Endogenous hormones in seed, leaf, and pod wall and their relationship to seed filling in soybeans
Bing Liu A B C , Xiao-bing Liu A E , Cheng Wang A , Jian Jin A and S. J. Herbert DA Key laboratory of Black Soil Ecology, Northeast Institute of Geography and Agroecology, Chinese Academy of Science, Harbin 150081, China.
B Graduate University of the Chinese Academy of Sciences, Beijing 100049, China.
C College of Life Science, Jilin Normal University, Siping 136000, China.
D Department of Plant, Soil, and Insect Sciences, University of Massachusetts, Amherst, MA 01003, USA.
E Corresponding author. Email: liuxb@neigae.ac.cn
Crop and Pasture Science 61(2) 103-110 https://doi.org/10.1071/CP09189
Submitted: 1 July 2009 Accepted: 6 November 2009 Published: 8 February 2010
Abstract
In order to investigate the possible relationship between endogenous hormones and seed filling in soybeans, concentrations of abscisic acid (ABA), gibberellins (GA3), indole-3-acetic acid (IAA), and cytokinins (ZR) in seed, leaf, and pod wall were determined during seed filling of 3 soybean cultivars differing in seed size and quality. All cultivars were grown at 3 densities. The large-seeded cultivar had a strong and greater ability to accumulate photosynthate during seed filling. The genetic trait of seed size was fully expressed at low density. The large-seeded cultivar had a much higher ABA concentration in seed than the moderate and small-seeded cultivars before physiological maturity. ABA concentration in the large-seeded cultivar seed was 40% greater than that of the small-seeded cultivar at 30 days after flowering. Higher densities increased ABA concentrations in seeds. Two peaks of seed GA3 concentration were observed during seed filling. GA3 concentrations at all densities were similar. The peaks of IAA concentration in the 3 cultivars uniformly occurred at 50 days after flowering. The large-seeded cultivar had greater peak concentrations of GA3 and IAA in seed than the other cultivars, while the peak concentration of ZR was highest in the small-seeded cultivar. The concentrations of ABA in leaf increased with time while that of GA3 decreased. The large-seeded cultivar had higher ABA and IAA concentration in leaf while the small-seeded cultivar consistently had higher GA3 concentration in leaf. ZR was present in a smaller amount in the leaf, and was not detected in the pod wall. The large-seeded cultivar maintained higher IAA concentration in pod wall. ABA concentration in seed was positively correlated with seed-filling rate (P < 0.01, r = 0.85**, 0.92**, and 0.83** for large-, moderate- and small-seeded cultivars respectively).The concentration of GA3 in seed was significantly correlated with the seed-filling rate in large- and moderate-seeded cultivars (P < 0.01, r = 0.87**; P < 0.05, r = 0.63*), and no correlation was found for the small-seeded cultivar. There was no correlation between the concentrations of seed IAA, ZR, and seed-filling rate. There was a parallel relationship between seed growth and leaf/pod wall ABA concentration. Thus, ABA might offer a driving force for photosynthate phloem unloading in the seed coat. Lower concentration of ABA and GA3 in the leaf than in seed suggests that most of the two hormones is transported to seed. The mechanism of IAA in seed growth and GA3 concentration and its dynamic in seed quality need further investigation.
Additional keywords: soybean, reproductive stage, plant hormone, seed growth.
Acknowledgments
This research was supported by the National Natural Science Foundation of China (30671315), Heilongjiang Province Natural Science Funds for Distinguished Young Scholar (JC2OO617).
Ackerson RC
(1984) Regulation of soybean embryogenesis by abscisic acid. Journal of Experimental Botany 35, 403–413.
| Crossref | GoogleScholarGoogle Scholar |
CAS |
Bano A, Harper JE
(2002) Plant growth regulators and phloem exudates modulate root nodulation of soybean. Functional Plant Biology 29, 1299–1307.
| Crossref | GoogleScholarGoogle Scholar |
CAS |
Burrows WJ, Carr DJ
(1970) Cytokinin content of pea seeds during their growth and development. Physiologia Plantarum 23, 1064–1070.
| Crossref | GoogleScholarGoogle Scholar |
CAS |
Cho MJ, Harper JE
(1993) Effect of abscisic acid application on root isoflavonoid concentration and nodulation of wild-type and nodulation-mutant soybean plants. Plant and Soil 153, 145–149.
| Crossref | GoogleScholarGoogle Scholar |
CAS |
Clifford PE,
Offler CE, Patrick JW
(1986) Growth regulators have rapid effects on photosynthate unloading from seed coats of Phaseolus vulgaris L. Plant Physiology 80, 635–637.
| Crossref | GoogleScholarGoogle Scholar |
CAS |
PubMed |
Cohen JD
(1982) Identification and quantitative analysis of indole-3-acetyl-aspartate from seed of Glycine max L. Plant Physiology 70, 749–753.
| Crossref | GoogleScholarGoogle Scholar |
CAS |
PubMed |
Dong ZX,
Fu JM, Zhang YX
(2001) Hormone regulating effect for cultivation physiology on soybean. Journal of Shihezi University 5, 339–341.
|
CAS |
Eeuwens CJ, Schwabe WW
(1975) Seed and pod wall development in Pisum sativum L. in relation to extracted and applied hormones. Journal of Experimental Botany 26, 1–14.
| Crossref | GoogleScholarGoogle Scholar |
CAS |
Gao SJ,
Wang WJ, Xie GJ
(2000) The changing rules of content of inner GA3, ABA in big kernel wheat variety. Journal of Henan Agricultural University 34, 213–219.
|
CAS |
Guldan SJ, Brun WA
(1987) Effect of abscisic acid on amino acid uptake and efflux in developing soybean seeds. Crop Science 27, 716–719.
|
CAS |
Hayata Y,
Li XX, Osajima Y
(2002) Pollination and CPPU treatment increase endogenous IAA and decrease endogenous ABA in Muskmelons during early development. Journal of the American Society for Horticultural Science 127, 908–911.
|
CAS |
Hein MB,
Brenner ML, Brun WA
(1984a) Concentrations of abscisic acid and indole-3-acetic acid in soybean seeds during development. Plant Physiology 76, 951–954.
| Crossref | GoogleScholarGoogle Scholar |
CAS |
PubMed |
Hein MB,
Brenner ML, Brun WA
(1984b) Effects of pod removal on the transport and accumulation of abscisic acid and indole-3-acetic acid in soybean leaves. Plant Physiology 76, 955–958.
| Crossref | GoogleScholarGoogle Scholar |
CAS |
PubMed |
Herzog H
(1982) Grain development and temporary dry matter storage in vegetative organs of wheat genotypes. Journal of Agronomy & Crop Science 151, 388–398.
Kannangara T,
Durley RC, Simpson GM
(1978) High performance liquid chromatographic analysis of cytokinins in Sorghum bicolor leaves. Physiologia Plantarum 44, 295–299.
| Crossref | GoogleScholarGoogle Scholar |
CAS |
Kovaleva LV,
Zakharova EV,
Skorobogatova IV, Karsunkina NP
(2002) Gametophyte-sporophyte interactions in the pollen-pistil system: 3. Hormonal status at the progamic phase of fertilization. Russian Journal of Plant Physiology: a Comprehensive Russian Journal on Modern Phytophysiology 49, 492–495.
| Crossref | GoogleScholarGoogle Scholar |
CAS |
Liang Y, Harris J
(2005) Response of root branching to abscisic acid is correlated with nodule formation both in legumes and nonlegumes. American Journal of Botany 92, 1675–1683.
| Crossref | GoogleScholarGoogle Scholar |
CAS |
Liu F,
Jensen CR, Andersen MN
(2004) Pod set related to phyotosynthetic rate and endogenous ABA in soybeans subjected to different water regimes and exogenous ABA and BA at early reproductive stage. Annals of Botany 94, 405–411.
| Crossref | GoogleScholarGoogle Scholar |
CAS |
PubMed |
Liu F,
Jensen CR, Andersen MN
(2005) A review of drought adaptation in crop plants: changes in vegetative and reproductive physiology induced by ABA-based chemical signals. Australian Journal of Agricultural Research 56, 1245–1252.
| Crossref | GoogleScholarGoogle Scholar |
CAS |
Nagel L,
Brewster R,
Riedell WE, Reese RN
(2001) Cytokinin regulation of flower and pod set in soybean (Glycine max (L.) Merr.). Annals of Botany 88, 27–31.
| Crossref | GoogleScholarGoogle Scholar |
CAS |
Pei Z, Kuchitsu K
(2005) Early ABA signaling events in guard cells. Journal of Plant Growth Regulation 24, 296–307.
| Crossref | GoogleScholarGoogle Scholar |
CAS |
Ross GS,
Minchin PEH, McWha JA
(1987) Direct evidence of abscisic acid affecting phloem unloading within the seed coat of peas. Journal of Plant Physiology 129, 435–441.
|
CAS |
Schussler JR,
Brenner ML, Brun WA
(1984) Abscisic acid and its relationship to seed filling in soybeans. Plant Physiology 76, 301–306.
| Crossref | GoogleScholarGoogle Scholar |
CAS |
PubMed |
Setter TL,
Brun WA, Brenner ML
(1981) Abscisic acid translocation and metabolism in soybeans following depodding and petiole girdling treatments. Plant Physiology 67, 774–779.
| Crossref | GoogleScholarGoogle Scholar |
CAS |
PubMed |
Strauss M, Arditti J
(1982) Postpollination phenomena in orchid flowers, transport and fate of auxin. Botanical Gazette 143, 286–293.
| Crossref | GoogleScholarGoogle Scholar |
CAS |
Suzuki A,
Akune M,
Kogiso M,
Imagama Y,
Osuki K,
Uchiumi T,
Higashi S,
Han S,
Yoshida S,
Asami T, Abe M
(2004) Control of nodule number by the phytohormone abscisic acid in the roots of two leguminous species. Plant & Cell Physiology 45, 914–922.
| Crossref | GoogleScholarGoogle Scholar |
CAS |
PubMed |
Tamas IA,
Engels CI,
Kaplan SL, Wallace DH
(1981) Role of indoleacetic acid and abscisic acid in the correlative control by fruits of axillary bud development and leaf senescence. Plant Physiology 68, 476–481.
| Crossref | GoogleScholarGoogle Scholar |
CAS |
PubMed |
Tanner W
(1980) On the possible role of ABA on phloem unloading. Berichte der Deutschen Botanischen Gesellschaft 93, 349–351.
|
CAS |
Vreugdenhil D
(1983) Abscisic acid inhibits phloem loading of sucrose. Physiologia Plantarum 57, 463–467.
| Crossref | GoogleScholarGoogle Scholar |
CAS |
Wang G,
Wang P, Wu Y
(2002) The effect of embryogenesis of immature cotyledon induced by auxins in soybean. Journal of Jinlin Agricultural Sciences 27, 7–10.
Wilkinson S, Davies W
(2002) ABA-based chemical signaling: the co-ordination of responses to stress in plants. Plant, Cell & Environment 25, 195–210.
| Crossref | GoogleScholarGoogle Scholar |
CAS |
PubMed |
Yang J,
Zhang J,
Wang Z, Zhu Q
(2003) Hormones in the grains in relation to sink strength and postanthesis development of spikelets in rice. Plant Growth Regulation 41, 185–195.
| Crossref | GoogleScholarGoogle Scholar |
CAS |
Yang J,
Zhang J,
Wang Z,
Zhu Q, Wang W
(2001) Hormonal changes in the grains of rice subjected to water stress during grain filling. Plant Physiology 127, 315–323.
| Crossref | GoogleScholarGoogle Scholar |
CAS |
PubMed |
Yang J,
Zhang J,
Ye Y,
Wang Z,
Zhu Q, Liu L
(2004) Involvement of abscisic acid and ethylene in the responses of rice grains to water stress during filling. Plant, Cell & Environment 27, 1055–1064.
| Crossref | GoogleScholarGoogle Scholar |
CAS |
Young TE, Gallie DR
(2000) Regulation of programmed cell death in maize endosperm by abscisic acid. Plant Molecular Biology 42, 397–414.
| Crossref | GoogleScholarGoogle Scholar |
CAS |
PubMed |
Zhang M,
Duan L,
Tian X,
He Z,
Li J,
Wang B, Li Z
(2007) Uniconazole-induced tolerance of soybean to water deficit stress in relation to changes in photosynthesis, hormones and antioxidant system. Journal of Plant Physiology 164, 709–717.
| Crossref | GoogleScholarGoogle Scholar |
CAS |
PubMed |
Zhang YZ,
Chen ZL,
Lu XZ,
Chen JG, Zhou X
(1999) Simultaneous determination of gibberellins A1 and A3 in foxtail millet seedlings by high performance liquid chromatography. Chinese Journal of Chromatography 17, 469–472.
|
CAS |
PubMed |