Browse > Article

Microspore Division and Plant Regeneration from Shed Pollen Culture in Rice  

Kim, Hyun-Soon (National Honam Agricultural Experiment Station, RDA)
Kang, Hyeon-Jung (Division of Research Coordination, RDA)
Lee, Young-Tae (National Honam Agricultural Experiment Station, RDA)
Lee, Seung-Yeob (Division of Plant Resources Science, Wonkwang University)
Nam, Jeong-Kwon (National Honam Agricultural Experiment Station, RDA)
Kim, Tae-Soo (National Honam Agricultural Experiment Station, RDA)
Rha, Eui-Shik (Research Center for Industrial Development of Bio Food Materials. Chonbuk National University)
Jin, Il-Doo (Coll. Of Agri. And Life Science, Sunchon national University)
Publication Information
KOREAN JOURNAL OF CROP SCIENCE / v.47, no.1, 2002 , pp. 62-67 More about this Journal
Abstract
An efficient system of rice microspore culture could contribute to the production of genetically modified rice. The microspores were isolated by mechanical or shed methods. The number of microspores per 100 anthers isolated at uninucleate stage was higher than (or similar to) those at binucleate stage in isolation method with pestle or spatular, but microspore divisions were not easily observed on both stages. On the other hand, pollen division in shed pollen culture was observed more frequently at uninuclear than at binuclear stage. Cold pretreatment at 1$0^{\circ}C$ for 10 days resulted in the best multicellular division to produce microcalli at 12.5% efficiency in shed microspores. Heat shock at 33$^{\circ}C$ for one hour before or after pollen shedding enhanced cell division and callus formation. Out of twelve green regenerants, two were haploids and ten were diploids based on the chromosome analysis of root tips. The size of stoma was 12$^{m}$ m in haploids and 15 ${\mu}{\textrm}{m}$ in diploids determined by scanning electron microscope (SEM).
Keywords
microspore isolation; shed pollen; cold treatment; heat treatment; ploidy;
Citations & Related Records
연도 인용수 순위
  • Reference
1 Pipeno, D. R. 1988. Phytolith analysis: An archaeological and geological perspective. San Diego Academic press, New York
2 Masaharu, K. and H. Hiroshi. 1985. Studies on conditions for cell division and embryogenesis in isolated pollen culture of Nicotiana rustica. Plnt physiol 79: 90-94   DOI   ScienceOn
3 Peng, M. and D. J. Wolyn. 1999. Improved callus formation and plant regeneration for shed microspore culture in asparagus (Asparagu officinalis L.) Plant Cell report 18 : 954-958   DOI   ScienceOn
4 Zapata, F. J. and L. B. Torrizo. 1986. Heat treatment to increase callus induction efficiency in anther culture of IR42. Intl. Rice Res.News. 11:25-26
5 Nishi, Y, Y. Yamada and E. Takahashi. 1968. Organ redifferentiation and plant restoration in rice callus. Nature (London) 219:508-509 Ogawa, T, H. Fukuoka, and Y. Ohkawa. 1994. Induction of cell division of isolated pollen grains by sugar starvation. Breeding Science 44: 75-77 Ogawa, T., T. Hagio and Y. Ohkawa. 1992. Plant regeneration from isolated pollen grains in indica type rice. Jpn. J. Breed. 42: 675-6790no, K. and S. Harashima. 1981. Induction of haploid callus from isolated microspores of peony in vitro. Ptant & Cell Physiol. 22(2) :337-341
6 regeneration in isolated pollen culture of rice (Oryza sativa L. cv. Taipei 309). Plant Science. 58 : 239-244   DOI   ScienceOn
7 Chen, C. H., F T. Chen, C. H. Chien, and C. H. Wang. 1978. Obtaining pollen plants of Hevea brasiliensis MUEll.-ARG (In: Plant Tissue Culture, Proceedings of the Beijing (Peking)Symposium. Pitman pl1-22. Chen, Y. 1983. Anther and pollenculture of rice in China (In. Cell and tissue culture techniques for cereal crop improvement). Science press & IRRL pp 11-25
8 Sathish, P, 0. L. Gamborg, and M. W. Nabors. 1995. Rice anther culture: callus initiation and androclonal variation in progenies of regenerated plants. Plant Cell Rep. 14: 432-436Sunder1and, N. and M. Roberts. 1977. New approach to pollen culture. Nature. 270: 236-238   DOI
9 Maeda, E. and H. Miyake. 1973. Surface structure of rice leaf blades observed through a scanning electron microscope. Proc. Crop Sci. Soc. Japan 42 : 327-333   DOI
10 Kim, H. S., Y. T. Lee, S. Y. Lee, and T. S. Kim. 1991. Anther culhire efficiency in different rice genotypes under different cold pretreatment duration and culture temperature. Res. Report (Biotec.) 33(1): 5-13Lee, S. Y, T. L. Lee, and B. T. Jun. 1991. Effect of preculture temperatures and isolation methods on callus formation and plant regeneration in microspore culture. Korean J. of Breeding 23(3): 205-210
11 Polsoni L., L. S. Kott, and W. D. Beversdorf. 1988. Large-scale microspore culture techniques for mutation-selection studies in Brassica napus. Can. J. Bot. Vol. 66: 1681-1684   DOI
12 Imamura, J., E. Okabe., K. Masaharu, and H. Harada. 1982.Embryogenesis and plantlet formation through direct culture of isolated pollen of Nicotiana tabacum cv. Samsun and Nicotiana rustica cv. Rustica. Plant and cell physiol. 23(4): 713-716
13 Cho, M. S. and F. J. Zapata. 1988. Callus formation and plant regeneration in isolated pollen culture of rice (Oryza sativa L. cv. Taipei 309). Plant Science. 58 : 239-244   DOI   ScienceOn
14 Chen, C. C., H. S. Tsay, and C. R. Huang. 1991. Factors affecting androgenesis in rice (Oryza sativa L). In: Y. P. S. Bajai(Ed.), Biotechnology in Agriculture and Forestry, Vol. 14, pp. 193-215. Springer-verlag. Berlin
15 Zhang, W. 1995. The observation of submicrostructure on leavesback in Oryza. Chinese J. Rice Sci. 9 : 71-76
16 Taguchi, T. and M. Mii. 1982. Effects of chilling, anther preculture and growth regulators on embryogenesis in isolated pollen culture of Nicotiana rustica L. Japan J. Breed., 32(4): 303-310   DOI
17 Reddy, Y. S., S. Leelavathi, and S. K. Sen. 1985. In fluence of genotype and culture medium on microspore callus, induction and green plant regeneration in anthers in Oryza sativa. Physiol. Plant. 63: 309-314Rha, E. S. and J. K. Kim. 1998. Characteristics of phytolith on rice leaf. Korean J. Crop Sci. 43 : 205-208