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Plants  2013 

TALE and Shape: How to Make a Leaf Different

DOI: 10.3390/plants2020317

Keywords: TALE, BLH, KNOX, homeobox transcription factors, target genes, leaf development, vascular development, cell fate, cell differentiation, shoot apical meristem

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Abstract:

The Three Amino acid Loop Extension (TALE) proteins constitute an ancestral superclass of homeodomain transcription factors conserved in animals, plants and fungi. In plants they comprise two classes, KNOTTED1-LIKE homeobox (KNOX) and BEL1-like homeobox (BLH or BELL, hereafter referred to as BLH), which are involved in shoot apical meristem (SAM) function, as well as in the determination and morphological development of leaves, stems and inflorescences. Selective protein-protein interactions between KNOXs and BLHs affect heterodimer subcellular localization and target affinity. KNOXs exert their roles by maintaining a proper balance between undifferentiated and differentiated cell state through the modulation of multiple hormonal pathways. A pivotal function of KNOX in evolutionary diversification of leaf morphology has been assessed. In the SAM of both simple- and compound-leafed seed species, downregulation of most class 1 KNOX ( KNOX1) genes marks the sites of leaf primordia initiation. However, KNOX1 expression is re-established during leaf primordia development of compound-leafed species to maintain transient indeterminacy and morphogenetic activity at the leaf margins. Despite the increasing knowledge available about KNOX1 protein function in plant development, a comprehensive view on their downstream effectors remains elusive. This review highlights the role of TALE proteins in leaf initiation and morphological plasticity with a focus on recent advances in the identification of downstream target genes and pathways.

References

[1]  Bertolino, E.; Reimund, B.; Wildt-Perinic, D.; Clerc, R.G. A novel homeobox protein which recognizes a TGT core and functionally interferes with a retinoid-responsive motif. J. Biol. Chem. 1995, 270, 31178–31188.
[2]  Burglin, T.R. Analysis of TALE superclass homeobox genes (MEIS, PBC, KNOX, Iroquois, TGIF) reveals a novel domain conserved between plants and animals. Nucleic Acids Res. 1997, 25, 4173–4180, doi:10.1093/nar/25.21.4173.
[3]  Burglin, T.R. The PBC domain contains a MEINOX domain: Coevolution of Hox and TALE homeobox genes? Dev. Genes Evol. 1998, 208, 113–116, doi:10.1007/s004270050161.
[4]  Laurent, A.; Bihan, R.; Omilli, F.; Deschamps, S.; Pellerin, I. PBX proteins: Much more than Hox cofactors. Int. J. Dev. Biol. 2008, 52, 9–20, doi:10.1387/ijdb.072304al.
[5]  Berthelsen, J.; Kilstrup-Nielsen, C.; Blasi, F.; Mavilio, F.; Zappavigna, V. The subcellular localization of PBX1 and EXD proteins depends on nuclear import and export signals and is modulated by association with PREP1 and HTH. Genes Dev. 1999, 13, 946–953, doi:10.1101/gad.13.8.946.
[6]  Saleh, M.; Huang, H.; Green, N.C.; Featherstone, M.S. A conformational change in PBX1A is necessary for its nuclear localization. Exp. Cell Res. 2000, 260, 105–115.
[7]  Bhatt, A.M.; Etchells, J.P.; Canales, C.; Lagodienko, A.; Dickinson, H. VAAMANA—A BEL1-like homeodomain protein, interacts with KNOX proteins BP and STM and regulates inflorescence stem growth in Arabidopsis. Gene 2004, 328, 103–111, doi:10.1016/j.gene.2003.12.033.
[8]  Cole, M.; Nolte, C.; Werr, W. Nuclear import of the transcription factor SHOOT MERISTEMLESS depends on heterodimerization with BLH proteins expressed in discrete sub-domains of the shoot apical meristem of Arabidopsis thaliana. Nucleic Acids Res. 2006, 34, 1281–1292, doi:10.1093/nar/gkl016.
[9]  Smith, H.M.; Boschke, I.; Hake, S. Selective interaction of plant homeodomain proteins mediates high DNA-binding affinity. Proc. Natl. Acad. Sci. USA 2002, 99, 9579–9584, doi:10.1073/pnas.092271599.
[10]  Smaczniak, C.; Immink, R.G.; Muino, J.M.; Blanvillain, R.; Busscher, M.; Busscher-Lange, J.; Dinh, Q.D.; Liu, S.; Westphal, A.H.; Boeren, S.; et al. Characterization of MADS-domain transcription factor complexes in Arabidopsis flower development. Proc. Natl. Acad. Sci. USA 2012, 109, 1560–1565, doi:10.1073/pnas.1112871109.
[11]  Mukherjee, K.; Brocchieri, L.; Burglin, T.R. A comprehensive classification and evolutionary analysis of plant homeobox genes. Mol. Biol. Evol. 2009, 26, 2775–2794, doi:10.1093/molbev/msp201.
[12]  Kerstetter, R.; Vollbrecht, E.; Lowe, B.; Veit, B.; Yamaguchi, J.; Hake, S. Sequence analysis and expression patterns divide the maize knotted1-like homeobox genes into two classes. Plant Cell 1994, 6, 1877–1887.
[13]  Reiser, L.; Sanchez-Baracaldo, P.; Hake, S. Knots in the family tree: Evolutionary relationships and functions of knox homeobox genes. Plant Mol. Biol. 2000, 42, 151–166, doi:10.1023/A:1006384122567.
[14]  Magnani, E.; Hake, S. KNOX lost the OX: The Arabidopsis KNATM gene defines a novel class of KNOX transcriptional regulators missing the homeodomain. Plant Cell 2008, 20, 875–887, doi:10.1105/tpc.108.058495.
[15]  Li, Y.; Pi, L.; Huang, H.; Xu, L. ATH1 and KNAT2 proteins act together in regulation of plant inflorescence architecture. J. Exp. Bot. 2012, 63, 1423–1433, doi:10.1093/jxb/err376.
[16]  Hackbusch, J.; Richter, K.; Muller, J.; Salamini, F.; Uhrig, J.F. A central role of Arabidopsis thaliana ovate family proteins in networking and subcellular localization of 3-aa loop extension homeodomain proteins. Proc. Natl. Acad. Sci. USA 2005, 102, 4908–4912, doi:10.1073/pnas.0501181102.
[17]  Bellaoui, M.; Pidkowich, M.S.; Samach, A.; Kushalappa, K.; Kohalmi, S.E.; Modrusan, Z.; Crosby, W.L.; Haughn, G.W. The Arabidopsis BELL1 and KNOX TALE homeodomain proteins interact through a domain conserved between plants and animals. Plant Cell 2001, 13, 2455–2470.
[18]  Di Giacomo, E.; Sestili, F.; Iannelli, M.A.; Testone, G.; Mariotti, D.; Frugis, G. Characterization of KNOX genes in Medicago truncatula. Plant Mol. Biol. 2008, 67, 135–150, doi:10.1007/s11103-008-9307-7.
[19]  Arabidopsis Interactome Mapping Consortium. Evidence for network evolution in an Arabidopsis interactome map. Science 2011, 333, 601–607, doi:10.1126/science.1203877.
[20]  Hake, S.; Smith, H.M.; Holtan, H.; Magnani, E.; Mele, G.; Ramirez, J. The role of knox genes in plant development. Annu. Rev. Cell Dev. Biol. 2004, 20, 125–151, doi:10.1146/annurev.cellbio.20.031803.093824.
[21]  Hay, A.; Tsiantis, M. KNOX genes: Versatile regulators of plant development and diversity. Development 2010, 137, 3153–3165, doi:10.1242/dev.030049.
[22]  Bharathan, G.; Goliber, T.E.; Moore, C.; Kessler, S.; Pham, T.; Sinha, N.R. Homologies in leaf form inferred from KNOXI gene expression during development. Science 2002, 296, 1858–1860, doi:10.1126/science.1070343.
[23]  Hamant, O.; Pautot, V. Plant development: A TALE story. C. R. Biol. 2010, 333, 371–381, doi:10.1016/j.crvi.2010.01.015.
[24]  Canales, C.; Barkoulas, M.; Galinha, C.; Tsiantis, M. Weeds of change: Cardamine hirsuta as a new model system for studying dissected leaf development. J. Plant Res. 2010, 123, 25–33, doi:10.1007/s10265-009-0263-3.
[25]  Blein, T.; Hasson, A.; Laufs, P. Leaf development: What it needs to be complex. Curr. Opin. Plant Biol. 2010, 13, 75–82, doi:10.1016/j.pbi.2009.09.017.
[26]  Efroni, I.; Eshed, Y.; Lifschitz, E. Morphogenesis of simple and compound leaves: A critical review. Plant Cell 2010, 22, 1019–1032.
[27]  Uchida, N.; Kimura, S.; Koenig, D.; Sinha, N. Coordination of leaf development via regulation of KNOX1 genes. J. Plant Res. 2010, 123, 7–14, doi:10.1007/s10265-009-0248-2.
[28]  Moon, J.; Hake, S. How a leaf gets its shape. Curr. Opin. Plant Biol. 2011, 14, 24–30, doi:10.1016/j.pbi.2010.08.012.
[29]  Burko, Y.; Ori, N. The tomato leaf as a model system for organogenesis. Methods Mol. Biol. 2013, 959, 1–19, doi:10.1007/978-1-62703-221-6_1.
[30]  Hasson, A.; Blein, T.; Laufs, P. Leaving the meristem behind: The genetic and molecular control of leaf patterning and morphogenesis. C. R. Biol. 2010, 333, 350–360, doi:10.1016/j.crvi.2010.01.013.
[31]  Wu, S.; Smith, M.S. Out of step:The function of TALE homeodomain transcription factors that regulate shoot meristem maintenance and meristem identity. Front Biol. 2012, 7, 144–154.
[32]  Winter, N.; Kollwig, G.; Zhang, S.; Kragler, F. MPB2C, a microtubule-associated protein, regulates non-cell-autonomy of the homeodomain protein KNOTTED1. Plant Cell 2007, 19, 3001–3018, doi:10.1105/tpc.107.044354.
[33]  Kim, J.Y.; Yuan, Z.; Cilia, M.; Khalfan-Jagani, Z.; Jackson, D. Intercellular trafficking of a KNOTTED1 green fluorescent protein fusion in the leaf and shoot meristem of Arabidopsis. Proc. Natl. Acad. Sci. USA 2002, 99, 4103–4108.
[34]  Kim, J.Y.; Yuan, Z.; Jackson, D. Developmental regulation and significance of KNOX protein trafficking in Arabidopsis. Development 2003, 130, 4351–4362, doi:10.1242/dev.00618.
[35]  Kim, J.Y.; Rim, Y.; Wang, J.; Jackson, D. A novel cell-to-cell trafficking assay indicates that the KNOX homeodomain is necessary and sufficient for intercellular protein and mRNA trafficking. Genes Dev. 2005, 19, 788–793, doi:10.1101/gad.332805.
[36]  Xu, X.M.; Wang, J.; Xuan, Z.; Goldshmidt, A.; Borrill, P.G.; Hariharan, N.; Kim, J.Y.; Jackson, D. Chaperonins facilitate KNOTTED1 cell-to-cell trafficking and stem cell function. Science 2011, 333, 1141–1144.
[37]  Vollbrecht, E.; Veit, B.; Sinha, N.; Hake, S. The developmental gene Knotted-1 is a member of a maize homeobox gene family. Nature 1991, 350, 241–243, doi:10.1038/350241a0.
[38]  Barton, M.K. Twenty years on: The inner workings of the shoot apical meristem, a developmental dynamo. Dev. Biol. 2010, 341, 95–113, doi:10.1016/j.ydbio.2009.11.029.
[39]  Long, J.A.; Moan, E.I.; Medford, J.I.; Barton, M.K. A member of the KNOTTED class of homeodomain proteins encoded by the STM gene of Arabidopsis. Nature 1996, 379, 66–69.
[40]  Clark, S.E.; Jacobsen, S.E.; Levin, J.Z.; Meyerowitz, E.M. The CLAVATA and SHOOT MERISTEMLESS loci competitively regulate meristem activity in Arabidopsis. Development 1996, 122, 1567–1575.
[41]  Endrizzi, K.; Moussian, B.; Haecker, A.; Levin, J.Z.; Laux, T. The SHOOT MERISTEMLESS gene is required for maintenance of undifferentiated cells in Arabidopsis shoot and floral meristems and acts at a different regulatory level than the meristem genes WUSCHEL and ZWILLE. Plant J. 1996, 10, 967–979.
[42]  Kanrar, S.; Onguka, O.; Smith, H.M. Arabidopsis inflorescence architecture requires the activities of KNOX-BELL homeodomain heterodimers. Planta 2006, 224, 1163–1173, doi:10.1007/s00425-006-0298-9.
[43]  Scofield, S.; Dewitte, W.; Murray, J.A. The KNOX gene SHOOT MERISTEMLESS is required for the development of reproductive meristematic tissues in Arabidopsis. Plant J. 2007, 50, 767–781, doi:10.1111/j.1365-313X.2007.03095.x.
[44]  Rutjens, B.; Bao, D.; van Eck-Stouten, E.; Brand, M.; Smeekens, S.; Proveniers, M. Shoot apical meristem function in Arabidopsis requires the combined activities of three BEL1-like homeodomain proteins. Plant J. 2009, 58, 641–654, doi:10.1111/j.1365-313X.2009.03809.x.
[45]  Ramirez, J.; Bolduc, N.; Lisch, D.; Hake, S. Distal expression of knotted1 in maize leaves leads to reestablishment of proximal/distal patterning and leaf dissection. Plant Physiol. 2009, 151, 1878–1888, doi:10.1104/pp.109.145920.
[46]  Takano, S.; Niihama, M.; Smith, H.M.; Tasaka, M.; Aida, M. gorgon, a novel missense mutation in the SHOOT MERISTEMLESS gene, impairs shoot meristem homeostasis in Arabidopsis. Plant Cell Physiol. 2010, 51, 621–634, doi:10.1093/pcp/pcq028.
[47]  Long, J.A.; Barton, M.K. The development of apical embryonic pattern in Arabidopsis. Development 1998, 125, 3027–3035.
[48]  Aida, M.; Ishida, T.; Tasaka, M. Shoot apical meristem and cotyledon formation during Arabidopsis embryogenesis: Interaction among the CUP-SHAPED COTYLEDON and SHOOT MERISTEMLESS genes. Development 1999, 126, 1563–1570.
[49]  Vollbrecht, E.; Reiser, L.; Hake, S. Shoot meristem size is dependent on inbred background and presence of the maize homeobox gene, knotted1. Development 2000, 127, 3161–3172.
[50]  Takada, S.; Hibara, K.; Ishida, T.; Tasaka, M. The CUP-SHAPED COTYLEDON1 gene of Arabidopsis regulates shoot apical meristem formation. Development 2001, 128, 1127–1135.
[51]  Poethig, R.S. Leaf morphogenesis in flowering plants. Plant Cell 1997, 9, 1077–1087, doi:10.1105/tpc.9.7.1077.
[52]  Dengler, N.; Kang, J. Vascular patterning and leaf shape. Curr. Opin. Plant Biol. 2001, 4, 50–56.
[53]  Holtan, H.E.; Hake, S. Quantitative trait locus analysis of leaf dissection in tomato using Lycopersicon pennellii segmental introgression lines. Genetics 2003, 165, 1541–1550.
[54]  Barkoulas, M.; Galinha, C.; Grigg, S.P.; Tsiantis, M. From genes to shape: Regulatory interactions in leaf development. Curr. Opin. Plant Biol. 2007, 10, 660–666, doi:10.1016/j.pbi.2007.07.012.
[55]  Shani, E.; Burko, Y.; Ben-Yaakov, L.; Berger, Y.; Amsellem, Z.; Goldshmidt, A.; Sharon, E.; Ori, N. Stage-specific regulation of Solanum lycopersicum leaf maturation by class 1 KNOTTED1-LIKE HOMEOBOX proteins. Plant Cell 2009, 21, 3078–3092, doi:10.1105/tpc.109.068148.
[56]  Gleissberg, H.A. Organogenetic capacity of leaves: The significance of marginal blastozones in angiosperms. Plant Syst. Evol. 1996, 199, 31.
[57]  Murray, J.A.; Jones, A.; Godin, C.; Traas, J. Systems analysis of shoot apical meristem growth and development: Integrating hormonal and mechanical signaling. Plant Cell 2012, 24, 3907–3919.
[58]  Fleming, A.J.; McQueen-Mason, S.; Mandel, T.; Kuhlemeier, C. Induction of leaf primordia by the cell wall protein expansin. Science 1997, 276, 1415–1418.
[59]  Reinhardt, D.; Wittwer, F.; Mandel, T.; Kuhlemeier, C. Localized upregulation of a new expansin gene predicts the site of leaf formation in the tomato meristem. Plant Cell 1998, 10, 1427–1437.
[60]  Pien, S.; Wyrzykowska, J.; McQueen-Mason, S.; Smart, C.; Fleming, A. Local expression of expansin induces the entire process of leaf development and modifies leaf shape. Proc. Natl. Acad. Sci. USA 2001, 98, 11812–11817.
[61]  Peaucelle, A.; Louvet, R.; Johansen, J.N.; Hofte, H.; Laufs, P.; Pelloux, J.; Mouille, G. Arabidopsis phyllotaxis is controlled by the methyl-esterification status of cell-wall pectins. Curr. Biol. 2008, 18, 1943–1948.
[62]  Peaucelle, A.; Louvet, R.; Johansen, J.N.; Salsac, F.; Morin, H.; Fournet, F.; Belcram, K.; Gillet, F.; Hofte, H.; Laufs, P.; et al. The transcription factor BELLRINGER modulates phyllotaxis by regulating the expression of a pectin methylesterase in Arabidopsis. Development 2011, 138, 4733–4741, doi:10.1242/dev.072496.
[63]  Elliott, R.C.; Betzner, A.S.; Huttner, E.; Oakes, M.P.; Tucker, W.Q.; Gerentes, D.; Perez, P.; Smyth, D.R. AINTEGUMENTA, an APETALA2-like gene of Arabidopsis with pleiotropic roles in ovule development and floral organ growth. Plant Cell 1996, 8, 155–168.
[64]  Lenhard, M.; Jurgens, G.; Laux, T. The WUSCHEL and SHOOTMERISTEMLESS genes fulfil complementary roles in Arabidopsis shoot meristem regulation. Development 2002, 129, 3195–3206.
[65]  Byrne, M.E.; Kidner, C.A.; Martienssen, R.A. Plant stem cells: Divergent pathways and common themes in shoots and roots. Curr. Opin. Genet. Dev. 2003, 13, 551–557, doi:10.1016/j.gde.2003.08.008.
[66]  Chuck, G.; Lincoln, C.; Hake, S. KNAT1 induces lobed leaves with ectopic meristems when overexpressed in Arabidopsis. Plant Cell 1996, 8, 1277–1289.
[67]  Ori, N.; Eshed, Y.; Chuck, G.; Bowman, J.L.; Hake, S. Mechanisms that control knox gene expression in the Arabidopsis shoot. Development 2000, 127, 5523–5532.
[68]  Kumar, R.; Kushalappa, K.; Godt, D.; Pidkowich, M.S.; Pastorelli, S.; Hepworth, S.R.; Haughn, G.W. The Arabidopsis BEL1-LIKE HOMEODOMAIN proteins SAW1 and SAW2 act redundantly to regulate KNOX expression spatially in leaf margins. Plant Cell 2007, 19, 2719–2735, doi:10.1105/tpc.106.048769.
[69]  Piazza, P.; Bailey, C.D.; Cartolano, M.; Krieger, J.; Cao, J.; Ossowski, S.; Schneeberger, K.; He, F.; de Meaux, J.; Hall, N.; et al. Arabidopsis thaliana leaf form evolved via loss of KNOX expression in leaves in association with a selective sweep. Curr. Biol. 2010, 20, 2223–2228, doi:10.1016/j.cub.2010.11.037.
[70]  Kawamura, E.; Horiguchi, G.; Tsukaya, H. Mechanisms of leaf tooth formation in Arabidopsis. Plant J. 2010, 62, 429–441, doi:10.1111/j.1365-313X.2010.04156.x.
[71]  Phelps-Durr, T.L.; Thomas, J.; Vahab, P.; Timmermans, M.C. Maize rough sheath2 and its Arabidopsis orthologue ASYMMETRIC LEAVES1 interact with HIRA, a predicted histone chaperone, to maintain knox gene silencing and determinacy during organogenesis. Plant Cell 2005, 17, 2886–2898, doi:10.1105/tpc.105.035477.
[72]  Xu, L.; Shen, W.H. Polycomb silencing of KNOX genes confines shoot stem cell niches in Arabidopsis. Curr. Biol. 2008, 18, 1966–1971, doi:10.1016/j.cub.2008.11.019.
[73]  Stahle, M.I.; Kuehlich, J.; Staron, L.; von Arnim, A.G.; Golz, J.F. YABBYs and the transcriptional corepressors LEUNIG and LEUNIG_HOMOLOG maintain leaf polarity and meristem activity in Arabidopsis. Plant Cell 2009, 21, 3105–3118, doi:10.1105/tpc.109.070458.
[74]  Causier, B.; Ashworth, M.; Guo, W.; Davies, B. The TOPLESS interactome: A framework for gene repression in Arabidopsis. Plant Physiol. 2012, 158, 423–438.
[75]  Ohta, M.; Matsui, K.; Hiratsu, K.; Shinshi, H.; Ohme-Takagi, M. Repression domains of class II ERF transcriptional repressors share an essential motif for active repression. Plant Cell 2001, 13, 1959–1968.
[76]  Kagale, S.; Rozwadowski, K. EAR motif-mediated transcriptional repression in plants: An underlying mechanism for epigenetic regulation of gene expression. Epigenetics 2011, 6, 141–146, doi:10.4161/epi.6.2.13627.
[77]  Hasson, A.; Plessis, A.; Blein, T.; Adroher, B.; Grigg, S.; Tsiantis, M.; Boudaoud, A.; Damerval, C.; Laufs, P. Evolution and diverse roles of the CUP-SHAPED COTYLEDON genes in Arabidopsis leaf development. Plant Cell 2011, 23, 54–68, doi:10.1105/tpc.110.081448.
[78]  Bilsborough, G.D.; Runions, A.; Barkoulas, M.; Jenkins, H.W.; Hasson, A.; Galinha, C.; Laufs, P.; Hay, A.; Prusinkiewicz, P.; Tsiantis, M. Model for the regulation of Arabidopsis thaliana leaf margin development. Proc. Natl. Acad. Sci. USA 2011, 108, 3424–3429, doi:10.1073/pnas.1015162108.
[79]  Hareven, D.; Gutfinger, T.; Parnis, A.; Eshed, Y.; Lifschitz, E. The making of a compound leaf: Genetic manipulation of leaf architecture in tomato. Cell 1996, 84, 735–744.
[80]  Kimura, S.; Koenig, D.; Kang, J.; Yoong, F.Y.; Sinha, N. Natural variation in leaf morphology results from mutation of a novel KNOX gene. Curr. Biol. 2008, 18, 672–677, doi:10.1016/j.cub.2008.04.008.
[81]  Hay, A.; Tsiantis, M. The genetic basis for differences in leaf form between Arabidopsis thaliana and its wild relative Cardamine hirsuta. Nat. Genet. 2006, 38, 942–947, doi:10.1038/ng1835.
[82]  Champagne, C.E.; Goliber, T.E.; Wojciechowski, M.F.; Mei, R.W.; Townsley, B.T.; Wang, K.; Paz, M.M.; Geeta, R.; Sinha, N.R. Compound leaf development and evolution in the legumes. Plant Cell 2007, 19, 3369–3378, doi:10.1105/tpc.107.052886.
[83]  Hofer, J.; Turner, L.; Hellens, R.; Ambrose, M.; Matthews, P.; Michael, A.; Ellis, N. UNIFOLIATA regulates leaf and flower morphogenesis in pea. Curr. Biol. 1997, 7, 581–587.
[84]  Wang, H.; Chen, J.; Wen, J.; Tadege, M.; Li, G.; Liu, Y.; Mysore, K.S.; Ratet, P.; Chen, R. Control of compound leaf development by FLORICAULA/LEAFY ortholog SINGLE LEAFLET1 in Medicago truncatula. Plant Physiol. 2008, 146, 1759–1772, doi:10.1104/pp.108.117044.
[85]  Moyroud, E.; Minguet, E.G.; Ott, F.; Yant, L.; Pose, D.; Monniaux, M.; Blanchet, S.; Bastien, O.; Thevenon, E.; Weigel, D.; et al. Prediction of regulatory interactions from genome sequences using a biophysical model for the Arabidopsis LEAFY transcription factor. Plant Cell 2011, 23, 1293–1306, doi:10.1105/tpc.111.083329.
[86]  Chen, J.; Yu, J.; Ge, L.; Wang, H.; Berbel, A.; Liu, Y.; Chen, Y.; Li, G.; Tadege, M.; Wen, J.; et al. Control of dissected leaf morphology by a Cys(2)His(2) zinc finger transcription factor in the model legume Medicago truncatula. Proc. Natl. Acad. Sci. USA 2010, 107, 10754–10759.
[87]  Peng, J.; Yu, J.; Wang, H.; Guo, Y.; Li, G.; Bai, G.; Chen, R. Regulation of compound leaf development in Medicago truncatula by fused compound leaf1, a class M KNOX gene. Plant Cell 2011, 23, 3929–3943, doi:10.1105/tpc.111.089128.
[88]  Chen, R. Plant Biology Division, The Samuel Roberts Noble Foundation: Ardmore, OK, USA, 2012.
[89]  Di Giacomo, E. Istituto di Biologia e Biotecnologia Agraria, UOS Roma, Consiglio Nazionale delle Ricerche: Monterotondo Scalo, Roma, Italy, 2011.
[90]  Smith, H.M.; Ung, N.; Lal, S.; Courtier, J. Specification of reproductive meristems requires the combined function of SHOOT MERISTEMLESS and floral integrators FLOWERING LOCUS T and FD during Arabidopsis inflorescence development. J. Exp. Bot. 2011, 62, 583–593, doi:10.1093/jxb/erq296.
[91]  Lal, S.; Pacis, L.B.; Smith, H.M. Regulation of the SQUAMOSA PROMOTER-BINDING PROTEIN-LIKE genes/microRNA156 module by the homeodomain proteins PENNYWISE and POUND-FOOLISH in Arabidopsis. Mol. Plant 2011, 4, 1123–1132.
[92]  Waites, R.; Selvadurai, H.R.; Oliver, I.R.; Hudson, A. The PHANTASTICA gene encodes a MYB transcription factor involved in growth and dorsoventrality of lateral organs in Antirrhinum. Cell 1998, 93, 779–789, doi:10.1016/S0092-8674(00)81439-7.
[93]  McConnell, J.R.; Barton, M.K. Leaf polarity and meristem formation in Arabidopsis. Development 1998, 125, 2935–2942.
[94]  Ha, C.M.; Jun, J.H.; Fletcher, J.C. Control of Arabidopsis leaf morphogenesis through regulation of the YABBY and KNOX families of transcription factors. Genetics 2010, 186, 197–206, doi:10.1534/genetics.110.118703.
[95]  Jun, J.H.; Ha, C.M.; Fletcher, J.C. BLADE-ON-PETIOLE1 coordinates organ determinacy and axial polarity in arabidopsis by directly activating ASYMMETRIC LEAVES2. Plant Cell 2010, 22, 62–76, doi:10.1105/tpc.109.070763.
[96]  Reinhardt, D.; Kuhlemeier, C. Plant architecture. EMBO Rep. 2002, 3, 846–851, doi:10.1093/embo-reports/kvf177.
[97]  Barkoulas, M.; Hay, A.; Kougioumoutzi, E.; Tsiantis, M. A developmental framework for dissected leaf formation in the Arabidopsis relative Cardamine hirsuta. Nat. Genet. 2008, 40, 1136–1141, doi:10.1038/ng.189.
[98]  Ben-Gera, H.; Ori, N. Auxin and LANCEOLATE affect leaf shape in tomato via different developmental processes. Plant Signal. Behav. 2012, 7, 1255–1257, doi:10.4161/psb.21550.
[99]  Peng, J.; Chen, R. Auxin efflux transporter MtPIN10 regulates compound leaf and flower development in Medicago truncatula. Plant Signal. Behav. 2011, 6, 1537–1544, doi:10.4161/psb.6.10.17326.
[100]  Zhou, C.; Han, L.; Hou, C.; Metelli, A.; Qi, L.; Tadege, M.; Mysore, K.S.; Wang, Z.Y. Developmental analysis of a Medicago truncatula smooth leaf margin1 mutant reveals context-dependent effects on compound leaf development. Plant Cell 2011, 23, 2106–2124, doi:10.1105/tpc.111.085464.
[101]  Ori, N.; Juarez, M.T.; Jackson, D.; Yamaguchi, J.; Banowetz, G.M.; Hake, S. Leaf senescence is delayed in tobacco plants expressing the maize homeobox gene knotted1 under the control of a senescence-activated promoter. Plant Cell 1999, 11, 1073–1080.
[102]  Frugis, G.; Giannino, D.; Mele, G.; Nicolodi, C.; Innocenti, A.M.; Chiappetta, A.; Bitonti, M.B.; Dewitte, W.; van Onckelen, H.; Mariotti, D. Are homeobox knotted-like genes and cytokinins the leaf architects? Plant Physiol. 1999, 119, 371–374, doi:10.1104/pp.119.2.371.
[103]  Sakamoto, T.; Kamiya, N.; Ueguchi-Tanaka, M.; Iwahori, S.; Matsuoka, M. KNOX homeodomain protein directly suppresses the expression of a gibberellin biosynthetic gene in the tobacco shoot apical meristem. Genes Dev. 2001, 15, 581–590, doi:10.1101/gad.867901.
[104]  Yanai, O.; Shani, E.; Dolezal, K.; Tarkowski, P.; Sablowski, R.; Sandberg, G.; Samach, A.; Ori, N. Arabidopsis KNOXI proteins activate cytokinin biosynthesis. Curr. Biol. 2005, 15, 1566–1571, doi:10.1016/j.cub.2005.07.060.
[105]  Jasinski, S.; Piazza, P.; Craft, J.; Hay, A.; Woolley, L.; Rieu, I.; Phillips, A.; Hedden, P.; Tsiantis, M. KNOX action in Arabidopsis is mediated by coordinate regulation of cytokinin and gibberellin activities. Curr. Biol. 2005, 15, 1560–1565, doi:10.1016/j.cub.2005.07.023.
[106]  Bolduc, N.; Hake, S. The maize transcription factor KNOTTED1 directly regulates the gibberellin catabolism gene ga2ox1. Plant Cell 2009, 21, 1647–1658, doi:10.1105/tpc.109.068221.
[107]  Hewelt, A.; Prinsen, E.; Thomas, M.; van Onckelen, H.; Meins, F., Jr. Ectopic expression of maize knotted1 results in the cytokinin-autotrophic growth of cultured tobacco tissues. Planta 2000, 210, 884–889, doi:10.1007/s004250050693.
[108]  Frugis, G.; Giannino, D.; Mele, G.; Nicolodi, C.; Chiappetta, A.; Bitonti, M.B.; Innocenti, A.M.; Dewitte, W.; van Onckelen, H.; Mariotti, D. Overexpression of KNAT1 in lettuce shifts leaf determinate growth to a shoot-like indeterminate growth associated with an accumulation of isopentenyl-type cytokinins. Plant Physiol. 2001, 126, 1370–1380, doi:10.1104/pp.126.4.1370.
[109]  Sakamoto, T.; Sakakibara, H.; Kojima, M.; Yamamoto, Y.; Nagasaki, H.; Inukai, Y.; Sato, Y.; Matsuoka, M. Ectopic expression of KNOTTED1-like homeobox protein induces expression of cytokinin biosynthesis genes in rice. Plant Physiol. 2006, 142, 54–62, doi:10.1104/pp.106.085811.
[110]  Shani, E.; Ben-Gera, H.; Shleizer-Burko, S.; Burko, Y.; Weiss, D.; Ori, N. Cytokinin regulates compound leaf development in tomato. Plant Cell 2010, 22, 3206–3217, doi:10.1105/tpc.110.078253.
[111]  Hay, A.; Kaur, H.; Phillips, A.; Hedden, P.; Hake, S.; Tsiantis, M. The gibberellin pathway mediates KNOTTED1-type homeobox function in plants with different body plans. Curr. Biol. 2002, 12, 1557–1565, doi:10.1016/S0960-9822(02)01125-9.
[112]  Chen, H.; Banerjee, A.K.; Hannapel, D.J. The tandem complex of BEL and KNOX partners is required for transcriptional repression of ga20ox1. Plant J. 2004, 38, 276–284, doi:10.1111/j.1365-313X.2004.02048.x.
[113]  Kessler, S.; Townsley, B.; Sinha, N. L1 division and differentiation patterns influence shoot apical meristem maintenance. Plant Physiol. 2006, 141, 1349–1362, doi:10.1104/pp.105.076075.
[114]  Jasinski, S.; Tattersall, A.; Piazza, P.; Hay, A.; Martinez-Garcia, J.F.; Schmitz, G.; Theres, K.; McCormick, S.; Tsiantis, M. PROCERA encodes a DELLA protein that mediates control of dissected leaf form in tomato. Plant J. 2008, 56, 603–612, doi:10.1111/j.1365-313X.2008.03628.x.
[115]  Bolduc, N.; Yilmaz, A.; Mejia-Guerra, M.K.; Morohashi, K.; O’Connor, D.; Grotewold, E.; Hake, S. Unraveling the KNOTTED1 regulatory network in maize meristems. Genes Dev. 2012, 26, 1685–1690, doi:10.1101/gad.193433.112.
[116]  Hay, A.; Barkoulas, M.; Tsiantis, M. PINning down the connections: Transcription factors and hormones in leaf morphogenesis. Curr. Opin. Plant Biol. 2006, 9, 443, doi:10.1016/j.pbi.2006.05.015.
[117]  Heisler, M.G.; Ohno, C.; Das, P.; Sieber, P.; Reddy, G.V.; Long, J.A.; Meyerowitz, E.M. Patterns of auxin transport and gene expression during primordium development revealed by live imaging of the Arabidopsis inflorescence meristem. Curr. Biol. 2005, 15, 1899–1911, doi:10.1016/j.cub.2005.09.052.
[118]  Gallavotti, A.; Yang, Y.; Schmidt, R.J.; Jackson, D. The Relationship between auxin transport and maize branching. Plant Physiol. 2008, 147, 1913–1923, doi:10.1104/pp.108.121541.
[119]  Vernoux, T.; Brunoud, G.; Farcot, E.; Morin, V.; van den Daele, H.; Legrand, J.; Oliva, M.; Das, P.; Larrieu, A.; Wells, D.; et al. The auxin signalling network translates dynamic input into robust patterning at the shoot apex. Mol. Syst. Biol. 2011, 7, 508.
[120]  Chapman, E.J.; Estelle, M. Mechanism of auxin-regulated gene expression in plants. Annu. Rev. Genet. 2009, 43, 265–285, doi:10.1146/annurev-genet-102108-134148.
[121]  Di Giacomo, E.; Serino, G.; Frugis, G. Emerging role of the ubiquitin proteasome system in the control of shoot apical meristem function. J. Integr. Plant Biol. 2013, 55, 7–20, doi:10.1111/jipb.12010.
[122]  Yadav, R.K.; Girke, T.; Pasala, S.; Xie, M.; Reddy, G.V. Gene expression map of the Arabidopsis shoot apical meristem stem cell niche. Proc. Natl. Acad. Sci. USA 2009, 106, 4941–4946.
[123]  Spinelli, S.V.; Martin, A.P.; Viola, I.L.; Gonzalez, D.H.; Palatnik, J.F. A mechanistic link between STM and CUC1 during Arabidopsis development. Plant Physiol. 2011, 156, 1894–1904.
[124]  Tsuda, K.; Ito, Y.; Sato, Y.; Kurata, N. Positive autoregulation of a KNOX gene is essential for shoot apical meristem maintenance in rice. Plant Cell 2011, 23, 4368–4381, doi:10.1105/tpc.111.090050.
[125]  Mele, G.; Ori, N.; Sato, Y.; Hake, S. The knotted1-like homeobox gene BREVIPEDICELLUS regulates cell differentiation by modulating metabolic pathways. Genes Dev. 2003, 17, 2088–2093, doi:10.1101/gad.1120003.
[126]  Groover, A.; Jones, A.M. Tracheary element differentiation uses a novel mechanism coordinating programmed cell death and secondary cell wall synthesis. Plant Physiol. 1999, 119, 375–384, doi:10.1104/pp.119.2.375.

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