed that EARLI1 might delay the flowering time through the autonomous pathway by maintaining the abundance of FLC transcripts.
     Hydrogen peroxide was used to treat Col-FRI-Sf2 and RNAi Col-FRI-Sf2 plants. The changes in germination rate of seeds, elongation of root length and other data were analyzed statistically. The results showed that RNA interference plants is much more sensitive to hydrogen peroxide than the wild type plants. Compared to wild-type plants, the seed germination rate of RNA interference lines under 5mmol/L hydrogen peroxide concentration decreased significantly. The root length elongation of RNAi lines subjected to O.lmmol/L, 0.5mmol/L hydrogen peroxide treatment was significantly lower than wild-type plants. RNA blotting analysis showed that the expression of EARLI1 gene could be induced definitely by 100mmol/L hydrogen peroxide for different time.
引文
[1]曹仪植.拟南芥.北京:高等教育出版社,2004:1-9
    [2]Zhang Y, Schlappi M. Cold responsive EARLI1 type HyPRPs improve freezing survival of yeast cells and form higher order complexes in plants. Planta,2007,227:233-43
    [3]Weyman PD, Pan Z, Feng Q, et al. A circadian rhythm-regulated tomato gene is induced by arachidonic acid and Phythophthora infestans infection. Plant Physiol,2006a, 140:235-248
    [4]Jose-Estanyol M, Gomis-Ruth FX, Puigdomenech P. The eight-cysteine motif, a versatile structure in plant proteins. Plant Physiol Biochem,2004,42:355-365
    [5]Richards KD, Gardner RC. pEARLI1:an Arabidopsis member of a conserved gene family. Plant Physiology,1995,109,1497.
    [6]Richards KD, Schott EJ, Sharma YK, et al. Aluminum induces oxidative stress genes in Arabidopsis thaliana. Plant Physiology,1998,116,409-418.
    [7]Wilkosz R, Schlappi M. A gene expression screen identifies EARLI1 as a novel vernalization-responsive gene in Arabidopsis thaliana. Plant Molecular Biology,2000, 44:777-787
    [8]Bubier J, Schlappi M. Cold induction of EARLI1, a putative Arabidopsis lipid transfer protein, is light and calcium dependent. Plant Cell Environ,2004,27:929-936
    [9]Vogel JT, Zarka DG, Van Buskirk HA, Fowler SG, Thomashow MF. Roles of the CBF2 and ZAT12 transcription factors in configuring the low temperature transcriptome of Arabidopsis. Plant J,2005,41:195-211
    [10]Wang H., Datla R, Georges F, Loewen M. Promoters from KIN1 and cor6.6, two homologous Arabidopsis thaliana genes:transcriptional regulation and gene expression induced by low temperature, ABA, osmoticum and dehydration. Plant Molecular Biology, 1995,28:605-617
    [11]Eulgem T, Victor JW, Chang H-S, et al. Gene expression signatures from three genetically separable resistance gene signaling pathways for downy mildew resistance. Plant Physiology,2004,135:1129-1144
    [12]Arondel V, Vergnolle C, Cantrel C, Kader JC. Lipid transfer proteins are encoded by a small multigene family in Arabidopsis thaliana. Plant Sci,2000,157:1-12
    [13]Celine C, Nawrath C, Metraux JP. Cuticular defects lead to full immunity to a major plant pathogen. The Plant Journal,2007,49:972-980
    [14]Jordan BS, Angie G, Eduardo B. DNA array analyses of Arabidopsis thaliana lacking a vacuolar Na+/H+antiporter:impact of AtNHX1 on gene expression. The Plant Journal, 2004,40:752-771
    [15]Jordan BS, Yehoshua S, Eduardo B. Impact of AtNHX1, a vacuolar Na+/H+antiporter, upon gene expression during short-and long-term salt stress in Arabidopsis thaliana. BMC Plant Biology 2007,7:18
    [16]Van Loon LC, Pierpoint WS, Boller T, Conejero V. Recommendation for naming plant pathogenesis-related proteins. Plant Mol Biol Rep,1994,12(Suppl 3):245-264.
    [17]Kav NNV, Srivastava S, Goonewardene L, Blade SF. Proteome-level changes in the roots of Pisum sativum in response to salinity. Ann Appl Biol,2004,145(Suppl 2):217-230.
    [18]Iturriaga EA, Leech MJ, Barratt DHP, Wang TL. Two ABA responsive proteins from pea (Pisum sativum L.) are closely related to intracellular pathogenesis-related proteins. Plant Mol Biol,1994,24(Suppl 1):235-240.
    [19]Sowmya SK, Sanjeeva S, Mohsen M, et al. Transcriptional profiling of pea ABR17 mediated changes in gene expression in Arabidopsis thaliana. BMC Plant Biology,2008, 8:91
    [20]Lewis NG, Yamamoto E. Lignin:occurrence, biogenesis and biodegradation. Annu Rev Plant Physiol Plant Mol Biol,1990,41:455-496.
    [21]Whetten R,Sederoff R. Lignin biosynthesis. The Plant Cell,1995,7:1001-1013.
    [22]Baucher M, Monties B, Van Montagu M, et al. Biosynthesis and genetic engineering of lignin. Critical Reviews in Plant Sciences,1998,17 (2):125-197
    [23]Minami E, Ozeki Y, Matsuoka M, Koizuka N, et al. Structure and some characterization of the gene for phenylalanine ammonia-lyase from rice plants. Euro J Biochem,1989, 185(1):19-25
    [24]Campbell MM, Sederoff RR. Variation in lignin content and composition. Mechanisms of control and implication for the genetic improvement of plants. Plant Physiol,1996, 110:3-13.
    [25]Boerjan W, Ralph J, Baucher M. Lignin biosynthesis. Annu Rev Plant Biol,2003, 54:519-546.
    [26]赵华燕,魏建华,宋艳茹.木质素生物合成及其基因工程研究进展.植物生理与分子生物学学报,2004,30:361-370.
    [27]Marita JM, Ralph J, Hatfield RD, et al. Structural and compositional modifications in lignin of transgenic alfalfa down-regulated in caffeic acid 3-O-methyltransferase and caffeoyl coenzyme A 3-O-methyltransferase Phytochemistry,2003,62:53-65
    [28]Fujiwara T, Lessard PA, Beachy RN. Inactivation of the nopaline synthase gene by double transformation:eactivation by segregation of the induced DNA. Plant Cell Rep, 1993,12:133-138
    [29]Wanner LA, Li G, Ware D, et al. The phenylalanine ammonia-lyase gene family in Arbidopsis Thaliana. Plant Mo Biol,1995,27:327-338
    [30]Zhu Q, Dabi T, Beeche A, et al. Cloning and properties of a rice gene encoding phenylalanine ammonia-lyase. Plant Mol Biol,1995,29:535-550
    [31]Sewalt VJH, et al. Reduced lignin content and altered lignin composition in transgenic tobacco down-regulated in expression of phenylalanine ammonia-lyase or cinnamate 4-hydroxylase. Plant Physiol,1997,115:41-57.
    [32]Rohde A, Morreel K, Ralph J, et al. Molecular phenotyping of the pall and pal2 mutants of Arabidopsis thaliana reveals far-reaching consequences on phenylpropanoid, amino acid,and carbohydrate metabolism. The Plant Cell,2004,16:2749-2771.
    [33]Howlasp A, Sewalt V. J. H, Paiva N. L,et al. Overexpression of L-pheny-lalanine ammonialyase in transgenic tobacco plants reveals control points for flux into phenylpropaniod biosynthesis. Plant physiol,1996,112:1617-1624.
    [34]Schoch G, Goepfert S, Morant M, et al. CYP98A3 from Arabidopsis thaliana is a 3-hydroxylase of phenolic esters, a missing link in the phenylpropanoid pathway. J Biol Chem,2001,276:36566-36574.
    [35]Ramesh B, N, Qun Xia, Cyril J, Kartha E. K, et al. Arabidopsis CYP98A3 mediating aromatic 3-hydroxylation. Developmental regulation of the gene, and expression in yeast. Plant Physiology,2002,130:210-220.
    [36]Franke R, Hemm MR, Denault JW, et al. Changes in secondary metabolism and deposition of an unusual lignin in the ref8 mutant of Arabidopsis. Plant J,2002, 30:47-59.
    [37]Franke R, Humphreys JM, Hemm MR, et al. The Arabidopsis REF8 gene encodes the 3-hydroxylase of phenylpropanoid metabolism. Plant J,2002b 30:33-45.
    [38]Chen F, Yasuda S, Fukushima K. Evidence for a novel biosynthetic pathway that regulates the ratio of syringyl to guaiacyl residues in lignin in the differentiating xylem of Magniolia kobus DC. Planta,1999, (207):597-603.
    [39]Ruegger M, Meyer K, Cusumano JC, et al. Regulation of ferulate-5-hydroxylase expression in Arabidopsis in the context of sinapate ester biosynthesis. Plant Physiol, 1999,119:101-110.
    [40]Lee D, Douglas CJ. Two divergent members of a tobacco 4-coumarate:coenzyme A ligase (4CL) gene family. Plant Physiol,1996,112:193-205.
    [41]Kajita S, Hishiyama S, Tomimura Y, et al. Structural characterization of modified lignin in transgenic tobacco plants in which the activity of 4-coumarate:coenzyme A ligase is depressed. Plant Physiology,1997,114:871-879.
    [42]Kajita S, KatayamaY, Omori S. Alteration in the biosynthesis of lignin in transgenic plants with chimeric genes for 4-coumarate:coenzymeA ligase. Plant and Cell Physiology,1996,37:957-965.
    [43]Hu WJ, Harding SA, Lung J, et al. Repression of lignin biosynthesis promotes accumulation and growth in transgenic trees. Nat Biotechnol,1999,17:808-812.
    [44]Goicoechea M, Lacombe E, Legay S, et al. EgMYB2,a new transcriptional activator from eucalyptus xylem, regulates secondary cell wall formation and lignin biosynthesis. The Plant Journal,2005,43:553-567.
    [45]Baucher M, Halpin C, Petit M, et al. Lignin:Genetic engineering and impact on pulping. Critical Reviews in Biochemistry and Molecular Biology,2003,38:305-350.
    [46]Laskar DD, Jourdes M, Patten AM, et al. The Arabidopsis cinnamoyl CoA reductase irx4 mutant has a delayed but coherent (normal) program of lignification. The Plant Journal, 2006,48:674-686.
    [47]Halpin C, Knight ME, Foxon GA, et al. Manipulation of lignin quality by down regulation of cinnamyl alcohol dehydrogenase. Plant J,1994,6:339-350.
    [48]Bernier G. The control of floral evocation and morphogenesis. Rev Plant Phys Plant Mol Biol,1988,39:175.
    [49]Mouradov A, Cremer F, Coupland G. Control of flowering time:Interacting pathways as a basis for diversity. Plant Cell,2002,14 (Suppl):S111-S130.
    [50]Boss PK, Bastow RM, Mylne JS, Dean C. Multiple pathways in the decision to flower: Enabling, promoting, and resetting. Plant Cell,2004,16:S18-S31.
    [51]Komeda Y. Genetic regulation of time to flower in Arabidopsis thaliana. Annu Rev Plant Biol,2004,55:521-535
    [52]Clack, T, Mathews, S, Sharrock RA. The phytochrome apoprotein family in Arabidopsis is encoded by five genes:the sequences and expression of PHYD and PHYE. Plant Mol Biol,1994,25:413
    [53]Lin C. Photoreceptors and regulation of flowering time. Plant Physiol,2000,123,39.
    [54]Quail PH. Phytochrome photosensory signalling networks. Nat Rev Mol Cell Biol,2002, 3:85-93
    [55]Mathews S. Phytochrome-mediated development in land plants:red light sensing evolves to meet the challenges of changing light environments. Mol Ecol,2006,15:3483-3503
    [56]Rockwell NC, Su YS, Lagarias JC. Phytochrome structure and signaling mechanisms. Annu Rev Plant Biol,2006,57:837-858
    [57]Reed JW, Nagpal P, Poole DS, Furuya M, Chory J. Mutations in the gene for the red/far-red light receptor phytochrome B alter cell elongation and physiological responses throughout Arabidopsis development. Plant Cell,1993,5:147-157
    [58]Reed JW, Nagatani A, Elich TD, Fagan M, Chory J. Phytochrome A and Phytochrome B have overlapping but distinct functions in Arabidopsis development. Plant Physiol,1994, 104:1139-1149
    [59]Neff MM, Chory J. Genetic interactions between phytochrome A, phytochrome B, and cryptochrome 1 during Arabidopsis development. Plant Physiol,1998,118:27-35
    [60]Aukerman MJ. A deletion in the PHYD gene of the Arabidopsis Wassilewskija ecotype defines a role for phytochrome D in red/far-red light sensing. Plant Cell,1997,9: 1317-1326
    [61]Devlin PF, Patel SR, Whitelam GC. Phytochrome E influences internode elongation and flowering time in Arabidopsis. Plant Cell,1998,10:1479-1487
    [62]Weller JL, Beauchamp N, Kerckhoffs LHJ, et al. Interaction of phytochromes A and B in the control of de-etiolation and flowering in pea. Plant J,2001,26:283-294
    [63]Childs KL, Miller FR, Cordonnier-Pratt MM, et al. The Sorghum bicolor photoperiod sensitive gene, Ma3, encodes a phytochrome B. Plant Physiol,1997,113:611-619
    [64]Tessadori F, Schulkes RK, Driel RV, et al. Light-regulated large-scale reorganization of chromatin during the floral transition in Arabidopsis. Plant J,2007,50:848-57.
    [65]Devlin PF, Kay SA. Cryptochromes are required for phytochrome signaling to the circadian clock but not for rhythmicity. Plant Cell,2000,12:2499-510.
    [66]Mas P, Devlin PF, Panda S, Kay SA. Functional interaction of phytochrome B and cryptochrome 2. Nature,2000,408:207-11
    [67]Somers DE, Devlin PF, Kay SA. Phytochromes and cryptochromes in the entrain ment of the Arabidopsis circadian clock. Science,1998,282:1488-90.
    [68]Alabadi D, Yanovsky MJ, Mas P, Harmer SL. Critical role for CCA1 and LHY in maintaining circadian rhythmicity in Arabidopsis. Curr Biol,2002,12:757-61.
    [69]Mizoguchi T, Wheatley K, Hanzawa Y, et al. LHY and CCA1 are partially redundant genes required to maintain circadian rhythms in Arabidopsis. Dev Cell,2002,2:629-41.
    [70]Alabadi D, Oyama T, Yanovsky MJ, et al. Reciprocal regulation between TOC1 and LHY/CCA1 within the Arabidopsis circadian clock. Science,2001,293:880-883.
    [71]Jang S, Marchal V, Panigrahi KC, et al. Arabidopsis COP1 shapes the temporal pattern of CO accumulation conferring a photoperiodic flowering response. EMBO,2008,27: 1277-1288
    [72]Liu LJ, Zhang YC, Li QH, et al. COP1-mediated ubiquitination of CONSTANS is implicated in cryptochrome regulation of flowering in Arabidopsis. Plant Cell,2008,20: 292-306
    [73]Mouradov A, Cremer F, Coupland G. Control of flowering time:Interacting pathways as a basis for diversity. The Plant Cell,2002,14 Suppl.S111-30
    [74]Parcy F. Flowering:a time for integration. Int J Dev Biol,2005,49:585-593
    [75]Michaels SD, He Y, Scortecci KC, Amasino RM. Attenuation of FLOWERING LOCUS C activity as a mechanism for the evolution of summer-annual flowering behavior in Arabidopsis. Proc Natl Acad Sci,2003,100:10102-10107
    [76]Johanson U, West J, Lister C, Michaels S, Amasino R, Dean C. Molecular analysis of FRIGIDA, a major determinant of natural variation in Arabidopsis flowering time. Science,2000,290:344-347.
    [77]Michaels SD, Amasino RM. FLOWERING LOCUS C encodes a novel MADS domain protein that acts as a repressor of flowering. Plant Cell,1999,11:949-956
    [78]Sheldon CC, Burn JE, Perez PP, et al. The FLF MADS box gene:a repressor of flowering in Arabidopsis regulated by vernalization and methylation. Plant Cell,1999,11: 445-458
    [79]Johanson U, West J, Lister C. Molecular analysis of FRIGIDA, a major determinant of natural variation in Arabidopsis flowering time. Science,2000,290:344
    [80]Michaels SD, Bezerra IC, Amasino RM. FRIGIDA-related genes are required for the winter-annual habit in Arabidopsis. Proc Natl Acad Sci,2004,101:3281-3285
    [81]Sung S, Amasino RM. Vernalization in Arabidopsis thaliana is mediated by the PHD finger protein VIN3. Nature,2004b,427:159-164
    [82]Gendall AR, Levy YY, Wilson A, Dean C. The VERNALIZATION 2 gene mediates the epigenetic regulation of vernalization in Arabidopsis. Cell,2001,107:525-535
    [83]Levy YY, Mesnage S, Mylne JS, Gendall AR, Dean C. Multiple roles of Arabidopsis VRN1 in vernalization and flowering time control. Science,2002,297:243-246.
    [84]张素芝,左建儒.拟南芥开花时间调控的研究进展.生物化学与生物物理进展,2006,33:301-309
    [85]Koornneef M, Hanhart CJ, van der Veen JH. A genetic and physiological analysis of late flowering mutants in Arabidopsis thaliana. Mol Gen Genet,1991,229:57-66
    [86]Koornneef M, Alonso-Blanco C, Blankestijn-De Vries H, et al. Genetic interactions among late-flowering mutants of Arabidopsis. Genetics,1998,148:885-892.
    [87]Lee I, Aukerman MJ, Gore SL, et al. Isolation of LUMINIDEPENDENS:a gene involved in the control of flowering time in Arabidopsis. Plant Cell,1994,6:75-83.
    [88]Sanda SL, Amasino RM:Ecotype-specific expression of a flowering mutant phenotype in Arabidopsis thaliana. Plant Physiol,1996,111:641-644.
    [89]LimMH, KimJ, KimYS, et al. A new Arabidopsis gene, FLK, encodes an RNA binding protein with K homology motifs and regulates flowering time via FLOWERING LOCUS C. Plant Cell,2004,16:731-740.
    [90]Macknight R, Bancroft I, Page T, et al. FCA, a gene controlling flowering time in Arabidopsis, encodes a protein containing RNA-binding domains. Cell,1997, 89:737-745
    [91]Ausin I, Alonso-Blanco C, Jarillo JA, et al. Regulation of flowering time by FVE, a retinoblastoma-associated protein. Nat Genet,2004,36:162-166
    [92]Simpson GG, Dean C. Arabidopsis, the Rosetta stone of flowering time? Science,2002, 296:285-289
    [93]Moon J, Suh SS, Lee H, et al. The SOC1 MADS-box gene integrates vernalization and gibberellin signals for flowering in Arabidopsis. Plant J,2003,35:613-623
    [94]Samach A, Onouchi H, Gold SE, et al. Distinct roles of CONSTANS target genes in reproductive development of Arabidopsis. Science,2000,288:1613-1616.
    [95]Reeves PH, Coupland G. Analysis of flowering time control in Arabidopsis by comparison of double and triple mutants. Plant Physiol,2001,126:1085-1091
    [96]Hepworth SR, Valverde F, Ravenscroft D, et al. Antagonistic regulation of flowering-time gene SOC1 by CONSTANS and FLC via separate promoter motifs. EMBO J,2002, 21:4327-4337.
    [97]Lang A. The effect of gibberellin upon flower formation. Proc Natl Acad Sci,1957, 43:709-717.
    [98]Wilson RN, Heckman JW, Somerville CR. Gibberellin is required for flowering in Arabidopsis thaliana under short days. Plant Physiol,1992,100:403-408.
    [99]Bolle C, Koncz C, Chua NH. PAT1, a new member of the GRAS family, is involved in phytochrome A signal transduction. Genes Dev,2000,14:1269-1278.
    [100]Olszewski N, Sun T, Gubler F. Gibberellin signaling:Biosynthesis, catabolism and response pathways. Plant Cell,2002,14:S61-S80.
    [101]Pineiro M, Coupland G. The control of flowering time and floral identity in Arabidopsis. Plant Physiol,1998,117:1-8
    [102]Blazquez MA, Weigel D. Integration of floral inductive signals in Arabidopsis. Nature, 2000,404:889-892.
    [103]Mittler R, Vanderauwera S, Gollery M, et al. Reactive oxygen gene network of plants. Trends Plant Sci,2004,9:490-498.
    [104]Vandenabeele S, Vanderauwera S, Vuylsteke M, et al. Catalase deficiency drastically affects high light-induced gene expression in Arabidopsis thaliana. Plant J,2004,39: 45-58
    [105]Pnueli L, Liang H, Rozenberg M. Growth suppression, altered stomatal responses, and augmented induction of heat shock proteins in cytosolic ascorbate peroxidase (Apx1)-deficient Arabidopsis plants. Plant J,2003,34:187-203.
    [106]Torres MA, Dangl JL, Jones JD. Arabidopsis gp91phox homologues AtrbohD and AtrbohF are required for accumulation of reactive oxygen intermediates in the plant defense response. Proc Natl Acad Sci,2002,99:517-522
    [107]Foreman J, Bothwell JH, Demidchik V, et al. Reactive oxygen species produced by NADPH oxidase regulate plant cell growth. Nature,2003,422:442-446.
    [108]Kwak JM, Mori IC, Pei ZM, et al. NADPH oxidase AtrbohD and AtrbohF genes function in ROS-dependent ABA signaling in Arabidopsis. EMBO,2003,22:2623-2633
    [109]Rizhsky L, Liang HJ, Mittler R. The water-water cycle is essential for chloroplasts protection in the absence of stress. J Biol Chem,2003,278:38921-38925
    [110]Shinozaki K, Yamaguchi-Shinozaki K. Molecular responses to dehydration and low temperature:differences and cross-talk between two stress signaling pathways. Curr Opin Plant Biol,3:217-223
    [111]Fujita M, Fujita Y, Maruyama K et al. A dehydration-induced NAC protein, RD26, is involved in a novel ABA-dependent stress-signaling pathway. Plant J,2004,39:863-876
    [112]Vandenabeele S, Van Der Kelen K, Dat J, et al. A comprehensive anlysis of hydrogen peroxide-induced gene expression in tobacco. Proc Natl Acad Sci,2003,100: 16113-16118.
    [113]Vanderauwera S, Zimmermann P, Rombauts S, et al. Genome-wide analysis of hydrogen peroxide-regulated gene expression in Arabidopsis reveals a high light-induced transcriptional cluster involved in anthocyanin biosynthesis. Plant Physiol,2005,139: 806-821
    [114]Gleave AP. A versatile binary vector system with a T-DNA organisational structure conducive to efficient integration of cloned DNA into the plant genome. Plant Mol Biol, 1992,20:1203-1207
    [115]Murashige T, Skoog F. A revised medium for rapid growth and bioassays with tobacco tissue cultures. Physiol Plant,1962,15:473-497
    [116]Guo S, Kemphues KJ. Par-1 a gene required for establishing polarity in C. elegans embryos, encodes a putative Ser/Thr kinase that is asymmetrically distributed. Cell,1995, 81:611-20
    [117]Napoli C, Lemieux C, Jorgensen R. Introduction of a chimeric chalcone synthase gene into petunia results in reversible co-suppression of homologous genes in trans. Plant Cell, 1990,2:279-89
    [118]Fire A, Xu S, Montgomery MK,写全.Potent and specific genetic interference by double-stranded RNA in Caenorhabditis elegans. Narture,1998,391:806-11.
    [119]李和平.植物纤维技术.北京:科学出版社,2009:78-85
    [120]Zhong RQ, Taylor JJ, Ye ZH. Disruption of interfascicular fiber differentiation in an Arabidopsis mutant. The Plant Cell,1997,9:2159-2170.
    [121]李靖,程周,杨晓伶等.紫外分光光度法测定微量人参木质素的含量.中药材,2006,29:239-241
    [122]Zhong RQ, Ye ZH. Regulation of cell wall biosynthesis. Current Opinion in Plant Biology,2007,10:1-9
    [123]Bessire M, Chassot C, Jacquat A C, et al. A permeable cuticle in Arabidopsis leads to a strong resistance to Botrytis cinerea. The EMBO Journal,2007,26:2158-2168
    [124]Sebastien B, Laurent H, Pierrette G, et al. Flavonoid accumulation in Arabidopsis repressed in lignin synthesis affects auxin transport and plant growth. The Plant Cell, 2007,19:148-162
    [125]Govrin EM, Levine A. The hypersensitive response facilitates plant infection by the necrotrophic pathogen Botrytis cinerea. Curr Biol,2000,10:751-757
    [126]Keller T, Damude HG, Werner D, et al. A plant homolog of the neutrophil NADPH oxidase gp91-phox subunit gene encodes a plasma membrane protein with Ca2+binding motifs. Plant Cell,1998,10:255-266.
    [127]Neill S, Desikan R, Clarke A. et al. Hydrogen peroxide and nitric oxide as signalling molecules in plants. J Exp Bot,2002,53:1237-1247.
    [128]Van BF, Vranova E, Dat JF, et al. The role of active oxygen species in plant signal transduction. Plant Sci,2001,161:405-414.
    [129]Pastori G.M, Foyer C.H. Common components, networks, and pathways of cross-tolerance to stress. The central role of "redox" and abscisic acid-mediated controls. Plant Physiol,2002,129:460-468.
    [130]Desikan R, Mackerness AHS, Hancock JT, et al. Regulation of the Arabidopsis transcriptome by oxidative stress. Plant Physiol,2001,127:159-172.
    [131]Finkelstein RR, Zeevaart JAD. Gibberellin and ab'scisic acid biosynthesis and response.In arabidopsis. Pp,1994,523-553
    [132]Doerner P, Jorgensen JE, You R, et al. Control of root growth and development by cyclin expression. Nature,1996,380:520-523

© 2004-2018 中国地质图书馆版权所有 京ICP备05064691号 京公网安备11010802017129号

地址:北京市海淀区学院路29号 邮编:100083

电话:办公室:(+86 10)66554848;文献借阅、咨询服务、科技查新:66554700