Summary
Auxin-induced cell elongation necessitates plasma membrane enlargement. The effect of auxin (10 μM 2,4-dichlorophenoxyacetic acid) treatment on amount, composition, and rate of synthesis of plasma membrane lipids was examined. Auxin-treated and control soybean (Glycine max L.) hypocotyl segments were incubated with [14C]acetate for times ranging from 0.5 to 18 h, prior to isolation of plasma membrane by aqueous two-phase partitioning. The composition of individual plasma membrane lipids in elongating segments did not differ from the composition in treatment time-matched control segments, except that after longer auxin treatments, phospholipids had more unsaturated fatty acids. Plasma membrane phospholipid and free sterol content both increased in elongating segments. The relative proportion of sterols and phospholipids in the plasma membrane primarily depended on time after segment excision, for both auxin-treated and control segments. Auxin enhanced the rate of lipid incorporation into the plasma membrane by 6 h, and stimulated the synthesis of some phospholipids and sterols.
Similar content being viewed by others
Abbreviations
- 2,4-D:
-
2,4-dichlorophenoxyacetic acid
- ER:
-
endoplasmic reticulum
- GC:
-
gas chromatography
- IAA:
-
indole-3-acetic acid
- PA:
-
phosphatidic acid
- PC:
-
phosphatidylcholine
- PE:
-
phosphatidylethanolamine
- PG:
-
phosphatidylglycerol
- PI:
-
phosphatidylinositol
- PM:
-
plasma membrane
- PS:
-
phosphatidylserine
References
Bowles DJ (1990) Endomembrane traffic and targetting in plant cells. Curr Opin Cell Biol 2: 673–680
Brummell DA, Hall JL (1987) Rapid cellular responses to auxin and the regulation of growth. Plant Cell Environ 10: 523–543
Cleland RE (1982) The mechanism of auxin-induced proton efflux. In: Wareing PF (ed) Plant growth substances. Academic Press, New York, pp 23–31
Cunninghame ME, Hall JL (1985) A quantitative stereological analysis of the effect of indoleacetic acid on the dictyosomes in pea stem epidermal cells. Protoplasma 125: 230–234
Evans ML (1985) The action of auxin on plant cell elongation. CRC Crit Rev Plant Sci 2: 317–365
Fenwick GR, Price KR, Tsukamoto C, Okubo K (1991) Saponins. In: D'Mello JPF, Duffus CM, Duffus JH (eds) Toxic substances in crop plants. Royal Society of Chemistry, Cambridge, pp285–327
Gawlik SR, Shen-Miller J (1974) Effects of indoleacetic acid on dictyosomes of apical and expanding cells of oat coleoptiles. Plant Physiol 54: 217–221
Geuns JMC, Vendrig JC (1974) Hormonal control of sterol biosynthesis inPhaseolus aureus. Phytochemistry 13: 919–922
Gogstad GO, Krutnes M-B (1982) Measurement of protein in cell suspensions using the Coomassie brilliant blue dye-binding assay. Anal Biochem 72: 248–254
Goodrich-Tanrikulu M (1993) A reevaluation of the effect of auxin on phospholipids in pea stem segments. Plant Sci 145: 59–65
—, Travis RL (1994) Plasma membrane protein composition and synthesis in soybean hypocotyl segments undergoing auxin-induced elongation. Protoplasma 177: 144–152
Hager A, Brich M, Debus G, Edel H-G, Priester T (1989) Membrane metabolism and growth. Phospholipases, protein kinases and exocytotic processes in coleoptiles ofZea mays. In: Plant water relations and growth under stress. Proceedings of the Yamada Conference XXII, Osaka, Japan. Yamada Science Foundation, Tokyo, pp 275–282
—, Debus G, Edel H-G, Stransky H, Serrano R (1991) Auxin induces exocytosis and the rapid synthesis of a high-turnover pool of plasma-membrane H+-ATPase. Planta 185: 527–537
Houslay MD, Stanley KK (1982) Dynamics of biological membranes. Influence on synthesis, structure and function. Wiley, Chichester
Jackson CK, Hall JL (1993) A fine structural analysis of auxin-induced elongation of cucumber hypocotyls, and the effects of calcium antagonists and ionophores. Ann Bot 72: 193–204
Kaluzny MA, Duncan LA, Merritt MV, Epps DE (1985) Rapid separation of lipid classes in high yield and purity using bonded phase columns. J Lipid Res 26: 135–140
Kates M (1986) Techniques of lipidology, 2nd edn. Elsevier, Amsterdam
Leshem Y (1987) Membrane phospholipid catabolism and Ca2+ activity in control of senescence. Physiol Plant 69: 551–559
Lynch DV, Steponkus PL (1987) Plasma membrane lipid alterations associated with cold acclimation of winter rye seedlings (Secale cereale L. cv Puma). Plant Physiol 83: 761–767
Mann JD, Pu M (1968) Inhibition of lipid synthesis by certain herbicides. Weed Sci 16: 197–198
Moore TS Jr, Price-Jones MJ, Harwood JL (1983) The effect of indoleacetic acid on phospholipid metabolism in pea stems. Phytochemistry 22: 2421–2425
Morré DJ, Gripshover B, Monroe A, Morré JT (1984) Phosphatidyl-inositol turnover in isolated soybean membranes stimulated by the synthetic growth hormone 2,4-dichlorophenoxyacetic acid. J Biol Chem 259: 15364–15368
Mudd JB (1980) Phospholipid biosynthesis. In: Tolbert NE (ed) The biochemistry of plants — a comprehensive treatise. Academic Press, New York, pp 249–282
Paliyath G, Lynch DV, Thompson JE (1987) Regulation of membrane phospholipid catabolism in senescing carnation flowers. Physiol Plant 71: 503–511
Pastan I, Friedman RM (1968) Actinomycin D; inhibition of phospholipid synthesis in chick embryo cells. Science 160: 316–317
Penny P, Penny D (1978) Rapid responses to phytohormones. In: Letham DS, Goodwin PB, Higgins TJV (eds) Phytohormones and related compounds — a comprehensive treatise, vol VII. Elsevier/North-Holland, Amsterdam, pp 537–597
Phillips GD, Preshaw C, Steer MW (1988) Dictyosome vesicle production and plasma membrane turnover in auxin-stimulated outer epidermal cells of coleoptile segments fromAvena saliva (L.). Protoplasma 145: 59–65
Price-Jones MJ, Harwood JL (1983) Hormonal regulation of phosphatidylcholine synthesis in plants. The inhibition of cytidyltransferase activity by indole-3-ylacetic acid. Biochem J 216: 627–631
Quaite E, Parker RE, Steer MW (1983) Plant cell extension: structural implications for the origin of the plasma membrane. Plant Cell Environ 6: 429–432
Rodriquez RJ, Parks LW (1985) High-performance liquid chromatography of sterols: yeast sterols. Methods Enzymol 111: 37–51
Sandstrom RP, Cleland RE (1989) Comparison of the lipid composition of oat root and coleoptile plasma membranes. Lack of short-term change in response to auxin. Plant Physiol 90: 1207–1213
Scherer GFE, André B (1989) A rapid response to a plant hormone: auxin stimulates phospholipase A2 in vivo and in vitro. Biochem Biophys Res Commun 163: 111–117
Sinyutina NF, Voloshina TV (1983) Effect of auxin on the phospholipids of corn coleoptile membranes. Leningrad Univ Vestn Ser Biol 1983 (1): 87–92 (in Russian)
—, Znamenskaya OV, Minayeva LA, Polevoi W (1980) Incorporation of 2-14C-acetate into lipids of corn coleoptile segments in the presence of indoleacetic acid. Leningrad Univ Vestn Ser Biol 1980 (1): 99–103 (in Russian)
Theologis A, Huynh TV, Davis RW (1985) Rapid induction of specific mRNAs by auxin in pea epicotyl tissue. J. Mol Biol 183: 53–68
van Meer G (1993) Transport and sorting of membrane lipids. Curr Opin Cell Biol 5: 661–673
Voloshina TV (1980) Effect of auxin on phospholipid and galactolipid metabolism of corn. Leningrad Univ Vestn Ser Biol 1980 (2): 66–69 (in Russian)
—, Sinyutina NF, Polevoi W (1980) The effect of auxin on lipid changes of membrane fractions of corn coleoptile segments. Biol Nauki (Moscow) 9: 90–94 (in Russian)
Wilson RF, Rinne RW (1976) Studies on lipid synthesis and degradation in developing soybean cotyledons. Plant Physiol 57: 375–381
Wolfe J, Dowgert MF, Steponkus PL (1985) Dynamics of membrane exchange of the plasma membrane and the lysis of isolated protoplasts during rapid expansion in area. J Membr Biol 86: 127–138
Yadav NS, Wierzbicki A, Aegerter M, Caster CS, Pérez-Grau L, Kinney AJ, Hitz WD, Booth JR Jr, Schweiger B, Stecca KL, Allen SM, Blackwell M, Reiter RS, Carlson TJ, Russell SH, Feldman KA, Pierce J, Browse J (1993) Cloning of higher plant ω-3 fatty acid desaturases. Plant Physiol 103: 467–476
Yamamoto KT (1994) Further characterization of auxin-regulated mRNAs in hypocotyl sections of mung bean [Vigna radiata (L.) Wilczek]: sequence homology to genes for fatty-acid desaturases and atypical late-embryogenesis-abundant protein, and the mode of expression of the mRNAs. Planta 192: 359–364
—, Mori H, Imaseki H (1992) Novel mRNA sequences induced by indole-3-acetic acid in sections of elongating hypocotyls of mung bean (Vigna radiata). Plant Cell Physiol 33: 13–20
Zbell B, Walter-Back C (1988) Signal transduction of auxin on isolated plant cell membranes: indications for a rapid polyphosphoinositide response stimulated by indoleacetic acid. J Plant Physiol 133: 353–360
Zimmerer RP, Hamilton RH (1965) The incorporation of32P orthophosphate into the phospholipids of elongatingAvena coleoptiles. Plant Cell Physiol 6: 681–687
Author information
Authors and Affiliations
Rights and permissions
About this article
Cite this article
Goodrich-Tanrikulu, M., Travis, R.L. Plasma membrane phospholipid and sterol synthesis in soybean hypocotyl segments undergoing auxin-induced elongation. Protoplasma 185, 83–92 (1995). https://doi.org/10.1007/BF01272756
Received:
Accepted:
Issue Date:
DOI: https://doi.org/10.1007/BF01272756