Abstract
Plant architecture determines grain production in rice (Oryza sativa) and is affected by important agronomic traits such as tillering, plant height, and panicle morphology. Many key genes involved in controlling the initiation and outgrowth of axillary buds, the elongation of stems, and the architecture of inflorescences have been isolated and analyzed. Previous studies have shown that SiPf40, which was identified from a foxtail millet (Setaria italica) immature seed cDNA library, causes extra branches and tillers in SiPf40-transgenic tobacco and foxtail millet, respectively. To reconfirm its function, we generated transgenic rice plants overexpressing SiPf40 under the control of the ubiquitin promoter. SiPf40-overexpressing transgenic plants have a greater tillering number and a wider tiller angle than wild-type plants. Their root architecture is modified by the promotion of lateral root development, and the distribution of xylem and phloem in the vascular bundle is affected. Analysis of hormone levels showed that the ratios of indole-3-acetic acid/zeatin (IAA/ZR) and IAA/gibberellic acid (IAA/GA) decreased in SiPf40-transgenic plants compared with wild-type plants. These findings strongly suggest that SiPf40 plays an important role in plant architecture.
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Eide D, Broderius M, Fett J, et al. A novel iron-regulated metal transporter from plants identified by functional expression in yeast. Proc Natl Acad Sci USA, 1996, 93: 5624–5628 1:CAS:528:DyaK28Xjt1Ojt7w%3D, 10.1073/pnas.93.11.5624, 8643627
Zhao H, Eide D. The yeast ZRT1 gene encodes the zinc transporter protein of a high-affinity uptake system induced by zinc limitation. Proc Natl Acad Sci USA, 1996a, 93: 2454–2458 1:CAS:528:DyaK28XhvVSktLY%3D, 10.1073/pnas.93.6.2454, 8637895
Zhao H, Eide D. The ZRT2 gene encodes the low affinity zinc transporter in Saccharomyces cerevisiae. J Biol Chem, 1996b, 271: 23203–23210 1:CAS:528:DyaK28XlvVCgs7s%3D, 10.1074/jbc.271.38.23203, 8798516
Grotz N, Fox T, Connolly E, et al. Identification of a family of zinc transporter genes from Arabidopsis that respond to zinc deficiency. Proc Natl Acad Sci USA, 1998, 95: 7220–7224 1:CAS:528:DyaK1cXjslymt7g%3D, 10.1073/pnas.95.12.7220, 9618566
Vert G, Briat J F, Curie C. Arabidopsis IRT2 gene encodes a root-periphery iron transporter. Plant J, 2001, 26: 181–189 1:CAS:528:DC%2BD3MXkvVSnsr0%3D, 10.1046/j.1365-313x.2001.01018.x, 11389759
Assunção A G L, Da Costa Martins P, De Folter S, et al. Elevated expression of metal transporter genes in three accessions of the metal hyperaccumulator Thlaspi caerulescens. Plant Cell Environ, 2001, 24: 217–226 10.1111/j.1365-3040.2001.00666.x
Pence N S, Larsen P B, Ebbs S D, et al. The molecular physiology of heavy metal transport in the Zn/Cd hyperaccumulator Thlaspi caerulescens. Proc Natl Acad Sci USA, 2000, 97: 4956–4960 1:CAS:528:DC%2BD3c**vFKisrk%3D, 10.1073/pnas.97.9.4956, 10781104
Plaza S, Tearall K L, Zhao F J, et al. Expression and functional analysis of metal transporter genes in two contrasting ecotypes of the hyperaccumulator Thlaspi caerulescens. J Exp Bot, 2007, 58: 1717–1728 1:CAS:528:DC%2BD2sXmsFeisrg%3D, 10.1093/jxb/erm025, 17404382
Cohen C K, Fox T C, Garvin D F, et al. The role of iron-deficiency stress responses in stimulating heavy-metal transport in plants. Plant Physiol, 1998, 116: 1063–1072 1:CAS:528:DyaK1c**tVOjs7g%3D, 10.1104/pp.116.3.1063, 9501139
Moreau S, Thomson R M, Kaiser B N, et al. GmZIP1 encodes a symbiosis-specific zinc transporter in soybean. J Biol Chem, 2002, 277: 4738–4746 1:CAS:528:DC%2BD38XhsFeqt7s%3D, 10.1074/jbc.M106754200, 11706025
Eckhardt U, Mas Marques A, Buckhout T J. Two iron-regulated cation transporters from tomato complement metal uptake-deficient yeast mutants. Plant Mol Biol, 45: 437–448
Schikora A, Thimm O, Linke B, et al. Expression, localization, and regulation of the iron transporter LeIRT1 in tomato roots. Planta, 2006, 284: 101–108 1:CAS:528:DC%2BD28XntF2is7Y%3D
Burleigh S H, Kristensen B K, Bechmann I E. A plasma membrane zinc transporter from Medicago truncatula is up-regulated in roots by Zn fertilization, yet down-regulated by arbuscular mycorrhizal colonization. Plant Mol Biol, 2003, 52: 1077–1088 1:CAS:528:DC%2BD3sXmvVais7k%3D, 10.1023/A:1025479701246, 14558666
Lo S F, Yang S Y, Chen K T, et al. A novel class of gibberellin 2-oxidases control semidwarfism, tillering, and root development in rice. Plant Cell, 2008, 20: 2603–2618 1:CAS:528:DC%2BD1cXhsFWms7nF, 10.1105/tpc.108.060913, 18952778
Bughio N, Yamaguchi H, Nishizawa N K, et al. Cloning an iron-regulated metal transporter from rice. J Exp Bot, 2002, 53: 1677–1682 1:CAS:528:DC%2BD38XlsFSmtr8%3D, 10.1093/jxb/erf004, 12096107
Ishimaru Y, Suzuki M, Kobayashi T, et al. OsZIP4, a novel zincregulated zinc transporter in rice. J Exp Bot, 2005, 56: 3207–3214 1:CAS:528:DC%2BD2MXht1GlsbfP, 10.1093/jxb/eri317, 16263903
Ramesh S A, Shin R, Eide D J, et al. Differential metal selectivity and gene expression of two zinc transporters from rice. Plant Physiol, 2003, 133: 126–134 1:CAS:528:DC%2BD3sXntlaitLs%3D, 10.1104/pp.103.026815, 12970480
Yang X, Huang J, Jiang Y, et al. Cloning and functional identification of two members of the ZIP (Zrt, Irt-like protein) gene family in rice (Oryza sativa L.). Mol Biol Rep, 2009, 36: 281–287 1:CAS:528:DC%2BD1cXhsFCmsLfF, 10.1007/s11033-007-9177-0, 18038191
Xu Y G, Wang B S, Yu J J, et al. Cloning and characterisation of ZmZLP1, a gene encoding an endoplasmic reticulum-localised zinc transporter in Zea mays. Fuctional Plant Biology, 2010, 37: 194–205 1:CAS:528:DC%2BC3c**sVCgu7o%3D, 10.1071/FP09045
Gitan R S, Shababi M, Kramer M, et al. A cytosolic domain of the yeast Zrt1 zinc transporter is required for its post-translational inactivation in response to zinc and cadmium. J Biol Chem, 2003, 278: 39558–39564 1:CAS:528:DC%2BD3sXnvFantLg%3D, 10.1074/jbc.M302760200, 12893829
Li X, Qian Q, Fu Z, et al. Control of tillering in rice. Nature, 2003, 422: 618–621 1:CAS:528:DC%2BD3s**slCgtL0%3D, 10.1038/nature01518, 12687001
Takeda T, Suwa Y, Suzuki M, et al. The OsTB1 gene negatively regulates lateral branching in rice. Plant J, 2003, 33: 513–520 1:CAS:528:DC%2BD3sXhslOgt7Y%3D, 10.1046/j.1365-313X.2003.01648.x, 12581309
Bolle C. The role of GRAS proteins in plant signal transduction and development. Planta, 2004, 218: 683–692 1:CAS:528:DC%2BD2cXhslGjsbc%3D, 10.1007/s00425-004-1203-z, 14760535
Richards D E, Peng J, Harberd N P. Plant GRAS and metazoan STATs: One family? Bioessays, 2000, 22: 573–577 1:CAS:528:DC%2BD3MXmslSiu70%3D, 10.1002/(SICI)1521-1878(200006)22:6<573::AID-BIES10>3.0.CO;2-H, 10842311
Aloni R, Aloni E, Langhans M, et al. Role of cytokinin and auxin in sha** root architecture: Regulating vascular differentiation, lateral root initiation, root apical dominance and root gravitropism. Ann Bot, 2006, 97: 883–893 1:CAS:528:DC%2BD28XmtFahtLY%3D, 10.1093/aob/mcl027, 16473866
Leyser O. Regulation of shoot branching by auxin. Trends Plant Sci, 2003, 8: 541–545 1:CAS:528:DC%2BD3sXos1Cnsrk%3D, 10.1016/j.tplants.2003.09.008, 14607099
Zhao Y, Hu Y, Dai M, et al. The WUSCHEL-related homeobox gene WOX11 is required to activate shoot-borne crown root development in rice. Plant Cell, 2009, 21: 736–748 1:CAS:528:DC%2BD1MXlsFyltbo%3D, 10.1105/tpc.108.061655, 19258439
Inukai Y, Sakamoto T, Ueguchi-Tanaka M, et al. Crown rootless1, which is essential for crown root formation in rice, is a target of an AUXIN RESPONSE FACTOR in auxin signaling. Plant Cell, 2005, 17: 1387–1396 1:CAS:528:DC%2BD2MXksVKksrY%3D, 10.1105/tpc.105.030981, 15829602
Liu H, Wang S, Yu X, et al. ARL1, a LOB-domain protein required for adventitious root formation in rice. Plant J, 2005, 43: 47–56 10.1111/j.1365-313X.2005.02434.x, 15960615
Liu Y, Feng X, Xu Y, et al. Overexpression of foxtail millet ZIP-like gene (SiPf40) affects lateral bud outgrowth in tobacco and foxtail millet. Plant Physiol Biochem, 2009, 47: 1051–1060 1:CAS:528:DC%2BD1MXhsVajsrbK, 10.1016/j.plaphy.2009.08.007, 19766013
Hiei Y, Ohta S, Komari T, et al. Efficient transformation of rice (Oryza sativa L.) mediated by Agrobacterium and sequence analysis of the boundaries of the T-DNA. Plant J, 1994, 6: 271–282 1:CAS:528:DyaK2MXhtlGntLc%3D, 10.1046/j.1365-313X.1994.6020271.x, 7920717
Saghai-Maroof M A, Soliman K M, Jorgensen R A, et al. Ribosomal DNA spacer-length polymorphisms in barley: Mendelian inheritance, chromosomal location, and population dynamics. Proc Natl Acad Sci USA, 81: 8014–818
Sambrook J, Fritsch E T, Maniatis T. Molecular Cloning: A Laboratory Manual. New York: Cold Spring Harbor Laboratory Press, 1989
Logemann J, Schell J, Willmitzer L. Improved method for the isolation of RNA from plant tissues. Anal Biochem, 1987, 163: 16–20 1:CAS:528:DyaL2sXktlKitr0%3D, 10.1016/0003-2697(87)90086-8, 2441623
Di Laurenzio L, Wysocka-Diller J, Malamy J E, et al. The SCARECROW gene regulates an asymmetric cell division that is essential for generating the radial organization of the Arabidopsis root. Cell, 1996, 86: 423–433 10.1016/S0092-8674(00)80115-4, 8756724
Sembdner G, Atzorn R, Schneider G. Plant hormone conjugation. Plant Mol Biol, 1994, 26: 1459–1481 1:CAS:528:DyaK2MXjvFeksr0%3D, 10.1007/BF00016485, 7858200
Monna L, Kitazawa N, Yoshino R, et al. Positional cloning of rice semidwarfing gene, sd-1: Rice “green revolution gene” encodes a mutant enzyme involved in gibberellin synthesis. DNA Res, 2002, 9: 11–17 1:CAS:528:DC%2BD38**t1Cmu7Y%3D, 10.1093/dnares/9.1.11, 11939564
Spielmeyer W, Ellis M H, Chandler P M. Semidwarf (sd-1), “green revolution” rice, contains a defective gibberellin 20-oxidase gene. Proc Natl Acad Sci USA, 2002, 99: 9043–9048 1:CAS:528:DC%2BD38XltF2hu74%3D, 10.1073/pnas.132266399, 12077303
Yamamuro C, Ihara Y, Wu X, et al. Loss of function of a rice brass-inosteroid insensitive1 homolog prevents internode elongation and bending of the lamina joint. Plant Cell, 2000, 12: 1591–1606 1:CAS:528:DC%2BD3cXnsVyltrw%3D, 10.1105/tpc.12.9.1591, 11006334
Yan J B, Tang H, Huang Y Q, et al. Comparative analyses of QTL for important agronomic traits between maize and rice. Acta Genetica Sin, 2004, 31: 1401–1407 1:CAS:528:DC%2BD2MXktlGjtro%3D
Biemelt S, Tschiersch H, Sonnewald U. Impact of altered gibberellin metabolism on biomass accumulation, lignin biosynthesis, and photosynthesis in transgenic tobacco plants. Plant Physiol, 2004, 135: 254–265 1:CAS:528:DC%2BD2cXkt12nurs%3D, 10.1104/pp.103.036988, 15122040
Eriksson S, Bjorkman J, Borg S, et al. Salmonella typhimurium mutants that downregulate phagocyte nitric oxide production. Cell Microbiol, 2000, 2: 239–250 1:CAS:528:DC%2BD3cXls1yrsrY%3D, 10.1046/j.1462-5822.2000.00051.x, 11207580
Grotz N, Guerinot M L. Molecular aspects of Cu, Fe and Zn homeostasis in plants. Biochim Biophys Acta, 2006, 1763: 595–608 1:CAS:528:DC%2BD28XotFGqurk%3D, 10.1016/j.bbamcr.2006.05.014, 16857279
Colangelo E P, Guerinot M L. Put the metal to the petal: Metal uptake and transport throughout plants. Curr Opin Plant Biol, 2006, 9: 322–330 1:CAS:528:DC%2BD28XktVGgur0%3D, 10.1016/j.pbi.2006.03.015, 16616607
**a Y F, Zhao Q, Yu J J. Study of subcellular localization of PF40. Prog Biochem Biophys, 2005, 32: 1020–1025 1:CAS:528:DC%2BD2sXms1Olsrs%3D
Lasswell J, Rogg L E, Nelson D C, et al. Cloning and characterization of IAR1, a gene required for auxin conjugate sensitivity in Arabidopsis. Plant Cell, 2000, 12: 2395–2408 1:CAS:528:DC%2BD3MXns1Shug%3D%3D, 10.1105/tpc.12.12.2395, 11148286
Yang G, Inoue A, Takasaki H, et al. A proteomic approach to analyze auxin- and zinc-responsive protein in rice. J Proteome Res, 2005, 4: 456–463 1:CAS:528:DC%2BD2MXhs1yrsb8%3D, 10.1021/pr049801h, 15822922
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Luan, Y., Wang, B., Zhao, Q. et al. Ectopic expression of foxtail millet zip-like gene, SiPf40, in transgenic rice plants causes a pleiotropic phenotype affecting tillering, vascular distribution and root development. Sci. China Life Sci. 53, 1450–1458 (2010). https://doi.org/10.1007/s11427-010-4090-5
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DOI: https://doi.org/10.1007/s11427-010-4090-5