Shade avoidance

Shade avoidance is a set of responses that plants display when they are subjected to the shade of another plant. It often includes elongation, altered flowering time, increased apical dominance and altered partitioning of resources. This set of responses is collectively called the shade-avoidance syndrome (SAS).

Shade responses display varying strength along a continuum. Most plants are neither extreme shade avoiders or tolerators, but possess a combination of the two strategies; this helps adapt them to their environment. However, the ability to perceive and respond to shade plays a very important role in all plants: they are sessile by nature and access to photosynthetically active radiation is essential for plant nutrition and growth.

Over the past few decades, major increases in grain yield have come largely through increasing planting densities. As planting densities increase so does the proportion of far red light in the canopy. Thus, it is likely that plant breeders have selected for lines with reduced SAS in their efforts to produce high yields at high density.

Sensing shade

Plants can tell the difference between the shade of an inanimate object (e.g. a rock) and the shade of another plant, as well as the presence of nearby plants that may compete with and shade it in the future.[1] In the shade of a plant, far red light is present in a higher irradiance than red light, as a result of the absorption of the red light by the pigments involved in photosynthesis, while a nearby plant forms an intermediate ratio. This is known as far red enrichment. Phytochrome can be used to measure the ratio of far red to red light, and thus to detect whether the plant is in the shade of another plant, so it can alter its growth strategy accordingly (photomorphogenesis). In Arabidopsis, phytochrome B is the predominant photoreceptor that regulates SAS.[2] Phytochromes exist in two forms: PR and PFR. It is synthesised as PR, but red light triggers a conformational change, producing PFR. Far red light causes the phytochrome to be converted back into PR. For a given red:far red light ratio, there will be a dynamic equilibrium in the relative quantities of PR and PFR present. Far red enrichment causes a build-up of PR. If PR is present above a species-specific threshold, shade avoidance signal transduction pathways will be activated.

Seedling response

Seedling response is the most well understood factor of shade avoidance. In the model organism Arabidopsis thaliana, the shade avoidance response varies at different points in the life cycle. Dry, dormant seeds will not germinate if they are in the shade. Once dormancy has been broken and they have imbibed water, the seeds are committed to germination. Water-imbibed seeds display hypocotyl elongation; if the shade were caused by excessive soil depth, this would help the seedling grow vertically very quickly and push up and out of the ground. If an Arabidopsis seedling becomes shaded, its petioles and internodes elongate. It may even lose rosette morphology.[3]

Pathway

Studies using Brassica rapa indicate that the light quality and ratio available to seedlings is sensed in the cotyledons, which upregulates the production of auxin. Arabidopsis was used to demonstrate PIF (Phytochrome Interacting Factor) involvement in auxin production. PIFs are transcription factors that regulate thousands of genes related to germination repression and shade avoidance, and PIF4, PIF5, and PIF7 directly regulate genes that code for the enzymes required in auxin synthesis. Other PIF proteins are thought to be involved in regulating auxin and the plant's response.[4] In shade conditions, PR induces the dephosphorylation of PIF proteins, which strengthens their ability to bind DNA and promote transcription of genes involved in shade avoidance response, including in the production of auxin and its receptors.[5] Auxin is transported to the hypocotyl to promote elongation, although the mechanism it uses to do so remains unclear.[6]

Adult response

Shade avoidance response in adult plants is less commonly studied than it is in seedlings, though adult Arabidopsis show more complex response patterns than seedlings. Shaded adults have elongated petioles at the rosette, smaller leaf blades, and suppressed axillary bud growth.[7] By elongating the petiole sideways, the plant repositions its leaves away from shading plants to absorb more red light, though there is a trade off in leaf size. The leaves can also bend upwards towards potential light sources as a result of higher growth on the underside of the petiole than the top, a process called hyponasty.[8] Flattening of leaves in plants with normally curled leaves also increases surface area for light absorption.[9]

If a mature plant becomes shaded, shade avoidance also often prompts changes in reproductive strategies. Plants may flower early, as it is unlikely that growing more structures will result in profitable nutrient gain in the short term.[10] In Arabidopsis, early flowering is linked to overall lower reproductive success due to lower seed production, smaller fruit, and lower germination rate of seeds,[11] although germination success is also dependent on genetic variation between individuals.[12]

Pathway

Like seedlings, adult plant shade avoidance involves several mechanisms acting together. Petiole elongation is both a result of cell expansion and cell division, though not at the same stage in petiole and leaf formation. In newly growing leaves, cell division is the primary factor, while fully formed leaves and petioles rely on cell expansion.[13] Xyloglucan endotransglucosylase/hydrolases (XTHs) are a family of cell wall modifying proteins. In shade conditions, the genes coding for XTH9, XTH15/XTR7, XTH16, XTH17, and XTH19 are up-regulated and these proteins act to hydrolyze and weaken the cell wall, allowing for expansion of the petiole cells.[14] Like in seedlings, PIF7 is involved in the regulation of petiole and leaf growth due to low R:FR, by up-regulating auxin-related and brassinosteroid-response genes which promote growth. Auxin signalling is also essential to hyponasty, though its role is not yet fully understood.[15]
Leaf curling is primarily a response to phytochrome B converting to PR in shade conditions, which promotes unequal proliferation and growth of cells on the upper and lower leaf sides. Two redundant genes, ATHB4 and HAT3, code for transcription factors that regulate leaf curling, with loss of function mutants having plants with leaves that curl downwards, and plants with over-expressive copies of these genes having leaves that curl strongly upwards.[16] By changing expression of these genes, plants can straighten their leaves in response to shade.

References

  1. ↑ Roig-Villanova, Irma; Martínez-García, Jaime F. (29 February 2016). "Plant Responses to Vegetation Proximity: A Whole Life Avoiding Shade". Frontiers in Plants Science. 7. doi:10.3389/fpls.2016.00236.
  2. ↑ Smith, H.; Whitelam, G. C. (1997). "The shade avoidance syndrome: Multiple responses mediated by multiple phytochromes". Plant, Cell and Environment. 20 (6): 840–844. doi:10.1046/j.1365-3040.1997.d01-104.x.
  3. ↑ Casal (2011). "Shade Avoidance". The Arabidopsis Book. 10: e0157. doi:10.1199/tab.0157. PMC 3350169Freely accessible. PMID 22582029.
  4. ↑ Leivar, P; Quail, PH (January 2011). "PIFs: pivotal components in a cellular signaling hub.". Trends in Plant Science. 16 (1): 19–28. doi:10.1016/j.tplants.2010.08.003. PMC 3019249Freely accessible. PMID 20833098.
  5. ↑ Roig-Villanova, Irma; Martínez-García, Jaime F. (29 February 2016). "Plant Responses to Vegetation Proximity: A Whole Life Avoiding Shade". Frontiers in Plants Science. 7. doi:10.3389/fpls.2016.00236.
  6. ↑ Procko, C; Crenshaw, CM; Ljung, K; Noel, JP; Chory, J (2 June 2014). "Cotyledon-Generated Auxin Is Required for Shade-Induced Hypocotyl Growth in Brassica rapa.". 165 (3): 1285–1301. doi:10.1104/pp.114.241844. PMC 4081337Freely accessible. PMID 24891610.
  7. ↑ González-Grandío, E; Poza-Carrión, C; Sorzano, CO; Cubas, P (March 2013). "BRANCHED1 promotes axillary bud dormancy in response to shade in Arabidopsis.". The Plant cell. 25 (3): 834–50. doi:10.1105/tpc.112.108480. PMC 3634692Freely accessible. PMID 23524661.
  8. ↑ Casal, JJ (2012). "Shade avoidance.". The Arabidopsis book / American Society of Plant Biologists. 10: e0157. doi:10.1199/tab.0157. PMC 3350169Freely accessible. PMID 22582029.
  9. ↑ Kozuka, T; Suetsugu, N; Wada, M; Nagatani, A (January 2013). "Antagonistic regulation of leaf flattening by phytochrome B and phototropin in Arabidopsis thaliana.". Plant & cell physiology. 54 (1): 69–79. doi:10.1093/pcp/pcs134. PMID 23054390.
  10. ↑ Casal (2011). "Shade Avoidance". The Arabidopsis Book. 10: e0157. doi:10.1199/tab.0157. PMC 3350169Freely accessible. PMID 22582029.
  11. ↑ Franklin, KA; Praekelt, U; Stoddart, WM; Billingham, OE; Halliday, KJ; Whitelam, GC (March 2003). "Phytochromes B, D, and E act redundantly to control multiple physiological responses in Arabidopsis.". Plant Physiology. 131 (3): 1340–6. doi:10.1104/pp.102.015487. PMC 166893Freely accessible. PMID 12644683.
  12. ↑ Miller, SM; Farrugia, G; Schmalz, PF; Ermilov, LG; Maines, MD; Szurszewski, JH (February 1998). "Heme oxygenase 2 is present in interstitial cell networks of the mouse small intestine.". Gastroenterology. 114 (2): 239–44. doi:10.1016/s0016-5085(98)70473-1. PMID 9453482.
  13. ↑ Roig-Villanova, Irma; Martínez-García, Jaime F. (29 February 2016). "Plant Responses to Vegetation Proximity: A Whole Life Avoiding Shade". Frontiers in Plants Science. 7. doi:10.3389/fpls.2016.00236.
  14. ↑ Sasidharan, R; Chinnappa, CC; Staal, M; Elzenga, JT; Yokoyama, R; Nishitani, K; Voesenek, LA; Pierik, R (October 2010). "Light quality-mediated petiole elongation in Arabidopsis during shade avoidance involves cell wall modification by xyloglucan endotransglucosylase/hydrolases.". Plant Physiology. 154 (2): 978–90. doi:10.1104/pp.110.162057. PMC 2949003Freely accessible. PMID 20688978.
  15. ↑ Casal, JJ (2012). "Shade avoidance.". The Arabidopsis book / American Society of Plant Biologists. 10: e0157. doi:10.1199/tab.0157. PMC 3350169Freely accessible. PMID 22582029.
  16. ↑ Bou-Torrent, J; Salla-Martret, M; Brandt, R; Musielak, T; Palauqui, JC; Martínez-García, JF; Wenkel, S (November 2012). "ATHB4 and HAT3, two class II HD-ZIP transcription factors, control leaf development in Arabidopsis.". Plant signaling & behavior. 7 (11): 1382–7. doi:10.4161/psb.21824. PMC 3548853Freely accessible. PMID 22918502.
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