PL EN


Preferencje help
Widoczny [Schowaj] Abstrakt
Liczba wyników
2012 | 81 | 3 |

Tytuł artykułu

Effect of osmotic stress on in vitro translational capacity of polysomes and on the composition of polysome-associated proteins in germinating seeds of pea (Pisum sativum L.)

Treść / Zawartość

Warianty tytułu

Języki publikacji

EN

Abstrakty

EN
Plant growth throughout the world is often limited by unfavourable environmental conditions. This paper reports results of a study on long- and short-term osmotic stress (−0.5 MPa) followed by a recovery on in vitro translational capacity of polysomes and on the composition of polysome-associated proteins in germinating pea (Pisum sativum L.) seeds. Here we show that, under osmotic stress, cytoskeleton-bound polysomes were charaterized by the highest translation activity, which may be indicative of an important role that this population of polysomes plays in the synthesis of the so-called “stress proteins”. We also find out that in response to osmotic stress, new proteins (22.01, 96.47 and 105.3 kDa), absent in the unstressed sample, associated with the total pool of polysomes, whereas the protein of 22.95 kDa, which was present in the embryonic tissue of seeds germinating under unstressed conditions, disappeared. These changes may have affected both the stability and the translational capacity of polysomes.

Wydawca

-

Rocznik

Tom

81

Numer

3

Opis fizyczny

p.185-191,fig.,ref.

Twórcy

  • Department of Biochemistry, University of Warmia and Mazury in Olsztyn, Oczapowskiego 2, 10-719 Olsztyn, Poland
autor

Bibliografia

  • 1. Howarth CJ, Ougham HJ. Gene expression under temperature stress. New Phytol. 1993;125(1):1–26. http://dx.doi. org/10.1111/j.1469-8137.1993.tb03862.x
  • 2. Bhatnagar-Mathur P, Rao JS, Vadez V, Sharma KK. Transgenic strategies for improved drought tolerance in legumes of semi-arid tropics. JCRIP. 2009;24(1):92–111. http:// dx.doi.org/10.1080/15427520903337095
  • 3. Szilagyi L. Influence of drought on seed yield components in common bean. Bulg J Plant Physiol. 2003;(special issue):320–330.
  • 4. Gepts P. Legumes as a model plant family. Genomics for food and feed report of the cross-legume advances through genomics conference. Plant Physiol. 2005;137(4):1228– 1235. http://dx.doi.org/10.1104/pp.105.060871
  • 5. Urbano G, López-Jurado M, Frejnagel S, Gómez-Villalva E, Porres JM, Frías J, et al. Nutritional assessment of raw and germinated pea (Pisum sativum L.) protein and carbohydrate by in vitro and in vivo techniques. Nutrition. 2005;21(2):230–239. http://dx.doi.org/10.1016/j. nut.2004.04.025
  • 6. Vidal-Valverde C, Frias J, Hernandez A, Martin-AlvarezPJ, Sierra I, Rodriguez C, et al. Assessment of nutritionalcompounds and antinutritional factors in pea (Pisum sativum)seeds. J Sci Food Agric. 2003;83(4):298–306. http://dx.doi.org/10.1002/jsfa.1309
  • 7. Hsiao TC. Rapid changes in levels of polyribosomes in zea mays in response to water stress. Plant Physiol.1970;46(2):281–285. http://dx.doi.org/10.1104/pp.46.2.281
  • 8. Mason HS, Mullet JE, Boyer JS. Polysomes, messenger RNA, and growth in soybean stems during development and water deficit. Plant Physiol. 1988;86(3):725–733. http:// dx.doi.org/10.1104/pp.86.3.725
  • 9. Uesono Y. Transient inhibition of translation initiation by osmotic stress. J Biol Chem. 2002;277(16):13848–13855. http://dx.doi.org/10.1074/jbc.M108848200
  • 10. Rhodes PR, Matsuda K. Water stress, rapid polyribosome reductions and growth. Plant Physiol. 1976;58(5):631–635. http://dx.doi.org/10.1104/pp.58.5.631
  • 11. Slaymaker DH, Hoppey CM. Reduced polysome levels and preferential recruitment of a defense gene transcript into polysomes in soybean cells treated with the syringolide elicitor. Plant Sci. 2006;170(1):54–60. http://dx.doi.org/10.1016/j.plantsci.2005.07.026
  • 12. Kawiak J, Mirecka J, Olszewska M, Warchoła J. Podstawy cytofizjologii. Warszawa: Polish Scientific Publishers PWN; 1997.
  • 13. Davies E, Fillingham BD, Abe S, Ito Y. Polyribosomes from peas. VII. Initial characterization of a population of polysomes associated with the cytoskeleton. Cell Biol Int Rep. 1991;17:331–340.
  • 14. Davies E, Fillingham B, Ito Y, Abe S. Evidence for the existence of cytoskeleton-bound polysomes in plants. Cell Biol Int Rep. 1991;15(10):973–981. http://dx.doi. org/10.1016/0309-1651(91)90147-B
  • 15. Davies E. Intercellular and intracellular signals and their transduction via the plasma membrane-cytoskeleton interface. Semin Cell Biol. 1993;4(2):139–147. http://dx.doi. org/10.1006/scel.1993.1017
  • 16. Hesketh JE, Pryme IF. Interaction between mRNA, ribosomes and the cytoskeleton. Biochem J. 1991;277:1–10.
  • 17. Nicchitta CV, Lerner RS, Stephens SB, Dodd RD, Pyhtila B. Pathways for compartmentalizing protein synthesis in eukaryotic cells: the template-partitioning model. Biochem Cell Biol. 2005;83(6):687–695. http://dx.doi.org/10.1139/ o05-147
  • 18. Adams A, Fey EG, Pike SF, Taylorson CJ, White HA, Rabin BR. Preparation and properties of a complex from rat liver of polyribosomes with components of the cytoskeleton. Biochem J. 1983;216(1):215–226.
  • 19. Davies E, Abe S, Larkins BA, Clore AM, Quatrano RS,Weidner S. The role of the cytoskeleton in protein synthesis. In: Bailey-Serres J, Gallie DR, editors. A look beyond transcription: mechanisms determining mRNA stabilityand translation in plants. Rockville MD: Amer Society ofPlant Physiologists; 1998. p. 115–124.
  • 20. Weidner S, Łukaszewicz D, Amarowicz R. Significant role for polysomes associated with the cytoskeleton in the control of protein synthesis during germination of triticale caryopses in the presence of abscisic acid. Acta Physiol Plant. 2000;22(2):185–193. http://dx.doi.org/10.1007/s11738-000-0075-5
  • 21. Weidner S, Frączek E, Romanowska M, Amarowicz R, Abe S, Davies E. The influence of abscisic acid on different polysomal populations in embryonal tissue during pea seeds germination. Acta Physiol Plant. 2003;25(1):5–12. http://dx.doi.org/10.1007/s11738-003-0030-3
  • 22. Abe S, Davies E. Isolation of F-actin from pea stems. Protoplasma.1991;163(1):51–61. http://dx.doi.org/10.1007/BF01323406
  • 23. Bailey-Serres J. Selective translation of cytoplasmic mRNAs in plants. Trends Plant Sci. 1999;4(4):142–148. http:// dx.doi.org/10.1016/S1360-1385(99)01386-2
  • 24. Hummel M, Rahmani F, Smeekens S, Hanson J. Sucrosemediated translational control. Ann Bot. 2009;104(1):1–7. http://dx.doi.org/10.1093/aob/mcp086
  • 25. Gong P, Wilke BM, Strozzi E, Fleischmann S. Evaluation and refinement of a continuous seed germination and early seedling growth test for the use in the ecotoxicological assessment of soils. Chemosphere. 2001;44(3):491–500.http://dx.doi.org/10.1016/S0045-6535(00)00280-0
  • 26. Davies E, Abe S. Methods for isolation and analysis of polyribosomes. Method Cell Biol. 1995;50:209–222. http:// dx.doi.org/10.1016/S0091-679X(08)61032-8
  • 27. Abe S, Ito Y, Davies E. Co-sedimentation of actin, tubulin andmembranes in the cytoskeleton fractions from peas and mouse 3T3 cells. J Exp Bot. 1992;43(7):941–949. http:// dx.doi.org/10.1093/jxb/43.7.941
  • 28. Bradford MM. A rapid and sensitive method for the quantitation of microgram quantities of protein utilizing the principle of protein-dye binding. Anal Biochem. 1976;72(1–2):248–254. http://dx.doi. org/10.1016/0003-2697(76)90527-3
  • 29. Laemmli UK. Cleavage of structural proteins during the assembly of the head of bacteriophage T4. Nature. 1970;227(5259):680–685. http://dx.doi. org/10.1038/227680a0
  • 30. Hamayuni M, Khan SA, Shinowari ZK, Khani AL, Ahmad N, Lee IJ. Effect of polyethylene glycol induced drought stress on physio-hormonal attributes of soybean. Pak J Bot. 2010;42:977–986.
  • 31. Türkan I, Bor M, Özdemir F, Koca H. Differential responses of lipid peroxidation and antioxidants in the leaves of drought-tolerant P. acutifolius Gray and drought-sensitive P. vulgaris L. subjected to polyethylene glycol mediated water stress. Plant Sci. 2005;168(1):223–231. http://dx.doi.org/10.1016/j.plantsci.2004.07.032
  • 32. Brosowska-Arendt W, Weidner S. Effect of osmotic stress on the formation of a population of polysomes and their stability in pea (Pisum sativum L.) seeds. Acta Physiol Plant. 2011;33(4):1475–1482. http://dx.doi.org/10.1007/s11738-010-0686-4
  • 33. Gill PK, Sharma AD, Singh P, Bhullar SS. Osmotic stressinduced changes in germination, growth and soluble sugar content of Sorghum bicolor (L.) moench seeds. Bulg J Plant Physiol. 2002;28:12–25.
  • 34. Gomes FE, Eneas FJ, Tarquínio PJ. Effects of osmotic stress on growth and ribonuclease activity in Vigna unguiculata (L.) Walp. seedlings differing in stress tolerance. Rev Bras Fisiol Veg. 1996;8:51–57.
  • 35. Khayatnezhad M, Gholamin R, Jamaati-e-Somarin S, Zabihi-e-Mahmoodabad R. Effects of peg stress on corn cultivars (Zea mays L.) at germination stage. World Appl Sci J. 2010;11:504–506.
  • 36. Kosowska M, Frączek E, Amarowicz R, Karama M, Abe S, Weidner S. Water-deficit-induced changes in cytoskeleton- bound and other polysomal populations in embryonic tissue during triticale caryopsis germination. ActaPhysiol Plant. 2004;26(1):67–74. http://dx.doi.org/10.1007/ s11738-004-0046-3
  • 37. Murillo-Amador B, Lopez-Aguilar R, Kaya C, Larrinaga-Mayoral J, Flores-Hernandez A. Comparative effects of nacl and polyethylene glycol on germination, emergence and seedling growth of cowpea. J Agron Crop Sci. 2002;188(4):235–247. http://dx.doi.org/10.1046/j.1439-037X.2002.00563.x
  • 38. Kawaguchi R, Williams AJ, Bray EA, Bailey-Serres J. Waterdeficit- induced translational control in Nicotiana tabacum. Plant Cell Environ. 2003;26(2):221–229. http://dx.doi. org/10.1046/j.1365-3040.2003.00952.x
  • 39. Klyachko N. Plant polysome binding to the actin cytoskeleton as a target for physiological regulation. Cell Biol Int. 2003;27(3):217–218. http://dx.doi.org/10.1016/ S1065-6995(02)00314-1
  • 40. Abe S, Azama K, Sugimoto H, Davies E. Protein accumulation in the maize endosperm: role of polyribosomes and the cytoskeleton. Plant Physiol Biochem. 2003;41(2):125–131. http://dx.doi.org/10.1016/S0981-9428(02)00016-5
  • 41. Klyachko N. Interaction of plant polysomes with the actin cytoskeleton. Cell Biol Int. 2000;24(6):351–358. http:// dx.doi.org/10.1006/cbir.1999.0517
  • 42. Weidner S, Każarnowicz M, Frączek E, Amarowicz R, Karamać M. Exogenous abscisic acid increases stability of polysomes in embryos of triticale caryopses during germination. Acta Physiol Plant. 2006;28(6):627–634. http://dx.doi.org/10.1007/s11738-006-0059-1
  • 43. Dai H, Lo YS, Lin YH, Ruddat M, Chiang KS. In vitro polysome translation analysis of heat shock proteins in higher plants. Bot Bull Acad Sin. 1996;37:261–264.
  • 44. Branco-Price C. Genome-wide analysis of transcript abundance and translation in arabidopsis seedlings subjected to oxygen deprivation. Ann Bot. 2005;96(4):647–660. http://dx.doi.org/10.1093/aob/mci217
  • 45. Kawaguchi R, Girke T, Bray EA, Bailey-Serres J. Differential mRNA translation contributes to gene regulation under non-stress and dehydration stress conditions in Arabidopsis thaliana. Plant J. 2004;38(5):823–839. http://dx.doi.org/10.1111/j.1365-313X.2004.02090.x
  • 46. Nicolai M. Large-scale analysis of mrna translation states during sucrose starvation in Arabidopsis cells identifies cell proliferation and chromatin structure as targets of translational control. Plant Physiol. 2006;141(2):663–673.http://dx.doi.org/10.1104/pp.106.079418
  • 47. Shenton D. Global translational responses to oxidative stress impact upon multiple levels of protein synthesis. J Biol Chem. 2006;281(39):29011–29021. http://dx.doi. org/10.1074/jbc.M601545200
  • 48. Perras M, Sarhan F. Polysome metabolism during cold acclimation in wheat. Plant Cell Physiol. 1990;31(8):1083–1089.
  • 49. Morelli JK, Shewmaker CK, Vayda ME. Biphasic stimulation of translational activity correlates with induction of translation elongation factor 1 subunit [alpha] upon wounding in potato tubers. Plant Physiol. 1994;106(3):897–903. http://dx.doi.org/10.1104/pp.106.3.897
  • 50. Spriggs KA, Stoneley M, Bushell M, Willis AE. Reprogramming of translation following cell stress allows IRES-mediated translation to predominate. Biol Cell. 2008;100(1):27–38. http://dx.doi.org/10.1042/BC20070098
  • 51. Morelli JK. Actin depolymerization affects stress-induced translational activity of potato tuber tissue. Plant Physiol. 1998;116(4):1227–1237. http://dx.doi.org/10.1104/ pp.116.4.1227

Typ dokumentu

Bibliografia

Identyfikatory

Identyfikator YADDA

bwmeta1.element.agro-08464811-8b5f-4a3e-a52b-814d87365aec
JavaScript jest wyłączony w Twojej przeglądarce internetowej. Włącz go, a następnie odśwież stronę, aby móc w pełni z niej korzystać.