The DOI matches its Crossref record; 59 of the 59 references it cites were found in a registry or an index.
Plant Gravitropism. Unraveling the Ups and Downs of a Complex Process
Open accessAbstract
Wind and heavy rain can have a devastating effect on crop production if they occur late during the life cycle of the plants. They often flatten the crop on the ground, leaving seed and other harvestable products at the mercy of soil moisture and pathogens and inaccessible to mechanical harvesting machinery. However, farmers will not worry much if a storm of similar strength hits a crop earlier in its cycle. They know that younger plants are able to straighten up and resume upward growth. This example illustrates the significance of tropism, or the ability of plant organs to direct their growth along a path that is dictated by their surrounding environment. In nature, plant organs can use a variety of environmental cues to guide their growth, including gravity, touch, light, gradients in temperature, humidity, ions, chemicals, and oxygen. In the example illustrated above, the stems of younger crops were able to perceive a change in their orientation within the gravity field. The corresponding information was then translated into a complex growth response called gravitropism that allowed them to straighten up and to eventually resume growth at a defined angle from the gravity vector, the gravitational set point angle (GSPA). The GSPA associated with specific plant organs is a function of the identity of the species and organ under consideration, its developmental phase, the physiological status of the plant, and a variety of environmental parameters to which the plant has been exposed. A plant organ is capable of detecting any deviation from its assigned GSPA and responds to the corresponding stimulus (gravitropic stimulus) by developing differential cellular elongation on opposite flanks, resulting in tip curvature and subsequent realignment with the GSPA (Firn and Digby, 1997). Gravitropism has been observed and analyzed in a variety of plant organs, including roots, hypocotyls, and inflorescence stems of dicots; roots, coleoptiles, and pulvini of monocots; and rhizoids and protonemata of algae and moss. It also has been observed and studied in fungal fruiting bodies. In 1999, an Update discussing the status of our understanding of gravitropism in roots of higher plants was published (Chen et al., 1999). Since then, there have been several developments in the field that have provided new insights on the different issues related to gravitropism in multiple plant systems. These breakthroughs are discussed in this Update. For a plant organ to guide its growth along a defined GSPA, it must perceive any change in its orientation within the gravity field. The corresponding physical information must be transduced into a physiological and/or biochemical signal, which must be transported to the response site where differential growth generates a curvature, allowing the growing tip to regain its orientation along the GSPA. As discussed in our previous Update (Chen et al., 1999), different cells are specialized to carry out these successive phases of gravitropism in monocots and dicots. For instance, in roots, gravity is perceived mainly by the columella cells of the root cap, whereas the differential growth response associated with gravistimulation occurs in the elongation zone (EZ; Figs. 1A and 2). In shoots, cells located in specialized tissues at the periphery of the vasculature, including the endodermis of hypocotyls (Fig. 1B), and the bundle sheath parenchyma in inflorescence stems and cereal pulvini perceive gravity and generate a signal that is transported laterally to the more peripheral tissues. There, the signal promotes the differential growth responsible for gravitropic curvature (Fig. 1B). On the other hand, in lower plants and algae exhibiting single-cell tip growth (i.e. rhizoids and protonemata), gravity perception and curvature response occur in the same cell (Fig. 1C). Hence, different species and organs adopt different molecular, cytological, and physiological strategies to guide their growth along specified GSPAs. Gravitropism in higher plants and algae. A, In roots of higher plants, the site of gravity sensing (i.e. the root cap) is spatially distinct from the site of the response (the EZ). Amyloplasts present in root columella cells settle to the bottom side of the cell (arrowheads) when the root is reoriented. There is overwhelming support that this process (starch-statolith hypothesis) constitutes one of the primary mechanisms of gravity sensing in plants. Depending on various environmental and endogenous factors, the reoriented root attains a specific GSPA with respect to the vertical. B, In shoots are located in the cell to the In rhizoids of the function of the in of which In to higher plants, the and response phases of gravitropism occur in the same of a root columella cell the and the It has been that the in the is in the physical information of to a physiological signal that to the gravity The of in In roots is transported the into the root where it in the of There, it is transported lat
Overview
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Integrity signals
Registry
Cites
Statistics
Verification
Claims the paper makes
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Self-check
Percentages, sums and reported differences re-computed from the paper’s own numbers.
The self-check needs the paper’s full text.
Citations
Cites
Lateral relocation of auxin efflux regulator PIN3 mediates tropism in Arabidopsis
Friml, J., Wiśniewska, J., Benková, E., Mendgen, K., & Palme, K. (2002) · Nature · doi:10.1038/415806a · Cited by 1,426
Auxin transport inhibitors block PIN1 cycling and vesicle trafficking
Geldner, N., Friml, J., Stierhof, Y.-D., Jürgens, G., & Palme, K. (2001) · Nature · doi:10.1038/35096571 · Cited by 1,241
Calcium at the Crossroads of Signaling
Sanders, D., Pelloux, J., Brownlee, C., & Harper, J. F. (2002) · The Plant Cell · doi:10.1105/tpc.002899 · Cited by 1,214
Neill, S. (2002) · Current Opinion in Plant Biology · doi:10.1016/s1369-5266(02)00282-0 · Cited by 1,207
Geldner, N., Anders, N., Wolters, H., Keicher, J., Kornberger, W., Muller, P., Delbarre, A., Ueda, T., Nakano, A., & Jürgens, G. (2003) · Cell · doi:10.1016/s0092-8674(03)00003-5 · Cited by 1,122
Tensegrity II. How structural networks influence cellular information processing networks
Ingber, D. E. (2003) · Journal of Cell Science · doi:10.1242/jcs.00360 · Cited by 839
Auxin transport — shaping the plant
Friml, J. (2003) · Current Opinion in Plant Biology · doi:10.1016/s1369526602000031 · Cited by 745
The Control of the Patterned Differentiation of Vascular Tissues
Sachs, T. (1981) · Advances in Botanical Research · doi:10.1016/s0065-2296(08)60351-1 · Cited by 656
Role of Auxin-Induced Reactive Oxygen Species in Root Gravitropism
Joo, J. H., Bae, Y. S., & Lee, J. S. (2001) · Plant Physiology · doi:10.1104/pp.126.3.1055 · Cited by 557
Gravity-regulated differential auxin transport from columella to lateral root cap cells
Ottenschläger, I., Wolff, P., Wolverton, C., Bhalerao, R. P., Sandberg, G., Ishikawa, H., Evans, M., & Palme, K. (2003) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0437936100 · Cited by 549
Noh, B., Murphy, A. S., & Spalding, E. P. (2001) · The Plant Cell · doi:10.1105/tpc.010350 · Cited by 527
Free oxygen radicals regulate plasma membrane Ca2+- and K+-permeable channels in plant root cells
Demidchik, V., Shabala, S. N., Coutts, K. B., Tester, M. A., & Davies, J. M. (2003) · Journal of Cell Science · doi:10.1242/jcs.00201 · Cited by 358
Sack, F. D. (1991) · International Review of Cytology · doi:10.1016/s0074-7696(08)60695-6 · Cited by 345
Mapping the Functional Roles of Cap Cells in the Response of Arabidopsis Primary Roots to Gravity1
Blancaflor, E. B., Fasano, J. M., & Gilroy, S. (1998) · Plant Physiology · doi:10.1104/pp.116.1.213 · Cited by 345
Self-citationMicrotubule basis for left-handed helical growth in Arabidopsis
Thitamadee, S., Tuchihara, K., & Hashimoto, T. (2002) · Nature · doi:10.1038/417193a · Cited by 300
Reversible Root Tip Rotation in Arabidopsis Seedlings Induced by Obstacle-Touching Stimulus
Okada, K., & Shimura, Y. (1990) · Science · doi:10.1126/science.250.4978.274 · Cited by 298
Enhanced gravi- and phototropism in plant mdr mutants mislocalizing the auxin efflux protein PIN1
Noh, B., Bandyopadhyay, A., Peer, W. A., Spalding, E. P., & Murphy, A. S. (2003) · Nature · doi:10.1038/nature01716 · Cited by 272
Rashotte, A. M., DeLong, A., & Muday, G. K. (2001) · The Plant Cell · doi:10.1105/tpc.010158 · Cited by 271
Gravitropism in Higher Plants1
Chen, R., Rosen, E., & Masson, P. H. (1999) · Plant Physiology · doi:10.1104/pp.120.2.343 · Cited by 264
Self-citationSanderfoot, A. A., Kovaleva, V., Bassham, D. C., & Raikhel, N. V. (2001) · Molecular Biology of the Cell · doi:10.1091/mbc.12.12.3733 · Cited by 258
Changes in Root Cap pH Are Required for the Gravity Response of the Arabidopsis Root
Fasano, J. M., Swanson, S. J., Blancaflor, E. B., Dowd, P. E., Kao, T.-H., & Gilroy, S. (2001) · The Plant Cell · doi:10.1105/tpc.13.4.907 · Cited by 257
Self-citationSedbrook, J. C., Carroll, K. L., Hung, K. F., Masson, P. H., & Somerville, C. R. (2002) · The Plant Cell · doi:10.1105/tpc.002360 · Cited by 240
Self-citationKato, T., Morita, M. T., Fukaki, H., Yamauchi, Y., Uehara, M., Niihama, M., & Tasaka, M. (2002) · The Plant Cell · doi:10.1105/tpc.010215 · Cited by 235
M OLECULAR G ENETICS OF A UXIN S IGNALING
Leyser, O. (2002) · Annual Review of Plant Biology · doi:10.1146/annurev.arplant.53.100301.135227 · Cited by 224
Touch modulates gravity sensing to regulate the growth of primary roots of Arabidopsis thaliana
Massa, G. D., & Gilroy, S. (2003) · The Plant Journal · doi:10.1046/j.1365-313x.2003.01637.x · Cited by 221
Sugimoto, K., Himmelspach, R., Williamson, R. E., & Wasteneys, G. O. (2003) · The Plant Cell · doi:10.1105/tpc.011593 · Cited by 220
Morita, M. T., Kato, T., Nagafusa, K., Saito, C., Ueda, T., Nakano, A., & Tasaka, M. (2002) · The Plant Cell · doi:10.1105/tpc.010216 · Cited by 219
Reorientation of Seedlings in the Earth's Gravitational Field Induces Cytosolic Calcium Transients
Plieth, C., & Trewavas, A. J. (2002) · Plant Physiology · doi:10.1104/pp.011007 · Cited by 195
Yano, D., Sato, M., Saito, C., Sato, M. H., Morita, M. T., & Tasaka, M. (2003) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1430749100 · Cited by 191
An Emerging Model of Auxin Transport Regulation
Muday, G. K., & Murphy, A. S. (2002) · The Plant Cell · doi:10.1105/tpc.140230 · Cited by 184
Boonsirichai, K., Sedbrook, J. C., Chen, R., Gilroy, S., & Masson, P. H. (2003) · The Plant Cell · doi:10.1105/tpc.015560 · Cited by 174
Self-citationIonic Signaling in Plant Responses to Gravity and Touch
Fasano, J. M., Massa, G. D., & Gilroy, S. (2002) · Journal of Plant Growth Regulation · doi:10.1007/s003440010049 · Cited by 158
The transient receptor potential channel on the yeast vacuole is mechanosensitive
Zhou, X., Batiza, A. F., Loukin, S. H., Palmer, C. P., Kung, C., & Saimi, Y. (2003) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1230540100 · Cited by 156
Actin cytoskeleton in plants: From transport networks to signaling networks
Volkmann, D., & ka, F. E. B. (1999) · Microscopy Research and Technique · doi:10.1002/(sici)1097-0029(19991015)47:2<135::aid-jemt6>3.0.co;2-1 · Cited by 150
Takahashi, N., Yamazaki, Y., Kobayashi, A., et al. (2003) · PLANT PHYSIOLOGY · doi:10.1104/pp.018853 · Cited by 149
Sedbrook, J. C., Chen, R., & Masson, P. (1999) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.96.3.1140 · Cited by 148
Self-citationPerera, I. Y., Heilmann, I., Chang, S. C., Boss, W. F., & Kaufman, P. B. (2001) · PLANT PHYSIOLOGY · doi:10.1104/pp.125.3.1499 · Cited by 148
Boonsirichai, K., Guan, C., Chen, R., & Masson, P. (2002) · Annual Review of Plant Biology · doi:10.1146/annurev.arplant.53.100301.135158 · Cited by 146
Self-citationScott, A. C., & Allen, N. S. (1999) · PLANT PHYSIOLOGY · doi:10.1104/pp.121.4.1291 · Cited by 142
Gravitropic Response of Inflorescence Stems in Arabidopsis thaliana
Fukaki, H., Fujisawa, H., & Tasaka, M. (1996) · PLANT PHYSIOLOGY · doi:10.1104/pp.110.3.933 · Cited by 137
Arabidopsis actin gene ACT7 plays an essential role in germination and root growth
Gilliland, L. U., Pawloski, L. C., Kandasamy, M. K., & Meagher, R. B. (2003) · The Plant Journal · doi:10.1046/j.1365-313x.2003.01626.x · Cited by 136
Enhanced Gravitropism of Roots with a Disrupted Cap Actin Cytoskeleton
Hou, G., Mohamalawari, D. R., & Blancaflor, E. B. (2003) · PLANT PHYSIOLOGY · doi:10.1104/pp.014423 · Cited by 127
Self-citationAno hydrotropic responseRoot Mutant that Responds Positively to Gravitropism in Arabidopsis1,
Eapen, D., Barroso, M. L. B., Campos, M. E., Ponce, G., Corkidi, G., DUBROVSKY, J. G., & Cassab, G. I. (2003) · PLANT PHYSIOLOGY · doi:10.1104/pp.011841 · Cited by 127
Ethylene Modulates Root-Wave Responses in Arabidopsis
Buer, C. S., Wasteneys, G. O., & Masle, J. (2003) · PLANT PHYSIOLOGY · doi:10.1104/pp.102.019182 · Cited by 125
Lee, H. Y., Bahn, S. C., Kang, Y.-M., Lee, K.-H., Kim, H. J., Noh, E. K., Palta, J. P., Shin, J. S., & Ryu, S. B. (2003) · The Plant Cell · doi:10.1105/tpc.014423 · Cited by 123
Interactions Between Gravitropism and Phototropism in Plants
Correll, M. J., & Kiss, J. Z. (2002) · Journal of Plant Growth Regulation · doi:10.1007/s003440010056 · Cited by 122
The Cytoskeleton and Gravitropism in Higher Plants
Blancaflor, E. B. (2002) · Journal of Plant Growth Regulation · doi:10.1007/s003440010041 · Cited by 121
Self-citationMoseyko, N., Zhu, T., Chang, H., Wang, X., & Feldman, L. J. (2002) · PLANT PHYSIOLOGY · doi:10.1104/pp.009688 · Cited by 112
Root gravitropism in response to a signal originating outside of the cap
Wolverton, C., Mullen, J. L., Ishikawa, H., & Evans, M. L. (2002) · Planta · doi:10.1007/s00425-001-0726-9 · Cited by 111
Yamamoto, K., & Kiss, J. Z. (2002) · PLANT PHYSIOLOGY · doi:10.1104/pp.010804 · Cited by 108
Guan, C., Rosen, E., Boonsirichai, K., Poff, K. L., & Masson, P. (2003) · PLANT PHYSIOLOGY · doi:10.1104/pp.103.023358 · Cited by 90
Self-citationCurvature in Arabidopsis Inflorescence Stems Is Limited to the Region of Amyloplast Displacement
Weise, S. E., Kuznetsov, O. A., Hasenstein, K. H., et al. (2000) · Plant and Cell Physiology · doi:10.1093/pcp/41.6.702 · Cited by 77
Graviorientation in Protists and Plants
Hemmersbach, R., Volkmann, D., & Häder, D. (1999) · Journal of Plant Physiology · doi:10.1016/s0176-1617(99)80311-3 · Cited by 75
Wyatt, S. E., Rashotte, A. M., Shipp, M. J., Robertson, D., & Muday, G. K. (2002) · PLANT PHYSIOLOGY · doi:10.1104/pp.102.010579 · Cited by 72
Cytoplasmic pH Dynamics in Maize Pulvinal Cells Induced by Gravity Vector Changes,
Johannes, E., Collings, D. A., Rink, J. C., & Allen, N. S. (2001) · PLANT PHYSIOLOGY · doi:10.1104/pp.127.1.119 · Cited by 65
Solving the puzzle of gravitropism — has a lost piece been found?
Firn, R. D., & Digby, J. (1997) · Planta · doi:10.1007/pl00008104 · Cited by 59
Monshausen, G. B., & Sievers, A. (2002) · Planta · doi:10.1007/s00425-002-0880-8 · Cited by 27
Contributions of Space Experiments to the Study of Gravitropism
Perbal, G., & Driss‐Ecole, D. (2002) · Journal of Plant Growth Regulation · doi:10.1007/s003440010055 · Cited by 19
Clore, A. M., TURNER, W. S., Morse, A. M., & Whetten, R. W. (2003) · Plant Cell & Environment · doi:10.1046/j.1365-3040.2003.00990.x · Cited by 11
Cited by
Flavonoids: New Roles for Old Molecules
Buer, C. S., Imin, N., & Djordjevic, M. A. (2010) · Journal of Integrative Plant Biology · doi:10.1111/j.1744-7909.2010.00905.x · Cited by 694
Auxin Receptors and Plant Development: A New Signaling Paradigm
Mockaitis, K., & Estelle, M. (2008) · Annual Review of Cell and Developmental Biology · doi:10.1146/annurev.cellbio.23.090506.123214 · Cited by 651
Swarup, R., Kramer, E. M., Perry, P., Knox, K., Leyser, H. M. O., Haseloff, J., Beemster, G. T. S., Bhalerao, R., & Bennett, M. J. (2005) · Nature Cell Biology · doi:10.1038/ncb1316 · Cited by 614
Buer, C. S., & Muday, G. K. (2004) · The Plant Cell · doi:10.1105/tpc.020313 · Cited by 398
Regulation of Root Growth by Plant Hormones—Roles for Auxin and Gibberellin
Tanimoto, E. (2005) · Critical Reviews in Plant Sciences · doi:10.1080/07352680500196108 · Cited by 356
Metadata
- Authors
- Blancaflor, E. B., & Masson, P. H.
- Venue
- Plant Physiology
- Publisher
- Oxford University Press (OUP)
- Published
- 2003-12-01
- Volume
- 133
- Issue
- 4
- Pages
- 1677-1690
- ISSN
- 0032-0889 (ISSN-L)
- 1532-2548
- OpenAlex
- W1987913274
- Cited by
- 332
- References
- 59
- FWCI
- 22.56
- Type
- journal article
- Language
- en
- Open access
- green
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
Statistics and arithmetic are recomputed, not judged.
Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.
What counts as a claim ›How we measure confidence ›How we check this ›
Are you an author, or do you see a problem with this page? Request a review
Data sources
Bibliographic data: Semantic Scholar, OpenAlex, Crossref.
Contains information from the Semantic Scholar Academic Graph Datasets, made available under the ODC Attribution License (ODC-BY 1.0).
Semantic Scholar’s data is described in: Kinney, R., et al. (2023). The Semantic Scholar Open Data Platform. arXiv:2301.10140.