Menu
×
John's Island Library
9 a.m. - 8 p.m.
Phone: (843) 559-1945
Main Library
9 a.m. - 8 p.m.
Phone: (843) 805-6930
West Ashley Library
9 a.m. - 7 p.m.
Phone: (843) 766-6635
Wando Mount Pleasant Library
9 a.m. - 8 p.m.
Phone: (843) 805-6888
Village Library
9 a.m. - 6 p.m.
Phone: (843) 884-9741
St. Paul's/Hollywood Library
9 a.m. - 8 p.m.
Phone: (843) 889-3300
Otranto Road Library
9 a.m. - 8 p.m.
Phone: (843) 572-4094
Mt. Pleasant Library
9 a.m. - 8 p.m.
Phone: (843) 849-6161
McClellanville Library
9 a.m. - 6 p.m.
Phone: (843) 887-3699
Keith Summey North Charleston Library
9 a.m. - 8 p.m.
Phone: (843) 744-2489
Hurd/St. Andrews Library
9 a.m. - 8 p.m.
Phone: (843) 766-2546
Folly Beach Library
9 a.m. - 5:30 p.m.
Phone: (843) 588-2001
Edisto Island Library
9 a.m. - 4 p.m.
Phone: (843) 869-2355
Dorchester Road Library
9 a.m. - 8 p.m.
Phone: (843) 552-6466
John L. Dart Library
9 a.m. - 7 p.m.
Phone: (843) 722-7550
Baxter-Patrick James Island
9 a.m. - 8 p.m.
Phone: (843) 795-6679
Bees Ferry West Ashley Library
9 a.m. - 8 p.m.
Phone: (843) 805-6892
Edgar Allan Poe/Sullivan's Island Library
Closed for renovations
Phone: (843) 883-3914
Mobile Library
9 a.m. - 5 p.m.
Phone: (843) 805-6909
Today's Hours
John's Island Library
9 a.m. - 8 p.m.
Phone: (843) 559-1945
Main Library
9 a.m. - 8 p.m.
Phone: (843) 805-6930
West Ashley Library
9 a.m. - 7 p.m.
Phone: (843) 766-6635
Wando Mount Pleasant Library
9 a.m. - 8 p.m.
Phone: (843) 805-6888
Village Library
9 a.m. - 6 p.m.
Phone: (843) 884-9741
St. Paul's/Hollywood Library
9 a.m. - 8 p.m.
Phone: (843) 889-3300
Otranto Road Library
9 a.m. - 8 p.m.
Phone: (843) 572-4094
Mt. Pleasant Library
9 a.m. - 8 p.m.
Phone: (843) 849-6161
McClellanville Library
9 a.m. - 6 p.m.
Phone: (843) 887-3699
Keith Summey North Charleston Library
9 a.m. - 8 p.m.
Phone: (843) 744-2489
Hurd/St. Andrews Library
9 a.m. - 8 p.m.
Phone: (843) 766-2546
Folly Beach Library
9 a.m. - 5:30 p.m.
Phone: (843) 588-2001
Edisto Island Library
9 a.m. - 4 p.m.
Phone: (843) 869-2355
Dorchester Road Library
9 a.m. - 8 p.m.
Phone: (843) 552-6466
John L. Dart Library
9 a.m. - 7 p.m.
Phone: (843) 722-7550
Baxter-Patrick James Island
9 a.m. - 8 p.m.
Phone: (843) 795-6679
Bees Ferry West Ashley Library
9 a.m. - 8 p.m.
Phone: (843) 805-6892
Edgar Allan Poe/Sullivan's Island Library
Closed for renovations
Phone: (843) 883-3914
Mobile Library
9 a.m. - 5 p.m.
Phone: (843) 805-6909
Patron Login
menu
Item request has been placed!
×
Item request cannot be made.
×
Processing Request
Differential root and cell regulation of maize aquaporins by the arbuscular mycorrhizal symbiosis highlights its role in plant water relations.
Item request has been placed!
×
Item request cannot be made.
×
Processing Request
- Author(s): Romero-Munar A;Romero-Munar A; Muñoz-Carrasco M; Muñoz-Carrasco M; Balestrini R; Balestrini R; De Rose S; De Rose S; Giovannini L; Giovannini L; Aroca R; Aroca R; Ruiz-Lozano JM; Ruiz-Lozano JM
- Source:
Plant, cell & environment [Plant Cell Environ] 2024 Nov; Vol. 47 (11), pp. 4337-4353. Date of Electronic Publication: 2024 Jul 04.- Publication Type:
Journal Article- Language:
English - Source:
- Additional Information
- Source: Publisher: John Wiley & Sons Ltd Country of Publication: United States NLM ID: 9309004 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1365-3040 (Electronic) Linking ISSN: 01407791 NLM ISO Abbreviation: Plant Cell Environ Subsets: MEDLINE
- Publication Information: Publication: Hoboken, NJ : John Wiley & Sons Ltd.
Original Publication: Oxford, UK : Blackwell Scientific Publications - Subject Terms: Zea mays*/microbiology ; Zea mays*/genetics ; Zea mays*/physiology ; Zea mays*/metabolism ; Mycorrhizae*/physiology ; Aquaporins*/metabolism ; Aquaporins*/genetics ; Symbiosis* ; Plant Roots*/microbiology ; Plant Roots*/metabolism ; Water*/metabolism ; Gene Expression Regulation, Plant*; Plant Proteins/metabolism ; Plant Proteins/genetics
- Abstract: This study aims to elucidate if the regulation of plant aquaporins by the arbuscular mycorrhizal (AM) symbiosis occurs only in roots or cells colonized by the fungus or at whole root system. Maize plants were cultivated in a split-root system, with half of the root system inoculated with the AM fungus and the other half uninoculated. Plant growth and hydraulic parameters were measured and aquaporin gene expression was determined in each root fraction and in microdissected cells. Under well-watered conditions, the non-colonized root fractions of AM plants grew more than the colonized root fraction. Total osmotic and hydrostatic root hydraulic conductivities (Lo and Lpr) were higher in AM plants than in non-mycorrhizal plants. The expression of most maize aquaporin genes analysed was different in the mycorrhizal root fraction than in the non-mycorrhizal root fraction of AM plants. At the cellular level, differential aquaporin expression in AM-colonized cells and in uncolonized cells was also observed. Results indicate the existence of both, local and systemic regulation of plant aquaporins by the AM symbiosis and suggest that such regulation is related to the availability of water taken up by fungal hyphae in each root fraction and to the plant need of water mobilization.
(© 2024 The Author(s). Plant, Cell & Environment published by John Wiley & Sons Ltd.) - References: Afzal, Z., Howton, T., Sun, Y. & Mukhtar, M. (2016) The roles of aquaporins in plant stress responses. Journal of Developmental Biology, 4, 9.
Aharon, R., Shahak, Y., Wininger, S., Bendov, R., Kapulnik, Y. & Galili, G. (2003) Overexpression of a plasma membrane aquaporin in transgenic tobacco improves plant vigor under favorable growth conditions but not under drought or salt stress. The Plant Cell, 15, 439–447.
Albacete, A., Ghanem, M.E., Martinez‐Andujar, C., Acosta, M., Sanchez‐Bravo, J., Martinez, V. et al. (2008) Hormonal changes in relation to biomass partitioning and shoot growth impairment in salinized tomato (Solanum lycopersicum L.) plants. Journal of Experimental Botany, 59, 4119–4131.
Allen, M.F. (2009) Bidirectional water flows through the soil‐fungal‐plant mycorrhizal continuum. New Phytologist, 182, 290–293.
Andersen, C.L., Jensen, J.L. & Ørntoft, T.F. (2004) Normalization of real‐time quantitative reverse transcription‐PCR data: a model‐based variance estimation approach to identify genes suited for normalization, applied to bladder and colon cancer data sets. Cancer Research, 64, 5245–5250.
Aroca, R., Bago, A., Sutka, M., Paz, J.A., Cano, C., Amodeo, G. et al. (2009) Expression analysis of the first arbuscular mycorrhizal fungi aquaporin described reveals concerted gene expression between salt‐stressed and nonstressed mycelium. Molecular Plant‐Microbe Interactions®, 22, 1169–1178.
Aroca, R., Porcel, R. & Ruiz‐Lozano, J.M. (2007) How does arbuscular mycorrhizal symbiosis regulate root hydraulic properties and plasma membrane aquaporins in Phaseolus vulgaris under drought, cold or salinity stresses? New Phytologist, 173, 808–816.
Aroca, R., Vernieri, P. & Ruiz‐Lozano, J.M. (2008) Mycorrhizal and non‐mycorrhizal Lactuca sativa plants exhibit contrasting responses to exogenous ABA during drought stress and recovery. Journal of Experimental Botany, 59, 2029–2041.
Augé, R.M. (2001) Water relations, drought and vesicular‐arbuscular mycorrhizal symbiosis. Mycorrhiza, 11, 3–42.
Augé, R.M. (2004) Arbuscular mycorrhizae and soil/plant water relations. Canadian Journal of Soil Science, 84, 373–381.
Augé, R.M., Stodola, A.J.W., Tims, J.E. & Saxton, A.M. (2001) Moisture retention properties of a mycorrhizal soil. Plant and Soil, 230, 87–97.
Augé, R.M., Sylvia, D.M., Park, S., Buttery, B.R., Saxton, A.M., Moore, J.L. et al. (2004) Partitioning mycorrhizal influence on water relations of Phaseolus vulgaris into soil and plant components. Canadian Journal of Botany, 82, 503–514.
Augé, R.M., Toler, H.D. & Saxton, A.M. (2015) Arbuscular mycorrhizal symbiosis alters stomatal conductance of host plants more under drought than under amply watered conditions: a meta‐analysis. Mycorrhiza, 25, 13–24.
Bahadur, A., Batool, A., Nasir, F., Jiang, S., Mingsen, Q., Zhang, Q. et al. (2019) Mechanistic insights into arbuscular mycorrhizal fungi‐mediated drought stress tolerance in plants. International Journal of Molecular Sciences, 20, 4199.
Balestrini, R., Gómez‐Ariza, J., Lanfranco, L. & Bonfante, P. (2007) Laser microdissection reveals that transcripts for five plant and one fungal phosphate transporter genes are contemporaneously present in arbusculated cells. Molecular Plant‐Microbe Interactions®, 20, 1055–1062.
Balestrini, R., Rosso, L.C., Veronico, P., Melillo, M.T., De Luca, F., Fanelli, E. et al. (2019) Transcriptomic responses to water deficit and nematode infection in mycorrhizal tomato roots. Frontiers in Microbiology, 10, 1807.
Bárzana, G., Aroca, R., Bienert, G.P., Chaumont, F. & Ruiz‐Lozano, J.M. (2014) New insights into the regulation of aquaporins by the arbuscular mycorrhizal symbiosis in maize plants under drought stress and possible implications for plant performance. Molecular Plant‐Microbe Interactions®, 27, 349–363.
Bárzana, G., Aroca, R., Paz, J.A., Chaumont, F., Martinez‐Ballesta, M.C., Carvajal, M. et al. (2012) Arbuscular mycorrhizal symbiosis increases relative apoplastic water flow in roots of the host plant under both well‐watered and drought stress conditions. Annals of Botany, 109, 1009–1017.
Bárzana, G., Aroca, R. & Ruiz‐Lozano, J.M. (2015) Localized and non‐localized effects of arbuscular mycorrhizal symbiosis on accumulation of osmolytes and aquaporins and on antioxidant systems in maize plants subjected to total or partial root drying. Plant, Cell & Environment, 38, 1613–1627.
Beaudette, P.C., Chlup, M., Yee, J. & Emery, R.J.N. (2007) Relationships of root conductivity and aquaporin gene expression in Pisum sativum: diurnal patterns and the response to HgCl2 and ABA. Journal of Experimental Botany, 58, 1291–1300.
Bedini, S., Pellegrino, E., Avio, L., Pellegrini, S., Bazzoffi, P., Argese, E. et al. (2009) Changes in soil aggregation and glomalin‐related soil protein content as affected by the arbuscular mycorrhizal fungal species Glomus mosseae and Glomus intraradices. Soil Biology and Biochemistry, 41, 1491–1496.
Chaumont, F. & Tyerman, S.D. (2014) Aquaporins: highly regulated channels controlling plant water relations. Plant Physiology, 164, 1600–1618.
Cheng, S., Zou, Y.‐N., Kuča, K., Hashem, A., Abd_Allah, E.‐F. & Wu, Q.‐S. (2021) Elucidating the mechanisms underlying enhanced drought tolerance in plants mediated by arbuscular mycorrhizal fungi. Frontiers in Microbiology, 12, 809473.
Cruz, C., Green, J.J., Watson, C.A., Wilson, F. & Martins‐Loução, M.A. (2004) Functional aspects of root architecture and mycorrhizal inoculation with respect to nutrient uptake capacity. Mycorrhiza, 14, 177–184.
Daryanto, S., Wang, L. & Jacinthe, P.A. (2016) Global synthesis of drought effects on maize and wheat production. PLoS One, 11, e0156362.
Das, S. & Sarkar, S. (2024) Arbuscular mycorrhizal fungal contribution towards plant resilience to drought conditions. Frontiers in Fungal Biology, 5, 1355999. https://doi.org/10.3389/ffunb.2024.1355999.
Domec, J.C., King, J.S., Carmichael, M.J., Overby, A.T., Wortemann, R., Smith, W.K. et al. (2021) Aquaporins, and not changes in root structure, provide new insights into physiological responses to drought, flooding, and salinity. Journal of Experimental Botany, 72, 4489–4501.
Ezawa, T. & Saito, K. (2018) How do arbuscular mycorrhizal fungi handle phosphate? New insight into fine‐tuning of phosphate metabolism. New Phytologist, 220, 1116–1121.
FAOSTAT. (2019) Food and Agriculture Organization of the United Nations (FAO), FAO Statistical Databases. Retrieved February 14, 2019, from http://www.fao.org/faostat/en/#data/QC.
Fiorilli, V., Volpe, V. & Balestrini, R. (2019) Microscopic techniques coupled to molecular and genetic approaches to highlight cell‐type specific differences in mycorrhizal symbiosis. In: Reinhardt, D. & Sharma, A. (Eds.) Methods in rhizosphere biology research. Rhizosphere biology. Singapore: Springer, pp. 197–225. https://doi.org/10.1007/978-981-13-5767-1_11.
Fochi, V., Falla, N., Girlanda, M., Perotto, S. & Balestrini, R. (2017) Cell‐specific expression of plant nutrient transporter genes in orchid mycorrhizae. Plant Science, 263, 39–45.
Foo, E., Ross, J.J., Jones, W.T. & Reid, J.B. (2013) Plant hormones in arbuscular mycorrhizal symbioses: an emerging role for gibberellins. Annals of Botany, 111, 769–779.
Forrest, K.L. & Bhave, M. (2007) Major intrinsic proteins (MIPs) in plants: a complex gene family with major impacts on plant phenotype. Functional & Integrative Genomics, 7, 263–289.
Fox, A.R., Maistriaux, L.C. & Chaumont, F. (2017) Toward understanding of the high number of plant aquaporin isoforms and multiple regulation mechanisms. Plant Science, 264, 179–187.
Genre, A., Chabaud, M., Timmers, T., Bonfante, P. & Barker, D.G. (2005) Arbuscular mycorrhizal fungi elicit a novel intracellular apparatus in Medicago truncatula root epidermal cells before infection. The Plant Cell, 17, 3489–3499.
Giovannetti, M., Balestrini, R., Volpe, V., Guether, M., Straub, D., Costa, A. et al. (2012) Two putative‐aquaporin genes are differentially expressed during arbuscular mycorrhizal symbiosis in Lotus japonicus. BMC Plant Biology, 12, 186.
Giovannetti, M. & Mosse, B. (1980) An evaluation of techniques for measuring vesicular arbuscular mycorrhizal infection in roots. New Phytologist, 84, 489–500.
Gupta, A., Rico‐Medina, A. & Caño‐Delgado, A.I. (2020) The physiology of plant responses to drought. Science, 368, 266–269.
Hallett, P.D., Feeney, D.S., Bengough, A.G., Rillig, M.C., Scrimgeour, C.M. & Young, I.M. (2009) Disentangling the impact of AM fungi versus roots on soil structure and water transport. Plant and Soil, 314, 183–196.
Hoagland, D.R. & Arnon, D.I. (1950) The water‐culture method for growing plants without soil. California Agricultural Experimental Station Circular, 347, 1–32.
Hogekamp, C., Arndt, D., Pereira, P.A., Becker, J.D., Hohnjec, N. & Küster, H. (2011) Laser microdissection unravels cell‐type‐specific transcription in arbuscular mycorrhizal roots, including CAAT‐box transcription factor gene expression correlating with fungal contact and spread. Plant Physiology, 157, 2023–2043.
Kakouridis, A., Hagen, J.A., Kan, M.P., Mambelli, S., Feldman, L.J., Herman, D.J. et al. (2022) Routes to roots: direct evidence of water transport by arbuscular mycorrhizal fungi to host plants. New Phytologist, 236, 210–221.
Khaosaad, T., Staehelin, C., Steinkellner, S., Hage‐Ahmed, K., Ocampo, J.A., Garcia‐Garrido, J.M. et al. (2010) The Rhizobium sp. strain NGR234 systemically suppresses arbuscular mycorrhizal root colonization in a split‐root system of barley (Hordeum vulgare). Physiologia Plantarum, 140, no.
Krajinski, F., Biela, A., Schubert, D., Gianinazzi‐Pearson, V., Kaldenhoff, R. & Franken, P. (2000) Arbuscular mycorrhiza development regulates the mRNA abundance of Mtaqp1 encoding a mercury‐insensitive aquaporin of Medicago truncatula. Planta, 211, 85–90.
Lesk, C., Rowhani, P. & Ramankutty, N. (2016) Influence of extreme weather disasters on global crop production. Nature, 529, 84–87.
Lian, H.L., Yu, X., Lane, D., Sun, W.N., Tang, Z.C. & Su, W.A. (2006) Upland rice and lowland rice exhibited different PIP expression under water deficit and ABA treatment. Cell Research, 16, 651–660.
Li, G., Santoni, V. & Maurel, C. (2014) Plant aquaporins: roles in plant physiology. Biochimica et Biophysica Acta (BBA)—General Subjects, 1840, 1574–1582.
Li, T., Hu, Y.‐J., Hao, Z.P., Li, H., Wang, Y.S. & Chen, B.D. (2013) First cloning and characterization of two functional aquaporin genes from an arbuscular mycorrhizal fungus Glomus intraradices. New Phytologist, 197, 617–630.
Liu, C.Y., Hao, Y., Wu, X.L., Dai, F.J., Abd‐Allah, E.F., Wu, Q.S. et al. (2024) Arbuscular mycorrhizal fungi improve drought tolerance of tea plants via modulating root architecture and hormones. Plant Growth Regulation, 102, 13–22.
Livak, K.J. & Schmittgen, T.D. (2001) Analysis of relative gene expression data using real‐time quantitative PCR and the 2‐ΔΔCT method. Methods, 25, 402–408.
Lobell, D.B., Burke, M.B., Tebaldi, C., Mastrandrea, M.D., Falcon, W.P. & Naylor, R.L. (2008) Prioritizing climate change adaptation needs for food security in 2030. Science, 319, 607–610.
Luang, S. & Hrmova, M. (2017) Structural basis of the permeation function of plant aquaporins. In plant aquaporins. From transport to signaling. In: Chaumont, F. & Tyerman, S.D. Signaling and communication in plants series. Cham, Switzerland: Springer International Publishing, pp. 1–28.
Marjanović, Ž., Uehlein, N., Kaldenhoff, R., Zwiazek, J.J., Weiß, M., Hampp, R. et al. (2005) Aquaporins in poplar: what a difference a symbiont makes! Planta, 222, 258–268.
Marulanda, A., Azcón, R. & Ruiz‐Lozano, J.M. (2003) Contribution of six arbuscular mycorrhizal fungal isolates to water uptake by Lactuca sativa plants under drought stress. Physiologia Plantarum, 119, 526–533.
Maurel, C., Boursiac, Y., Luu, D.‐T., Santoni, V., Shahzad, Z. & Verdoucq, L. (2015) Aquaporins in plants. Physiological Reviews, 95, 1321–1358.
Maurel, C. & Plassard, C. (2011) Aquaporins: for more than water at the plant–fungus interface? New Phytologist, 190, 815–817.
Maurel, C., Verdoucq, L., Luu, D.‐T. & Santoni, V. (2008) Plant aquaporins: membrane channels with multiple integrated functions. Annual Review of Plant Biology, 59, 595–624.
Munné‐Bosch, S. & Müller, M. (2013) Hormonal cross‐talk in plant development and stress responses. Frontiers in Plant Science, 4, 529.
Neumann, E., Schmid, B., Römheld, V. & George, E. (2009) Extraradical development and contribution to plant performance of an arbuscular mycorrhizal symbiosis exposed to complete or partial root zone drying. Mycorrhiza, 20, 13–23.
Ortiz‐Delvasto, N., García‐Gomez, P., Carvajal, M. & Bárzana, G. (2024) Aquaporins‑mediated water availability in substrates for cannabis cultivation in relation to CBD yield. Plant and Soil, 495, 469–485.
Oxborough, K. & Baker, N.R. (1997) Resolving chlorophyll a fluorescence images of photosynthetic efficiency into photochemical and non‐photochemical components—calculation of qP and Fv’/Fm’ without measuring Fo’. Photosynthesis Research, 54, 135–142.
Phillips, J.M. & Hayman, D.S. (1970) Improved procedures for clearing roots and staining parasitic and vesicular‐arbuscular mycorrhizal fungi for rapid assessment of infection. Transactions of the British Mycological Society, 55, 158–IN18.
Porcel, R., Aroca, R., Azcón, R. & Ruiz‐Lozano, J.M. (2006) PIP aquaporin gene expression in arbuscular mycorrhizal Glycine max and Lactuca sativa plants in relation to drought stress tolerance. Plant Molecular Biology, 60, 389–404.
Pozo, M.J., López‐Ráez, J.A., Azcón‐Aguilar, C. & García‐Garrido, J.M. (2015) Phytohormones as integrators of environmental signals in the regulation of mycorrhizal symbioses. New Phytologist, 205, 1431–1436.
Prado, K., Boursiac, Y., Tournaire‐Roux, C., Monneuse, J.M., Postaire, O., Da Ines, O. et al. (2013) Regulation of Arabidopsis leaf hydraulics involves light‐dependent phosphorylation of aquaporins in veins. The Plant Cell, 25, 1029–1039.
Püschel, D., Bitterlich, M., Rydlová, J. & Jansa, J. (2020) Facilitation of plant water uptake by an arbuscular mycorrhizal fungus: a Gordian knot of roots and hyphae. Mycorrhiza, 30, 299–313.
Quiroga, G., Erice, G., Aroca, R., Chaumont, F. & Ruiz‐Lozano, J.M. (2017) Enhanced drought stress tolerance by the arbuscular mycorrhizal symbiosis in a drought‐sensitive maize cultivar is related to a broader and differential regulation of host plant aquaporins than in a drought‐tolerant cultivar. Frontiers in Plant Science, 8, 1056.
Quiroga, G., Erice, G., Aroca, R., Chaumont, F. & Ruiz‐Lozano, J.M. (2019) Contribution of the arbuscular mycorrhizal symbiosis to the regulation of radial root water transport in maize plants under water deficit. Environmental and Experimental Botany, 167, 103821.
Quiroga, G., Erice, G., Aroca, R., Zamarreño, Á.M., García‐Mina, J.M. & Ruiz‐Lozano, J.M. (2018) Arbuscular mycorrhizal symbiosis and salicylic acid regulate aquaporins and root hydraulic properties in maize plants subjected to drought. Agricultural Water Management, 202, 271–284.
Quiroga, G., Erice, G., Aroca, R., Zamarreño, Á.M., García‐Mina, J.M. & Ruiz‐Lozano, J.M. (2020) Radial water transport in arbuscular mycorrhizal maize plants under drought stress conditions is affected by indole‐acetic acid (IAA) application. Journal of Plant Physiology, 246–247, 153115.
Quiroga, G., Erice, G., Ding, L., Chaumont, F., Aroca, R. & Ruiz‐Lozano, J.M. (2019) The arbuscular mycorrhizal symbiosis alters aquaporins activity and root cell water permeability in maize plants subjected to water deficit. Plant, Cell and Environment, 42, 2274–2290.
Recchia, G.H., Konzen, E.R., Cassieri, F., Caldas, D.G.G. & Tsai, S.M. (2018) Arbuscular mycorrhizal symbiosis leads to differential regulation of drought‐responsive genes in tissue‐specific root cells of common bean. Frontiers in Microbiology, 9, 1339.
Rillig, M.C., Wright, S.F. & Eviner, V.T. (2002) The role of arbuscular mycorrhizal fungi and glomalin in soil aggregation: comparing effects of five plant species. Plant and Soil, 238, 325–333.
Ruiz‐Lozano, J.M. & Aroca, R. (2017) Plant aquaporins and mycorrhizae: Their regulation and involvement in plant physiology and performance. In: Chaumont, F. & Tyerman, S.D. Plant aquaporins. From transport to signaling. Signaling and communication in plants series. Cham, Switzerland: Springer International Publishing, pp. 333–353.
Ruiz‐Lozano, J.M., del Mar Alguacil, M., Bárzana, G., Vernieri, P. & Aroca, R. (2009) Exogenous ABA accentuates the differences in root hydraulic properties between mycorrhizal and non‐mycorrhizal maize plants through regulation of PIP aquaporins. Plant Molecular Biology, 70, 565–579.
Ruiz‐Lozano, J.M., Porcel, R., Azcón, R., Bárzana, G. & Aroca, R. (2012) Contribution of arbuscular mycorrhizal symbiosis to plant drought tolerance: state of the art. In: Aroca, R. Plant responses to drought stress: From morphological to molecular features. Heidelberg, Germany: Springer‐Verlag, pp. 335–362.
Ruiz‐Lozano, J.M., Quiroga, G., Erice, G., Pérez‐Tienda, J., Zamarreño, Á.M., García‐Mina, J.M. et al. (2022) Using the maize nested association mapping (NAM) population to partition arbuscular mycorrhizal effects on drought stress tolerance into hormonal and hydraulic components. International Journal of Molecular Sciences, 23, 9822.
Ruth, B., Khalvati, M. & Schmidhalter, U. (2011) Quantification of mycorrhizal water uptake via high‐resolution on‐line water content sensors. Plant and Soil, 342, 459–468.
Sack, L. & Holbrook, N.M. (2006) Leaf hydraulics. Annual Review of Plant Biology, 57, 361–381.
Sánchez‐Blanco, M.J., Ferrández, T., Morales, M.A., Morte, A. & Alarcón, J.J. (2004) Variations in water status, gas exchange, and growth in Rosmarinus officinalis plants infected with Glomus deserticola under drought conditions. Journal of Plant Physiology, 161, 675–682.
Sánchez‐Romera, B., Ruiz‐Lozano, J.M., Li, G., Luu, D.T., Martínez‐Ballesta, M.D.C., Carvajal, M. et al. (2014) Enhancement of root hydraulic conductivity by methyl jasmonate and the role of calcium and abscisic acid in this process. Plant, Cell & Environment, 37, 995–1008.
Sánchez‐Romera, B., Ruiz‐Lozano, J.M., Zamarreño, Á.M., García‐Mina, J.M. & Aroca, R. (2016) Arbuscular mycorrhizal symbiosis and methyl jasmonate avoid the inhibition of root hydraulic conductivity caused by drought. Mycorrhiza, 26, 111–122.
Santander, C., Aroca, R., Ruiz‐Lozano, J.M., Olave, J., Cartes, P., Borie, F. et al. (2017) Arbuscular mycorrhiza effects on plant performance under osmotic stress. Mycorrhiza, 27, 639–657.
Shatil‐Cohen, A., Sibony, H., Draye, X., Chaumont, F., Moran, N. & Moshelion, M. (2014) Measuring the osmotic water permeability coefficient (Pf) of spherical cells: isolated plant protoplasts as an example. Journal of Visualized Experiments, 8, e51652.
Shi, J., Gao, H., Wang, H., Lafitte, H.R., Archibald, R.L., Yang, M. et al. (2017) ARGOS8 variants generated by CRISPR‐Cas9 improve maize grain yield under field drought stress conditions. Plant Biotechnology Journal, 15, 207–216.
Singh, R.K., Deshmukh, R., Muthamilarasan, M., Rani, R. & Prasad, M. (2020) Versatile roles of aquaporin in physiological processes and stress tolerance in plants. Plant Physiology and Biochemistry, 149, 178–189.
Smart, L.B., Moskal, W.A., Cameron, K.D. & Bennett, A.B. (2001) Mip genes are down‐regulated under drought stress in Nicotiana glauca. Plant and Cell Physiology, 42, 686–693.
Steudle, E., Oren, R. & Schulze, E.‐D. (1987) Water transport in maize roots. Plant Physiology, 84, 1220–1232.
Steudle, E. & Peterson, C.A. (1998) How does water get through roots? Journal of Experimental Botany, 49, 775–788.
Trenberth, K.E., Dai, A., van der Schrier, G., Jones, P.D., Barichivich, J., Briffa, K.R. et al. (2014) Global warming and changes in drought. Nature Climate Change, 4, 17–22.
Ullah, A., Manghwar, H., Shaban, M., Khan, A.H., Akbar, A., Ali, U. et al. (2018) Phytohormones enhanced drought tolerance in plants: a coping strategy. Environmental Science and Pollution Research, 25, 33103–33118.
Varma, A. (2008) Mycorrhiza. State of the art, genetics and molecular biology, eco‐funcion, biotecnology, eco‐physiology, structure and systematics, 3rd edition. Berlin, Heidelberg: Springer‐Verlag.
Wu, C., Bi, Y. & Zhu, W. (2024) Is the amount of water transported by arbuscular mycorrhizal fungal hyphae negligible? Insights from a compartmentalized experimental study. Plant and Soil, 499, 537–552. https://doi.org/10.1007/s11104-024-06477-1.
Zwiazek, J.J., Xu, H., Tan, X., Navarro‐Ródenas, A. & Morte, A. (2017) Significance of oxygen transport through aquaporins. Scientific Reports, 7, 40411. - Grant Information: PHENOLAB 4.0; FEDER 'A way to make Europe'; Ministerio de Ciencia e Innovación
- Contributed Indexing: Keywords: arbusculated cell; colonized root fraction; drought; laser microdissection; mycorrhiza; uncolonized root fraction
- Accession Number: 0 (Aquaporins)
059QF0KO0R (Water)
0 (Plant Proteins) - Publication Date: Date Created: 20240705 Date Completed: 20241001 Latest Revision: 20241001
- Publication Date: 20241002
- Accession Number: 10.1111/pce.15029
- Accession Number: 38965812
- Source:
Contact CCPL
Copyright 2022 Charleston County Public Library Powered By EBSCO Stacks 3.3.0 [350.3] | Staff Login
No Comments.