Graviperception in maize plants: is amyloplast sedimentation a red herring?
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Land plants perceive gravity and respond to it in an organ-specific way; shoots typically direct growth upwards, roots typically downwards. Historically, at least with respect to maize plants, this phenomenon is attributed to three sequential processes, namely graviperception, the transduction of the perceived signal, and the graviresponse, resulting in a typical (re)positioning of the organ or entire plant body relative to the gravivector. For decades, sedimentation of starch-containing plastids within the cells of special tissues has been regarded as the primary and initiating process fundamental for gravitropic growth (starch-statolith hypothesis). Based on Popper’s falsification principle, uncompromising experiments were executed. The results indicate that the model of graviperception based on amyloplast sedimentation does not apply to maize seedlings.
KeywordsGraviperception Gravitropism Gravi-model Plant signal transduction Gravitropic growth Starch-statolith hypothesis Tensegrity model Ethylene
The successful development of a land plant depends from the very beginning on the right direction of growth and positioning of the seedling organs relative to the gravivector. This capacity ensures the plant anchors its roots in the soil (providing nutrients and water) and adjusts light-harvesting shoot organs optimally above ground (enabling photosynthesis).
Growth dependence on gravity—so-called gravitropic growth—is from its early investigations formally divided into three sequential processes: graviperception, the transduction of the perceived stimulus, and the growth response, adjusting the growth and the position of cells or organs according to prevailing graviconditions (Kutschera 2001). The way plants supposedly perceive gravity stems from a long-standing model which arose from the early discoveries of the function of statocyts in animals, when Noll (1892) suggested that plant cells might contain microscopic particles which may function in the same way as animal statoliths. Soon, it was demonstrated that gravisensitive organs of land plants possessed cells containing starch grains which, unlike normal storage starch, sedimented to the cell bottom whatever the position of the organ (Haberlandt 1900; Nemec 1900; Darwin 1903; Rawitscher 1932). From then on, sedimentation of these dense structures within specialized cells (statocytes) of certain tissues has been postulated as the graviperceiving step, supposedly providing the necessary information to optimally position the organs relative to gravity by appropriate growth (responses) and by this to ensure the survival of the individual plant (Wilkins 1966).
In roots, statolith-containing statocytes are ascribed to the columella cells at the very tip of the roots—the so-called root cap—whereas in shoots, cells containing sedimentable amyloplasts are restricted to the so-called starch sheath surrounding the vascular bundles (Noll 1892).
This tissue-restricted and organ-specific model of plant graviperception has since been repeatedly substantiated in a great many of apparent, yet indirect experiments. Both, occurrence of amyloplasts and their sedimentation developed a dogmatic character, disregarding models not involving this cybernetic principle. Yet, how sedimentation yields positional information and how this may eventually induce a hypothetical, factually unknown signal transduction is still, after more than 100 years, speculative. Various modifications of the classical hypothesis of the graviperceiving process are typified in the topographic model, the kinetic model, and the deformation model, and many other versions, all of which aim to rationalize the existence and dependence of these plastids on gravity. In support of such a sedimentation scenario, the cytoskeleton of the cells was claimed to play a crucial role leading to the so-called tensegrity model (Yoder et al. 2001; Ingber 2003), which was suggested to interfere with mechanosensitive ion channels within the cell plasma membrane of plant cells (Yoder et al. 2001). Contradicting this, Yamamoto and Kiss (2002) suggested actin filaments were not involved in gravitropism of stems and hypocotyls. Also, molecular genetic approaches employing knockouts of actin showed no effect on gravitropism (Gilliland et al. 2003) despite demonstrated impacts on auxin transport and altered cycling of PIN1, an auxin transport protein (Muday and Murphy 2002). Although it has also been repeatedly demonstrated that starchless Arabidopsis mutants respond gravitropically and therefore do not depend on starch-containing amyloplast sedimentation for graviperception (Caspar and Pickard 1989), the long-standing model developed a dogma-like character, excluding and preventing any models not involving amyloplast sedimentation in specialized cells for graviperception.
As briefly outlined, graviperception via organ-specific plastid sedimentation was always considered “compulsory” for the rationale of any graviperception model. Yet, despite its putatively obvious and, therefore, tempting plausibility, no binding causal processes, i.e., steps causally being induced by sedimentation and themselves inducing processes eventually leading to differential growth, have so far been demonstrated. After more than 100 years, no answers exist to questions such as “what processes represent the signal transduction steps as induced by sedimentation eventually leading to gravitropic differential growth?” or “what signal(s) pass from the site of perception to the site of action?” (Cleland 1997) and “how are sedimenting starch particles related to PIN/auxin redistribution supposedly accomplishing unequal growth of opposing organ flanks?” In fact, despite apparently overwhelming evidence consistently reiterated in favor of the outlined model, we do not know what sedimentation actually does — yet, it is dictating experimental approaches and excluding alternative scenarios. The possible fatal consequences of such a strategy have already been pointed out by August Weismann (1868) saying “although a scientific hypothesis can never be proved, it can be refuted if false, and it therefore raises the question whether facts cannot be taught which are inextricably contradictory with one of the two hypotheses and thus bring it to a collapse....”
If sedimentation of statoliths within the statocytes of the root cap represents the graviperceiving step of gravitropic growth regulation in roots, then its removal should eliminate gravitropic growth.
If sedimentation of statoliths within the vascular bundle sheath cells represents the graviperceiving step of gravitropic growth regulation in shoots, then their removal should eliminate gravitropic growth.
The system of choice is the classical system for the analyses of graviperception, namely coleoptiles of maize (Wolverton et al. 2002), as well as roots of maize, characterized by so-called closed root caps (Barlow 2002). Both systems allowed surgical removal without destruction, damage, or impairment of the responding tissues.
Materials and methods
Maize kernels (Hybridmais, Ronaldinio, KWS) were germinated in darkness at room temperature (~ 21–24 °C) by rolling them in moistened sheets of filter paper (MN 710; 580 × 580 mm). For this, 20 kernels were placed in rows at interval distances of 1–1.5 cm on chromatography paper sheets (40 × 10 cm). The rolled sheets were placed vertically in 200-mL glass beakers and filled with distilled water to a depth of 1 cm. The beakers were then covered with aluminum foil. After 2–3 days, the germinated seedlings with developed coleoptiles and also exhibiting roots with lengths in the range of 2 to 3 cm were selected for the experiments (for details, also see Hahn et al. 2006).
Coleoptiles, 2–3 cm in length, were harvested in dim white light. Segments, 2.5 cm in length including the tips, were cut and the primary leaves removed. Coleoptiles were placed in holes in Perspex blocks and stabilized with “plastic-fermit” (Installationskitt; Nissen & Volk, Hamburg, Germany). The blocks were placed in Perspex containers so that the coleoptiles were in a horizontal position. The containers were filled with 350 mL of distilled water, sufficient to cover the coleoptiles, and aerated.
Decalyptration of the roots was carried out by a faint partial lateral cut in the zone between the root tip and the beginning of the root cap by pressing the root gently under a binocular on to a vertically fixed razor blade without cutting but causing a predetermined breaking crack. Thereafter, the root cap was carefully removed by squeezing it off between the fingernails.
Root gravitropic growth of both, intact and decapped roots by horizontally placing seedlings on water-imbibed filter paper on top of Styrofoam stands within PET containers (“Gerda-Dosen”). The container bottoms were covered with water-imbibed filter paper in order to guarantee water-saturated air conditions. Decapped roots were preincubated with the roots immersed in Eppendorf caps in solutions of 10 μM latrunculin for 1 h before placing them similar to controls.
Results and discussion
After 9 h of incubation, both, intact and coleoptiles without amyloplast-containing tissues exhibit identical graviresponses, which tended to be, but—but not statistically significant — slightly earlier in coleoptiles lacking the vascular bundle sheath tissue established compared to intact coleoptiles, i.e., faster, which might be interpreted by more favorable mechanical conditions for bending.
As illustrated in Figs. 2 and 3, both organs lacking the presumed graviperceiving tissues exhibit graviresponsive growth. Sedimenting, starch-filled amyloplasts are quite obviously not necessary for growth dependent on gravity.
Based on these clear and unequivocal findings, one may ask: what other or further removal of a claimed graviperceiving system has to be carried out in order to demonstrate its absence as irrelevant for gravitropic growth? Or—vice versa—“why should we attribute to a tissue or an organ a regulatory function when its elimination does not result in a deletion or strongly impeded graviresponse?”
Consistent with earlier presented data (Firn and Digby 1977) in which the loss of gravitropic growth was demonstrated by removal of the epidermal tissues, the finding implies that not only accomplishment of gravibending, but also anticipatory perception of gravity takes place within the peripheral tissue—without sedimentation of amyloplasts. In support of this, Wolverton et al. (2002) demonstrated the existence of root-borne graviperception, yet without any idea on “the nature of the signal originating outside the root cap.”
It therefore appears appropriate to search for alternative mechanisms for graviperception (also) immanent to peripheral cells, irrespective of the lack of sedimentable amyloplasts.
There are apprehensible explanations for the rationale of the ancient model of graviperception. By then, in the absence of any other measurable effect accompanying reorientation of a plant organ, the obvious (re)sedimentation in dependence of the cells position relative to the gravivector provided a most plausible scenario as the graviperceiving step. However, as in context with many other scientific problems, plausibility can be a tempting, yet a “dangerous teacher.”
In fact, the model of graviperception or gravitropic growth regulation in general might look very different had scientists in the early days of exploring gravitropism known about and had the chance to detect and to measure ethylene. It has been reported that inhibiting ethylene synthesis results in a concentration-dependent manner, in a corresponding reduction of gravitropic growth of (Edelmann and Roth 2006). The more ethylene synthesis inhibited, the less pronounced gravicurvature. How these ethylene-dependent phenomena are brought about is still speculative. Nevertheless, it may be worthwhile to address ethylene as a serious candidate for graviperception.
In support of this, according to results of more recent studies (reviewed by Sato et al. 2015), models of gravitropic growth regulation based on (re)sedimentation of amyloplasts in columella cells are redundant: PIN—proteins facilitating gravi-dependent auxin transport—redistribute per se dependent on gravity (Gälweiler et al. 1998; Müller et al. 1998; Friml et al. 2002). This effect does not depend on sedimentation of amyloplasts, the (ir)relevance of which seems deliberately not addressed—at least not in cybernetical detail—since it is obviously not needed for the gravitropic scenario.
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