Роль универсальных регуляторов роста и развития растений DELLA-белков в контроле симбиозов
- Авторы: Долгих А.В.1, Долгих Е.А.1
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Учреждения:
- ФГБНУ «Всероссийский научно-исследовательский институт сельскохозяйственной микробиологии»
- Выпуск: Том 17, № 1 (2019)
- Страницы: 33-41
- Раздел: Генетические основы эволюции экосистем
- URL: https://journals.rcsi.science/ecolgenet/article/view/10588
- DOI: https://doi.org/10.17816/ecogen17133-41
- ID: 10588
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Аннотация
Универсальными участниками сигнальных путей, координирующими процессы роста и развития растений, являются регуляторы гиббереллинового ответа DELLA-белки. Эта регуляция обеспечивается путем интеграции внешних воздействий, а также внутренних сигналов, таких как изменение в уровне фитогормонов и вторичных мессенджеров. Поскольку DELLA-белки чрезвычайно чувствительны к повышению или же снижению эндогенного уровня гибберелловой кислоты (ГК), их прямое взаимодействие с транскрипционными факторами модулирует активность последних, а следовательно, и уровень экспрессии генов-мишеней в ответ на внешние воздействия, вызывающие изменения в уровне ГК. Одна из наиболее важных функций, которые выполняют DELLA-белки, связана с их участием в регуляции развития симбиозов растений с азотфиксирующими клубеньковыми бактериями и грибами арбускулярной микоризы. Однако молекулярные механизмы влияния DELLA-белков на развитие симбиозов остаются малоизученными. В обзоре проведен анализ классических и современных данных о функционировании DELLA-белков у растений.
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Александра Вячеславовна Долгих
ФГБНУ «Всероссийский научно-исследовательский институт сельскохозяйственной микробиологии»
Email: sqshadol@gmail.com
ORCID iD: 0000-0003-1845-9701
студент, лаборатория молекулярной и клеточной биологии
Россия, 196608, г. Санкт-Петербург, Пушкин 8, ш. Подбельского, д.3Елена Анатольевна Долгих
ФГБНУ «Всероссийский научно-исследовательский институт сельскохозяйственной микробиологии»
Автор, ответственный за переписку.
Email: dol2helen@yahoo.com
ORCID iD: 0000-0002-5375-0943
SPIN-код: 4453-2060
Scopus Author ID: 6603496335
ResearcherId: G-6363-2017
д-р биол. наук, ведущий научный сотрудник лаборатории молекулярной и клеточной биологии
Россия, 196608, г. Санкт-Петербург, Пушкин 8, ш. Подбельского, д.3Список литературы
- Xue L, Cui H, Buer B, et al. Network of GRAS transcription factors involved in the control of arbuscule development in Lotus japonicus. Plant Phy siol. 2015;167(3):854-871. https://doi.org/10.1104/pp.114.255430.
- Hirsch S, Oldroyd GED. GRAS-domain transcription factors that regulate plant development. Plant Signaling & Behavior. 2014;4(8):698-700. https://doi.org/10.4161/psb.4.8.9176.
- Hirsch S, Oldroyd GED. GRAS-domain transcription factors that regulate plant development. Plant Signaling & Behavior. 2014;4(8):698-700. https://doi.org/10.4161/psb.4.8.9176.
- Vera-Sirera F, Gomez MD, Perez-Amador MA. DELLA proteins, a group of GRAS transcription regulators that mediate gibberellin signaling. In: Plant Transcription Factors. Elsevier; 2016. P. 313-328. https://doi.org/10.1016/B978-0-12-800854-6.00020-8.
- Daviere JM, Achard P. Gibberellin signaling in plants. Development. 2013;140(6):1147-1151. https://doi.org/10.1242/dev.087650.
- Briones-Moreno A, Hernandez-Garcia J, Vargas-Chavez C, et al. Evolutionary analysis of DELLA-associated transcriptional networks. Front Plant Sci. 2017;8:626. https://doi.org/10.3389/fpls.2017.00626.
- Sun TP. The molecular mechanism and evolution of the GA-GID1-DELLA signaling module in plants. Curr Biol. 2011;21(9):R338-345. https://doi.org/10.1016/j.cub.2011.02.036.
- Dill A, Thomas SG, Hu J, et al. The Arabidopsis F-box protein SLEEPY1 targets gibberellin signaling repressors for gibberellin-induced degradation. Plant Cell. 2004;16(6):1392-1405. https://doi.org/10.1105/tpc.020958.
- Hirano K, Kouketu E, Katoh H, et al. The suppressive function of the rice DELLA protein SLR1 is dependent on its transcriptional activation activity. Plant J. 2012;71(3):443-453. https://doi.org/10.1111/j.1365-313X.2012.05000.x.
- Fleck B, Harberd NP. Evidence that the Arabidopsis nuclear gibberellin signalling protein GAI is not destabilised by gibberellin. The Plant Journal. 2002;32(6):935-947. https://doi.org/10.1046/j.1365-313X.2002.01478.x.
- Wen CK. Arabidopsis RGL1 encodes a negative regulator of gibberellin responses. Plant Cell. 2002;14(1):87-100. https://doi.org/10.1105/tpc.010325.
- Hedden P, Thomas SG. Gibberellin biosynthesis and its regulation. Biochem J. 2012;444(1):11-25. https://doi.org/10.1042/BJ20120245.
- Livne S, Lor VS, Nir I, et al. Uncovering DELLA-independent gibberellin responses by characterizing new tomato procera mutants. Plant Cell. 2015;27(6):1579-94. https://doi.org/10.1105/tpc.114.132795.
- Gubler F, Chandler PM, White RG, et al. Gibberellin signaling in barley aleurone cells. Control of SLN1 and GAMYB expression. Plant Physiol. 2002;129(1): 191-200. https://doi.org/10.1104/pp.010918.
- Floss DS, Levy JG, Levesque-Tremblay V, et al. DELLA proteins regulate arbuscule formation in arbuscular mycorrhizal symbiosis. Proc Natl Acad Sci USA. 2013;110(51):E5025-5034. https://doi.org/10.1073/pnas.1308973110.
- Weston DE, Elliott RC, Lester DR, et al. The Pea DELLA proteins LA and CRY are important regulators of gibberellin synthesis and root growth. Plant Phy siol. 2008;147(1):199-205. https://doi.org/10.1104/pp.108.115808.
- Zhang ZL, Ogawa M, Fleet CM, et al. Scarecrow-like 3 promotes gibberellin signaling by antagonizing master growth repressor DELLA in Arabidopsis. Proc Natl Acad Sci U S A. 2011;108(5):2160-2165. https://doi.org/10.1073/pnas.1012232108.
- Zentella R, Zhang ZL, Park M, et al. Global analysis of della direct targets in early gibberellin signaling in Arabidopsis. Plant Cell. 2007;19(10):3037-3057. https://doi.org/10.1105/tpc.107.054999.
- Hirano K, Nakajima M, Asano K, et al. The GID1-mediated gibberellin perception mechanism is conserved in the Lycophyte Selaginella moellendorffii but not in the Bryophyte Physcomitrella patens. Plant Cell. 2007;19(10):3058-3079. https://doi.org/10.1105/tpc.107.051524.
- Yasumura Y, Crumpton-Taylor M, Fuentes S, Harberd NP. Step-by-step acquisition of the gibberellin-DELLA growth-regulatory mechanism during land-plant evolution. Curr Biol. 2007;17(14):1225-1230. https://doi.org/10.1016/j.cub.2007.06.037.
- Vandenbussche F, Fierro AC, Wiedemann G, et al. Evolutionary conservation of plant gibberellin signalling pathway components. BMC Plant Biol. 2007;7:65. https://doi.org/10.1186/1471-2229-7-65.
- Gallego-Bartolome J, Minguet EG, Marin JA, et al. Transcriptional diversification and functional conservation between DELLA proteins in Arabidopsis. Mol Biol Evol. 2010;27(6):1247-1256. https://doi.org/10.1093/molbev/msq012.
- Frigerio M, Alabadi D, Perez-Gomez J, et al. Transcriptional regulation of gibberellin metabolism genes by auxin signaling in Arabidopsis. Plant Physiol. 2006;142(2):553-563. https://doi.org/10.1104/pp.106.084871.
- Plant Hormones: Physiology, Biochemistry and Molecular Biology. Ed. by P.J. Davies. Springer; 2013.
- Brian PW, Hemming HG. Complementary action of Gibberellic acid and auxins in pea internode extension. Ann Bot. 1958;22(1):1-17. https://doi.org/10.1093/oxfordjournals.aob.a083592.
- Fu X, Harberd NP. Auxin promotes Arabidopsis root growth by modulating gibberellin response. Nature. 2003;421(6924):740-743. https://doi.org/10.1038/nature01387.
- Achard P, Vriezen WH, Van Der Straeten D, Harberd NP. Ethylene regulates arabidopsis development via the modulation of DELLA protein growth repressor function. Plant Cell. 2003;15(12):2816-2825. https://doi.org/10.1105/tpc.015685.
- Hua J, Meyerowitz EM. Ethylene responses are negatively regulated by a receptor gene family in Arabidopsis thaliana. Cell. 1998;94(2):261-271. https://doi.org/10.1016/s0092-8674(00)81425-7.
- Gallego-Bartolome J, Minguet EG, Marin JA, et al. Transcriptional diversification and functional conservation between DELLA proteins in Arabidopsis. Mol Biol Evol. 2010;27(6):1247-1256. https://doi.org/10.1093/molbev/msq012.
- Saibo NJM, Vriezen WH, Beemster GTS, Van Der Straeten D. Growth and stomata development of Arabidopsis hypocotyls are controlled by gibberellins and modulated by ethylene and auxins. Plant J. 2003;33(6):989-1000. https://doi.org/10.1046/j.1365-313X.2003.01684.x.
- Moubayidin L, Perilli S, Dello Ioio R, et al. The rate of cell differentiation controls the Arabidopsis root meristem growth phase. Curr Biol. 2010;20(12):1138-43. https://doi.org/10.1016/j.cub.2010.05.035.
- Dello Ioio R, Linhares FS, Sabatini S. Emerging role of cytokinin as a regulator of cellular differentiation. Curr Opin Plant Biol. 2008;11(1):23-27. https://doi.org/10.1016/j.pbi.2007.10.006.
- Lofke C, Luschnig C, Kleine-Vehn J. Posttranslational modification and trafficking of PIN auxin efflux carriers. Mech Dev. 2013;130(1):82-94. https://doi.org/10.1016/j.mod.2012.02.003.
- Kleine-Vehn J, Leitner J, Zwiewka M, et al. Differential degradation of PIN2 auxin efflux carrier by retromer-dependent vacuolar targeting. Proc Natl Acad Sci USA. 2008;105(46):17812-17817. https://doi.org/10.1073/pnas.0808073105.
- Salanenka Y, Verstraeten I, Lofke C, et al. Gibberellin DELLA signaling targets the retromer complex to redirect protein trafficking to the plasma membrane. Proc Natl Acad Sci U S A. 2018;115(14):3716-3721. https://doi.org/10.1073/pnas.1721760115.
- Lundin VF, Srayko M, Hyman AA, Leroux MR. Efficient chaperone-mediated tubulin biogenesis is essential for cell division and cell migration in C. ele gans. Dev Biol. 2008;313(1):320-334. https://doi.org/10.1016/j.ydbio.2007.10.022.
- Torres MA, Jones JD, Dangl JL. Reactive oxygen species signaling in response to pathogens. Plant Phy siol. 2006;141(2):373-378. https://doi.org/10.1104/pp.106.079467.
- Roy Choudhury S, Pandey S. Phosphatidic acid binding inhibits RGS1 activity to affect specific signaling pathways in Arabidopsis. Plant J. 2017;90(3):466-477. https://doi.org/10.1111/tpj.13503.
- Achard P, Renou JP, Berthome R, et al. Plant DELLAs restrain growth and promote survival of adversity by reducing the levels of reactive oxygen species. Curr Biol. 2008;18(9):656-660. https://doi.org/10.1016/j.cub.2008.04.034.
- Tsukagoshi H. Control of root growth and development by reactive oxygen species. Curr Opin Plant Biol. 2016;29:57-63. https://doi.org/10.1016/j.pbi.2015.10.012.
- Madsen EB, Madsen LH, Radutoiu S, et al. A receptor kinase gene of the LysM type is involved in legume perception of rhizobial signals. Nature. 2003;425(6958):637-640. https://doi.org/10.1038/nature02045.
- Zhukov V, Radutoiu S, Madsen LH, et al. The pea Sym37 receptor kinase gene controls infection-thread initiation and nodule development. Mol Plant Microbe Interact. 2008;21(12):1600-1608. https://doi.org/10.1094/MPMI-21-12-1600.
- Kirienko AN, Porozov YB, Malkov NV, et al. Role of a receptor-like kinase K1 in pea Rhizobium symbiosis development. Planta. 2018;248(5):1101-1120. https://doi.org/10.1007/s00425-018-2944-4.
- Oldroyd GE, Murray JD, Poole PS, Downie JA. The rules of engagement in the legume-rhizobial symbiosis. Annu Rev Genet. 2011;45:119-144. https://doi.org/10.1146/annurev-genet-110410-132549.
- Grunwald U, Nyamsuren O, Tamasloukht M, et al. Identification of mycorrhiza-regulated genes with arbuscule development-related expression profile. Plant Mol Biol. 2004;55(4):553-566. https://doi.org/10.1007/s11103-004-1303-y.
- Plet J, Wasson A, Ariel F, et al. MtCRE1-dependent cytokinin signaling integrates bacterial and plant cues to coordinate symbiotic nodule organogenesis in Medicago truncatula. Plant J. 2011;65(4):622-633. https://doi.org/10.1111/j.1365-313X.2010.04447.x.
- Hirsch AM, Bhuvaneswari TV, Torrey JG, Bisse ling T. Early nodulin genes are induced in alfalfa root outgrowths elicited by auxin transport inhibitors. Proc Natl Acad Sci USA. 1989;86(4):1244-1248. https://doi.org/10.1073/pnas.86.4.1244.
- Gamas P, Brault M, Jardinaud MF, Frugier F. Cytokinins in Symbiotic Nodulation: When, Where, What for? Trends Plant Sci. 2017;22(9):792-802. https://doi.org/10.1016/j.tplants.2017.06.012.
- McAdam EL, Reid JB, Foo E. Gibberellins promote nodule organogenesis but inhibit the infection stages of nodulation. J Exp Bot. 2018;69(8):2117-2130. https://doi.org/10.1093/jxb/ery046.
- Fonouni-Farde C, Tan S, Baudin M, et al. DELLA-media ted gibberellin signalling regulates Nod factor signalling and rhizobial infection. Nat Commun. 2016;7:12636. https://doi.org/10.1038/ncomms12636.
- Ferguson BJ, Ross JJ, Reid JB. Nodulation phenotypes of gibberellin and brassinosteroid mutants of pea. Plant Physiol. 2005;138(4):2396-2405. https://doi.org/10.1104/pp.105.062414.
- Fonouni-Farde C, Kisiala A, Brault M, et al. DELLA1-mediated gibberellin signaling regulates cytokinin-dependent symbiotic nodulation. Plant Physiol. 2017;175(4):1795-1806. https://doi.org/10.1104/pp.17.00919.
- Jin Y, Liu H, Luo D, et al. DELLA proteins are common components of symbiotic rhizobial and mycorrhizal signalling pathways. Nat Commun. 2016;7:12433. https://doi.org/10.1038/ncomms12433.
- Harrison MJ. Cellular programs for arbuscular mycorrhizal symbiosis. Curr Opin Plant Biol. 2012;15(6):691-8. https://doi.org/10.1016/j.pbi.2012.08.010.
- Smith SE, Smith FA. Roles of arbuscular mycorrhizas in plant nutrition and growth: new paradigms from cellular to ecosystem scales. Annu Rev Plant Biol. 2011;62:227-250. https://doi.org/10.1146/annurev-arplant-042110-103846.
- Levy J, Bres C, Geurts R, et al. A putative Ca2+ and calmodulin-dependent protein kinase required for bacterial and fungal symbioses. Science. 2004;303(5662):1361-1364. https://doi.org/10.1126/science.1093038.
- Banba M, Gutjahr C, Miyao A, et al. Divergence of evolutionary ways among common sym genes: CASTOR and CCaMK show functional conservation between two symbiosis systems and constitute the root of a common signaling pathway. Plant Cell Physiol. 2008;49(11): 1659-71. https://doi.org/10.1093/pcp/pcn153.
- Harrison MJ. A phosphate transporter from Medicago truncatula involved in the acquisition of phosphate released by Arbuscular mycorrhizal fungi. Plant Cell. 2002;14(10):2413-2429. https://doi.org/10.1105/tpc.004861.
- Floss DS, Levesque-Tremblay V, Park HJ, Harrison MJ. DELLA proteins regulate expression of a subset of AM symbiosis-induced genes in Medicago truncatula. Plant Signal Behav. 2016;11(4):e1162369. https://doi.org/10.1080/15592324.2016.1162369.
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