Systemic control of cell division and endoreduplication by NAA and BAP by modulating CDKs in root tip cells of Allium cepa

BioMed Research International

Volumn 2014, Issue , 2014, Pages

  Tank, Jigna G ^a   Thaker, Vrinda S ^a  

^a SAURASHTRA UNIVERSITY   (India)

Author keywords

[No Author keywords available]

Indexed keywords

AUXIN; COLCHICINE; CYCLIN DEPENDENT KINASE; CYTOKININ; PLANT DNA; PLANT RNA; INDOLEACETIC ACID DERIVATIVE; PHYTOHORMONE;

AGAR GEL ELECTROPHORESIS; ANAPHASE; ARTICLE; C TUMOR; CARCINOGENESIS; CDKA 1 GENE; CDKA 2 GENE; CDKB2 1 GENE; CDKB2 2 GENE; CDKD1 1 GENE; CDKD1 3 GENE; CELL DIVISION; CELL ELONGATION; CELL SIZE; CELL STRUCTURE; CONTROLLED STUDY; CYCLIN DEPENDENT KINASE GENE; CYTOKINESIS; CYTOLOGY; DNA ISOLATION; DNA REPLICATION; DOWN REGULATION; ENDOREDUPLICATION; G2 PHASE CELL CYCLE CHECKPOINT; GENE EXPRESSION; M PHASE CELL CYCLE CHECKPOINT; MERISTEMATIC CELL; METAPHASE; NONHUMAN; NUCLEAR SIZE; ONION; PLANT CELL; PLANT GENE; PLANT ROOT; PLANT TUMOR; PROPHASE; RNA ISOLATION; ROOT CELL; TELOPHASE; VEGETATIVE GROWTH; BIOSYNTHESIS; DRUG EFFECTS; GENE EXPRESSION REGULATION; GENETICS; GROWTH, DEVELOPMENT AND AGING; MERISTEM; METABOLISM;

CELL DIVISION; CYTOKININS; ENDOREDUPLICATION; GENE EXPRESSION REGULATION, PLANT; INDOLEACETIC ACIDS; MERISTEM; ONIONS; PLANT GROWTH REGULATORS; PLANT ROOTS;

EID: 84902138435     PISSN: 23146133     EISSN: 23146141     Source Type: Journal    
DOI: 10.1155/2014/453707     Document Type: Article

References (60)

1. Jasinski S., Riou-Khamlichi C., Roche O., Perennes C., Bergounioux C., Glab N., The CDK inhibitor NtKIS1a is involved in plant development, endoreduplication and restores normal development of cyclin D3;1-overexpressing plants. Journal of Cell Science 2002 115 5 973 982 2-s2.0-0036500183 (Pubitemid 34257382)
2. Lammens T., Boudolf V., Kheibarshekan L., Zalmas L. P., Gaamouche T., Maes S., Vanstraelen M., Kondorosi E., La Thangue N. B., Govaerts W., Inzé D., de Veylder L., Atypical E2F activity restrains APC/CCCS52A2 function obligatory for endocycle onset. Proceedings of the National Academy of Sciences of the United States of America 2008 105 38 14721 14726 2-s2.0-55749101203 10.1073/pnas.0806510105
3. Sanchez M. D. L. P., Caro E., Desvoyes B., Ramirez-Parra E., Gutierrez C., Chromatin dynamics during the plant cell cycle. Seminars in Cell and Developmental Biology 2008 19 6 537 546 2-s2.0-54549104349 10.1016/j.semcdb. 2008.07.014
4. Nieuwland J., Scofield S., Murray J. A. H., Control of division and differentiation of plant stem cells and their derivatives. Seminars in Cell and Developmental Biology 2009 20 9 1134 1142 2-s2.0-70449635122 10.1016/j.semcdb.2009.09.011
5. Tominaga R., Iwata M., Sano R., Inoue K., Okada K., Wada T., Arabidopsis CAPRICE-LIKE MYB 3 (CPL3) controls endoreduplication and flowering development in addition to trichome and root hair formation. Development 2008 135 7 1335 1345 2-s2.0-43049104534 10.1242/dev.017947 (Pubitemid 351622477)
6. Larkins B. A., Dilkes B. P., Dante R. A., Coelho C. M., Woo Y.-M., Liu Y., Investigating the hows and whys of DNA endoreduplication. Journal of Experimental Botany 2001 52 355 183 192 2-s2.0-0035058313 (Pubitemid 32337455)
7. Jakoby M., Schnittger A., Cell cycle and differentiation. Current Opinion in Plant Biology 2004 7 6 661 669 2-s2.0-6044220205 10.1016/j.pbi.2004.09.015 (Pubitemid 39379509)
8. Lee H. O., Davidson J. M., Duronio R. J., Endoreplication: polyploidy with purpose. Genes and Development 2009 23 21 2461 2477 2-s2.0-70350629054 10.1101/gad.1829209
9. Gendreau E., Höfte H., Grandjean O., Brown S., Traas J., Phytochrome controls the number of endoreduplication cycles in the Arabidopsis thaliana hypocotyl. The Plant Journal 1998 13 2 221 230 2-s2.0-0031905339 10.1046/j.1365-313X.1998.00030.x (Pubitemid 28073327)
10. Hülskamp M., Misera S., Jürgens: G., Genetic dissection of trichome development in Arabidopsis. Cell 1994 76 555 566 10.1016/0092-8674(94) 90118-X (Pubitemid 24064175)
11. Melaragno J. E., Mehrotra B., Coleman A. W., Relationship between endopolyploidy and cell size in epidermal tissue of Arabidopsis. The Plant Cell 1993 5 11 1661 1668 2-s2.0-0027145426 10.1105/tpc.5.11.1661 (Pubitemid 2021821)
12. Kowles R. V., McMullen M. D., Yerk G., Phillips R. L., Kraemer S., Srienc F., Endosperm mitotic activity and endoreduplication in maize affected by defective kernel mutations. Genome 1992 35 1 68 77 2-s2.0-0026579218
13. Inzé D., de Veylder L., Cell cycle regulation in plant development. Annual Review of Genetics 2006 40 77 105 2-s2.0-33845634412 10.1146/annurev.genet.40.110405.090431 (Pubitemid 44956780)
14. Beemster G. T. S., de Vusser K., de Tavernier E., de Bock K., Inzé D., Variation in growth rate between Arabidopsis ecotypes is correlated with cell division and a-type cyclin-dependent kinase activity. Plant Physiology 2002 129 2 854 864 2-s2.0-0035983674 10.1104/pp.002923 (Pubitemid 34689165)
15. Wolff J., Knipling L., Sackett D. L., Charge shielding and the "paradoxical" stimulation of tubulin polymerization by guanidine hydrochloride. Biochemistry 1996 35 5910 5920 10.1021/bi9527395 (Pubitemid 26143685)
16. Screpanti E., Santaguida S., Nguyen T., Silvestri R., Gussio R., Musacchio A., Hamel E., de Wulf P., A screen for kinetochore-microtubule interaction inhibitors identifies novel antitubulin compounds. PLoS ONE 2010 5 7 2-s2.0-77955407826 10.1371/journal.pone.0011603 e11603
17. Caperta A. D., Delgado M., Ressurreição F., Meister A., Jones R. N., Viegas W., Houben A., Colchicine-induced polyploidization depends on tubulin polymerization in c-metaphase cells. Protoplasma 2006 227 2-4 147 153 2-s2.0-33744466290 10.1007/s00709-005-0137-z (Pubitemid 43807447)
18. Weingartner M., Binarova P., Drykova D., Schweighofer A., David J.-P., Heberle-Bors E., Doonan J., Bögre L., Dynamic recruitment of Cdc2 to specific microtubule structures during mitosis. The Plant Cell 2001 13 8 1929 1943 2-s2.0-0034877395 10.1105/tpc.13.8.1929 (Pubitemid 32781999)
19. Sadhan K. C., Sibdas G., Monoclonal antibody raised against human mitotic cyclin B1, identifies cyclin B-like mitotic proteins in synchronized onion (Allium cepa L.) root meristem. Cell Biology International 1997 21 3 159 166 10.1006/cbir.1996.0121 (Pubitemid 27202299)
20. Yamaguchi M., Kato H., Yoshida S., Yamamura S., Uchimiya H., Umeda M., Control of in vitro organogenesis by cyclin-dependent kinase activities in plants. Proceedings of the National Academy of Sciences of the United States of America 2003 100 13 8019 8023 2-s2.0-0037595619 10.1073/pnas.1332637100 (Pubitemid 36760087)
21. 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 Regulation 2000 32 2-3 129 141 2-s2.0-0034461074 10.1023/A:1010793226030 (Pubitemid 32241277)
22. Haberer G., Kieber J. J., Cytokinins. New insights into a classic phytohormone. Plant Physiology 2002 128 2 354 362 2-s2.0-0036008891 10.1104/pp.128.2.354 (Pubitemid 34190852)
23. Stals H., Inzé D., When plant cells decide to divide. Trends in Plant Science 2001 6 8 359 364 2-s2.0-0035213401 10.1016/S1360-1385(01)02016-7 (Pubitemid 33141648)
24. Pines J., Cyclins and cyclin-dependent kinases: a biochemical view. Biochemical Journal 1995 308 3 697 711 2-s2.0-0029000579
25. Tank J. G., Thaker V. S., Changes in DNA and RNA level with endoreduplication can be determined using α -naphthyl red dye. Cibtech Journal of Bio-Protocols 2012 1 1 23 31
26. Umeda M., Shimotohno A., Yamaguchi M., Control of cell division and transcription by cyclin-dependent kinase-activating kinases in plants. Plant and Cell Physiology 2005 46 9 1437 1442 2-s2.0-26444470797 10.1093/pcp/pci170 (Pubitemid 41436585)
27. Joubès J., Chevalier C., Dudits D., Heberle-Bors E., Inzé D., Umeda M., Renaudin J.-P., CDK-related protein kinases in plants. Plant Molecular Biology 2000 43 5-6 607 620 2-s2.0-0033776984
28. Joubès J., Lemaire-Chamley M., Delmas F., Walter J., Hernould M., Mouras A., Raymond P., Chevalier C., A new C-type cyclin-dependent kinase from tomato expressed in dividing tissues does not interact with mitotic and G1 cyclins. Plant Physiology 2001 126 4 1403 1415 2-s2.0-0034877049 10.1104/pp.126.4.1403 (Pubitemid 32752370)
29. Colasanti J., Tyers M., Sundaresan V., Isolation and characterization of cDNA clones encoding a functional p34(cdc2) homologue from Zea mays. Proceedings of the National Academy of Sciences of the United States of America 1991 88 8 3377 3381 2-s2.0-0026356177 (Pubitemid 21916624)
30. Miao G.-H., Hong Z., Verma D. P. S., Two functional soybean genes encoding p34(cdc2) protein kinases are regulated by different plant developmental pathways. Proceedings of the National Academy of Sciences of the United States of America 1993 90 3 943 947 2-s2.0-0027446265 10.1073/pnas.90.3.943 (Pubitemid 23053926)
31. Francis D., Sorrell D. A., The interface between the cell cycle and plant growth regulators: a mini review. Plant Growth Regulation 2001 33 1 1 12 2-s2.0-0035057951 10.1023/A:1010762111585 (Pubitemid 32320055)
32. Mironov V., de Veylder L., van Montagu M., Inzé D., Cyclin-dependent kinases and cell division in plants-the nexus. The Plant Cell 1999 11 4 509 521 2-s2.0-0032697004 10.1105/tpc.11.4.509
33. Zhiponova M. K., Pettkó-Szandtner A., Stelkovics É., Neer Z., Bottka S., Krenács T., Dudits D., Fehér A., Szilák L., Mitosis-specific promoter of the alfalfa cyclin-dependent kinase gene (Medsa;CDKB2;1) is activated by wounding and ethylene in a non-cell division-dependent manner. Plant Physiology 2006 140 2 693 703 2-s2.0-33646827878 10.1104/pp.105.072173 (Pubitemid 43956288)
34. Kono A., Umeda-Hara C., Lee J., Ito M., Uchimiya H., Umeda M., Arabidopsis D-type cyclin CYCD4;1 is a novel cyclin partner of B2-type cyclin-dependent kinase. Plant Physiology 2003 132 3 1315 1321 2-s2.0-0038376835 10.1104/pp.103.020644 (Pubitemid 36872881)
35. Meszaros T., Miskolczi P., Ayaydin F., Pettko-Szandtner A., Peres A., Magyar Z., Horvath G. V., Bako L., Feher A., Dudits D., Multiple cyclin-dependent kinase complexes and phosphatases control G2/M progression in alfalfa cells. Plant Molecular Biology 2000 43 5-6 595 605 2-s2.0-0033772794
36. Takatsuka H., Ohno R., Umeda M., The Arabidopsis cyclin-dependent kinase-activating kinase CDKF;1 is a major regulator of cell proliferation and cell expansion but is dispensable for CDKA activation. The Plant Journal 2009 59 3 475 487 2-s2.0-67651230832 10.1111/j.1365-313X.2009.03884.x
37. Fabian-Marwedel T., Umeda M., Sauter M., The rice cyclin-dependent kinase-activating kinase R2 regulates S-phase progression. The Plant Cell 2002 14 1 197 210 2-s2.0-0036007920 10.1105/tpc.010386 (Pubitemid 34140407)
38. Hirt H., Páy A., Bögre L., Meskiene I., Heberle-Bors E., Cdc2MsB, a cognate cdc2 gene from alfalfa, complements the G1/S but not the G2/M transition of budding yeast cdc28 mutants. The Plant Journal 1993 4 1 61 69 2-s2.0-0027633236
39. Umeda M., Umeda-Hara C., Yamaguchi M., Hashimoto J., Uchimiya H., Differential expression of genes for cyclin-dependent protein kinases in rice plants. Plant Physiology 1999 119 1 31 40 2-s2.0-0032873026 (Pubitemid 29384578)
40. Carle S. A., Bates G. W., Shannon T. A., Hormonal control of gene expression during reactivation of the cell cycle in tobacco mesophyll protoplasts. Journal of Plant Growth Regulation 1998 17 4 221 230 2-s2.0-0032437032 (Pubitemid 29032583)
41. Kapros T., Bögre L., Németh K., Bakó L., Györgyey J., Wu S. C., Dudits D., Differential expression of histone H3 gene variants during cell cycle and somatic embryogenesis in alfalfa. Plant Physiology 1992 98 2 621 625 2-s2.0-0000283274
42. Soni R., Carmichael J. P., Shah Z. H., Murray J. A., A family of cyclin D homologs from plants differentially controlled by growth regulators and containing the conserved retinoblastoma protein interaction motif. The Plant Cell 1995 7 1 85 103 2-s2.0-0029107653 10.1105/tpc.7.1.85
43. Dello Ioio R., Nakamura K., Moubayidin L., Perilli S., Taniguchi M., Morita M. T., Aoyama T., Costantino P., Sabatini S., A genetic framework for the control of cell division and differentiation in the root meristem. Science 2008 322 5906 1380 1384 2-s2.0-57149091945 10.1126/science.1164147 (Pubitemid 352775250)
44. Perrot-Rechenmann C., Cellular responses to auxin: division versus expansion. Cold Spring Harbor Perspectives in Biology 2010 2 5 a001446 2-s2.0-77955273142 10.1101/cshperspect.a001446
45. Maheshwari M. G., Nooden L. D., A requirement for DNA synthesis during auxin induction of cell enlargement in tobacco pith tissue. Physiologia Plantarum 1971 24 2 282 287 10.1111/j.1399-3054.1971.tb03492.x
46. Quélo A.-H., Bryant J. A., Verbelen J.-P., Endoreduplication is not inhibited but induced by aphidicolin in cultured cells of tobacco. Journal of Experimental Botany 2002 53 369 669 675 2-s2.0-0036009372 (Pubitemid 34253559)
47. Valente P., Tao W., Verbelen J.-P., Auxins and cytokinins control DNA endoreduplication and deduplication in single cells of tobacco. Plant Science 1998 134 2 207 215 2-s2.0-0032486486 10.1016/S0168-9452(98)00062-4 (Pubitemid 28319551)
48. Horváth B. M., Magyar Z., Zhang Y., Hamburger A. W., Bakó L., Visser R. G. F., Bachem C. W. B., Bögre L., EBP1 regulates organ size through cell growth and proliferation in plants. EMBO Journal 2006 25 20 4909 4920 2-s2.0-33750219419 10.1038/sj.emboj.7601362 (Pubitemid 44607035)
49. Barbier-Brygoo H., Ephritikhine G., Klämbt D., Maurel C., Palme K., Schell J., Guern J., Perception of the auxin signal at the plasma membrane of tobacco mesophyll protoplasts. The Plant Journal 1991 1 1 83 93 2-s2.0-0001991444 (Pubitemid 121001035)
50. Evans M. L., Ishikawa H., Estelle M. A., Responses of Arabidopsis roots to auxin studied with high temporal resolution: comparison of wild type and auxin-response mutants. Planta 1994 194 2 215 222 2-s2.0-0028105282 (Pubitemid 2099051)
51. Hemerly A., de Almeida Engler J., Bergounioux C., van Montagu M., Engler G., Inzé D., Ferreira P., Dominant negative mutants of the Cdc2 kinase uncouple cell division from iterative plant development. EMBO Journal 1995 14 16 3925 3936 2-s2.0-0029093029
52. Das N. K., Patau K., Skoog F., Autoradiographic and microspectrophotometric studies of DNA synthesis in excised tobacco pith tissue. Chromosoma 1957 9 1 606 617 2-s2.0-51649204910 10.1007/BF02568095
53. Jahlonski J. R., Skoog F., Cell enlargement and cell division in excised tobacco pith tissue. Physiologia Plantarum 1954 7 1 16 24 10.1111/j.1399-3054. 1954.tb07552.x
54. Silberger J. Jr., Skoog F., Changes induced by indoleacetic acid in nucleic acid contents and growth of tobacco pith tissue. Science 1953 118 3068 443 444 2-s2.0-0005221645
55. Bradley M. V., Crane J. C., The effect of 2, 4, 5-trichlorophenoxyacetic acid on cell and nuclear size and endopolyploidy in parenchyma of apricot fruits. American Journal of Botany 1955 42 3 273 281 10.2307/2438563
56. Liscum E., Hangarter R. P., Arabidopsis mutants lacking blue light-dependent inhibition of hypocotyl elongation. The Plant Cell 1991 3 7 685 694 2-s2.0-0001121272 (Pubitemid 21913733)
57. John P. C. L., Zhang K., Dong C., Diederich L., Wightman F., p34cdc2 related proteins in control of cell cycle progression, the switch between division and differentiation in tissue development, and stimulation of division by auxin and cytokinin. Australian Journal of Plant Physiology 1993 20 4-5 503 526 2-s2.0-0027142251 (Pubitemid 2010307)
58. Yoshizumi T., Nagata N., Shimada H., Matsui M., An Arabidopsis cell cycle-dependent kinase-related gene, CDC2b, plays a role in regulating seedling growth in darkness. The Plant Cell 1999 11 10 1883 1895 2-s2.0-0033213009 10.1105/tpc.11.10.1883
59. Ohri D., Fritsch R. M., Hanelt P., Evolution of genome size in allium (alliaceae). Plant Systematics and Evolution 1998 210 1-2 57 86 2-s2.0-0031959574 (Pubitemid 28209212)
60. Andersen S. U., Buechel S., Zhao Z., Ljung K., Novák O., Busch W., Schuster C., Lohmanna J. U., Requirement of B2-type cyclin-dependent kinases for meristem integrity in Arabidopsis thaliana. The Plant Cell 2008 20 1 88 100 2-s2.0-43549108405 10.1105/tpc.107.054676 (Pubitemid 352844036)