Acid-growth hypothesis explained

The acid-growth hypothesis is a theory that explains the expansion dynamics of cells and organs in plants. It was originally proposed by Achim Hager and Robert Cleland in 1971.[1] [2] They hypothesized that the naturally occurring plant hormone, auxin (indole-3-acetic acid, IAA), induces H+ proton extrusion into the apoplast. Such derived apoplastic acidification then activates a range of enzymatic reactions which modifies the extensibility of plant cell walls. Since its formulation in 1971, the hypothesis has stimulated much research and debate. Most debates have concerned the signalling role of auxin and the molecular nature of cell wall modification. The current version holds that auxin activates small auxin-up RNA (SAUR) proteins, which in turn regulate protein phosphatases that modulate proton-pump activity. Acid growth is responsible for short-term (seconds to minutes) variation in growth rate, but many other mechanisms influence longer-term growth.[3]

History and development of the theory

Early development

Emergence of theory

Auxin was known to be a growth stimulant, but it was not until the year 1971 that Hager and Cleland proposed the "acid-growth hypothesis," which primarily suggested the correlation between auxin and apoplast acidification. The hypothesis states that susceptible coleoptile cells expel H+ protons through membrane-bound proton pumps into the apoplast (space between plant cell wall and cytoplasm) at an accelerated pace, causing a decrease in the apoplastic pH value. The following precise natural mechanism of the wall-loosening process; however, remained unknown at the time. With reference to auxin-induced elongation regarded as "acid-growth," Hager based his experiment on plasmolyzed hypocotyls from sunflower (Helianthus annuus). Subsequently, the wall-acidification model initiated continual controversy among scientists, and act as the blueprint for further re-examination. By 1900s, four core pieces of qualitative evidences solidified the core concept of the theory, as summarized below:[4] [5] [6] [7] [8]

  1. In auxin-treated coleoptile and stem (hypocotyl) sections, auxin induces proton extrusion into the apoplast, which could decrease the pH value by as much as one full unit.
  2. Infiltration of neutral buffer (pH~7) into the apoplast could inhibit auxin-induced elongation and growth.
  3. Acidic buffers of pH 5.0 could accelerate cell elongation at the same or even greater rate in comparison to that induced by auxin.
  4. Fusiococcin (Fc) could also induce rapid cell elongation and growth, despite its primary role in promoting extensive acidification of the apoplast.

Constraints and interpretation

Within the 20-year timespan, many scientists have actively contributed to examining and reevaluating Hager's acid-growth hypothesis. Despite the accumulation of observations that evidently identify the final target of the auxin-induced action to be H+-ATPase, which excretes H+ protons to the apoplast and take in K+ ions through its rectifying K+ channel in the following years, the controversy has been carried over till today as an ongoing debate.[9]

Ongoing development

Discovery of hydrolytic enzyme

With H+ protons being excreted to the apoplast as one of the wall-loosening factors (WLF), scientists believed that the mechanism involves activation of hydrolytic enzymes through possible hydrolysis of bonds. Back in the year 1971, Hager anticipated the possible existence of enzymes from his experiment which involves heat-killing and denaturation of enzyme inhibitors. However, it wasn't until 1992 when Simon McQueen-Mason and his collaborators discovered the most pH-responsive substance in the apoplast- expansin.[10] Expansin is a pH-dependent hormone that could cause irreversible wall extension and wall stress relaxation without displaying any enzymatic activity. It is activated after detecting the acidification in cell wall solution, consequently breaking down hydrogen bonds or covalent bonds in the cell wall to allow xyloglucan slipping- a mechanism that allows microfibrils to slip into the cell wall matrix without extension. Meanwhile, it could also loosen the cellulose microfibrils within the cell wall to enable the cell to take in more water and expand via turgor and osmosis.[11] [12]

Transcriptional control

Transcriptional modification is crucial in the growth and development of cells When a plant is treated with auxin treatment, auxin-induced transcriptional changes occurs within minutes, which indicates that both transcription and translation is necessary for auxin-induced growth. One of the major mechanisms for auxin control in plant is the transport inhibitor response through singling from F-box (regulatory protein)[13] When auxin level raise to a certain concentration, auxin will interact with F-Box protein and stimulate the auxin transcriptional repressors. This leads to degradation of auxin protein. Nevertheless, transcriptional response does not only regulate auxin itself but also mediate the gene expression for protein encoded for cell-wall modification (cell wall-remodelling agents). It was found that when treated plant with exogenous auxin, the expression of pectin methylesterases, expansins and other protein that changes cell wall's shape and size.[14]

Modern interpretation

See main article: Acid growth.

This acid-growth model has been updated to account for new mechanistic understanding. The decrease in apoplast pH value leads to cell-wall modification; the resulting increased extensibility of cell wall results in cell growth.[15] The reduction in apoplastic pH is mediated by auxin-induced mechanisms. With auxin acting as the primary signalling tool, it initiates apoplastic acidification via two mechanisms. Auxin stimulates the activity of the plasma-membrane proton pump (H+-ATPase), acidifying the wall. Auxin changes the cell wall's composition directly by increasing the transcription of wall-modifying agents.

Unsolved questions

There are several aspects of the theory that remain contentious. These include:

  1. Measurement of pH value: Despite optimal high-sensitivity detection brought by the implementation of fluorescent pH sensors, there is a lack of reliable method in quantifying the absolute apoplast pH value in plants. For instance, scientists made use of whole-organ resolution as part of their apoplastic pH measurement.[16] However, such research methods on the cellular level wouldn't establish equivalent validity at the quantitative level due to the plausible leaking of the signal from the endomembrane system into those originating from the apoplast.[17]
  2. Limitations on particular plant organs: Most of the research has been limited to the aerial organs of plants. Instead of studying the growth-promoting effect that auxin brings to the aerial organs, David Pacheco Villalobos discovers the inhibitory effect auxin has on root elongation.[18]
  3. Narrow coverage of plant species: Data that supported the early development of the theory initially originated from coleoptiles, epicotyls, and hypocotyls of a wide range of monocot and dicot species. To note, it all began with observations from sunflower. The importance to expand the research territory beyond angiosperm species to more ancient members within the plant family tree is undeniable. Latter observations on different plant species could help identify conserved hormones and genes, or underlying mechanisms that support the theory, with the confirmation of SAUR19's role in auxin-induced hypocotyl elongation in tomatoes being one of the more recent discoveries.[19] [20]

See also

Notes and References

  1. Hager A, Menzel H, Krauss A . [Experiments and hypothesis concerning the primary action of auxin in elongation growth] . Planta . 100 . 1 . 47–75 . March 1971 . 24488103 . 10.1007/BF00386886 .
  2. Cleland R . 1971-06-01. Cell Wall Extension . Annual Review of Plant Physiology. 22. 1. 197–222. 10.1146/annurev.pp.22.060171.001213 .
  3. Du M, Spalding EP, Gray WM . 2020-03-04. Rapid Auxin-Mediated Cell Expansion . Annual Review of Plant Physiology. 71. 379–402. 10.1146/annurev.pp.22.060171.001213 . 32131604.
  4. Rayle DL, Cleland R . Enhancement of wall loosening and elongation by acid solutions. . Plant Physiol . 46 . 250–253 . 1970 . 2 . 16657445 . 10.1104/pp.46.2.250 . 396573 . free .
  5. Durand H, Rayle DL . Physiological evidence for auxin-induced hydrogen-ion secretion and the epidermal paradox . Planta . 114 . 2 . 185–93 . June 1973 . 24458722 . 10.1007/BF00387475 .
  6. Hager A, Debus G, Edel HG, Stransky H, Serrano R . Auxin induces exocytosis and the rapid synthesis of a high-turnover pool of plasma-membrane H(+)-ATPase . Planta . 185 . 4 . 527–37 . November 1991 . 24186531 . 10.1007/BF00202963 .
  7. Rayle DL . Auxin-induced hydrogen-ion secretion in Avena coleoptiles and its implications . Planta . 114 . 1 . 63–73 . March 1973 . 24458665 . 10.1007/BF00390285 .
  8. Rayle DL, Cleland R . Control of plant cell enlargement by hydrogen ions . Current Topics in Developmental Biology . 11 . 187–214 . 1977 . 20280 . 10.1016/S0070-2153(08)60746-2 .
  9. Hager A . Role of the plasma membrane H+-ATPase in auxin-induced elongation growth: historical and new aspects . Journal of Plant Research . 116 . 6 . 483–505 . December 2003 . 12937999 . 10.1007/s10265-003-0110-x .
  10. McQueen-Mason S, Durachko DM, Cosgrove DJ . Two endogenous proteins that induce cell wall extension in plants . The Plant Cell . 4 . 11 . 1425–33 . November 1992 . 11538167 . 160229 . 10.1105/tpc.4.11.1425 .
  11. Cosgrove DJ . Loosening of plant cell walls by expansins . Nature . 407 . 6802 . 321–6 . September 2000 . 11014181 . 10.1038/35030000 . 2000Natur.407..321C .
  12. Yennawar NH, Li LC, Dudzinski DM, Tabuchi A, Cosgrove DJ . Crystal structure and activities of EXPB1 (Zea m 1), a beta-expansin and group-1 pollen allergen from maize . Proceedings of the National Academy of Sciences of the United States of America . 103 . 40 . 14664–71 . October 2006 . 16984999 . 1595409 . 10.1073/pnas.0605979103 .
  13. Arsuffi G, Braybrook SA . 5 January 2018. Acid growth: an ongoing trip . Journal of Experimental Botany. 69. 2. 137–146 . 10.1093/jxb/erx390 . 29211894. free.
  14. Bosch M, Hepler PK . Pectin methylesterases and pectin dynamics in pollen tubes . The Plant Cell . 17 . 12 . 3219–26 . December 2005 . 16322606 . 1315365 . 10.1105/tpc.105.037473 .
  15. Prat R, Gueissaz MB, Goldberg R . 1984-12-01. Effects of Ca2+ and Mg2+ on Elongation and H+ Secretion of Vigna radiata Hypocotyl Sections . Plant and Cell Physiology . 25 . 8 . 1459–1467 . 10.1093/oxfordjournals.pcp.a076858 .
  16. Villiers F, Kwak JM . Rapid apoplastic pH measurement in Arabidopsis leaves using a fluorescent dye . Plant Signaling & Behavior . 8 . 1 . e22587 . January 2013 . 23221761 . 3745564 . 10.4161/psb.22587 .
  17. Gjetting KS, Ytting CK, Schulz A, Fuglsang AT . Live imaging of intra- and extracellular pH in plants using pHusion, a novel genetically encoded biosensor . Journal of Experimental Botany . 63 . 8 . 3207–18 . May 2012 . 22407646 . 3350929 . 10.1093/jxb/ers040 .
  18. Pacheco-Villalobos D, Díaz-Moreno SM, van der Schuren A, Tamaki T, Kang YH, Gujas B, Novak O, Jaspert N, Li Z, Wolf S, Oecking C, Ljung K, Bulone V, Hardtke CS . The Effects of High Steady State Auxin Levels on Root Cell Elongation in Brachypodium . The Plant Cell . 28 . 5 . 1009–24 . May 2016 . 27169463 . 4904674 . 10.1105/tpc.15.01057 .
  19. Spartz AK, Lor VS, Ren H, Olszewski NE, Miller ND, Wu G, Spalding EP, Gray WM . Constitutive Expression of Arabidopsis SMALL AUXIN UP RNA19 (SAUR19) in Tomato Confers Auxin-Independent Hypocotyl Elongation . Plant Physiology . 173 . 2 . 1453–1462 . February 2017 . 27999086 . 5291034 . 10.1104/pp.16.01514 .
  20. https://academic.oup.com/view-large/figure/107451136/erx39003.jpg Table 1

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