期刊论文详细信息
BMC Genomics
Gene expression profiling in juvenile and mature cuttings of Eucalyptus grandis reveals the importance of microtubule remodeling during adventitious root formation
Einat Sadot3  Ron Ophir3  Joseph Riov1  Mor Rubinstein3  Saar Levinkron3  Yossi Yaniv3  Inna Mordehaev3  David Szwerdszarf2  Mohamad Abu-Abied3 
[1] The Robert H. Smith Institute of Plant Sciences and Genetics in Agriculture, The Robert H. Smith Faculty of Agriculture, Food and Environment, The Hebrew University of Jerusalem, Rehovot 7610001, Israel;Current address: Syngenta Seeds – R&D, Valle de Azapa Km 17, Arica, Chile;The Institute of Plant Sciences, Volcani Center, PO Box 6, Bet-Dagan 5025000, Israel
关键词: Microtubule;    Microarray analysis;    Adventitious-roots formation;    Juvenile-to-mature phase change;    Eucalyptus grandis;   
Others  :  1139492
DOI  :  10.1186/1471-2164-15-826
 received in 2014-04-01, accepted in 2014-09-23,  发布年份 2014
PDF
【 摘 要 】

Background

The ability to form adventitious roots (AR) is an economically important trait that is lost during the juvenile-to-mature phase change in woody plants. Auxin treatment, which generally promotes rooting in juvenile cuttings, is often ineffective when applied to mature cuttings. The molecular basis for this phenomenon in Eucalyptus grandis was addressed here.

Results

A comprehensive microarray analysis was performed in order to compare gene-expression profiles in juvenile and mature cuttings of E. grandis, with or without auxin treatment on days, 0, 1, 3, 6, 9 and 12 post AR induction. Under these conditions AR primordia were formed only in auxin-treated juvenile cuttings. However, clustering the expression profiles revealed that the time after induction contributed more significantly to the differences in expression than the developmental phase of the cuttings or auxin treatment. Most detected differences which were related to the developmental phase and auxin treatment occurred on day 6, which correlated with the kinetics of AR-primordia formation. Among the functional groups of transcripts that differed between juvenile and mature cuttings was that of microtubules (MT). The expression of 42 transcripts annotated as coding for tubulin, MT-associated proteins and kinesin motor proteins was validated in the same RNA samples. The results suggest a coordinated developmental and auxin dependent regulation of several MT-related transcripts in these cuttings. To determine the relevance of MT remodeling to AR formation, MTs were subjected to subtle perturbations by trifluralin, a MT disrupting drug, applied during auxin induction. Juvenile cuttings were not affected by the treatment, but rooting of mature cuttings increased from 10 to more than 40 percent.

Conclusions

The data suggest that juvenile-specific MT remodeling is involved in AR formation in E. grandis.

【 授权许可】

   
2014 Abu-Abied et al.; licensee BioMed Central Ltd.

【 预 览 】
附件列表
Files Size Format View
20150321135721274.pdf 1766KB PDF download
Figure 6. 67KB Image download
Figure 5. 96KB Image download
Figure 4. 107KB Image download
Figure 3. 56KB Image download
Figure 2. 52KB Image download
Figure 1. 151KB Image download
【 图 表 】

Figure 1.

Figure 2.

Figure 3.

Figure 4.

Figure 5.

Figure 6.

【 参考文献 】
  • [1]Day ME, Greenwood MS, Diaz-Sala C: Age- and size-related trends in woody plant shoot development: regulatory pathways and evidence for genetic control. Tree Physiol 2002, 22(8):507-513.
  • [2]Hackett WP: Juvenility, maturation and rejuvenation in woody plants. Hort Rev 1985, 7:109-155.
  • [3]McGowran E, Douglas GC, Parkinson M: Morphological and physiological markers of juvenility and maturity in shoot cultures of oak (Quercus robur and Q. petraea). Tree Physiol 1998, 18(4):251-257.
  • [4]Poethig RS: The past, present, and future of vegetative phase change. Plant Physiol 2010, 154(2):541-544.
  • [5]Poethig RS: Phase change and the regulation of shoot morphogenesis in plants. Science 1990, 250(4983):923-930.
  • [6]Greenwood MS: Rejuvenation of forest trees. Plant Growth Regul 1987, 6:1-12.
  • [7]da Costa CT, de Almeida MR, Ruedell CM, Schwambach J, Maraschin FS, Fett-Neto AG: When stress and development go hand in hand: main hormonal controls of adventitious rooting in cuttings. Front Plant Sci 2013, 4:133.
  • [8]Riov J, Szwerdszarf D, Abu-Abied M, Sadot E: The molecular mechanisms involved in adventitious root formation. In Plant Roots: The Hidden Half. 4th edition. Edited by Eshel A, Beeckman T. Taylor & Francis; 2013:11.11-11.14.
  • [9]Blakesley D, Weston GD, Hall JF: The role of endogenous auxin in root initiation Part I. Evidence from studies on auxin application, and analysis of endogenous levels. Plant Growth Regul 1991, 10:341-353.
  • [10]De Klerk GJ, Van der Krieken W, de Jong JC: The formation of adventitious roots: new concepts, new possibilities. In Vitro Cell Dev Biol Plant 1999, 35:189-199.
  • [11]Ballester A, San-Jose MC, Vidal N, Fernandez-Lorenzo JL, Vieitez AM: Anatomical and biochemical events during in vitro rooting of microcuttings from juvenile and mature phases of chestnut. Ann Bot 1999, 83:619-629.
  • [12]Vidal N, Arellano G, San-Jose MC, Vieitez AM, Ballester A: Developmental stages during the rooting of in-vitro-cultured Quercus robur shoots from material of juvenile and mature origin. Tree Physiol 2003, 23(18):1247-1254.
  • [13]Greenwood MS, Cui X, Xu F: Response to auxin changes during maturation-related loss of adventitious rooting competence in loblolly pine (Pinus taeda) stem cuttings. Physiol Plant 2001, 111(3):373-380.
  • [14]Ramirez-Carvajal GA, Morse AM, Dervinis C, Davis JM: The cytokinin type-B response regulator PtRR13 is a negative regulator of adventitious root development in Populus. Plant Physiol 2009, 150(2):759-771.
  • [15]Rigal A, Yordanov YS, Perrone I, Karlberg A, Tisserant E, Bellini C, Busov VB, Martin F, Kohler A, Bhalerao R, Legue V: The AINTEGUMENTA LIKE1 homeotic transcription factor PtAIL1 controls the formation of adventitious root primordia in poplar. Plant Physiol 2012, 160(4):1996-2006.
  • [16]Trupiano D, Yordanov Y, Regan S, Meilan R, Tschaplinski T, Scippa GS, Busov V: Identification, characterization of an AP2/ERF transcription factor that promotes adventitious, lateral root formation in Populus. Planta 2013, 238:271-282.
  • [17]Liu B, Wang L, Zhang J, Li J, Zheng H, Chen J, Lu M: WUSCHEL-related Homeobox genes in Populus tomentosa: diversified expression patterns and a functional similarity in adventitious root formation. BMC Genomics 2014, 15(1):296. BioMed Central Full Text
  • [18]Brinker M, van Zyl L, Liu W, Craig D, Sederoff RR, Clapham DH, von Arnold S: Microarray analyses of gene expression during adventitious root development in Pinus contorta. Plant Physiol 2004, 135(3):1526-1539.
  • [19]Sanchez C, Vielba JM, Ferro E, Covelo G, Sole A, Abarca D, de Mier BS, Diaz-Sala C: Two SCARECROW-LIKE genes are induced in response to exogenous auxin in rooting-competent cuttings of distantly related forest species. Tree Physiol 2007, 27(10):1459-1470.
  • [20]Vielba JM, Diaz-Sala C, Ferro E, Rico S, Lamprecht M, Abarca D, Ballester A, Sanchez C: CsSCL1 is differentially regulated upon maturation in chestnut microshoots and is specifically expressed in rooting-competent cells. Tree Physiol 2013, 31(10):1152-1160.
  • [21]Sole A, Sanchez C, Vielba JM, Valladares S, Abarca D, Diaz-Sala C: Characterization and expression of a Pinus radiata putative ortholog to the Arabidopsis SHORT-ROOT gene. Tree Physiol 2008, 28(11):1629-1639.
  • [22]Fett-Neto AG, Fett JP, Veira Goulart LW, Pasquali G, Termignoni RR, Ferreira AG: Distinct effects of auxin and light on adventitious root development in Eucalyptus saligna and Eucalyptus globulus. Tree Physiol 2001, 21(7):457-464.
  • [23]Ruedell CM, Schwambach J, Corrêa LR, Fett-Neto AG: Strategies for adventitious rooting in clonal propagation of Eucalyptus. In Adventitious Root Formation of Forest Trees and Horticultural Plants - From Genes to Applications. Edited by Niemi K, Scagel C. India: Research Signpost; 2009:337-358.
  • [24]Paton DM, Willing RR, Nichols W, Pryor LD: Rooting of stem cuttings of Eucalyptus: a rooting inhibitor in adult tissue. Aus J Bot 1970, 18:175-183.
  • [25]Abu-Abied M, Szwerdszarf D, Mordehaev I, Levy A, Stelmakh OR, Belausov E, Yaniv Y, Uliel S, Katzenellenbogen M, Riov J, Ophir R, Sadot E: Microarray analysis revealed upregulation of nitrate reductase in juvenile cuttings of Eucalyptus grandis, which correlated with increased nitric oxide production and adventitious root formation. Plant J 2012, 71:787-799.
  • [26]Levy A, Szwerdszarf D, Abu-Abied M, Mordehaev I, Yaniv Y, Riov J, Arazi T, Sadot E: Profiling microRNAs in Eucalyptus grandis reveals no mutual relationship between alterations in miR156 and miR172 expression and adventitious root induction during development. BMC Genomics 2014, 15(1):524. BioMed Central Full Text
  • [27]Geiss GK, Bumgarner RE, Birditt B, Dahl T, Dowidar N, Dunaway DL, Fell HP, Ferree S, George RD, Grogan T, James JJ, Maysuria M, Mitton JD, Oliveri P, Osborn JL, Peng T, Ratcliffe AL, Webster PJ, Davidson EH, Hood L, Dimitrov K: Direct multiplexed measurement of gene expression with color-coded probe pairs. Nat Biotechnol 2008, 26(3):317-325.
  • [28]Rasmussen CG, Humphries JA, Smith LG: Determination of symmetric and asymmetric division planes in plant cells. Annu Rev Plant Biol 2011, 62:387-409.
  • [29]Wasteneys GO: Microtubule organization in the green kingdom: chaos or self-order? J Cell Sci 2002, 115(Pt 7):1345-1354.
  • [30]Wasteneys GO: Progress in understanding the role of microtubules in plant cells. Curr Opin Plant Biol 2004, 7(6):651-660.
  • [31]Wasteneys GO, Collings DA: Expanding beyond the great divide: the cytoskeletonand axial growth. In The Plant and Cytoskeleton in Cell Differentiation and Development. Edited by Hussey PJ. Oxford.uk: Blackwell Publishing; 2004:83-116. vol. 10
  • [32]Wasteneys GO, Fujita M: Establishing and maintaining axial growth: wall mechanical properties and the cytoskeleton. J Plant Res 2006, 119(1):5-10.
  • [33]Landrein B, Hamant O: How mechanical stress controls microtubule behavior and morphogenesis in plants: history, experiments and revisited theories. Plant J 2013, 7:324-338.
  • [34]Myburg AA, Grattapaglia D, Tuskan GA, Hellsten U, Hayes RD, Grimwood J, Jenkins J, Lindquist E, Tice H, Bauer D, Goodstein DM, Dubchak I, Poliakov A, Mizrachi E, Kullan AR, Hussey SG, Pinard D, van der Merwe K, Singh P, van Jaarsveld I, Silva-Junior OB, Togawa RC, Pappas MR, Faria DA, Sansaloni CP, Petroli CD, Yang X, Ranjan P, Tschaplinski TJ, Ye CY, et al.: The genome of Eucalyptus grandis. Nature 2014, 509(7505):356-362.
  • [35]Diaz-Sala C, Hutchison KW, Goldfarb B, Greenwood MS: Maturation-related loss in rooting competence by loblolly pine stem cuttings: the role of auxin transport, metabolism and tissue sensitivity. Physiol Plant 1996, 97:481-490.
  • [36]Wierzba MP, Tax FE: Notes from the underground: receptor-like kinases in Arabidopsis root development. J Integr Plant Biol 2013, 55:1224-1237.
  • [37]Greenwood MS, Diaz-Sala C, Singer PB, Decker A, Hutchison KW: Differential gene expression during maturation-caused decline in adventitious rooting ability in loblolly pine. In Biology of Root Formation and Development. Edited by Altman A, Weisel Y. New York: Plenum Press; 1997:203-207.
  • [38]Diaz-Sala C, Garrido G, Sabater B: Age-related loss of rooting capability in Arabidopsis thaliana and its reversal by peptides containing the Arg-Gly-Asp (RGD) motif. Physiol Plant 2002, 114(4):601-607.
  • [39]Ho CM, Lee YR, Kiyama LD, Dinesh-Kumar SP, Liu B: Arabidopsis microtubule-associated protein MAP65-3 cross-links antiparallel microtubules toward their plus ends in the phragmoplast via its distinct C-terminal microtubule binding domain. Plant Cell 2012, 24(5):2071-2085.
  • [40]Van Damme D, De Rybel B, Gudesblat G, Demidov D, Grunewald W, De Smet I, Houben A, Beeckman T, Russinova E: Arabidopsis alpha Aurora kinases function in formative cell division plane orientation. Plant Cell 2011, 23(11):4013-4024.
  • [41]Rasmussen CG, Wright AJ, Muller S: The role of the cytoskeleton and associated proteins in determination of the plant cell division plane. Plant J 2013, 75(2):258-269.
  • [42]De Smet I, Beeckman T: Asymmetric cell division in land plants and algae: the driving force for differentiation. Nat Rev Mol Cell Biol 2011, 12(3):177-188.
  • [43]Fujita M, Himmelspach R, Hocart CH, Williamson RE, Mansfield SD, Wasteneys GO: Cortical microtubules optimize cell-wall crystallinity to drive unidirectional growth in Arabidopsis. Plant J 2011, 66(6):915-928.
  • [44]Ambrose C, Ruan Y, Gardiner J, Tamblyn LM, Catching A, Kirik V, Marc J, Overall R, Wasteneys GO: CLASP interacts with sorting nexin 1 to link microtubules and auxin transport via PIN2 recycling in Arabidopsis thaliana. Dev Cell 2013, 24(6):649-659.
  • [45]Grover R, Wolt JD, Cessna AJ, Schiefer HB: Environmental fate of trifluralin. Rev Environ Contam Toxicol 1997, 153:1-64.
  • [46]Southerton SG, Marshall H, Mouradov A, Teasdale RD: Eucalypt MADS-Box genes expressed in developing flowers. Plant Physiol 1998, 118(2):365-372.
  • [47]Smyth GK: Linear models and empirical bayes methods for assessing differential expression in microarray experiments. Stat Appl Genet Mol Biol 2004, 3:Article3.
  • [48]Benjamini Y, Hochberg Y: Controlling the false discovery rate: a practical and powerful approach to multiple testing. J Ro Stat Soc B 1995, 57:289-300.
  文献评价指标  
  下载次数:15次 浏览次数:7次