Patterns of Stem Cell Divisions Contribute to Plant Longevity

Current Biology

Volumn 26, Issue 11, 2016, Pages 1385-1394

  Burian, Agata ^a,b   Barbier de Reuille, Pierre ^a   Kuhlemeier, Cris ^a  

^a UNIVERSITY OF BERN   (Switzerland)

^b UNIVERSITY OF SILESIA   (Poland)

Author keywords

[No Author keywords available]

Indexed keywords

ARABIDOPSIS; CELL DIVISION; CELL LINEAGE; CYTOLOGY; GROWTH, DEVELOPMENT AND AGING; LONGEVITY; MERISTEM; PHYSIOLOGY; TOMATO;

ARABIDOPSIS; CELL DIVISION; CELL LINEAGE; LONGEVITY; LYCOPERSICON ESCULENTUM; MERISTEM;

EID: 84964940338     PISSN: 09609822     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.cub.2016.03.067     Document Type: Article

References (68)

1. 1 Lanner, R.M., Why do trees live so long?. Ageing Res. Rev. 1 (2002), 653–671.
2. 2 Lynch, A.J.J., Barnes, R.W., Cambecedes, J., Vaillancourt, R.E., Genetic evidence that Lomatia tasmanica (Proteaceae) is an ancient clone. Aust. J. Bot. 46 (1998), 25–33.
3. 3 Munne-Bosch, S., Aging in perennials. Crit. Rev. Plant Sci. 26 (2007), 123–138.
4. 4 Munné-Bosch, S., Perennial roots to immortality. Plant Physiol. 166 (2014), 720–725.
5. 5 Jones, O.R., Scheuerlein, A., Salguero-Gómez, R., Camarda, C.G., Schaible, R., Casper, B.B., Dahlgren, J.P., Ehrlén, J., García, M.B., Menges, E.S., et al. Diversity of ageing across the tree of life. Nature 505 (2014), 169–173.
6. 6 Felsenstein, J., The evolutionary advantage of recombination. Genetics 78 (1974), 737–756.
7. 7 Gabriel, W., Lynch, M., Burger, R., Muller's ratchet and mutational meltdowns. Evolution 47 (1993), 1744–1757.
8. 8 Lynch, M., Bürger, R., Butcher, D., Gabriel, W., The mutational meltdown in asexual populations. J. Hered. 84 (1993), 339–344.
9. 9 Domagalska, M.A., Leyser, O., Signal integration in the control of shoot branching. Nat. Rev. Mol. Cell Biol. 12 (2011), 211–221.
10. 10 Wang, Q., Hasson, A., Rossmann, S., Theres, K., Divide et impera: boundaries shape the plant body and initiate new meristems. New Phytol. 209 (2016), 485–498.
11. 11 Wang, Q., Kohlen, W., Rossmann, S., Vernoux, T., Theres, K., Auxin depletion from the leaf axil conditions competence for axillary meristem formation in arabidopsis and tomato. Plant Cell 26 (2014), 2068–2079.
12. 12 Wang, Y., Wang, J., Shi, B., Yu, T., Qi, J., Meyerowitz, E.M., Jiao, Y., The stem cell niche in leaf axils is established by auxin and cytokinin in arabidopsis. Plant Cell 26 (2014), 2055–2067.
13. 13 Borchert, R., Slade, N.A., Bifurcation ratios and the adaptive geometry of trees. Bot. Gaz. 142 (1981), 394–401.
14. 14 Godin, C., Costes, E., Sinoquet, H., A method for describing plant architecture which integrates topology and geometry. Ann. Bot. (Lond.) 84 (1999), 343–357.
15. 15 Leopold, L.B., Trees and streams: the efficiency of branching patterns. J. Theor. Biol. 31 (1971), 339–354.
16. 16 Furner, I.J., Pumfrey, J.E., Cell fate in the shoot apical meristem of Arabidopsis thaliana. Development 115 (1992), 755–764.
17. 17 Irish, V.F., Sussex, I.M., A fate map of the Arabidopsis embryonic shoot apical meristem. Development 115 (1992), 745–753.
18. 18 McDaniel, C.N., Poethig, R.S., Cell-lineage patterns in the shoot apical meristem of the germinating maize embryo. Planta 175 (1988), 13–22.
19. 19 Schnittger, A., Grini, P.E., Folkers, U., Hülskamp, M., Epidermal fate map of the Arabidopsis shoot meristem. Dev. Biol. 175 (1996), 248–255.
20. 20 Esau, K., Plant Anatomy. 1953, Wiley.
21. 21 McConnell, J.R., Barton, M.K., Leaf polarity and meristem formation in Arabidopsis. Development 125 (1998), 2935–2942.
22. 22 Bobiwash, K., Schultz, S.T., Schoen, D.J., Somatic deleterious mutation rate in a woody plant: estimation from phenotypic data. Heredity (Edinb.) 111 (2013), 338–344.
23. 23 Scofield, D.G., Medial pith cells per meter in twigs as a proxy for mitotic growth rate (Phi/m) in the apical meristem. Am. J. Bot. 93 (2006), 1740–1747.
24. 24 Scofield, D.G., Schultz, S.T., Mitosis, stature and evolution of plant mating systems: low-Phi and high-Phi plants. Proc. Biol. Sci. 273 (2006), 275–282.
25. 25 Kwiatkowska, D., Dumais, J., Growth and morphogenesis at the vegetative shoot apex of Anagallis arvensis L. J. Exp. Bot. 54 (2003), 1585–1595.
26. 26 Greb, T., Clarenz, O., Schafer, E., Muller, D., Herrero, R., Schmitz, G., Theres, K., Molecular analysis of the LATERAL SUPPRESSOR gene in Arabidopsis reveals a conserved control mechanism for axillary meristem formation. Genes Dev. 17 (2003), 1175–1187.
27. 27 Keller, T., Abbott, J., Moritz, T., Doerner, P., Arabidopsis REGULATOR OF AXILLARY MERISTEMS1 controls a leaf axil stem cell niche and modulates vegetative development. Plant Cell 18 (2006), 598–611.
28. 28 Müller, D., Schmitz, G., Theres, K., Blind homologous R2R3 Myb genes control the pattern of lateral meristem initiation in Arabidopsis. Plant Cell 18 (2006), 586–597.
29. 29 Raman, S., Greb, T., Peaucelle, A., Blein, T., Laufs, P., Theres, K., Interplay of miR164, CUP-SHAPED COTYLEDON genes and LATERAL SUPPRESSOR controls axillary meristem formation in Arabidopsis thaliana. Plant J. 55 (2008), 65–76.
30. 30 Long, J., Barton, M.K., Initiation of axillary and floral meristems in Arabidopsis. Dev. Biol. 218 (2000), 341–353.
31. 31 Edwards, P.B., Wanjura, W.J., Brown, W.V., Dearn, J.M., Mosaic resistance in plants. Nature, 347, 1990 434–434.
32. 32 Padovan, A., Lanfear, R., Keszei, A., Foley, W.J., Külheim, C., Differences in gene expression within a striking phenotypic mosaic Eucalyptus tree that varies in susceptibility to herbivory. BMC Plant Biol., 13, 2013, 29.
33. 33 Szymkowiak, E.J., Sussex, I.M., What chimeras can tell us about plant development. Annu. Rev. Plant Physiol. Plant Mol. Biol. 47 (1996), 351–376.
34. 34 Pineda-Krch, M., Fagerstrom, T., On the potential for evolutionary change in meristematic cell lineages through intraorganismal selection. J. Evol. Biol. 12 (1999), 681–688.
35. 35 Whitham, T.G., Slobodchikoff, C.N., Evolution by individuals, plant-herbivore interactions, and mosaics of genetic variability- The adaptive significance of somatic mutations in plants. Oecologia 49 (1981), 287–292.
36. 36 White, J., The Plant as a Metapopulation. Annu. Rev. Ecol. Syst. 10 (1979), 109–145.
37. 37 Newman, I.V., Pattern in the meristems of vascular plants: III. Pursuing the patterns in the apical meristem where no cell is a permanent cell. Journal of the Linnean Society of London. Botany 59 (1965), 185–214.
38. 38 Ruth, J., Klekowski, E.J., Stein, O.L., Impermanent initials of the shoot apex and diplontic selection in a juniper chimera. Am. J. Bot. 72 (1985), 1127–1135.
39. 39 Zagorska-Marek, B., Turzanska, M., Clonal analysis provides evidence for transient initial cells in shoot apical meristems of seed plants. J. Plant Growth Regul. 19 (2000), 55–64.
40. 40 Stewart, R.N., Dermen, H., Determination of number and mitotic activity of shoot apical initial cells by analysis of mericlinal chimeras. Am. J. Bot. 57 (1970), 816–826.
41. 41 Klekowski, E.J., Kazarinova-Fukshansky, N., Shoot apical meristems - selective loss of disadvantageous cell genotypes. Am. J. Bot. 71 (1984), 28–34.
42. 42 Klekowski, E.J., Kazarinova-Fukshansky, N., Shoot apical meristems and mutation - fixation of selectively neutral genotypes. Am. J. Bot. 71 (1984), 22–27.
43. 43 Petit, R.J., Hampe, A., Some evolutionary consequences of being a tree. Annu. Rev. Ecol. Evol. Syst. 37 (2006), 187–214.
44. 44 Grbic, V., Axillary meristem development. McManus, M.T., Veit, B.E., (eds.) Meristematic Tissues in Plant Growth and Development, 2002, Sheffield Academic Press, 142–171.
45. 45 Christianson, M.L., Fate map of the organizing shoot apex in Gossypium. Am. J. Bot. 73 (1986), 947–958.
46. 46 Johri, M.M., Coe, E.H. Jr., Clonal analysis of corn plant development. I. The development of the tassel and the ear shoot. Dev. Biol. 97 (1983), 154–172.
47. 47 Fink, S., Some cases of delayed or induced development of axillary buds from persisting detached meristems in conifers. Am. J. Bot. 71 (1984), 44–51.
48. 48 Romberger, J.A., Meristems, Growth, and Development in Woody Plants: An Analytical Review of Anatomical, Physiological, and Morphogenic Aspects, USDA Technical Bulletin 1293. 1963, US Government Printing Office.
49. 49 Otto, S.P., Walbot, V., DNA methylation in eukaryotes: kinetics of demethylation and de novo methylation during the life cycle. Genetics 124 (1990), 429–437.
50. 50 Hoffman, P.D., Leonard, J.M., Lindberg, G.E., Bollmann, S.R., Hays, J.B., Rapid accumulation of mutations during seed-to-seed propagation of mismatch-repair-defective Arabidopsis. Genes Dev. 18 (2004), 2676–2685.
51. 51 Poethig, R.S., Clonal analysis of cell lineage patterns in plant development. Am. J. Bot. 74 (1987), 581–594.
52. 52 Palubicki, W., Horel, K., Longay, S., Runions, A., Lane, B., Mech, R., Prusinkiewicz, P., Self-organizing tree models for image synthesis. ACM Trans. Graph. 28 (2009), 1–10.
53. 53 Ossowski, S., Schneeberger, K., Lucas-Lledó, J.I., Warthmann, N., Clark, R.M., Shaw, R.G., Weigel, D., Lynch, M., The rate and molecular spectrum of spontaneous mutations in Arabidopsis thaliana. Science 327 (2010), 92–94.
54. 54 Lanfear, R., Ho, S.Y.W., Jonathan Davies, T., Moles, A.T., Aarssen, L., Swenson, N.G., Warman, L., Zanne, A.E., Allen, A.P., Taller plants have lower rates of molecular evolution. Nat. Commun., 4, 2013, 1879.
55. 55 Smith, S.A., Donoghue, M.J., Rates of molecular evolution are linked to life history in flowering plants. Science 322 (2008), 86–89.
56. 56 Ally, D., Ritland, K., Otto, S.P., Aging in a long-lived clonal tree. PLoS Biol., 8, 2010, 8.
57. 57 Barrett, S.C.H., Influences of clonality on plant sexual reproduction. Proc. Natl. Acad. Sci. USA 112 (2015), 8859–8866.
58. 58 Greaves, M., Maley, C.C., Clonal evolution in cancer. Nature 481 (2012), 306–313.
59. 59 Martincorena, I., Campbell, P.J., Somatic mutation in cancer and normal cells. Science 349 (2015), 1483–1489.
60. 60 Nowell, P.C., The clonal evolution of tumor cell populations. Science 194 (1976), 23–28.
61. 61 Shendure, J., Akey, J.M., The origins, determinants, and consequences of human mutations. Science 349 (2015), 1478–1483.
62. 62 Fulcher, N., Sablowski, R., Hypersensitivity to DNA damage in plant stem cell niches. Proc. Natl. Acad. Sci. USA 106 (2009), 20984–20988.
63. 63 Vernoux, T., Brunoud, G., Farcot, E., Morin, V., Van den Daele, H., Legrand, J., Oliva, M., Das, P., Larrieu, A., Wells, D., et al. The auxin signalling network translates dynamic input into robust patterning at the shoot apex. Mol. Syst. Biol., 7, 2011, 508.
64. 64 Reddy, G.V., Meyerowitz, E.M., Stem-cell homeostasis and growth dynamics can be uncoupled in the Arabidopsis shoot apex. Science 310 (2005), 663–667.
65. 65 Müller, B., Sheen, J., Cytokinin and auxin interaction in root stem-cell specification during early embryogenesis. Nature 453 (2008), 1094–1097.
66. 66 Shani, E., Ben-Gera, H., Shleizer-Burko, S., Burko, Y., Weiss, D., Ori, N., Cytokinin regulates compound leaf development in tomato. Plant Cell 22 (2010), 3206–3217.
67. 67 Barbier de Reuille, P., Routier-Kierzkowska, A.-L., Kierzkowski, D., Bassel, G.W., Schüpbach, T., Tauriello, G., Bajpai, N., Strauss, S., Weber, A., Kiss, A., et al. MorphoGraphX: A platform for quantifying morphogenesis in 4D. eLife, 4, 2015, 05864.
68. 68 Kuchen, E.E., Fox, S., de Reuille, P.B., Kennaway, R., Bensmihen, S., Avondo, J., Calder, G.M., Southam, P., Robinson, S., Bangham, A., Coen, E., Generation of leaf shape through early patterns of growth and tissue polarity. Science 335 (2012), 1092–1096.