Gravitropism (also known as geotropism) is a coordinated process of differential growth by a plant in response to gravity pulling on it. It also occurs in fungi. Gravity can be either "artificial gravity" or natural gravity. It is a general feature of all higher and many lower plants as well as other organisms. Charles Darwin was one of the first to scientifically document that roots show positive gravitropism and stems show negative gravitropism. [1] That is, roots grow in the direction of gravitational pull (i.e., downward) and stems grow in the opposite direction (i.e., upwards). This behavior can be easily demonstrated with any potted plant. When laid onto its side, the growing parts of the stem begin to display negative gravitropism, growing (biologists say, turning; see tropism) upwards. Herbaceous (non-woody) stems are capable of a degree of actual bending, but most of the redirected movement occurs as a consequence of root or stem growth outside. The mechanism is based on the Cholodny–Went model which was proposed in 1927, and has since been modified. [2] Although the model has been criticized and continues to be refined, it has largely stood the test of time.[ citation needed ]
Root growth occurs by division of stem cells in the root meristem located in the tip of the root, and the subsequent asymmetric expansion of cells in a shoot-ward region to the tip known as the elongation zone. Differential growth during tropisms mainly involves changes in cell expansion versus changes in cell division, although a role for cell division in tropic growth has not been formally ruled out. Gravity is sensed in the root tip and this information must then be relayed to the elongation zone so as to maintain growth direction and mount effective growth responses to changes in orientation to and continue to grow its roots in the same direction as gravity. [4]
Abundant evidence demonstrates that roots bend in response to gravity due to a regulated movement of the plant hormone auxin known as polar auxin transport. [5] This was described in the 1920s in the Cholodny-Went model. The model was independently proposed by the Ukrainian scientist N. Cholodny of the University of Kyiv in 1927 and by Frits Went of the California Institute of Technology in 1928, both based on work they had done in 1926. [6] Auxin exists in nearly every organ and tissue of a plant, but it has been reoriented in the gravity field, can initiate differential growth resulting in root curvature.
Experiments show that auxin distribution is characterized by a fast movement of auxin to the lower side of the root in response to a gravity stimulus at a 90° degree angle or more. However, once the root tip reaches a 40° angle to the horizontal of the stimulus, auxin distribution quickly shifts to a more symmetrical arrangement. This behavior is described as a "tipping point" mechanism for auxin transport in response to a gravitational stimulus. [3]
Gravitropism is an integral part of plant growth, orienting its position to maximize contact with sunlight, as well as ensuring that the roots are growing in the correct direction. Growth due to gravitropism is mediated by changes in concentration of the plant hormone auxin within plant cells.
As plants mature, gravitropism continues to guide growth and development along with phototropism. While amyloplasts continue to guide plants in the right direction, plant organs and function rely on
phototropic responses to ensure that the leaves are receiving enough light to perform basic functions such as photosynthesis. In complete darkness, mature plants have little to no sense of gravity, unlike seedlings that can still orient themselves to have the shoots grow upward until light is reached when development can begin. [8]
Differential sensitivity to auxin helps explain Darwin's original observation that stems and roots respond in the opposite way to the forces of gravity. In both roots and stems, auxin accumulates towards the gravity vector on the lower side. In roots, this results in the inhibition of cell expansion on the lower side and the concomitant curvature of the roots towards gravity (positive gravitropism). [4] [9] In stems, the auxin also accumulates on the lower side, however in this tissue it increases cell expansion and results in the shoot curving up (negative gravitropism). [10]
A recent study showed that for gravitropism to occur in shoots, a lot of an inclination, instead of a weak gravitational force, is necessary. This finding sets aside gravity sensing mechanisms that would rely on detecting the pressure of the weight of statoliths. [11]
A few species of fruit exhibit negative geotropism. Bananas are one well-known example. [12] Once the canopy that covers the fruit dries, the bananas will begin to curve upwards, towards sunlight, in what is known as phototropism. The specific chemical that initiates the upward curvature is a phytohormone in the banana called Auxin. When the banana is first exposed to sunlight after the leaf canopy dries, one face of the fruit is shaded. On exposure to sunlight, auxin in the banana migrates from the sunlight side to the shaded side. Since auxin is a powerful plant growth hormone, the increased concentration promotes cell division and causes the plant cells on the shaded side to grow. [13] This asymmetrical distribution of auxin is responsible for the upward curvature of the banana. [13] [14]
Plants possess the ability to sense gravity in several ways, one of which is through statoliths. Statoliths are dense amyloplasts, organelles that synthesize and store starch involved in the perception of gravity by the plant (gravitropism), that collect in specialized cells called statocytes. Statocytes are located in the starch parenchyma cells near vascular tissues in the shoots and in the columella in the caps of the roots. [15] These specialized amyloplasts are denser than the cytoplasm and can sediment according to the gravity vector. The statoliths are enmeshed in a web of actin and it is thought that their sedimentation transmits the gravitropic signal by activating mechanosensitive channels. [4] The gravitropic signal then leads to the reorientation of auxin efflux carriers and subsequent redistribution of auxin streams in the root cap and root as a whole. [16] Auxin moves toward higher concentrations on the bottom side of the root and suppresses elongation. The asymmetric distribution of auxin leads to differential growth of the root tissues, causing the root to curve and follow the gravity stimuli. Statoliths are also found in the endodermic layer of the hypocotyl, stem, and inflorescence stock. The redistribution of auxin causes increased growth on the lower side of the shoot so that it orients in a direction opposite that of the gravity stimuli.
Phytochromes are red and far-red photoreceptors that help induce changes in certain aspects of plant development. Apart being itself the tropic factor (phototropism), light may also suppress the gravitropic reaction. [17] In seedlings, red and far-red light both inhibit negative gravitropism in seedling hypocotyls (the shoot area below the cotyledons) causing growth in random directions. However, the hypocotyls readily orient towards blue light. This process may be caused by phytochrome disrupting the formation of starch-filled endodermal amyloplasts and stimulating their conversion to other plastid types, such as chloroplasts or etiolaplasts. [17]
Bending mushroom stems follow some regularities that are not common in plants. After turning into horizontal the normal vertical orientation the apical part (region C in the figure below) starts to straighten. Finally this part gets straight again, and the curvature concentrates near the base of the mushroom. [18] This effect is called compensation (or sometimes, autotropism). The exact reason of such behavior is unclear, and at least two hypotheses exist.
Both models fit the initial data well, but the latter was also able to predict bending from various reorientation angles. Compensation is less obvious in plants, but in some cases it can be observed combining exact measurements with mathematical models. The more sensitive roots are stimulated by lower levels of auxin; higher levels of auxin in lower halves stimulate less growth, resulting in downward curvature (positive gravitropism).
Mutants with altered responses to gravity have been isolated in several plant species including Arabidopsis thaliana (one of the genetic model systems used for plant research). These mutants have alterations in either negative gravitropism in hypocotyls and/or shoots, or positive gravitropism in roots, or both. [10] Mutants have been identified with varying effects on the gravitropic responses in each organ, including mutants which nearly eliminate gravitropic growth, and those whose effects are weak or conditional. In the same way that gravity has an effect on winding and circumnutating, thus aspects of morphogenesis have defects on the mutant. Once a mutant has been identified, it can be studied to determine the nature of the defect (the particular difference(s) it has compared to the non-mutant 'wildtype'). This can provide information about the function of the altered gene, and often about the process under study. In addition the mutated gene can be identified, and thus something about its function inferred from the mutant phenotype.
Gravitropic mutants have been identified that affect starch accumulation, such as those affecting the PGM1 (which encodes the enzyme phosphoglucomutase) gene in Arabidopsis, causing plastids – the presumptive statoliths – to be less dense and, in support of the starch-statolith hypothesis, less sensitive to gravity. [20] Other examples of gravitropic mutants include those affecting the transport or response to the hormone auxin. [10] In addition to the information about gravitropism which such auxin-transport or auxin-response mutants provide, they have been instrumental in identifying the mechanisms governing the transport and cellular action of auxin as well as its effects on growth.
There are also several cultivated plants that display altered gravitropism compared to other species or to other varieties within their own species. Some are trees that have a weeping or pendulate growth habit; the branches still respond to gravity, but with a positive response, rather than the normal negative response. Others are the lazy (i.e. ageotropic or agravitropic) varieties of corn ( Zea mays ) and varieties of rice, barley and tomatoes, whose shoots grow along the ground.
In vascular plants, the roots are the organs of a plant that are modified to provide anchorage for the plant and take in water and nutrients into the plant body, which allows plants to grow taller and faster. They are most often below the surface of the soil, but roots can also be aerial or aerating, that is, growing up above the ground or especially above water.
Auxins are a class of plant hormones with some morphogen-like characteristics. Auxins play a cardinal role in coordination of many growth and behavioral processes in plant life cycles and are essential for plant body development. The Dutch biologist Frits Warmolt Went first described auxins and their role in plant growth in the 1920s. Kenneth V. Thimann became the first to isolate one of these phytohormones and to determine its chemical structure as indole-3-acetic acid (IAA). Went and Thimann co-authored a book on plant hormones, Phytohormones, in 1937.
Amyloplasts are a type of plastid, double-enveloped organelles in plant cells that are involved in various biological pathways. Amyloplasts are specifically a type of leucoplast, a subcategory for colorless, non-pigment-containing plastids. Amyloplasts are found in roots and storage tissues, and they store and synthesize starch for the plant through the polymerization of glucose. Starch synthesis relies on the transportation of carbon from the cytosol, the mechanism by which is currently under debate.
In biology, a tropism is a phenomenon indicating the growth or turning movement of an organism, usually a plant, in response to an environmental stimulus. In tropisms, this response is dependent on the direction of the stimulus. Tropisms are usually named for the stimulus involved; for example, a phototropism is a movement to the light source, and an anemotropism is the response and adaptation of plants to the wind.
Phytochromes are a class of photoreceptor proteins found in plants, bacteria and fungi. They respond to light in the red and far-red regions of the visible spectrum and can be classed as either Type I, which are activated by far-red light, or Type II that are activated by red light. Recent advances have suggested that phytochromes also act as temperature sensors, as warmer temperatures enhance their de-activation. All of these factors contribute to the plant's ability to germinate.
Coleoptile is the pointed protective sheath covering the emerging shoot in monocotyledons such as grasses in which few leaf primordia and shoot apex of monocot embryo remain enclosed. The coleoptile protects the first leaf as well as the growing stem in seedlings and eventually, allows the first leaf to emerge. Coleoptiles have two vascular bundles, one on either side. Unlike the flag leaves rolled up within, the pre-emergent coleoptile does not accumulate significant protochlorophyll or carotenoids, and so it is generally very pale. Some preemergent coleoptiles do, however, accumulate purple anthocyanin pigments.
In plant biology, thigmotropism is a directional growth movement which occurs as a mechanosensory response to a touch stimulus. Thigmotropism is typically found in twining plants and tendrils, however plant biologists have also found thigmotropic responses in flowering plants and fungi. This behavior occurs due to unilateral growth inhibition. That is, the growth rate on the side of the stem which is being touched is slower than on the side opposite the touch. The resultant growth pattern is to attach and sometimes curl around the object which is touching the plant. However, flowering plants have also been observed to move or grow their sex organs toward a pollinator that lands on the flower, as in Portulaca grandiflora.
Hydrotropism is a plant's growth response in which the direction of growth is determined by a stimulus or gradient in water concentration. A common example is a plant root growing in humid air bending toward a higher relative humidity level.
In developmental biology, photomorphogenesis is light-mediated development, where plant growth patterns respond to the light spectrum. This is a completely separate process from photosynthesis where light is used as a source of energy. Phytochromes, cryptochromes, and phototropins are photochromic sensory receptors that restrict the photomorphogenic effect of light to the UV-A, UV-B, blue, and red portions of the electromagnetic spectrum.
Frits Warmolt Went was a Dutch biologist whose 1928 experiment demonstrated the existence of auxin in plants.
A primordium in embryology, is an organ or tissue in its earliest recognizable stage of development. Cells of the primordium are called primordial cells. A primordium is the simplest set of cells capable of triggering growth of the would-be organ and the initial foundation from which an organ is able to grow. In flowering plants, a floral primordium gives rise to a flower.
Lateral roots, emerging from the pericycle, extend horizontally from the primary root (radicle) and over time makeup the iconic branching pattern of root systems. They contribute to anchoring the plant securely into the soil, increasing water uptake, and facilitate the extraction of nutrients required for the growth and development of the plant. Lateral roots increase the surface area of a plant's root system and can be found in great abundance in several plant species. In some cases, lateral roots have been found to form symbiotic relationships with rhizobia (bacteria) and mycorrhizae (fungi) found in the soil, to further increase surface area and increase nutrient uptake.
The law of the prolonged sine was observed when measuring strength of the reaction of the plant stems and roots in response to turning from their usual vertical orientation. Such organisms maintained their usual vertical growth, and, if turned, start bending back toward the vertical. The prolonged sine law was observed when measuring the dependence of the bending speed from the angle of reorientation.
Polar auxin transport is the regulated transport of the plant hormone auxin in plants. It is an active process, the hormone is transported in cell-to-cell manner and one of the main features of the transport is its asymmetry and directionality (polarity). The polar auxin transport functions to coordinate plant development; the following spatial auxin distribution underpins most of plant growth responses to its environment and plant growth and developmental changes in general. In other words, the flow and relative concentrations of auxin informs each plant cell where it is located and therefore what it should do or become.
Statocytes are gravity-sensing (gravitropic) cells in higher plants. They contain amyloplasts-statoliths – starch-filled amyloplastic organelles – which sediment at the lowest part of the cells. In the roots, sedimentation of the statoliths towards the lower part of the statocytes constitutes a signal for the production and redistribution of auxin. When stems or roots are not exactly aligned with the gravity vector, statoliths move and adjust to gravity. This is followed by a triggering of the asymmetrical distribution of auxin that causes the curvature and growth of stems against the gravity vector, as well as growth of roots along the gravity vector. Statocytes are present in the elongating region of coleoptiles, shoots and inflorescence stems. In roots, the root cap is the only place where sedimentation is observed, and only the central columella cells of the root cap serve as gravity-sensing statocytes. They can initiate differential growth patterns, bending the root towards the vertical axis.
In biology, phototropism is the growth of an organism in response to a light stimulus. Phototropism is most often observed in plants, but can also occur in other organisms such as fungi. The cells on the plant that are farthest from the light contain a hormone called auxin that reacts when phototropism occurs. This causes the plant to have elongated cells on the furthest side from the light. Phototropism is one of the many plant tropisms, or movements, which respond to external stimuli. Growth towards a light source is called positive phototropism, while growth away from light is called negative phototropism. Negative phototropism is not to be confused with skototropism, which is defined as the growth towards darkness, whereas negative phototropism can refer to either the growth away from a light source or towards the darkness. Most plant shoots exhibit positive phototropism, and rearrange their chloroplasts in the leaves to maximize photosynthetic energy and promote growth. Some vine shoot tips exhibit negative phototropism, which allows them to grow towards dark, solid objects and climb them. The combination of phototropism and gravitropism allow plants to grow in the correct direction.
In botany, the Cholodny–Went model, proposed in 1927, is an early model describing tropism in emerging shoots of monocotyledons, including the tendencies for the shoot to grow towards the light (phototropism) and the roots to grow downward (gravitropism). In both cases the directional growth is considered to be due to asymmetrical distribution of auxin, a plant growth hormone. Although the model has been criticized and continues to be refined, it has largely stood the test of time.
Randy O. Wayne is an associate professor of plant biology at Cornell University. Along with his former colleague Peter K. Hepler, Wayne established the role of calcium in regulating plant growth. Their 1985 article Calcium and Plant Development was awarded the "Citation Classic" award from Current Contents magazine. They researched how plant cells sense gravity through pressure, the water permeability of plant membranes, light microscopy, as well as the effects of calcium on plant development. Wayne authored two textbooks, including Plant Cell Biology: From Astronomy to Zoology and Light and Video Microscopy.
PIN proteins are integral membrane proteins in plants that transport the anionic form of the hormone auxin across membranes. The discovery of the initial member of the PIN gene family, PIN1, occurred through the identification of the pin-formed1 (pin1) mutation in Arabidopsis thaliana. This mutation led to a stem that lacked almost all organs, including leaves and flowers.
John Z. Kiss is an American biologist known for his work on the gravitational and space biology of plants. Kiss is dean of the College of Arts & Sciences at the University of North Carolina Greensboro. Previously, he was a professor of biology and dean of the Graduate School at the University of Mississippi. and distinguished professor and chair of the botany department at Miami University. He has worked with NASA since 1987 and served as principal investigator on eight spaceflight experiments on the Space Shuttle, the former Russian space station Mir, and on the International Space Station. His research focuses on the sensory physiology of plants in space. He received the NASA Outstanding Public Leadership Medal in 2014. In 2021, Asteroid Kiss 8267 was named in his honor, a recognition that coincided with his receipt of the 2021 COSPAR International Cooperation Medal. His international collaboration on a spaceflight project with NASA and the European Space Agency has led to the discovery of novel sensory mechanisms in plants.
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