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The control of developmental phase transitions in plants

Huijser, Peter, Schmid, Markus·2011·Development

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Abstract

Plant development progresses through distinct phases: vegetative growth, followed by a reproductive phase and eventually seed set and senescence. The transitions between these phases are controlled by distinct genetic circuits that integrate endogenous and environmental cues. In recent years, however, it has become evident that the genetic networks that underlie these phase transitions share some common factors. Here, we review recent advances in the field of plant phase transitions, highlighting the role of two microRNAs – miR156 and miR172 – and their respective targets during these transitions. In addition, we discuss the evolutionary conservation of the functions of these miRNAs in regulating the control of plant developmental phase transitions.

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miRBase: integrating microRNA annotation and deep-sequencing data
Kozomara, A., & Griffiths-Jones, S. (2011) · Nucleic Acids Research · doi:10.1093/nar/gkq1027 · Cited by 3,634
A gene expression map of Arabidopsis thaliana development
Schmid, M., Davison, T. S., Henz, S. R., Pape, U. J., Demar, M., Vingron, M., Schölkopf, B., Weigel, D., & Lohmann, J. U. (2005) · Nature Genetics · doi:10.1038/ng1543 · Cited by 2,523
Self-citation
Prediction of Plant MicroRNA Targets
Rhoades, M. W., Reinhart, B. J., Lim, L. P., Burge, C. B., Bartel, B., & Bartel, D. P. (2002) · Cell · doi:10.1016/s0092-8674(02)00863-2 · Cited by 2,283
Target mimicry provides a new mechanism for regulation of microRNA activity
Franco-Zorrilla, J. M., Valli, A., Todesco, M., Mateos, I., Puga, M. I., Rubio-Somoza, I., Leyva, A., Weigel, D., García, J. A., & Paz-Ares, J. (2007) · Nature Genetics · doi:10.1038/ng2079 · Cited by 2,069
Regulation of Flowering Time and Floral Organ Identity by a MicroRNA and Its APETALA2 -Like Target Genes
Aukerman, M. J., & Sakai, H. (2003) · The Plant Cell · doi:10.1105/tpc.016238 · Cited by 1,946
A MicroRNA as a Translational Repressor of APETALA2 in Arabidopsis Flower Development
Chen, X. (2004) · Science · doi:10.1126/science.1088060 · Cited by 1,770
The Sequential Action of miR156 and miR172 Regulates Developmental Timing in Arabidopsis
Wu, G., Park, M. Y., Conway, S. R., Wang, J.-W., Weigel, D., & Poethig, R. S. (2009) · Cell · doi:10.1016/j.cell.2009.06.031 · Cited by 1,678
Regulation of OsSPL14 by OsmiR156 defines ideal plant architecture in rice
Jiao, Y., Wang, Y., Xue, D., Wang, J., Yan, M., Liu, G., Dong, G., Zeng, D., Lu, Z., Zhu, X., et al. (2010) · Nature Genetics · doi:10.1038/ng.591 · Cited by 1,528
miR156-Regulated SPL Transcription Factors Define an Endogenous Flowering Pathway in Arabidopsis thaliana
Wang, J.-W., Czech, B., & Weigel, D. (2009) · Cell · doi:10.1016/j.cell.2009.06.014 · Cited by 1,489
Specific effects of microRNAs on the plant transcriptome
Schwab, R., Palatnik, J. F., Riester, M., Schommer, C., Schmid, M., & Weigel, D. (2005) · Developmental Cell · doi:10.1016/j.devcel.2005.01.018 · Cited by 1,467
Self-citation
A naturally occurring epigenetic mutation in a gene encoding an SBP-box transcription factor inhibits tomato fruit ripening
Manning, K., Tör, M., Poole, M., Hong, Y., Thompson, A. J., King, G. J., Giovannoni, J. J., & Seymour, G. B. (2006) · Nature Genetics · doi:10.1038/ng1841 · Cited by 1,310
CARPEL FACTORY, a Dicer Homolog, and HEN1, a Novel Protein, Act in microRNA Metabolism in Arabidopsis thaliana
Park, W., Li, J., Song, R., Messing, J., & Chen, X. (2002) · Current Biology · doi:10.1016/s0960-9822(02)01017-5 · Cited by 1,244
High-Throughput Sequencing of Arabidopsis microRNAs: Evidence for Frequent Birth and Death of MIRNA Genes
Fahlgren, N., Howell, M. D., Kasschau, K. D., Chapman, E. J., Sullivan, C. M., Cumbie, J. S., Givan, S. A., Law, T. F., Grant, S. R., Dangl, J. L., et al. (2007) · PLoS ONE · doi:10.1371/journal.pone.0000219 · Cited by 1,197
Genetic interactions among floral homeotic genes of Arabidopsis
Bowman, J. L., Smyth, D. R., & Meyerowitz, E. M. (1991) · Development · doi:10.1242/dev.112.1.1 · Cited by 1,166
Control of Arabidopsis flower and seed development by the homeotic gene APETALA2.
Jofuku, K. D., den Boer, B. G., Van Montagu, M., & Okamuro, J. K. (1994) · The Plant Cell · doi:10.1105/tpc.6.9.1211 · Cited by 1,137
OsSPL14 promotes panicle branching and higher grain productivity in rice
Miura, K., Ikeda, M., Matsubara, A., Song, X.-J., Ito, M., Asano, K., Matsuoka, M., Kitano, H., & Ashikari, M. (2010) · Nature Genetics · doi:10.1038/ng.592 · Cited by 1,104
Temporal regulation of shoot development in Arabidopsis thaliana by miR156 and its target SPL3
Wu, G., & Poethig, R. S. (2006) · Development · doi:10.1242/dev.02521 · Cited by 1,074
Regulation of flowering time: all roads lead to Rome
Srikanth, A., & Schmid, M. (2011) · Cellular and Molecular Life Sciences · doi:10.1007/s00018-011-0673-y · Cited by 1,039
Self-citation
Negative Regulation of Anthocyanin Biosynthesis in Arabidopsis by a miR156-Targeted SPL Transcription Factor
Gou, J.-Y., Felippes, F. F., Liu, C.-J., Weigel, D., & Wang, J.-W. (2011) · The Plant Cell · doi:10.1105/tpc.111.084525 · Cited by 953
Seasonal and developmental timing of flowering
Amasino, R. (2010) · The Plant Journal · doi:10.1111/j.1365-313x.2010.04148.x · Cited by 894
Evolution and Functional Diversification of MIRNA Genes
Cuperus, J. T., Fahlgren, N., & Carrington, J. C. (2011) · The Plant Cell · doi:10.1105/tpc.110.082784 · Cited by 727
Conservation and divergence of plant microRNA genes
Zhang, B., Pan, X., Cannon, C. H., Cobb, G. P., & Anderson, T. A. (2006) · The Plant Journal · doi:10.1111/j.1365-313x.2006.02697.x · Cited by 725
Expression of Arabidopsis MIRNA Genes
Xie, Z., Allen, E., Fahlgren, N., Calamar, A., Givan, S. A., & Carrington, J. C. (2005) · Plant Physiology · doi:10.1104/pp.105.062943 · Cited by 707
Multiple Pathways in the Decision to Flower: Enabling, Promoting, and Resetting
Boss, P. K. (2004) · THE PLANT CELL ONLINE · doi:10.1105/tpc.015958 · Cited by 706
Role of SVP in the control of flowering time by ambient temperature in Arabidopsis
Lee, J. H., Yoo, S. J., Park, S. H., Hwang, I., Lee, J. S., & Ahn, J. H. (2007) · Genes & Development · doi:10.1101/gad.1518407 · Cited by 682
Genomic Organization, Differential Expression, and Interaction of SQUAMOSA Promoter-Binding-Like Transcription Factors and microRNA156 in Rice
Xie, K., Wu, C., & Xiong, L. (2006) · Plant Physiology · doi:10.1104/pp.106.084475 · Cited by 680
Nuclear processing and export of microRNAs in Arabidopsis
Park, M. Y., Wu, G., Gonzalez-Sulser, A., Vaucheret, H., & Poethig, R. S. (2005) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0405570102 · Cited by 669
The heterochronic maize mutant Corngrass1 results from overexpression of a tandem microRNA
Chuck, G., Cigan, A. M., Saeteurn, K., & Hake, S. (2007) · Nature Genetics · doi:10.1038/ng2001 · Cited by 652
The MicroRNA-Regulated SBP-Box Transcription Factor SPL3 Is a Direct Upstream Activator of LEAFY, FRUITFULL, and APETALA1
Yamaguchi, A., Wu, M.-F., Yang, L., Wu, G., Poethig, R. S., & Wagner, D. (2009) · Developmental Cell · doi:10.1016/j.devcel.2009.06.007 · Cited by 646
Regulation of AUXIN RESPONSE FACTOR3 by TAS3 ta-siRNA Affects Developmental Timing and Patterning in Arabidopsis
Fahlgren, N., Montgomery, T. A., Howell, M. D., Allen, E., Dvorak, S. K., Alexander, A. L., & Carrington, J. C. (2006) · Current Biology · doi:10.1016/j.cub.2006.03.065 · Cited by 639
The SOC1 MADS‐box gene integrates vernalization and gibberellin signals for flowering in Arabidopsis
Moon, J., Suh, S., Lee, H., Choi, K., Hong, C. B., Paek, N., Kim, S., & Lee, I. (2003) · The Plant Journal · doi:10.1046/j.1365-313x.2003.01833.x · Cited by 625
Conserved noncoding genomic sequences associated with a flowering-time quantitative trait locus in maize
Salvi, S., Sponza, G., Morgante, M., Tomes, D., Niu, X., Fengler, K. A., Meeley, R., Ananiev, E. V., Svitashev, S., Bruggemann, E., et al. (2007) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0704145104 · Cited by 615
Molecular Characterization of the Major Wheat Domestication Gene Q
Simons, K. J., Fellers, J. P., Trick, H. N., Zhang, Z., Tai, Y.-S., Gill, B. S., & Faris, J. D. (2006) · Genetics · doi:10.1534/genetics.105.044727 · Cited by 615
The miRNA156/157 recognition element in the 3′ UTR of the Arabidopsis SBP box gene SPL3 prevents early flowering by translational inhibition in seedlings
Gandikota, M., Birkenbihl, R. P., Höhmann, S., Cardon, G. H., Saedler, H., & Huijser, P. (2007) · The Plant Journal · doi:10.1111/j.1365-313x.2006.02983.x · Cited by 615
Self-citation
Phase Change and the Regulation of Shoot Morphogenesis in Plants
Poethig, R. S. (1990) · Science · doi:10.1126/science.250.4983.923 · Cited by 611
The origin of the naked grains of maize
Wang, H., Nussbaum-Wagler, T., Li, B., Zhao, Q., Vigouroux, Y., Faller, M., Bomblies, K., Lukens, L., & Doebley, J. F. (2005) · Nature · doi:10.1038/nature03863 · Cited by 603
Antiquity of MicroRNAs and Their Targets in Land Plants
Axtell, M. J., & Bartel, D. P. (2005) · The Plant Cell · doi:10.1105/tpc.105.032185 · Cited by 593
The Control Of Floral Evocation And Morphogenesis
Bernier, G. (1988) · Annual Review of Plant Physiology and Plant Molecular Biology · doi:10.1146/annurev.arplant.39.1.175 · Cited by 589
Canalization of development by microRNAs
Hornstein, E., & Shomron, N. (2006) · Nature Genetics · doi:10.1038/ng1803 · Cited by 578
Auxin Response Factors Mediate Arabidopsis Organ Asymmetry via Modulation of KANADI Activity
Pekker, I., Alvarez, J. P., & Eshed, Y. (2005) · The Plant Cell · doi:10.1105/tpc.105.034876 · Cited by 550
The microRNA regulated SBP-box genes SPL9 and SPL15 control shoot maturation in Arabidopsis
Schwarz, S., Grande, A. V., Bujdoso, N., Saedler, H., & Huijser, P. (2008) · Plant Molecular Biology · doi:10.1007/s11103-008-9310-z · Cited by 520
Self-citation
The GIGANTEA -Regulated MicroRNA172 Mediates Photoperiodic Flowering Independent of CONSTANS in Arabidopsis
Jung, J.-H., Seo, Y.-H., Seo, P. J., Reyes, J. L., Yun, J., Chua, N.-H., & Park, C.-M. (2007) · The Plant Cell · doi:10.1105/tpc.107.054528 · Cited by 519
Dual Effects of miR156-Targeted SPL Genes and CYP78A5/KLUH on Plastochron Length and Organ Size in Arabidopsis thaliana
Wang, J.-W., Schwab, R., Czech, B., Mica, E., & Weigel, D. (2008) · The Plant Cell · doi:10.1105/tpc.108.058180 · Cited by 513
Dissection of floral induction pathways using global expression analysis
Schmid, M., Uhlenhaut, N. H., Godard, F., Demar, M., Bressan, R., Weigel, D., & Lohmann, J. U. (2003) · Development · doi:10.1242/dev.00842 · Cited by 505
Self-citation
Orchestration of the Floral Transition and Floral Development in Arabidopsis by the Bifunctional Transcription Factor APETALA2
Yant, L., Mathieu, J., Dinh, T. T., Ott, F., Lanz, C., Wollmann, H., Chen, X., & Schmid, M. (2010) · The Plant Cell · doi:10.1105/tpc.110.075606 · Cited by 505
Self-citation
Phase change and the regulation of trichome distribution in Arabidopsis thaliana
Telfer, A., Bollman, K. M., & Poethig, R. S. (1997) · Development · doi:10.1242/dev.124.3.645 · Cited by 470
Deep sequencing of tomato short RNAs identifies microRNAs targeting genes involved in fruit ripening
Moxon, S., Jing, R., Szittya, G., Schwach, F., Rusholme Pilcher, R. L., Moulton, V., & Dalmay, T. (2008) · Genome Research · doi:10.1101/gr.080127.108 · Cited by 470
Repression of Flowering by the miR172 Target SMZ
Mathieu, J., Yant, L. J., Mürdter, F., Küttner, F., & Schmid, M. (2009) · PLoS Biology · doi:10.1371/journal.pbio.1000148 · Cited by 467
Self-citation
microRNA172 down-regulates glossy15 to promote vegetative phase change in maize
Lauter, N., Kampani, A., Carlson, S., Goebel, M., & Moose, S. P. (2005) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0503927102 · Cited by 460
FLOWERING LOCUS T duplication coordinates reproductive and vegetative growth in perennial poplar
Hsu, C.-Y., Adams, J. P., Kim, H., No, K., Ma, C., Strauss, S. H., Drnevich, J., Vandervelde, L., Ellis, J. D., Rice, B. M., et al. (2011) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1104713108 · Cited by 453
Evolution of plant microRNAs and their targets
Axtell, M. J., & Bowman, J. L. (2008) · Trends in Plant Science · doi:10.1016/j.tplants.2008.03.009 · Cited by 452
Molecular characterisation of the Arabidopsis SBP-box genes
Cardon, G., Höhmann, S., Klein, J., Nettesheim, K., Saedler, H., & Huijser, P. (1999) · Gene · doi:10.1016/s0378-1119(99)00308-x · Cited by 450
Self-citation
Cloning and characterization of the maize An1 gene.
Bensen, R. J., Johal, G. S., Crane, V. C., Tossberg, J. T., Schnable, P. S., Meeley, R. B., & Briggs, S. P. (1995) · The Plant Cell · doi:10.1105/tpc.7.1.75 · Cited by 448
MiRNA Control of Vegetative Phase Change in Trees
Wang, J.-W., Park, M. Y., Wang, L.-J., Koo, Y., Chen, X.-Y., Weigel, D., & Poethig, R. S. (2011) · PLoS Genetics · doi:10.1371/journal.pgen.1002012 · Cited by 424
The maize tasselseed4 microRNA controls sex determination and meristem cell fate by targeting Tasselseed6/indeterminate spikelet1
Chuck, G., Meeley, R., Irish, E., Sakai, H., & Hake, S. (2007) · Nature Genetics · doi:10.1038/ng.2007.20 · Cited by 399
A Collection of Target Mimics for Comprehensive Analysis of MicroRNA Function in Arabidopsis thaliana
Todesco, M., Rubio-Somoza, I., Paz-Ares, J., & Weigel, D. (2010) · PLoS Genetics · doi:10.1371/journal.pgen.1001031 · Cited by 394
A new family of DNA binding proteins includes putative transcriptional regulators of theAntirrhinum majus floral meristem identity geneSQUAMOSA
Klein, J., Saedler, H., & Huijser, P. (1996) · Molecular and General Genetics MGG · doi:10.1007/bf02191820 · Cited by 376
Self-citation
FLOWERING LOCUS C (FLC) regulates development pathways throughout the life cycle of Arabidopsis
Deng, W., Ying, H., Helliwell, C. A., Taylor, J. M., Peacock, W. J., & Dennis, E. S. (2011) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1103175108 · Cited by 375
Floral organ identity: 20 years of ABCs
Causier, B., Schwarz-Sommer, Z., & Davies, B. (2010) · Seminars in Cell & Developmental Biology · doi:10.1016/j.semcdb.2009.10.005 · Cited by 374
Identification and characterization of small RNAs from the phloem of Brassica napus
Buhtz, A., Springer, F., Chappell, L., Baulcombe, D. C., & Kehr, J. (2008) · The Plant Journal · doi:10.1111/j.1365-313x.2007.03368.x · Cited by 370
Trans-acting siRNA-mediated repression of ETTIN and ARF4 regulates heteroblasty in Arabidopsis
Hunter, C., Willmann, M. R., Wu, G., Yoshikawa, M., de la Luz Gutiérrez-Nava, M., & Poethig, S. R. (2006) · Development · doi:10.1242/dev.02491 · Cited by 367
miR156-Targeted and Nontargeted SBP-Box Transcription Factors Act in Concert to Secure Male Fertility in Arabidopsis
Xing, S., Salinas, M., Höhmann, S., Berndtgen, R., & Huijser, P. (2011) · The Plant Cell · doi:10.1105/tpc.110.079343 · Cited by 365
Self-citation
MicroRNAs prevent precocious gene expression and enable pattern formation during plant embryogenesis
Nodine, M. D., & Bartel, D. P. (2010) · Genes & Development · doi:10.1101/gad.1986710 · Cited by 362
Effects of Sugar on Vegetative Development and Floral Transition in Arabidopsis
Ohto, M.-A., Onai, K., Furukawa, Y., Aoki, E., Araki, T., & Nakamura, K. (2001) · Plant Physiology · doi:10.1104/pp.127.1.252 · Cited by 348
Temporal Control of Trichome Distribution by MicroRNA156-Targeted SPL Genes in Arabidopsis thaliana
Yu, N., Cai, W.-J., Wang, S., Shan, C.-M., Wang, L.-J., & Chen, X.-Y. (2010) · The Plant Cell · doi:10.1105/tpc.109.072579 · Cited by 343
Functional analysis of the Arabidopsis thaliana SBP‐box gene SPL3: a novel gene involved in the floral transition
Cardon, G. H., Höhmann, S., Nettesheim, K., Saedler, H., & Huijser, P. (1997) · The Plant Journal · doi:10.1046/j.1365-313x.1997.12020367.x · Cited by 335
Self-citation
MicroRNA networks and developmental plasticity in plants
Rubio-Somoza, I., & Weigel, D. (2011) · Trends in Plant Science · doi:10.1016/j.tplants.2011.03.001 · Cited by 331
Juvenility, Maturation, and Rejuvenation in Woody Plants
Hackett, W. P. (1985) · Horticultural reviews · doi:10.1002/9781118060735.ch3 · Cited by 309
Graft-transmissible induction of potato tuberization by the microRNA miR172
Martin, A., Adam, H., Díaz-Mendoza, M., Żurczak, M., González-Schain, N. D., & Suárez-López, P. (2009) · Development · doi:10.1242/dev.031658 · Cited by 296
Arabidopsis SBP-Box Genes SPL10, SPL11 and SPL2 Control Morphological Change in Association with Shoot Maturation in the Reproductive Phase
Shikata, M., Koyama, T., Mitsuda, N., & Ohme-Takagi, M. (2009) · Plant and Cell Physiology · doi:10.1093/pcp/pcp148 · Cited by 280
Structure-Function Relationships in Highly Modified Shoots of Cactaceae
MAUSETH, J. D. (2006) · Annals of Botany · doi:10.1093/aob/mcl133 · Cited by 271
Cloning and characterization of micro‐RNAs from moss
Arazi, T., Talmor‐Neiman, M., Stav, R., Riese, M., Huijser, P., & Baulcombe, D. C. (2005) · The Plant Journal · doi:10.1111/j.1365-313x.2005.02499.x · Cited by 264
Self-citation
The role of carbohydrates in the induction of flowering in Arabidopsis thaliana : comparison between the wild type and a starchless mutant
Corbesier, L., Lejeune, P., & Bernier, G. (1998) · Planta · doi:10.1007/s004250050383 · Cited by 261
Differential Regulation of Trichome Formation on the Adaxial and Abaxial Leaf Surfaces by Gibberellins and Photoperiod in Arabidopsis thaliana (L.) Heynh
Chien, J. C., & Sussex, I. M. (1996) · PLANT PHYSIOLOGY · doi:10.1104/pp.111.4.1321 · Cited by 259
On reconciling the interactions between APETALA2 , miR172 and AGAMOUS with the ABC model of flower development
Wollmann, H., Mica, E., Todesco, M., Long, J. A., & Weigel, D. (2010) · Development · doi:10.1242/dev.036673 · Cited by 258
Glossy15, an APETALA2-like gene from maize that regulates leaf epidermal cell identity.
Moose, S. P., & Sisco, P. H. (1996) · Genes & Development · doi:10.1101/gad.10.23.3018 · Cited by 246
Genetic framework for flowering-time regulation by ambient temperature-responsive miRNAs in Arabidopsis
Lee, H., Yoo, S. J., Lee, J. H., Kim, W., Yoo, S. K., Fitzgerald, H., Carrington, J. C., & Ahn, J. H. (2010) · Nucleic Acids Research · doi:10.1093/nar/gkp1240 · Cited by 245
The maize SBP-box transcription factor encoded by tasselsheath4 regulates bract development and the establishment of meristem boundaries
Chuck, G., Whipple, C., Jackson, D., & Hake, S. (2010) · Development · doi:10.1242/dev.048348 · Cited by 244
Regulation of plant biomass production
Demura, T., & Ye, Z.-H. (2010) · Current Opinion in Plant Biology · doi:10.1016/j.pbi.2010.03.002 · Cited by 242
Genome-wide identification and evolutionary analysis of the plant specific SBP-box transcription factor family
Guo, A.-Y., Zhu, Q.-H., Gu, X., Ge, S., Yang, J., & Luo, J. (2008) · Gene · doi:10.1016/j.gene.2008.03.016 · Cited by 240
Heteroblasty—A Review
Zotz, G., Wilhelm, K., & Becker, A. (2011) · The Botanical Review · doi:10.1007/s12229-010-9062-8 · Cited by 217
Building Beauty
Lohmann, J. U., & Weigel, D. (2002) · Developmental Cell · doi:10.1016/s1534-5807(02)00122-3 · Cited by 214
The more and smaller cells mutants of Arabidopsis thaliana identify novel roles for SQUAMOSA PROMOTER BINDING PROTEIN-LIKE genes in the control of heteroblasty
Usami, T., Horiguchi, G., Yano, S., & Tsukaya, H. (2009) · Development · doi:10.1242/dev.028613 · Cited by 210
Control of Arabidopsis Flower and Seed Development by the Homeotic Gene APETALA2
Jofuku, K. D., den Boer, B. G. W., Montagu, M. V., & Okamuro, J. K. (1994) · The Plant Cell · doi:10.2307/3869820 · Cited by 206
Over-expression of sly-miR156a in tomato results in multiple vegetative and reproductive trait alterations and partial phenocopy of the sft mutant
Zhang, X., Zou, Z., Zhang, J., Zhang, Y., Han, Q., Hu, T., Xu, X., Liu, H., Li, H., & Ye, Z. (2011) · FEBS Letters · doi:10.1016/j.febslet.2010.12.036 · Cited by 197
microRNAs: small molecules with big roles –C. elegans to human cancer
Kato, M., & Slack, F. J. (2008) · Biology of the Cell · doi:10.1042/bc20070078 · Cited by 185
Vegetative phase change is mediated by a leaf-derived signal that represses the transcription of miR156
Yang, L., Conway, S. R., & Poethig, R. S. (2011) · Development · doi:10.1242/dev.058578 · Cited by 183
Modulation of sugar metabolism by an INDETERMINATE DOMAIN transcription factor contributes to photoperiodic flowering in Arabidopsis
Seo, P. J., Ryu, J., Kang, S. K., & Park, C. (2011) · The Plant Journal · doi:10.1111/j.1365-313x.2010.04432.x · Cited by 179
Rice embryogenic calli express a unique set of microRNAs, suggesting regulatory roles of microRNAs in plant post‐embryogenic development
Luo, Y.-C., Zhou, H., Li, Y., Chen, J.-Y., Yang, J.-H., Chen, Y.-Q., & Qu, L.-H. (2006) · FEBS Letters · doi:10.1016/j.febslet.2006.08.046 · Cited by 168
miRNAs in the biogenesis of trans-acting siRNAs in higher plants
Allen, E. M., & Howell, M. D. (2010) · Seminars in Cell and Developmental Biology · doi:10.1016/j.semcdb.2010.03.008 · Cited by 161
The Past, Present, and Future of Vegetative Phase Change
Poethig, R. S. (2010) · PLANT PHYSIOLOGY · doi:10.1104/pp.110.161620 · Cited by 145
Evidence for the rapid expansion of microRNA-mediated regulation in early land plant evolution
Fattash, I., Voß, B., Reski, R., Hess, W. R., & Frank, W. (2007) · BMC Plant Biology · doi:10.1186/1471-2229-7-13 · Cited by 127
Comparative analysis of the SBP-box gene families in P. patens and seed plants
Riese, M., Höhmann, S., Saedler, H., Münster, T., & Huijser, P. (2007) · Gene · doi:10.1016/j.gene.2007.06.018 · Cited by 124
Self-citation
Heteroblasty in Arabidopsis thaliana (L.) Heynh
Tsukaya, H., Shoda, K., Kim, G., & Uchimiya, H. (2000) · Planta · doi:10.1007/s004250050042 · Cited by 87
From Decision to Commitment: The Molecular Memory of Flowering
Adrian, J., Torti, S., & Turck, F. (2009) · Molecular Plant · doi:10.1093/mp/ssp031 · Cited by 87
Feminized tassels of maize mop1 and ts1 mutants exhibit altered levels of miR156 and specific SBP-box genes
Hultquist, J. F., & Dorweiler, J. E. (2008) · Planta · doi:10.1007/s00425-008-0813-2 · Cited by 80
SQUAMOSA-PROMOTER BINDING PROTEIN 1 initiates flowering in Antirrhinum majus through the activation of meristem identity genes
Preston, J. C., & Hileman, L. C. (2010) · The Plant Journal · doi:10.1111/j.1365-313x.2010.04184.x · Cited by 74
Leaf development in Arabidopsis
Lijsebettens, M. V., & Clarke, J. (1998) · Plant Physiology and Biochemistry · doi:10.1016/s0981-9428(98)80090-9 · Cited by 74
15 Leaf Development in Arabidopsis
Telfer, A., & Poethig, R. S. (1994) · Medical Entomology and Zoology · doi:10.1101/087969428.27.379 · Cited by 67
The microRNA156 and microRNA172 gene regulation cascades at post-germinative stages inArabidopsis
Martin, R. C., Asahina, M., Liu, P., Kristof, J. R., Coppersmith, J. L., Pluskota, W. E., Bassel, G. W., Goloviznina, N. A., Nguyen, T. T., Martínez‐Andújar, C., et al. (2010) · Seed Science Research · doi:10.1017/s0960258510000085 · Cited by 64

Research works printed but not linked: 15

Diggle, 2002, A developmental morphologist's perspective on plasticity, Evol. Ecol., 16, 267, 10.1023/A:1019680527788 · doi:10.1023/a:1019680527788
Doorenbos, 1965, Juvenile and adult phases in woody plants, Encycl. Plant Physiol., 15, 1222
Goebel, 1889, Über die Jugendzustände der Pflanzen, Flora, 72, 1
Jaya, 2010, Vegetative phase change and photosynthesis in Eucalyptus occidentalis: architectural simplification prolongs juvenile traits, Tree Physiol., 30, 393, 10.1093/treephys/tpp128 · doi:10.1093/treephys/tpp128
Jones, 1999, An essay on juvenility, phase change, and heteroblasty in seed plants, Int. J. Plant Sci., 160, S105, 10.1086/314215 · doi:10.1086/314215
Martin, 2010, The regulation of post-germinative transition from the cotyledon-to vegetative-leaf stages by microRNA-targeted SQUAMOSA PROMOTER-BINDING PROTEIN LIKE13 in Arabidopsis, Seed Sci. Res., 20, 89, 10.1017/S0960258510000073 · doi:10.1017/s0960258510000073
Martinez-Zapater, 1995, Arabidopsis late-flowering fve mutants are affected both in vegetative and reproductive development, Plant J., 7, 543, 10.1046/j.1365-313X.1995.7040543.x · doi:10.1046/j.1365-313x.1995.7040543.x
Mozley, 1995, Developmental and photobiological factors affecting photoperiodic induction in Arabidopsis-thaliana Heynh Landsberg Erecta, J. Exp. Bot., 46, 173, 10.1093/jxb/46.2.173 · doi:10.1093/jxb/46.2.173
Preston, 2010, Evolutionary genetics of core eudicot inflorescence and flower development, Int. J. Plant Dev. Biol., 4, 17
Röbbelen, 1957, Über Heterophyllie bei Arabidopsis thaliana (L.) Heynh, Ber. Dtsch. Bot. Ges., 70, 39, 10.1111/j.1438-8677.1957.tb01293.x · doi:10.1111/j.1438-8677.1957.tb01293.x
Steynen, 2001, Alteration in flowering time causes accelerated or decelerated progression through Arabidopsis vegetative phases, Can. J. Bot., 79, 657
Thompson, 2010, An Arabidopsis flavonoid transporter is required for anther dehiscence and pollen development, J. Exp. Bot., 61, 439, 10.1093/jxb/erp312 · doi:10.1093/jxb/erp312
Tooke, 2005, Mechanisms and function of flower and inflorescence reversion, J. Exp. Bot., 56, 2587, 10.1093/jxb/eri254 · doi:10.1093/jxb/eri254
Vella M. C. , SlackF. J. (2005). C. elegans microRNAs (September 21, 2005). In WormBook (ed. The C. elegans Research Community, Wormbook), pp. 1-9. http://www.wormbook.org.
Willmann, 2011, The effect of the floral repressor FLC on the timing and progression of vegetative phase change in Arabidopsis, Development, 138, 677, 10.1242/dev.057448 · doi:10.1242/dev.057448

Gibberellin Regulates the Arabidopsis Floral Transition through miR156-Targeted SQUAMOSA PROMOTER BINDING–LIKE Transcription Factors
Yu, S., Galvão, V. C., Zhang, Y.-C., Horrer, D., Zhang, T.-Q., Hao, Y.-H., Feng, Y.-Q., Wang, S., Schmid, M., & Wang, J.-W. (2012) · The Plant Cell · doi:10.1105/tpc.112.101014 · Cited by 469
Self-citation
New insights into gibberellin signaling in regulating flowering in Arabidopsis
Bao, S., Hua, C., Shen, L., & Yu, H. (2020) · Journal of Integrative Plant Biology · doi:10.1111/jipb.12892 · Cited by 386
The multifaceted roles of FLOWERING LOCUS T in plant development
PIN, P. A., & NILSSON, O. (2012) · Plant, Cell & Environment · doi:10.1111/j.1365-3040.2012.02558.x · Cited by 384
Regulation of flowering time by the miR156-mediated age pathway
Wang, J.-W. (2014) · Journal of Experimental Botany · doi:10.1093/jxb/eru246 · Cited by 379
Multiple pathways regulate shoot branching
Rameau, C., Bertheloot, J., Leduc, N., Andrieu, B., Foucher, F., & Sakr, S. (2015) · Frontiers in Plant Science · doi:10.3389/fpls.2014.00741 · Cited by 357

See all 673

Authors: Huijser, P., & Schmid, M.
Venue: Development
Publisher: The Company of Biologists
Published: 2011-10-01
Volume: 138
Issue: 19
Pages: 4117-4129
ISSN: 0950-1991 (ISSN-L)
1477-9129
DOI: 10.1242/dev.063511
OpenAlex: W2010396990
Cited by: 673
References: 100
FWCI: 39.60
Type: journal article
Language: en
Open access: closed

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The control of developmental phase transitions in plants

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