[1]Inoue H, Higuchi K, Takahashi M, Nakanishi H, Mori S, Nishizawa N K. Three rice nicotianamine synthase genes, OsNAS1, OsNAS2 and OsNAS3, are expressed in cells involved in long distance transport of iron and differentially regulated by iron. The Plant Journal, 2003, 36: 366-381.[2]Higuchi K, Kanazawa K, Nishizawa K, Mori S. The role of nicotianamine synthase in response to Fe nutrition status in Gramineae. Plant and Soil, 1996, 178 (2): 171-177.[3]Yuan D S, Stearman R, Dancis A, Dunn T, Beeler T, Klausner R D. The Menkes/Wilson disease gene homologue in yeast provides copper to a ceruloplasmin-like oxidase required for iron uptake. Proceedings of the National Academy of Sciences of the USA, 1995, 92: 2632-2636.[4]Takahashi M, Terada Y, Nakai I, Nakanishi H, Yoshimura E, Mori S, Nishizawa N K. Role of nicotianamine in the intracellular delivery of metals and plant reproductive development. The Plant Cell, 2003, 15: 1263-1280.[5]Pianelli K, Mari S, Marques L, Lebrun M, Czernic P. Nicotianamine overaccumulation confers resistance to nickel in Arabidopsis thaliana. Transgenic Research, 2005, 14: 739-748.[6]Mari S, Gendre D, Pianelli K, Ouerdane L, Lobinski R, Briat J F, Lebrun M, Czernic P. Root-to-shoot long-distance circulation of nicotianamine and nicotianamine-nickel chelates in the metal hyperaccumulator Thlaspi caerulescens. Journal of Experimental Botany, 2006, 57: 4111-4122.[7]Dreyfus C, Lemaire D, Mari S, Pignol D, Arnoux P. Crystallographic snapshots of iterative substrate translocations during nicotianamine synthesis in archaea. Proceedings of the National Academy of Sciences of the USA, 2009, 22: 16180-16184.[8]Douchkovd D, Gryczka C, Stephan U W, Hell R, Bäumlein H. Ectopic expression of nicotianamine synthase genes results in improved iron accumulation and increased nickel tolerance in transgenic tobacco. Plant Cell and Environment, 2005, 28(3): 365-374.[9]Masuda H, Usuda K, Kobayashi T, Ishimaru Y, Kakei Y, Takahashi M, Higuchi K, Nakanishi H, Mori S, Nishizawa N K. Overexpression of the barley nicotianamine synthase gene HvNAS1 increases iron and zinc concentrations in rice grains. Rice, 2009, 2(4): 155-166.[10]Johnson A A, Kyriacou B, Callahan D L, Carruthers L, Stangoulis J, Lombi E, Tester M. Constitutive overexpression of the OsNAS gene family reveals single-gene strategies for effective iron- and Zinc-biofortification of rice endosperm. PLoS ONE, 2011, 6: e24476. [11]李力. 烟酰胺合酶基因在植物胁迫耐受性应答反应中的功能鉴定[D]. 北京: 中国科学院遗传与发育研究所, 2004.Li L. Nicotianamine synthase gene plays an important role in plant stress tolerance [D]. Beijing: Institute of Genetics and Developmental Biology, 2004. (in Chinese)[12]王育花, 陈芬, 储成才, 肖国樱. 转大麦烟酰胺合成酶基因提高水稻逆境胁迫耐受性的研究. 广西农业生物科学, 2008, 27(1): 25-30.Wang Y H, Chen F, Chu C C, Xiao G Y. Study on improving stress tolerances of rice by transformation of barley nicotianamine synthase gene. Journal of Guangxi Agriculture and Biology Science, 2008, 27(1): 25-30. (in Chinese)[13]骆萍, 王国栋, 陈晓亚. 亚洲棉C4H同源cDNA的分离和表达特征分析. 植物学报, 2001, 43(1): 77-81.Luo P, Wang G D, Chen X Y. Isolation and expression analysis of two cDNAs encoding C4H homologues from Gossypium arboretum. Acta Botanica Sinica, 2001, 43(1): 77-81. (in Chinese) [14]陈天子, 吴慎杰, 李飞飞, 郭旺珍, 张天真. 新疆棉花4 个主栽品种的体细胞胚胎发生及植株再生. 作物学报, 2008, 34(8): 1374-1380.Chen T Z, Wu S J, Li F F, Guo W Z, Zhang T Z. In vitro regeneration of four commercial cotton (Gossypium hirsutum L.) cultivars grown in Xinjiang, China. Acta Agronomica Sinica, 2008, 34(8): 1374-1380. (in Chinese)[15]Chen S B, Songkumarn P, Liu J L, Wang G L. A versatile zero background t-vector system for gene cloning and functional genomics. Plant Physiology, 2009, 150: 1111-1121. [16]Clough S J, Bent A F. Floral dip: A simplified method for Agrobacterium-mediated transformation of Arabidopsis thaliana. The Plant Journal, 1998, 16: 735-743.[17]Jefferson R A, Kavanagh T A, Bevan M W. GUS fusions: β-Glucuronidase as a sensitive and versatile gene fusion marker in higher plants. The EMBO Journal, 1987, 6: 3901-3907.[18]Kang J Y, Choi H I, Im M Y, Kim S Y. Arabidopsis basic leucine zipper proteins that mediate stress-responsive abscisic acid signaling. The Plant Cell, 2002, 14: 343-357.[19]Simpson S D, Nakashima K, Narusaka Y, Seki M, Shinozaki K, Yamaguchi-Shinozaki K. Two different novel cis-acting elements of erd1, a clpA homologous Arabidopsis gene function in induction by dehydration stress and dark-induced senescence. The Plant Journal, 2003, 33: 259-270.[20]Ulmasov T, Hagen G, Guilfoyle T J. Dimerization and DNA binding of auxin response factors. The Plant Journal, 1999, 19: 309-319. [21]Despres C, Chubak C, Rochon A, Clark R, Bethune T, Desveaux D, Fobert P R. The Arabidopsis NPR1 disease resistance protein is a novel cofactor that confers redox regulation of DNA binding activity to the basic domain/leucine zipper transcription factor TGA1. The Plant Cell, 2003, 15: 2181-2191.[22]Luo H, Song F, Goodman R M, Zheng Z. Up-regulation of OsBIHD1, a rice gene encoding BELL homeodomain transcriptional factor, in disease resistance responses. Plant Biology, 2005, 7: 459-468.[23]Quinn J M, Barraco P, Eriksson M, Merchant S. Coordinate copper- and oxygen-responsive Cyc6 and Cpx1 expression in Chlamydomonas is mediated by the same element. The Journal of Biological Chemistry, 2000, 275: 6080-6089.[24]Hartmann U, Sagasser M, Mehrtens F, Stracke R, Weisshaar B. Differential combinatorial interactions of cis-acting elements recognized by R2R3-MYB, BZIP, and BHLH factors control light-responsive and tissue-specific activation of phenylpropanoid biosynthesis genes. Plant Molecular Biology, 2005, 57: 155-171.[25]Laloi C, Mestres-Ortega D, Marco Y, Meyer Y, Reichheld J P. The Arabidopsis cytosolic thioredoxin h5 gene induction by oxidative stress and its W-box-mediated response to pathogen elicitor. Plant Physiology, 2004, 134: 1006-1016.[26]Itzhaki H, Maxson J M, Woodson W R. An ethylene-responsive enhancer element is involved in the senescence-related expression of the carnation glutathione-S-transferase (GSTI) gene. Proceedings of the National Academy of Sciences of the USA, 1994, 91: 8925-8929. [27]Ogawa M, Hanada A, Yamauchi Y, Kuwahara A, Kamiya Y, Yamaguchi S. Gibberellin biosynthesis and response during Arabidopsis seed germination. The Plant Cell, 2003, 15: 1591-1604. [28]Terzaghi W B, Cashmore A R. Light-regulated transcription. Annual Review of Plant Biology, 1995, 46: 445-474.[29]Rogers H J, Bate N, Combe J, Sullivan J, Sweetman J, Swan C, Lonsdale D M, Twell D. Functional analysis of cis-regulatory elements within the promoter of the tobacco late pollen gene g10. Plant Molecular Biology, 2001, 45: 577-585.[30]Ogo Y, Itai R N, Nakanishi H, Inoue H, Kobayashi T, Suzuki M, Takahashi M, Mori S, Nishizawa N K. Isolation and characterization of IRO2, a novel iron-regulated bHLH transcription factor in graminaceous plants. Journal of Experimental Botany, 2006, 57: 2867-2878. [31]Abe M, Takahashi T, Komeda Y. Identification of a cis-regulatory element for L1 layer-specific gene expression, which is targeted by an L1-specific homeodomain protein. The Plant Journal, 2001, 26: 487-494. [32]Abe H, Urao T, Ito T, Seki M, Shinozaki K, Yamaguchi-Shinozaki K. Arabidopsis AtMYC2 (bHLH) and AtMYB2 (MYB) function as transcriptional activators in abscisic acid signaling. The Plant Cell, 2003, 15: 63-78.[33]Sandal N N, Bojsen K, Marcker K A. A small family of nodule specific genes from soybean. Nucleic Acids Research, 1987, 15: 1507-1519. [34]Bate N, Twell D. Functional architecture of a late pollen promoter: Pollen-specific transcription is developmentally regulated by multiple stage-specific and co-dependent activator elements. Plant Molecular Biology, 1998, 37: 859-869.[35]Elmayan T, Tepfer M. Evaluation in tobacco of the organ specificity and strength of the rol D promoter, domain A of the 35S promoter and the 35S promoter. Transgenic Research, 1995, 4: 388-396.[36]Maruyama-Nakashita A, Nakamura Y, Watanabe-Takahashi A, Inoue E, Yamaya T, Takahashi H. Identification of a novel cis-acting element conferring sulfur deficiency response in Arabidopsis roots. The Plant Journal, 2005, 42: 305-314.[37]Yu D, Chen C, Chen Z. Evidence for an important role of WRKY DNA binding proteins in the regulation of NPR1 gene expression. The Plant Cell, 2001, 13: 1527-1540.[38]Zhang Z L, Xie Z, Zou X, Casaretto J, Ho T H, Shen Q J. A rice WRKY gene encodes a transcriptional repressor of the gibberellin signaling pathway in aleurone cells. Plant Physiology, 2004, 134: 1500-1513.[39]Ko J H, Beers E P, Han K H. Global comparative transcriptome analysis identifies gene network regulating secondary xylem development in Arabidopsis thaliana. Molecular Genetics and Genomics, 2006, 276: 517-531.[40]Han D G, Yang G H, Xu K D, Shao Q, Yu Z Y, Wang B, Ge Q L, Yu Y. Overexpression of a Malus xiaojinensis Nas1 gene influences flower development and tolerance to iron stress in transgenic tobacco. Plant Molecular Biology Reporter, 2013, 31(4): 802-809. [41]Zhou M L, Qi L P, Pang J F, Zhang Q, Lei Z, Tang Y X, Zhu X M, Shao J R, Wu Y M. Nicotianamine synthase gene family as central components in heavy metal and phytohormone response in maize. Functional & Integrative Genomics, 2013, 13: 229-239. [42]Marschner H, Rmheld V, Kissel M. Strategies of plants for acquisition of iron. Plant Soil, 1994, 165: 261-274.[43]MORI S. Iron acquisition by plants. Current Opinion in Plant Biology, 1999, 2: 250-253.[44]张士荣, 白灯莎•买买提艾力, 冯固. 新疆棉花幼叶黄化现象及其铁锌含量差异分析. 植物营养与肥料学报, 2007, 13(4): 745-748.Zhang S R, Bai D S, Feng G. The phenomenon of chlorosis and analysis of difference in Fe and Zn content of cotton in Xinjiang. Plant Nutrition and Fertilizer Science, 2007, 13(4): 745-748. (in Chinese) |