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Radial Patterning of Arabidopsis Shoots by Class III HD-ZIP and KANADI Genes
Open accessAbstract
Background Shoots of all land plants have a radial pattern that can be considered to have an adaxial (central)-abaxial (peripheral) polarity. In Arabidopsis, gain-of-function alleles of PHAVOLUTA and PHABULOSA, members of the class III HD-ZIP gene family, result in adaxialization of lateral organs. Conversely, loss-of-function alleles of the KANADI genes cause an adaxialization of lateral organs. Thus, the class III HD-ZIP and KANADI genes comprise a genetic system that patterns abaxial-adaxial polarity in lateral organs produced from the apical meristem. Results We show that gain-of-function alleles of REVOLUTA, another member of the class III HD-ZIP gene family, are characterized by adaxialized lateral organs and alterations in the radial patterning of vascular bundles in the stem. The gain-of-function phenotype can be obtained by changing only the REVOLUTA mRNA sequence and without changing the protein sequence; this finding indicates that this phenotype is likely mediated through an interference with microRNA binding. Loss of KANADI activity results in similar alterations in vascular patterning as compared to REVOLUTA gain-of-function alleles. Simultaneous loss-of-function of PHABULOSA, PHAVOLUTA, and REVOLUTA abaxializes cotyledons, abolishes the formation of the primary apical meristem, and in severe cases, eliminates bilateral symmetry; these phenotypes implicate these three genes in radial patterning of both embryonic and postembryonic growth. Conclusions Based on complementary vascular and leaf phenotypes of class III HD-ZIP and KANADI mutants, we propose that a common genetic program dependent upon miRNAs governs adaxial-abaxial patterning of leaves and radial patterning of stems in the angiosperm shoot. This finding implies that a common patterning mechanism is shared between apical and vascular meristems.
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“However, its effect on axillary meristem formation may be secondary and the primary function of REV is the control of radial patterning (Emery et al., 2003; Bennett and Leyser, 2006).”
From Shaping plant architecture (2015) · cites this paper as Emery et al., 2003
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Cites
Prediction of Plant MicroRNA Targets
Jones-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 2,263
MicroRNAs in plantsPreprint
Reinhart, B. J., Weinstein, E. G., Jones-Rhoades, M. W., Bartel, B., & Bartel, D. P. (2002) · Genes & Development · doi:10.1101/gad.1004402 · Cited by 2,052
Cleavage of Scarecrow-like mRNA Targets Directed by a Class of Arabidopsis miRNA
Llave, C., Xie, Z., Kasschau, K. D., & Carrington, J. C. (2002) · Science · doi:10.1126/science.1076311 · Cited by 1,627
Genes involved in organ separation in Arabidopsis: an analysis of the cup-shaped cotyledon mutant.
Aida, M., Ishida, T., Fukaki, H., Fujisawa, H., & Tasaka, M. (1997) · The Plant Cell · doi:10.1105/tpc.9.6.841 · Cited by 1,486
Role of PHABULOSA and PHAVOLUTA in determining radial patterning in shoots
McConnell, J. R., Emery, J. F., Eshed, Y., Bao, N., Bowman, J. L., & Barton, M. K. (2001) · Nature · doi:10.1038/35079635 · Cited by 1,104
Self-citationA biochemical framework for RNA silencing in plantsPreprint
Tang, G., Reinhart, B. J., Bartel, D. P., & Zamore, P. D. (2003) · Genes & Development · doi:10.1101/gad.1048103 · Cited by 994
Members of the YABBY gene family specify abaxial cell fate in Arabidopsis
Siegfried, K. R., Eshed, Y., Baum, S. F., Otsuga, D., Drews, G. N., & Bowman, J. L. (1999) · Development · doi:10.1242/dev.126.18.4117 · Cited by 744
Self-citationT-DNA as an Insertional Mutagen in Arabidopsis
Krysan, P. J., Young, J. C., & Sussman, M. R. (1999) · The Plant Cell · doi:10.1105/tpc.11.12.2283 · Cited by 722
Establishment of polarity in lateral organs of plants
Eshed, Y., Baum, S. F., Perea, J. V., & Bowman, J. L. (2001) · Current Biology · doi:10.1016/s0960-9822(01)00392-x · Cited by 635
Self-citationKANADI regulates organ polarity in Arabidopsis
Kerstetter, R. A., Bollman, K. M., Taylor, R. A., Bomblies, K., & Poethig, R. S. (2001) · Nature · doi:10.1038/35079629 · Cited by 600
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- Sussex, 1955, Morphogenesis in Solanum tuberosum L, Phytomorphology, 5, 286
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Regulation of Small RNA Accumulation in the Maize Shoot Apex
Nogueira, F. T. S., Chitwood, D. H., Madi, S., Ohtsu, K., Schnable, P. S., Scanlon, M. J., & Timmermans, M. C. P. (2009) · PLoS Genetics · doi:10.1371/journal.pgen.1000320 · Cited by 144
On the mechanisms of development in monocot and eudicot leaves
Conklin, P. A., Strable, J., Li, S., & Scanlon, M. J. (2018) · New Phytologist · doi:10.1111/nph.15371 · Cited by 147
From genes to shape: regulatory interactions in leaf development
Barkoulas, M., Galinha, C., Grigg, S. P., & Tsiantis, M. (2007) · Current Opinion in Plant Biology · doi:10.1016/j.pbi.2007.07.012 · Cited by 144
Lahrmann, U., Strehmel, N., Langen, G., Frerigmann, H., Leson, L., Ding, Y., Scheel, D., Herklotz, S., Hilbert, M., & Zuccaro, A. (2015) · New Phytologist · doi:10.1111/nph.13411 · Cited by 143
Plant primary meristems: shared functions and regulatory mechanisms
Stahl, Y., & Simon, R. G. (2009) · Current Opinion in Plant Biology · doi:10.1016/j.pbi.2009.09.008 · Cited by 142
Ribosomal proteins promote leaf adaxial identity
Yao, Y., Ling, Q., Wang, H., & Huang, H. Y. (2008) · Development · doi:10.1242/dev.017913 · Cited by 142
Braybrook, S. A., & Kuhlemeier, C. J. (2010) · The Plant Cell · doi:10.1105/tpc.110.073924 · Cited by 142
The role of ARGONAUTE1 (AGO1) in meristem formation and identity
Kidner, C. A., & Martienssen, R. A. (2005) · Developmental Biology · doi:10.1016/j.ydbio.2005.01.031 · Cited by 142
Pattern formation during early ovule development in Arabidopsis thaliana
Sieber, P., Gheyselinck, J., Groß‐Hardt, R., Laux, T., Grossniklaus, U., & Schneitz, K. (2004) · Developmental Biology · doi:10.1016/j.ydbio.2004.05.037 · Cited by 142
Spatio‐temporal accumulation of microRNAs is highly coordinated in developing plant tissues
Válóczi, A., Várallyay, É., Kauppinen, S., Burgyán, J., & Havelda, Z. (2006) · The Plant Journal · doi:10.1111/j.1365-313x.2006.02766.x · Cited by 141
Qiu, C. X., Xie, F. L., Zhu, Y., Guo, K., Huang, S. Q., Nie, L., & Yang, Z. M. (2007) · Gene · doi:10.1016/j.gene.2007.01.034 · Cited by 140
A Molecular Framework for the Embryonic Initiation of Shoot Meristem Stem Cells
Zhang, Z., Tucker, E. J., Hermann, M., & Laux, T. (2017) · Developmental Cell · doi:10.1016/j.devcel.2017.01.002 · Cited by 143
Brandt, R., Salla‐Martret, M., Bou‐Torrent, J., Musielak, T., Stahl, M., Lanz, C., Ott, F., Schmid, M., Greb, T., Schwarz, M., et al. (2012) · The Plant Journal · doi:10.1111/j.1365-313x.2012.05049.x · Cited by 136
Yan, J., Zhao, C., Zhou, J., Yang, Y., Wang, P., Zhu, X., Tang, G., Bressan, R. A., & Zhu, J. (2016) · PLoS Genetics · doi:10.1371/journal.pgen.1006416 · Cited by 136
Pandey, S. P., & Baldwin, I. T. (2007) · The Plant Journal · doi:10.1111/j.1365-313x.2007.03030.x · Cited by 136
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Shoot Meristem Function and Leaf Polarity: The Role of Class III HD–ZIP Genes
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Harrison, C. J., & Morris, J. L. (2017) · Philosophical Transactions of the Royal Society B Biological Sciences · doi:10.1098/rstb.2016.0496 · Cited by 138
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Merelo, P., Ram, H., Caggiano, M. P., Ohno, C. K., Ott, F., Straub, D., Graeff, M., Cho, S. K., Yang, S. W., Wenkel, S., et al. (2016) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1516110113 · Cited by 132
Something on the Side: Axillary Meristems and Plant Development
Bennett, T., & Leyser, O. (2006) · Plant Molecular Biology · doi:10.1007/s11103-005-2763-4 · Cited by 131
Zhu, Y., Song, D., Sun, J., Wang, X., & Li, L. (2013) · Molecular Plant · doi:10.1093/mp/sss164 · Cited by 131
Tsukaya, H. (2013) · The Arabidopsis Book · doi:10.1199/tab.0163 · Cited by 135
Leaf adaxial-abaxial polarity specification and lamina outgrowth: evolution and development
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Turchi, L., Carabelli, M., Ruzza, V., Possenti, M., Sassi, M., Peñalosa, A., Sessa, G., Salvi, S., Forte, V., Morelli, G., et al. (2013) · Development · doi:10.1242/dev.092833 · Cited by 131
Mukherjee, K., & Bürglin, T. R. (2006) · PLANT PHYSIOLOGY · doi:10.1104/pp.105.073833 · Cited by 130
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Caño‐Delgado, A. I., Lee, J., & Demura, T. (2010) · Annual Review of Cell and Developmental Biology · doi:10.1146/annurev-cellbio-100109-104107 · Cited by 135
Chen, C., Liu, M., Jiang, L., Liu, X., Zhao, J., Yan, S., Yang, S., Ren, H., Liu, R., & Zhang, X. (2014) · Journal of Experimental Botany · doi:10.1093/jxb/eru258 · Cited by 128
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Li, C., Chen, C., Gao, L., Yang, S., Nguyen, V., Shi, X., Siminovitch, K. A., Kohalmi, S. E., Huang, S., Wu, K., et al. (2015) · PLoS Genetics · doi:10.1371/journal.pgen.1004944 · Cited by 126
Ren, W., Wu, F., Bai, J., Li, X., Yang, X., Xue, W., Liu, H., & He, Y. (2020) · Horticulture Research · doi:10.1038/s41438-019-0222-7 · Cited by 125
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Iwasaki, M., Takahashi, H., Iwakawa, H., Nakagawa, A., Ishikawa, T., Tanaka, H., Matsumura, Y., Pekker, I., Eshed, Y., Vial-Pradel, S., et al. (2013) · Development · doi:10.1242/dev.085365 · Cited by 123
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Frazier, T., Xie, F., Freistaedter, A., Burklew, C. E., & Zhang, B. (2010) · Planta · doi:10.1007/s00425-010-1255-1 · Cited by 119
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Zhou, Y., Honda, M., Zhu, H., Zhang, Z., Guo, X., Li, T., Li, Z., Peng, X., Nakajima, K., Duan, L., et al. (2015) · Cell Reports · doi:10.1016/j.celrep.2015.02.047 · Cited by 118
The roles of HD-ZIP proteins in plant abiotic stress tolerance
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Gillmor, C. S., Park, M. Y., Smith, M., Pepitone, R., Kerstetter, R. A., & Poethig, R. S. (2009) · Development · doi:10.1242/dev.043174 · Cited by 118
Huang, T., Harrar, Y., Lin, C., Reinhart, B. J., Newell, N. R., Talavera-Rauh, F., Hokin, S. A., Barton, M. K., & Kerstetter, R. A. (2014) · The Plant Cell · doi:10.1105/tpc.113.111526 · Cited by 124
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Hibara, K., Obara, M., Hayashida, E., Abe, M., Ishimaru, T., Satoh, H., Itoh, J., & Nagato, Y. (2009) · Developmental Biology · doi:10.1016/j.ydbio.2009.07.042 · Cited by 117
Wang, W., Xu, B., Wang, H., Li, J., Huang, H. Y., & Xu, L. (2011) · PLANT PHYSIOLOGY · doi:10.1104/pp.111.186395 · Cited by 117
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Luo, M., Yu, C. W., Chen, F.-F., Zhao, L., Tian, G., Liu, X., Cui, Y., Yang, J., & Wu, K. (2012) · PLoS Genetics · doi:10.1371/journal.pgen.1003114 · Cited by 117
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Yu, Y., Ji, L., Le, B. H., Zhai, J., Chen, J., Luscher, E., Gao, L., Liu, C., Cao, X., Mo, B., et al. (2017) · PLoS Biology · doi:10.1371/journal.pbio.2001272 · Cited by 114
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Wang, H., Goué, N., Saïdi, M. N., Legay, S., Sivadon, P., Goffner, D., & Grima‐Pettenati, J. (2013) · Frontiers in Plant Science · doi:10.3389/fpls.2013.00189 · Cited by 116
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Singh, A., Roy, S., Singh, S., Das, S. S., Gautam, V., Yadav, S., Kumar, A., Singh, A., Samantha, S., & Sarkar, A. K. (2017) · Scientific Reports · doi:10.1038/s41598-017-03632-w · Cited by 108
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Hur, Y., Um, J., Kim, S., Kim, K., Park, H., Lim, J., Kim, W., Jun, S. E., Yoon, E. K., Lim, J., et al. (2014) · New Phytologist · doi:10.1111/nph.12998 · Cited by 100
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Garcia, D. (2008) · Seminars in Cell and Developmental Biology · doi:10.1016/j.semcdb.2008.07.013 · Cited by 104
Reichel, M., Li, Y., Li, J., & Millar, A. A. (2015) · Plant Biotechnology Journal · doi:10.1111/pbi.12327 · Cited by 101
Husbands, A. Y., Benkovics, A. H., Nogueira, F. T. S., Lodha, M., & Timmermans, M. C. P. (2015) · The Plant Cell · doi:10.1105/tpc.15.00454 · Cited by 102
Small Regulatory RNAs May Sharpen Spatial Expression Patterns
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Metadata
- Authors
- Emery, J. F., Floyd, S. K., Alvarez, J., Eshed, Y., Hawker, N. P., Izhaki, A., Baum, S. F., & Bowman, J. L.
- Affiliations
- University of California, Davis (US)
- Corresponding author
- Bowman, John L.
- Venue
- Current Biology
- Publisher
- Elsevier BV
- Published
- 2003-10
- Volume
- 13
- Issue
- 20
- Pages
- 1768-1774
- ISSN
- 0960-9822 (ISSN-L)
- OpenAlex
- W2002212941
- Cited by
- 1,143
- References
- 31
- Citations by year
- 2026: 23 · 2025: 24 · 2024: 33 · 2023: 30 · 2022: 62 · 2021: 38 · 2020: 54 · 2019: 42 · 2018: 42 · 2017: 59 · 2016: 38 · 2015: 56 · 2014: 46 · 2013: 59 · 2012: 63
- FWCI
- 79.29
- Type
- journal article
- Language
- en
- Open access
- bronze
- doi.org
- Licence
- www.elsevier.com/tdm/userlicense/1.0/ (tdm)
- www.elsevier.com/legal/tdmrep-license (tdm)
- www.elsevier.com/open-access/userlicense/1.0/ (vor, 3577 d)
- doi.org/10.15223/policy-017 (stm-asf)
- doi.org/10.15223/policy-037 (stm-asf)
- doi.org/10.15223/policy-012 (stm-asf)
- doi.org/10.15223/policy-029 (stm-asf)
- doi.org/10.15223/policy-004 (stm-asf)
- Locations
- Current Biology (publishedVersion)
- PubMed (publishedVersion)
- Funders
- National Science Foundation (00 77984, 99 86054)
- Topics
- Life Sciences › Agricultural and Biological Sciences › Plant Science › Plant Molecular Biology Research
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Developmental Biology and Gene Regulation
- Life Sciences › Agricultural and Biological Sciences › Plant Science › Plant Parasitism and Resistance
- Keywords
- radial patterning, adaxial-abaxial polarity, REVOLUTA, microRNA binding, vascular patterning, cotyledon development, apical meristem, bilateral symmetry, shoot development, Arabidopsis thaliana
- MeSH terms
- Base Sequence, Models, Molecular, Molecular Sequence Data, Phylogeny, Transcription Factors, Arabidopsis, Plant Shoots, Body Patterning, Gene Expression Profiling, Arabidopsis Proteins, MicroRNAs
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