Физиология растений, 2023, T. 70, № 4, стр. 433-448
Клеточный цикл растений: молекулярные события, регуляция внешними факторами и фитогормонами
А. В. Носов a, *, А. А. Фоменков a, **
a Федеральное государственное бюджетное учреждение науки Институт физиологии
растений им. К.А. Тимирязева Российской академии наук
Москва, Россия
* E-mail: alexv.nosov@mail.ru
** E-mail: artem.fomenkov@gmail.com
Поступила в редакцию 21.11.2022
После доработки 21.11.2022
Принята к публикации 21.11.2022
- EDN: IBGHGJ
- DOI: 10.31857/S0015330322600681
Полные тексты статей выпуска доступны в ознакомительном режиме только авторизованным пользователям.
Аннотация
В данной лекции представлены классические сведения и новые данные о молекулярных событиях “базового” (core) клеточного цикла (КЦ) растений. Кратко рассмотрено влияние водного дефицита, CO2, света и температуры на КЦ. Представлены данные о регуляции пролиферации клеток ауксинами, цитокининами, абсцизовой кислотой, гиббереллинами, брассиностероидами и этиленом. Обсуждаются закономерности и особенности влияния фитогормонов на КЦ в разных органах и тканях.
Полные тексты статей выпуска доступны в ознакомительном режиме только авторизованным пользователям.
Список литературы
Wilson E.B. The Cell in Development and Inheritance. New York: Macmillan, 1911. 483 p.
Vercruysse J., Baekelandt A., Gonzalez N., Inzé D. Molecular networks regulating cell division during Arabidopsis leaf growth // J. Exp. Bot. 2020. V. 71. P. 2365. https://doi.org/10.1093/jxb/erz522
Ivanov V.B., Dubrovsky J.G. Longitudinal zonation pattern in plant roots: conflicts and solutions // Trends Plant Sci. 2013. V. 18. P. 237. https://doi.org/10.1016/j.tplants.2012.10.002
Sablowski R. Coordination of plant cell growth and division: collective control or mutual agreement? // Curr. Opin. Plant Biol. V. 34. P. 54. https://doi.org/10.1016/j.pbi.2016.09.004
Howard A., Pelc S.R. Synthesis of deoxyribonucleic acid in normal and irradiated cells and its relation to chromosome breakage // Heredity (Edinb.) Suppl. 1953. V. 6. P. 261.
Swift H.H. The constancy of desoxyribose nucleic acid in plant nuclei // Proc. Natl. Acad. Sci. USA. 1950. V. 36. P. 643. https://doi.org/10.1073/pnas.36.11.643
Greilhuber J., Dolezel J., Lysák M.A., Bennett M.D. The origin, evolution and proposed stabilization of the terms “genome size” and “C-value” to describe nuclear DNA contents // Ann. Bot. V. 95. P. 255. https://doi.org/10.1093/aob/mci019
Kejnovsky E., Leitch I.J., Leitch A.R. Contrasting evolutionary dynamics between angiosperm and mammalian genomes // Trends Ecol. Evol. 2009. V. 24. P. 572. https://doi.org/10.1016/j.tree.2009.04.010
Pellicer J., Fay M.F., Leitch I.J. The largest eukaryotic genome of them all? // Bot. J. Linn. Soc. 2010. V. 164. P. 10. https://doi.org/10.1111/j.1095-8339.2010.01072.x
Bechhoefer J., Rhind N. Replication timing and its emergence from stochastic processes // Trends Genet. 2012. V. 28. P. 374. https://doi.org/10.1016/j.tig.2012.03.011
Greenberg A., Simon I. S phase duration is determined by local rate and global organization of replication // Biology. 2022. V. 11. 718. https://doi.org/10.3390/biology11050718
Lehti-Shiu M.D., Shiu S.-H. Diversity, classification and function of the plant protein kinase superfamily // Philos. Trans. R. Soc. Lond., B, Biol. Sci. 2012. V. 367. P. 2619. https://doi.org/10.1098/rstb.2012.0003
Cross F., Roberts J., Weintraub H. Simple and complex cell cycles // Annu. Rev. Cell Biol. 1989. V. 5. P. 341. https://doi.org/10.1146/annurev.cb.05.110189.002013
Satyanarayana A., Kaldis P. Mammalian cell-cycle regulation: several Cdks, numerous cyclins and diverse compensatory mechanisms // Oncogene. 2009. V. 28. P. 2925. https://doi.org/10.1038/onc.2009.170
Van’t Hof J. The regulation of cell division in higher plants // Brookhaven Symp. Biol. 1973. V. 25. P. 152.
Polyn S., Willems A., De Veylder L. Cell cycle entry, maintenance, and exit during plant development // Curr. Opin. Plant Biol. 2015. V. 23. P. 1. https://doi.org/10.1016/j.pbi.2014.09.012
Scholes D.R., Paige K.N. Plasticity in ploidy: a generalized response to stress // Trends Plant Sci. 2015. V. 20. P. 165. https://doi.org/10.1016/j.tplants.2014.11.007
Carneiro A.K., Montessoro P.D.F., Fusaro A.F., Araújo B.G., Hemerly A.S. Plant CDKs – driving the cell cycle through climate change // Plants. 2021. V. 10. 1804. https://doi.org/10.3390/plants10091804
Sablowski R., Gutierrez C. Cycling in a crowd: coordination of plant cell division, growth, and cell fate // Plant Cell. 2022. V. 34. P. 193. https://doi.org/10.1093/plcell/koab222
Blomme J., Inzé D., Gonzalez N. The cell-cycle interactome: a source of growth regulators? // J. Exp. Bot. 2014. V. 65. P. 2715. https://doi.org/10.1093/jxb/ert388
Van Leene J., Hollunder J., Eeckhout D., Persiau G., Van De Slijke E., Stals H., Van Isterdael G., Verkest A., Neirynck S., Buffel Y., De Bodt S., Maere S., Laukens K., Pharazyn A., Ferreira P.C.G., et al. Targeted interactomics reveals a complex core cell cycle machinery in Arabidopsis thaliana // Mol. Syst. Biol. 2010. V. 6. 397. https://doi.org/10.1038/msb.2010.53
Jia R.-D., Guo C.-C., Xu G.-X., Shan H.-Y., Kong H.-Z. Evolution of the cyclin gene family in plants // J. Syst. Evol. 2014. V. 52. P. 651. https://doi.org/10.1111/jse.12112
Vandepoele K., Raes J., De Veylder L., Rouzé P., Rombauts S., Inzé D. Genome-wide analysis of core cell cycle genes in Arabidopsis // Plant Cell. 2002. V. 14. P. 903. https://doi.org/10.1105/tpc.010445
Desvoyes B., De Mendoza A., Ruiz-Trillo I., Gutierrez C. Novel roles of plant RETINOBLASTOMA-RELATED (RBR) protein in cell proliferation and asymmetric cell division // J. Exp. Bot. 2014. V. 65. P. 2657. https://doi.org/10.1093/jxb/ert411
Desvoyes B., Gutierrez C. Roles of plant retinoblastoma protein: cell cycle and beyond // EMBO J. 2020. V. 39. e105802. https://doi.org/10.15252/embj.2020105802
Romeiro Motta M., Zhao X.A., Pastuglia M., Belcram K., Roodbarkelari F., Komaki M., Harashima H., Komaki S., Kumar M., Bulankova P., Heese M., Riha K., Bouchez D., Schnittger A. B1-type cyclins control microtubule organization during cell division in Arabidopsis // EMB-O Rep. 2022. V. 23. e53995. https://doi.org/10.15252/embr.202153995
Menges M., De Jager S.M., Gruissem W., Murray J.A.H. Global analysis of the core cell cycle regulators of Arabidopsis identifies novel genes, reveals multiple and highly specific profiles of expression and provides a coherent model for plant cell cycle control // Plant J. 2005. V. 41. P. 546. https://doi.org/10.1111/j.1365-313X.2004.02319.x
Ito M. Expression of mitotic cyclins in higher plants: transcriptional and proteolytic regulation // Plant Biotechnol. Rep. 2014. V. 8. P. 9. https://doi.org/10.1007/s11816-013-0297-9
Araki S., Ito M., Soyano T., Nishihama R., Machida Y. Mitotic cyclins stimulate the activity of c-Myb-like factors for transactivation of G2/M phase-specific genes in tobacco // J. Biol. Chem. 2004. V. 279. P. 32979. https://doi.org/10.1074/jbc.M403171200
Umeda M., Shimotohno A., Yamaguchi M. Control of cell division and transcription by cyclin-dependent kinase-activating kinases in plants // Plant Cell Physiol. 2005. V. 46. P. 1437. https://doi.org/10.1093/pcp/pci170
Pedroza-Garcia J.A., Xiang Y., De Veylder L. Cell cycle checkpoint control in response to DNA damage by environmental stresses // Plant J. 2022. V. 109. P. 490. https://doi.org/10.1111/tpj.15567
De Veylder L., Larkin J.C., Schnittger A. Molecular control and function of endoreplication in development and physiology // Trends Plant Sci. 2011. V. 16. P. 624. https://doi.org/10.1016/j.tplants.2011.07.001
De Veylder L., Beeckman T., Beemster G.T., Krols L., Terras F., Landrieu I., Van Der Schueren E., Maes S., Naudts M., Inzé D. Functional analysis of cyclin-dependent kinase inhibitors of Arabidopsis // Plant Cell. 2001. V. 13. P. 1653. https://doi.org/10.1105/tpc.010087
Churchman M.L., Brown M.L., Kato N., Kirik V., Hülskamp M., Inzé D., De Veylder L., Walker J.D., Zheng Z., Oppenheimer D.G., Gwin T., Churchman J., Larkin J.C. SIAMESE, a plant-specific cell cycle regulator, controls endoreplication onset in Arabidopsis thaliana // Plant Cell. 2006. V. 18. P. 3145. https://doi.org/10.1105/tpc.106.044834
Peres A., Churchman M.L., Hariharan S., Himanen K., Verkest A., Vandepoele K., Magyar Z., Hatzfeld Y., Van Der Schueren E., Beemster G.T.S., Frankard V., Larkin J.C., Inzé D., De Veylder L. Novel plant-specific cyclin-dependent kinase inhibitors induced by biotic and abiotic stresses // J. Biol. Chem. 2007. V. 282. P. 25588. https://doi.org/10.1074/jbc.M703326200
Han S.K., Herrmann A., Yang J., Iwasaki R., Sakamoto T., Desvoyes B., Kimura S., Gutierrez C., Kim E.-D., Torii K.U. Deceleration of the cell cycle underpins a switch from proliferative to terminal divisions in plant stomatal lineage // Dev. Cell. 2022. V. 57. P. 569. https://doi.org/10.1016/j.devcel.2022.01.014
Shoaib M., Nair N., Sørensen C.S. Chromatin landscaping at mitotic exit orchestrates genome function // Front. Genet. 2020. V. 11. 103. https://doi.org/10.3389/fgene.2020.00103
Buschmann H., Müller S. Update on plant cytokinesis: rule and divide // Curr. Opin. Plant Biol. 2019. V. 52. P. 97. https://doi.org/10.1016/j.pbi.2019.07.003
Jakoby M., Schnittger A. Cell cycle and differentiation // Curr. Opin. Plant Biol. 2004. V. 7. P. 661. https://doi.org/10.1016/j.pbi.2004.09.015
Maluszynska J., Kolano B., Sas-Nowosielska H. Endopolyploidy in plants // Plant Genome Diversity. V. 2 / Eds. J. Greilhuber et al. Springer. 2013. P. 99. https://doi.org/10.1007/978-3-7091-1160-4_7
Breuer C., Braidwood L., Sugimoto K. Endocycling in the path of plant development // Curr. Opin. Plant Bio-l. 2014. V. 17. P. 78. https://doi.org/10.1016/j.pbi.2013.11.007
Jiang S., Wei J., Li N., Wang Z., Zhang Y., Xu R., Zhou L., Huang X., Wang L., Guo S., Wang Y., Song C.-P., Qian W., Li Y. The UBP14-CDKB1;1-CDKG2 cascade controls endoreduplication and cell growth in Arabidopsis // Plant Cell. 2022. V. 34. P. 1308. https://doi.org/10.1093/plcell/koac002
Duan S., Hu L., Dong B., Jin H.L., Wang H.B. Signaling from plastid genome stability modulates endoreplication and cell cycle during plant development // Cell Rep. 2020. V. 32. 108019. https://doi.org/10.1016/j.celrep.2020.108019
Mahapatra K., Roy S. SOG1 transcription factor promotes the onset of endoreduplication under salinity stress in Arabidopsis // Sci. Rep. 2021. V. 11. 11659. https://doi.org/10.1038/s41598-021-91293-1
Barow M., Meister A. Endopolyploidy in seed plants is differently correlated to systematics, organ, life strategy and genome size // Plant Cell Environ. 2003. V. 26. P. 571. https://doi.org/10.1046/j.1365-3040.2003.00988.x
Melaragno J., Mehrotra B., Coleman A. Relationship between endopolyploidy and cell size in epidermal tissue of Arabidopsis // Plant Cell. 1993. V. 5. P. 1661. https://doi.org/10.1105/tpc.5.11.1661
Sugimoto-Shirasu K., Roberts K. “Big it up”: endoreduplication and cell-size control in plants // Curr. Opin. Plant Biol. 2003. V. 6. P. 544. https://doi.org/10.1016/j.pbi.2003.09.009
Granier C., Cookson S.J., Tardieu F., Muller B. Cell cycle and environmental stresses // Cell cycle control and plant development. Annu. Plant Rev. V. 32 / Ed. D. Inzé. Blackwell. 2007. P. 335. https://doi.org/10.1002/9781119312994.apr0346
Moreno S., Canales J., Hong L., Robinson D., Roeder A.H., Gutiérrez R.A. Nitrate defines shoot size through compensatory roles for endoreplication and cell division in Arabidopsis thaliana // Curr. Biol. 2020. V. 30. P. 1988. https://doi.org/10.1016/j.cub.2020.03.036
Tenorio Berrío R., Nelissen H., Inzé D., Dubois M. Increasing yield on dry fields: molecular pathways with growing potential // Plant J. 2022. V. 109. P. 323. https://doi.org/10.1111/tpj.15550
Kinsman E.A., Lewis C., Davies M.S., Young J.E., Francis D., Vilhar B., Ougham H.J. Elevated CO2 stimulates cells to divide in grass meristems: a differential effect in two natural populations of Dactylis glomerata // Plant Cell Environ. 1997. V. 20. P. 1309. https://doi.org/10.1046/j.1365-3040.1997.d01-21.x
Taylor G., Tricker P.J., Zhang F.Z., Alston V.J., Miglietta F., Kuzminsky E. Spatial and temporal effects of free-air CO2 enrichment (POPFACE) on leaf growth, cell expansion, and cell production in a closed canopy of poplar // Plant Physiol. 2003. V. 131. P. 177. https://doi.org/10.1104/pp.011296
Maksymowych R. Analysis of leaf development // Developmental and cell biology / Eds. M. Abercrombie et al. Cambridge University Press. 1973. 109 p.
López-Juez E., Dillon E., Magyar Z., Khan S., Hazeldine S., de Jager S.M., Murray J.A.H., Beemster G.T.S., Bögre L., Shanahan H. Distinct light-initiated gene expression and cell cycle programs in the shoot apex and cotyledons of Arabidopsis // Plant Cell. 2008. V. 20. P. 947. https://doi.org/10.1105/tpc.107.057075
Bao L., Inoue N., Ishikawa M., Gotoh E., Teh O.-K., Higa T., Morimoto T., Ginanjar E.F., Harashima H., Noda N., Watahiki M., Hiwatashi Y., Sekine M., Hasebe M., Wada M., Fujita T. A PSTAIRE-type cyclin-dependent kinase controls light responses in land plants // Sci. Adv. 2022. V. 8. eabk2116. https://doi.org/10.1126/sciadv.abk2116
Fung-Uceda J., Lee K., Seo P.J., Polyn S., De Veylder L., Mas P. The circadian clock sets the time of DNA replication licensing to regulate growth in Arabidopsis // Dev. Cell. 2018. V. 45. P. 101. https://doi.org/10.1016/j.devcel.2018.02.022
Nishihama R., Kohchi T. Evolutionary insights into photoregulation of the cell cycle in the green lineage // Curr. Opin. Plant Biol. 2013. V. 16. P. 630. https://doi.org/10.1016/j.pbi.2013.07.006
Beel B., Prager K., Spexard M., Sasso S., Weiss D., Müller N., Heinnickel M., Dewez D., Ikoma D., Grossman A.R., Kottke T., Mittag M. A flavin binding cryptochrome photoreceptor responds to both blue and red light in Chlamydomonas reinhardtii // Plant Cell. 2012. V. 24. P. 2992. https://doi.org/10.1105/tpc.112.098947
Qiao F., Petrasek J., Nick P. Light can rescue auxin-dependent synchrony of cell division in a tobacco cell line // J. Exp. Bot. 2010. V. 61. P. 503. https://doi.org/10.1093/jxb/erp319
Okello R.C.O., de Visser P.H.B., Heuvelink E., Marcelis L.F.M., Struik P.C. Light mediated regulation of cell division, endoreduplication and cell expansion // Environ. Exp. Bot. 2016. V. 121. P. 39. https://doi.org/10.1016/j.envexpbot.2015.04.003
Granier C., Tardieu F. Is thermal time adequate for expressing the effects of temperature on sunflower leaf development? // Plant Cell Environ. 1998. V. 21. P. 695. https://doi.org/10.1046/j.1365-3040.1998.00319.x
Grif V.G., Ivanov V.B., Machs E.M. Cell cycle and its parameters in flowering plants // Tsitologiia. 2002. V. 44. P. 936.
Thimann K.V. Antagonisms and similarities between cytokinins, abscisic acid and auxin (mini review) // Physiology and biochemistry of cytokinins in plants / Eds. M. Kaminek et al. SPB Academic Publishing. 1992. P. 395.
Van de Poel B., Smet D., Van Der Straeten D. Ethylene and hormonal cross talk in vegetative growth and development // Plant Physiol. 2015. V. 169. P. 61. https://doi.org/10.1104/pp.15.00724
Zluhan-Martínez E., López-Ruíz B.A., García-Gómez M.L., García-Ponce B., de la Paz Sánchez M., Álvarez-Buylla E.R., Garay-Arroyo A. Integrative roles of phytohormones on cell proliferation, elongation and differentiation in the Arabidopsis thaliana primary root // Front. Plant Sci. 2021. V. 12. 659155. https://doi.org/10.3389/fpls.2021.659155
Jiang K., Guo H., Zhai J. Interplay of phytohormones and epigenetic regulation: a recipe for plant development and plasticity // J. Integr. Plant Biol. 2022. https://doi.org/10.1111/jipb.13384
Péret B., De Rybel B., Casimiro I., Benková E., Swarup R., Laplaze L., Beeckman T., Bennett M.J. Arabidopsis lateral root development: an emerging story // Trends Plant Sci. 2009. V. 14. P. 399. https://doi.org/10.1016/j.tplants.2009.05.002
Hemerly A.S., Ferreira P., de Almeida Engler J., Van Montagu M., Engler G., Inzé D. cdc2a expression in Arabidopsis is linked with competence for cell division // Plant Cell. 1993. V. 5. P. 1711. https://doi.org/10.1105/tpc.5.12.1711
Brumos J., Robles L.M., Yun J., Vu T.C., Jackson S., Alonso J.M., Stepanova A.N. Local auxin biosynthesis is a key regulator of plant development // Dev. Cell. 2018. V. 47. P. 306. https://doi.org/10.1016/j.devcel.2018.09.022
Ivanov V.B., Filin A.N. Cytokinins regulate root growth through its action on meristematic cell proliferation but not on the transition to differentiation // Funct. Plant Biol. 2017. V. 45. P. 215. https://doi.org/10.1071/FP16340
Schaller G.E., Street I.H., Kieber J.J. Cytokinin and the cell cycle // Curr. Opin. Plant Biol. 2014. V. 21. P. 7. https://doi.org/10.1016/j.pbi.2014.05.015
Pasternak T., Miskolczi P., Ayaydin F., Mészáros T., Dudits D., Fehér A. Exogenous auxin and cytokinin dependent activation of CDKs and cell division in leaf protoplast-derived cells of alfalfa // Plant Growth Regul. 2000. V. 32. P. 129. https://doi.org/10.1023/A:1010793226030
Richard C., Lescot M., Inzé D., De Veylder L. Effect of auxin, cytokinin, and sucrose on cell cycle gene expression in Arabidopsis thaliana cell suspension cultures // Plant Cell. Tissue Organ Cult. 2002. V. 69. P. 167. https://doi.org/10.1023/A:1015241709145
Mészáros T., Miskolczi P., Ayaydin F., Pettkó-Szandtner A., Peres A., Magyar Z., Horváth G.V., Bakó L., Fehér A., Dudits D. Multiple cyclin-dependent kinase complexes and phosphatases control G2/M progression in alfalfa cells // Plant Mol. Biol. 2000. V. 43. P. 595. https://doi.org/10.1023/a:1006412413671
Hartig K., Beck E. Endogenous cytokinin oscillations control cell cycle progression of tobacco BY-2 cells // Plant Biol. 2005. V. 7. P. 33. https://doi.org/10.1055/s-2004-830474
Riou-Khamlichi C., Huntley R., Jacqmard A., Murray J.A. Cytokinin activation of Arabidopsis cell division through a D-type cyclin // Science. 1999. V. 283. P. 1541. https://doi.org/10.1126/science.283.5407.1541
Menges M., Samland A.K., Planchais S., Murray J.A.H. The D-Type Cyclin CYCD3;1 Is Limiting for the G1-to-S-Phase Transition in Arabidopsis // Plant Cell. 2006. V. 18. P. 893. https://doi.org/10.1105/tpc.105.039636
Chen C.C., Fu S.F., Lee Y.I., Lin C.Y., Lin W.C., Huang H.J. Transcriptome analysis of age-related gain of callus-forming capacity in Arabidopsis hypocotyls // Plant Cell Physiol. 2012. V. 53. P. 1457. https://doi.org/10.1093/pcp/pcs090
Cho H.-J., Kwon H.-K., Wang M.-H. Expression of Kip-related protein 4 gene (KRP4) in response to auxin and cytokinin during growth of Arabidopsis thaliana // BMB Rep. 2010. V. 43. P. 273. https://doi.org/10.5483/bmbrep.2010.43.4.273
Magyar Z., De Veylder L., Atanassova A., Bakó L., Inzé D., Bögre L. The role of the Arabidopsis E2FB transcription factor in regulating auxin-dependent cell division // Plant Cell. 2005. V. 17. P. 2527. https://doi.org/10.1105/tpc.105.033761
Jurado S., Abraham Z., Manzano C., López-Torrejón G., Pacios L.F., Del Pozo J.C. The Arabidopsis cell cycle F‑box protein SKP2A binds to auxin // Plant Cell. 2010. V. 22. P. 3891. https://doi.org/10.1105/tpc.110.078972
Del Pozo J.C., Manzano C. Auxin and the ubiquitin pathway. Two players-one target: the cell cycle in action // J. Exp. Bot. 2014. V. 65. P. 2617. https://doi.org/10.1093/jxb/ert363
Sauer M., Kleine-Vehn J. AUXIN BINDING PROTEIN1: the outsider // Plant Cell. 2011. V. 23. P. 2033. https://doi.org/10.1105/tpc.111.087064
Huang R., Zheng R., He J., Zhou Z., Wang J., Xiong Y., Xu T. Noncanonical auxin signaling regulates cell division pattern during lateral root development // Proc. Natl. Acad. Sci. USA. 2019. V. 116. P. 21285. https://doi.org/10.1073/pnas.1910916116
Takahashi N., Kajihara T., Okamura C., Kim Y., Katagiri Y., Okushima Y., Matsunaga S., Hwang I., Umeda M. Cytokinins control endocycle onset by promoting the expression of an APC/C activator in Arabidopsis roots // Curr. Biol. 2013. V. 23. P. 1812. https://doi.org/10.1016/j.cub.2013.07.051
Yang W., Cortijo S., Korsbo N., Roszak P., Schiessl K., Gurzadyan A., Wightman R., Jönsson H., Meyerowitz E. Molecular mechanism of cytokinin-activated cell division in Arabidopsis // Science. 2021. V. 371. P. 1350. https://doi.org/10.1126/science.abe2305
Park J., Lee S., Park G., Cho H., Choi D., Umeda M., Choi Y., Hwang D., Hwang I. CYTOKININ-RESPONSIVE GROWTH REGULATOR regulates cell expansion and cytokinin-mediated cell cycle progression // Plant Physiol. 2021. V. 186. P. 1734. https://doi.org/10.1093/plphys/kiab180
Humplík J.F., Bergougnoux V., Van Volkenburgh E. To stimulate or inhibit? That is the question for the function of abscisic acid // Trends Plant Sci. 2017. V. 22. P. 830. https://doi.org/10.1016/j.tplants.2017.07.009
Sun L.R., Wang Y.B., He S.B., Hao F.S. Mechanisms for abscisic acid inhibition of primary root growth // Plant Signal. Behav. 2018. V. 13. e1500069. https://doi.org/10.1080/15592324.2018.1500069
Tanaka Y., Nose T., Jikumaru Y., Kamiya Y. ABA inhibits entry into stomatal-lineage development in Arabidopsis leaves // Plant J. 2013. V. 74. P. 448. https://doi.org/10.1111/tpj.12136
Xie Q., Essemine J., Pang X., Chen H., Cai W. Exogenous application of abscisic acid to shoots promotes primary root cell division and elongation // Plant Sci. 2020. V. 292. 110385. https://doi.org/10.1016/j.plantsci.2019.110385
Luo X., Xu J., Zheng C., Yang Y., Wang L., Zhang R., Ren X., Wei S., Aziz U., Du J., Liu W., Tan W., Shu K. Abscisic acid inhibits primary root growth by impairing ABI4-mediated cell cycle and auxin biosynthesis // Plant Physiol. 2022. https://doi.org/10.1093/plphys/kiac407
Novikova G.V., Stepanchenko N.S., Zorina A.A., Nosov A.V., Rakitin V.Y., Moshkov I.E., Los D.A. Coupling of cell division and differentiation in Arabidopsis thaliana cultured cells with interaction of ethylene and ABA signaling pathways // Life. 2020. V. 10. 15. https://doi.org/10.3390/life10020015
Shtin M., Dello Ioio R., Del Bianco M. It’s time for a change: the role of gibberellin in root meristem development // Front. Plant Sci. 2022. V. 13. 882517 https://doi.org/10.3389/fpls.2022.882517
Claeys H., De Bodt S., Inzé D. Gibberellins and DELLAs: central nodes in growth regulatory networks // Trends Plant Sci. 2014. V. 19. P. 231. https://doi.org/10.1016/j.tplants.2013.10.001
Oh M.-H., Honey S.H., Tax F.E. The control of cell expansion, cell division, and vascular development by brassinosteroids: a historical perspective // Int. J. Mol. Sci. 2020. V. 21. 1743. https://doi.org/10.3390/ijms21051743
Hu Y., Bao F., Li J. Promotive effect of brassinosteroids on cell division involves a distinct CycD3-induction pathway in Arabidopsis // Plant J. 2000. V. 24. P. 693. https://doi.org/10.1046/j.1365-313x.2000.00915.x
Zhiponova M.K., Vanhoutte I., Boudolf V., Betti C., Dhondt S., Coppens F., Mylle E., Maes S., González-García M., Caño-Delgado A.I., Inzé D., Beemster G.T.S., De Veylder L., Russinova E. Brassinosteroid production and signaling differentially control cell division and expansion in the leaf // New Phytol. 2013. V. 197. P. 490. https://doi.org/10.1111/nph.12036
Apelbaum A., Burg S.P. Effect of ethylene on cell division and deoxyribonucleic acid synthesis in Pisum sativum // Plant Physiol. 1972. V. 50. P. 117. https://doi.org/10.1104/pp.50.1.117
Herbert R.J., Vilhar B., Evett C., Orchard C.B., Rogers H.J., Davies M.S., Francis D. Ethylene induces cell death at particular phases of the cell cycle in the tobacco TBY-2 cell line // J. Exp. Bot. 2001. V. 52. P. 1615. https://doi.org/10.1093/jxb/52.361.1615
Street I.H., Aman S., Zubo Y., Ramzan A., Wang X., Shakeel S.N., Kieber J.J., Schaller G.E. Ethylene inhibits cell proliferation of the Arabidopsis root meristem // Plant Physiol. 2015. V. 169. P. 338. https://doi.org/10.1104/pp.15.00415
Stoynova-Bakalova E., Bakalov D.V., Baskin T.I. Ethylene represses the promoting influence of cytokinin on cell division and expansion of cotyledons in etiolated Arabidopsis thaliana seedlings // PeerJ. 2022. V. 10. e14315. https://doi.org/10.7717/peerj.14315
Dan H., Imaseki H., Wasteneys G.O., Kazama H. Ethylene stimulates endoreduplication but inhibits cytokinesis in cucumber hypocotyl epidermis // Plant Physiol. 2003. V. 133. P. 1726. https://doi.org/10.1104/pp.103.025783
Ortega-Martínez O., Pernas M., Carol R.J., Dolan L. Ethylene modulates stem cell division in the Arabidopsis thaliana root // Science. 2007. V. 317. P. 507. https://doi.org/10.1126/science.1143409
Kazama H., Dan H., Imaseki H., Wasteneys G.O. Transient exposure to ethylene stimulates cell division and alters the fate and polarity of hypocotyl epidermal cells // Plant Physiol. 2004. V. 134. P. 1614. https://doi.org/10.1104/pp.103.031088
Love J., Björklund S., Vahala J., Hertzberg M., Kangasjärvi J., Sundberg B. Ethylene is an endogenous stimulator of cell division in the cambial meristem of Populus // Proc. Natl. Acad. Sci. USA. 2009. V. 106. P. 5984. https://doi.org/10.1073/pnas.0811660106
Bystrova E.I., Zhukovskaya N.V., Rakitin V.J. Ivanov V.B. Role of ethylene in activation of cell division in quiescent center of excised maize roots // Russ. J. Dev. Biol. 2015. V. 46. P. 60. https://doi.org/10.1134/S1062360415020034
Etchells J.P., Provost C.M., Turner S.R. Plant vascular cell division is maintained by an interaction between PXY and ethylene signaling // PLoS Genet. 2012. V. 8. e1002997. https://doi.org/10.1371/journal.pgen.1002997
Fomenkov A.A., Nosov A.V., Rakitin V.Y., Mamaeva A.S., Novikova G.V. Cytophysiological characteristics of Arabidopsis thaliana cultivated cells with disable perception of ethylene signal by the ETR1 receptor // Russ. J. Plant Physiol. 2014. V. 61. P. 598. https://doi.org/10.1134/S1021443714050070
Fomenkov A.A., Nosov A.V., Rakitin V.Y., Sukhanova E.S., Mamaeva A.S., Sobol’kova G.I., Nosov A.M., Novikova G.V. Ethylene in the proliferation of cultured plant cells: regulating or just going along? // Russ. J. Plant Physiol. 2015. V. 62. P. 815. https://doi.org/10.1134/S1021443715060059
Komaki S., Sugimoto K. Control of the plant cell cycle by developmental and environmental cues // Plant Cell Physiol. 2012. V. 53. P. 953. https://doi.org/10.1093/pcp/pcs070
Velappan Y., Signorelli S., Considine M.J. Cell cycle arrest in plants: what distinguishes quiescence, dormancy and differentiated G1? // Ann. Bot. 2017. V. 120. P. 495. https://doi.org/10.1093/aob/mcx082
Gutierrez C. The Arabidopsis cell division cycle // Arabidopsis Book. 2009. V. 7. e0120. https://doi.org/10.1199/tab.0120
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