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出典(authority):フリー百科事典『ウィキペディア(Wikipedia)』「2015/04/23 16:36:56」(JST)
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Drought rhizogenesis is an adaptive root response to drought stress. New emerging roots are short, swollen, and hairless, capable of retaining turgor pressure and resistant to prolonged desiccation. Upon rewatering, they are capable of quickly forming an absorbing root surface and hair growth. This rhizogenesis has been called a drought tolerance strategy for after-stress recovery.[1][2]
Structural features
These drought induced short roots can be found on either both the tap root and lateral roots or on lateral roots only. These patterns are mostly likely a reflection of the plants' individual ability to maintain meristematic activity under low water potential.[3]
This morphological phenomenon was found in some families of Angiosperm dicot perennials and has been documented in Arabidopsis thaliana.[4]
References
- ^ Vartanian, N. (1996), "The Drought Rhizogenesis", in Waisel, Yoav; Eshel, Amram; Kafkafi, Uzi, Plant Roots: The Hidden Half, CRC Press (published March 2002), pp. 471–482, ISBN 0-8247-0631-5
- ^ Vartanian, N., "Some aspects of structural and functional modifications induced by drought in root systems", Plant Soil 63 (1981): 83-92.
- ^ Balestrini, S. and N. Vartanian, "Rhizogenic activity during water stress-induced senescence in Brassica napus var. oleifera", Physiologie Vegetale 21, volume 2 (1983a): 269-277.
- ^ Vartanian, N., L. Marcotte, and J. Giraudat (1994), Drought Rhizogenesis in Arabidopsis thaliana. Differential responses of hormonal mutants, Plant Physiology, 104, 761-767. Available online: http://www.plantphysiol.org/content/104/2/761.full.pdf
English Journal
- Pattern of antioxidant enzyme activities and hydrogen peroxide content during developmental stages of rhizogenesis from hypocotyl explants of Mesembryanthemum crystallinum L.
- Konieczny R1, Banaś AK, Surówka E, Michalec Ż, Miszalski Z, Libik-Konieczny M.Author information 1Department of Plant Cytology and Embryology, Institute of Botany, Jagiellonian University, Gronostajowa 9, 30-387, Kraków, Poland.AbstractKEY MESSAGE: H2O2 is necessary to elicit rhizogenic action of auxin. Activities of specific catalase and manganese superoxide dismutase forms mark roots development. Hypocotyl explants of Mesembryanthemum crystallinum regenerated roots on medium containing 2,4-dichlorophenoxyacetic acid. Explants became competent to respond to the rhizogenic action of auxin on day 3 of culture, when hydrogen peroxide content in cultured tissue was the highest. L-Ascorbic acid added to the medium at 5 μM lowered the H2O2 level, inhibited rhizogenesis and induced non-regenerative callus, suggesting that certain level of H2O2 is required to promote root initiation. Coincident with the onset of rhizogenic determination, meristemoids formed at the periphery of the hypocotyl stele and the activity of the manganese form of superoxide dismutase, MnSOD-2 was induced. Once induced, MnSOD-2 activity was maintained through the post-determination phase of rooting, involving root growth. MnSOD-2 activity was not found in non-rhizogenic explants maintained in the presence of AA. Analyses of the maximum photochemical efficiency of photosystem II and the oxygen uptake rate revealed that the explants were metabolically arrested during the predetermination stage of rhizogenesis. Respiratory and photosynthetic rates were high during root elongation and maturation. Changes in catalase and peroxidase activities correlated with fluctuations of endogenous H2O2 content throughout rhizogenic culture. Expression of a specific CAT-2 form accompanied the post-determination stage of rooting and a high rate of carbohydrate metabolism during root growth. On the other hand, the occurrence of MnSOD-2 activity did not depend on the metabolic status of explants. The expression of MnSOD-2 activity throughout root development seems to relate it specifically to root metabolism and indicates it as a molecular marker of rhizogenesis in M. crystallinum.
- Plant cell reports.Plant Cell Rep.2014 Jan;33(1):165-77. doi: 10.1007/s00299-013-1520-4. Epub 2013 Oct 18.
- KEY MESSAGE: H2O2 is necessary to elicit rhizogenic action of auxin. Activities of specific catalase and manganese superoxide dismutase forms mark roots development. Hypocotyl explants of Mesembryanthemum crystallinum regenerated roots on medium containing 2,4-dichlorophenoxyacetic acid. Explants be
- PMID 24135858
- Assessing the response of indigenous loquat cultivar Mardan to phytohormones for in vitro shoot proliferation and rooting.
- Abbasi NA1, Pervaiz T, Hafiz IA, Yaseen M, Hussain A.Author information 1Plant Tissue Culture Laboratory, Department of Horticulture, Pir Mehr Ali Shah-Arid Agriculture University, Rawalpindi 46300, Pakistan.AbstractIn vitro cultures of loquat cultivar Mardan were established using shoot apices after treating with NaOCl (5%, 7%, 10%, 12%, 14% (v/v)) for 12 min and HgCl2 (0.01%, 0.05%, 0.10%, 0.20%, 0.25% (w/v)) for 2 min. A maximum survival rate of 70% was recorded after surface sterilization with 10% NaOCl. Caulogenic response was assessed on Murashige and Skoog (MS) medium fortified with assorted combinations of the cytokinins, benzylaminopurine (BAP), kinetin, and N6-(2-isopentyl)adenine (2iP). Treatment of BAP 1.5 mg/L combined with 2iP 9.0 mg/L and kinetin 1.5 mg/L was found to be optimum for shoot morphogenesis in terms of the number and subsequent growth of shoots, while the highest shoot length was yielded by the combination of BAP 0.5 mg/L, kinetin 0.5 mg/L, and 2iP 3 mg/L. Higher levels of cytokinins induced callogenesis, vitrification and stunted growth to some extent. For rhizogenesis, uniform sized micro-shoots were excised and transferred to half-strength MS medium containing auxins. The best rooting expression was observed with naphthaleneacetic acid (NAA) 1 mg/L combined with indole-3-butyric acid (IBA) 2 mg/L and paclobutrazol (PBZ) 1 mg/L.
- Journal of Zhejiang University. Science. B.J Zhejiang Univ Sci B.2013 Sep;14(9):774-84. doi: 10.1631/jzus.B1200277.
- In vitro cultures of loquat cultivar Mardan were established using shoot apices after treating with NaOCl (5%, 7%, 10%, 12%, 14% (v/v)) for 12 min and HgCl2 (0.01%, 0.05%, 0.10%, 0.20%, 0.25% (w/v)) for 2 min. A maximum survival rate of 70% was recorded after surface sterilization with 10% NaOCl. Ca
- PMID 24009197
- Comparative studies on cellular behaviour of carnation (Dianthus caryophyllus Linn. cv. Grenadin) grown in vivo and in vitro for early detection of somaclonal variation.
- Yaacob JS1, Taha RM, Khorasani Esmaeili A.Author information 1Institute of Biological Sciences, Faculty of Science, University of Malaya, 50603 Kuala Lumpur, Malaysia. jam_sya@yahoo.comAbstractThe present study deals with the cytological investigations on the meristematic root cells of carnation (Dianthus caryophyllus Linn.) grown in vivo and in vitro. Cellular parameters including the mitotic index (MI), chromosome count, ploidy level (nuclear DNA content), mean cell and nuclear areas, and cell doubling time (Cdt) were determined from the 2 mm root tip segments of this species. The MI value decreased when cells were transferred from in vivo to in vitro conditions, perhaps due to early adaptations of the cells to the in vitro environment. The mean chromosome number was generally stable (2n = 2x = 30) throughout the 6-month culture period, indicating no occurrence of early somaclonal variation. Following the transfer to the in vitro environment, a significant increase was recorded for mean cell and nuclear areas, from 26.59 ± 0.09 μm² to 35.66 ± 0.10 μm² and 142.90 ± 0.59 μm² to 165.05 ± 0.58 μm², respectively. However, the mean cell and nuclear areas of in vitro grown D. caryophyllus were unstable and fluctuated throughout the tissue culture period, possibly due to organogenesis or rhizogenesis. Ploidy level analysis revealed that D. caryophyllus root cells contained high percentage of polyploid cells when grown in vivo and maintained high throughout the 6-month culture period.
- TheScientificWorldJournal.ScientificWorldJournal.2013 May 22;2013:686752. doi: 10.1155/2013/686752. Print 2013.
- The present study deals with the cytological investigations on the meristematic root cells of carnation (Dianthus caryophyllus Linn.) grown in vivo and in vitro. Cellular parameters including the mitotic index (MI), chromosome count, ploidy level (nuclear DNA content), mean cell and nuclear areas, a
- PMID 23766703
Japanese Journal
- Tissue-specific localization and dynamic changes of endogenous IAA during poplar leaf rhizogenesis revealed by in situ immunohistochemistry
- Dong Ningguang,Pei Dong,Yin Weilun
- Plant biotechnology reports 6(2), 165-174, 2012-04
- NAID 40019231107
- Genetic difference in adventitious rhizogenesis in Albizia procera Benth. with IBA treatment
- ANSARI Shamim Akhtar,SINGH Sanjay
- Journal of forest research 13(1), 79-82, 2008-02-01
- NAID 10027225327
- 96(P14) 9-デオキシコチレノール誘導体の合成と活性(ポスター発表の部)
- 李 峰,竹下 齊,加藤 修雄,中沢 哲,森 章,佐々 武史
- 天然有機化合物討論会講演要旨集 (40), 565-570, 1998-08-31
- … These compounds widen the stomatal pore, stimulate cell elongation, break seed dormancy, and stimulate rhizogenesis. …
- NAID 110006679702
Related Links
- ... Thesaurus; Spanish; Medical; Concise Encyclopedia. rhizogenesis. About Our Definitions: All forms of a word (noun, verb, etc.) are now displayed on one page. rhi·zo·genesis. noun \ˌrīzə+\. Definition of RHIZOGENESIS. : root development ...
- Drought rhizogenesis is an adaptive root response to drought stress. New emerging roots are short, swollen, and hairless, capable of retaining turgor pressure and resistant to prolonged desiccation. Upon rewatering, they are capable of ...
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