Gene related to regeneration ability of plants and uses thereof

Multicellular living organisms and unmodified parts thereof and – Method of introducing a polynucleotide molecule into or...

Reexamination Certificate

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C800S298000, C800S290000, C536S023600, C435S320100, C435S419000

Reexamination Certificate

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10264341

ABSTRACT:
The objective is to isolate and identify a gene relating to the regeneration ability of a plant, and to provide the gene and methods of use thereof. Isogenic lines to which culture characteristics of Konansou was introduced were produced by backcrossing. Culture cells were induced from this isogenic line and its parent variety. After confirming the regeneration ability of culture cells cultured for 3 to 6 months, isolation of a gene expressed in culture cells derived from Konansou and an isogenic line having a high regeneration ability, but not expressed in culture cells derived from Sasanishiki and Koshihikari was conducted using the differential display method. As a result, a regeneration-related gene was successfully cloned.

REFERENCES:
patent: 3-7599 (1991-01-01), None
Fourgoux-Nicol et al (1999, Plant Molecular Biology 40 :857-872).
Bowie et al, Science 247:1306-1310, 1990.
McConnell et al, Nature 411 (6838):709-713, 2001.
Alexander et al (1994 Planta 192(4):519-525).
Kawahigashi, H. et al., “RFLP analysis of Koshihikari isogenic lines with high ability of regeneration,”Breeding Science 3, Suppl. 2, p. 10, Japanese Society of Breeding (Oct. 7, 2001).
Ozawa, K. et al., “Cloning and analysis of the genes correlated with the regeneration ability using the differential display inOryza sativa,” Breeding Science 3, Suppl. 2, p. 131, Japanese Society of Breeding (Oct. 7, 2001).
English translation of Kawahigashi, H. et al., “RFLP analysis of Koshihikari isogenic lines with high ability of regeneration,”Breeding Science 3, Suppl. 2, p. 10, Japanese Society of Breeding (Oct. 7, 2001).
English translation of Ozawa, K. et al., “Cloning and analysis of the genes correlated with the regeneration ability using the differential display inOryza sativa,” Breeding Science 3, Suppl. 2, p. 131, Japanese Society of Breeding (Oct. 7, 2001).
English language abstract of JP-7599 A, cited on Form PTO/SB/08A as document AL1.
Kwon, Y.-S., et al., “Marker-assisted Selection for Identification of Plant Regeneration Ability of Seed-derived Calli in Rice (Oryza sativaL.),”Mol. Cells 12:103-106, Korean Society for Molecular Biology (Aug. 2001).
Toshinori, A., “Genetic control of Dedifferentiation/Redifferentiation of rice,”Idenshi Igaku5:32-38, Ine Idengaku no Saikochiku (1995).
Unverified English translation of Toshinori, A., “Genetic control of Dedifferentiation/Redifferentiation of rice,”Idenshi Igaku5:32-38, Ine Idengaku no Saikochiku (1995), document AR3.
Ozawa et al., “Genetic analyses of the redifferentiation ability of rice and development of breeding materials for high redifferentiation ability,”Nougyoseibutsushigenkenkyujo Shuyo-na-kenkyu-seika, pp. 82-83, National Institute of Agrobiological Sciences (May 2002).
Unverified English translation of Ozawa et al., “Genetic analyses of the redifferentiation ability of rice and development of breeding materials for high redifferentiation ability,”Nougyoseibutsushigenkenkyujo Shuyo-na-kenkyu-seika, pp. 82-83, National Institute of Agrobiological Sciences (May 2002).
Yoshida, K.T., et al., “cDNA Cloning of Regeneration-Specific Genes in Rice by Differential Screening of Randomly Amplified cDNAa Using RAPD Primers,”Plant Cell Physiol. 35:1003-1009, Oxford University Press (1994).
Office Action for Japanese Patent Application No. 2002-314937, Japanese Patent Office.
Partial English Translation of Office Action for Japanese Patent Application No. 2002-314937.

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