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The Relationship between Auxin Transport and Maize Branching
Open accessAbstract
Maize (Zea mays) plants make different types of vegetative or reproductive branches during development. Branches develop from axillary meristems produced on the flanks of the vegetative or inflorescence shoot apical meristem. Among these branches are the spikelets, short grass-specific structures, produced by determinate axillary spikelet-pair and spikelet meristems. We investigated the mechanism of branching in maize by making transgenic plants expressing a native expressed endogenous auxin efflux transporter (ZmPIN1a) fused to yellow fluorescent protein and a synthetic auxin-responsive promoter (DR5rev) driving red fluorescent protein. By imaging these plants, we found that all maize branching events during vegetative and reproductive development appear to be regulated by the creation of auxin response maxima through the activity of polar auxin transporters. We also found that the auxin transporter ZmPIN1a is functional, as it can rescue the polar auxin transport defects of the Arabidopsis (Arabidopsis thaliana) pin1-3 mutant. Based on this and on the groundbreaking analysis in Arabidopsis and other species, we conclude that branching mechanisms are conserved and can, in addition, explain the formation of axillary meristems (spikelet-pair and spikelet meristems) that are unique to grasses. We also found that BARREN STALK1 is required for the creation of auxin response maxima at the flanks of the inflorescence meristem, suggesting a role in the initiation of polar auxin transport for axillary meristem formation. Based on our results, we propose a general model for branching during maize inflorescence development.
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Bartlett, M. E., Williams, S. K., Taylor, Z., DeBlasio, S. L., Goldshmidt, A., Hall, D. H., Schmidt, R. J., Jackson, D. P., & Whipple, C. (2015) · The Plant Cell · doi:10.1105/tpc.15.00679 · Cited by 54
Self-citationGenetic control of branching patterns in grass inflorescences
Kellogg, E. A. (2022) · The Plant Cell · doi:10.1093/plcell/koac080 · Cited by 50
Meristem identity and phyllotaxis in inflorescence development
Bartlett, M. E., & Thompson, B. E. (2014) · Frontiers in Plant Science · doi:10.3389/fpls.2014.00508 · Cited by 50
Translating auxin responses into ovules, seeds and yield: Insight from Arabidopsis and the cereals
Shirley, N. J., Aubert, M. K., Wilkinson, L. G., Bird, D. C., Lora, J., Yang, X., & Tucker, M. R. (2018) · Journal of Integrative Plant Biology · doi:10.1111/jipb.12747 · Cited by 50
Laureyns, R., Joossens, J., Herwegh, D., Pevernagie, J., Pavie, B., Demuynck, K., Debray, K., Coussens, G., Pauwels, L., Hautegem, T. V., et al. (2021) · PLANT PHYSIOLOGY · doi:10.1093/plphys/kiab533 · Cited by 48
Divergent Roles for Maize PAN1 and PAN2 Receptor-Like Proteins in Cytokinesis and Cell Morphogenesis
Sutimantanapi, D., Pater, D., & Smith, L. G. (2014) · PLANT PHYSIOLOGY · doi:10.1104/pp.113.232660 · Cited by 45
Stephenson, E., Estrada, S., Meng, X., Ourada, J., Muszynski, M. G., Habben, J. E., & Danilevskaya, O. N. (2019) · PLoS ONE · doi:10.1371/journal.pone.0203728 · Cited by 45
TALE and Shape: How to Make a Leaf Different
Giacomo, E. D., Iannelli, M. A., & Frugis, G. (2013) · Plants · doi:10.3390/plants2020317 · Cited by 43
Local auxin biosynthesis regulates brace root angle and lodging resistance in maize
Zheng, Z., Wang, B., Zhuo, C., Xie, Y., Zhang, X., Liu, Y., Zhang, G., Ding, H., Zhao, B., Tian, M., et al. (2023) · New Phytologist · doi:10.1111/nph.18733 · Cited by 43
Martinez, C. C., Koenig, D., Chitwood, D. H., & Sinha, N. R. (2016) · Developmental Biology · doi:10.1016/j.ydbio.2016.08.011 · Cited by 40
Wang, X., Feng, J., White, P. J., Shen, J., & Cheng, L. (2019) · Annals of Botany · doi:10.1093/aob/mcz154 · Cited by 41
Tissue-specific transcriptomics reveal functional differences in floral development
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Pressoir, G., Brown, P. J., Zhu, W., Upadyayula, N., Rocheford, T., Buckler, E. S., & Kresovich, S. (2009) · The Plant Journal · doi:10.1111/j.1365-313x.2009.03802.x · Cited by 38
What Has Been Seen Cannot Be Unseen—Detecting Auxin In Vivo
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“In the monocot maize, ZmPIN1a, b, and c are involved in auxin transport during embryogenesis and vegetative development (Carraro et al., 2006; Gallavotti et al., 2008; Forestan et al., 2010).”
Hormonal control of medial–lateral growth and vein formation in the maize leaf
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Metadata
- Authors
- Gallavotti, A., Yang, Y., Schmidt, R. J., & Jackson, D.
- Affiliations
- Cold Spring Harbor Laboratory (US)
- Venue
- Plant Physiology
- Publisher
- Oxford University Press (OUP)
- Published
- 2008-06-11
- Volume
- 147
- Issue
- 4
- Pages
- 1913-1923
- ISSN
- 0032-0889 (ISSN-L)
- 1532-2548
- PMC
- PMC2492655
- OpenAlex
- W2017000081
- Cited by
- 227
- References
- 49
- Citations by year
- 2026: 6 · 2025: 12 · 2024: 15 · 2023: 17 · 2022: 13 · 2021: 13 · 2020: 14 · 2019: 11 · 2018: 13 · 2017: 11 · 2016: 8 · 2015: 13 · 2014: 15 · 2013: 15 · 2012: 13
- FWCI
- 14.96
- Type
- journal article
- Language
- en
- Open access
- hybrid
- doi.org
- Locations
- PLANT PHYSIOLOGY (publishedVersion, cc-by)
- PubMed Central (publishedVersion)
- PubMed (publishedVersion)
- Cold Spring Harbor Laboratory Institutional Repository (Cold Spring Harbor Laboratory) (acceptedVersion)
- Funders
- National Science Foundation
- U.S. Department of Agriculture
- Iowa State University
- Topics
- Life Sciences › Agricultural and Biological Sciences › Plant Science › Plant Molecular Biology Research
- Life Sciences › Agricultural and Biological Sciences › Plant Science › Plant Parasitism and Resistance
- Life Sciences › Agricultural and Biological Sciences › Plant Science › Plant nutrient uptake and metabolism
- Keywords
- polar auxin transport, auxin efflux transporters, axillary meristem, inflorescence development
- MeSH terms
- Biological Transport, Zea mays, Indoleacetic Acids, Models, Biological, Mutation, Phthalimides, Plant Proteins, Up-Regulation, Arabidopsis, Genes, Reporter, Meristem, Plants, Genetically Modified
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