Osaka Kyoiku University Researcher Information
日本語 | English
研究者業績
基本情報
研究キーワード
4経歴
6-
2008年
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2008年
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1986年 - 1996年
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1996年
学歴
4-
- 1975年
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- 1975年
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- 1973年
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- 1973年
委員歴
2-
2007年 - 2008年
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2000年
MISC
111-
PLANT JOURNAL 66(5) 890-902 2011年6月
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GENES & GENETIC SYSTEMS 85(6) 377-382 2010年12月
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JOURNAL OF CEREAL SCIENCE 51(2) 182-188 2010年3月
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Chromosome Science 13(1) 27-29 2010年Onion, Allium cepa, is a model plant for experimental observation of mitotic cell division in practice of fundamental biology, because its chromosome is big and easy to observe. In order to develop new academic tools for visualization of plant cytokinesis, molecular cloning of onion mitotic genes, which are related to cell division, cell cycle, and chromosome segregation, is indispensable. Here we isolated CDC48 cDNA (AcCDC48) from onion seedlings, which encodes an AAA-ATPase chaperone and is known to play a role in cell division in broad species of organism. To characterize AcCDC48, we performed phylogenetic and DNA gel blot analyses, and discussed about the possible application of mammalian antibodies to detect it. The full-length onion CDC48 sequence provides useful information for future development of molecular markers to visualize cell division by using antibodies or GFP-fusion proteins.
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Chromosome science 13(1) 27-29 2010年Onion, Allium cepa, is a model plant for experimental observation of mitotic cell division in practice of fundamental biology, because its chromosome is big and easy to observe. In order to develop new academic tools for visualization of plant cytokinesis, molecular cloning of onion mitotic genes, which are related to cell division, cell cycle, and chromosome segregation, is indispensable. Here we isolated CDC48 cDNA (AcCDC48) from onion seedlings, which encodes an AAA-ATPase chaperone and is known to play a role in cell division in broad species of organism. To characterize AcCDC48, we performed phylogenetic and DNA gel blot analyses, and discussed about the possible application of mammalian antibodies to detect it. The full-length onion CDC48 sequence provides useful information for future development of molecular markers to visualize cell division by using antibodies or GFP-fusion proteins.
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PLANT BIOTECHNOLOGY 26(4) 421-425 2009年9月
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PLANT CELL REPORTS 28(5) 759-768 2009年5月
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GENES & GENETIC SYSTEMS 82(3) 241-248 2007年6月
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Chromosome Science 10(3) 75-81 2007年Four spontaneous chromosomal translocations were previously detected in tetraploid (Triticum turgidum L., 2n=4x=28) wheat landraces from Ethiopia. We identified here the chromosomes involved in the translocations through the application of meiotic analysis using the double-ditelosomic series of the durum wheat variety LD222. The landrace wheat lines, K-1-1, B-3-11 and CD-7 carried 2A/2B, 7A/7B and 4A/4B (?) translocations, respectively. The landrace variety DZ-04-118 carried a cyclic translocation involving three chromosomes, 2A/2B/4B. Translocation 2A/2B in K-1-1 and in DZ-04-118 has the same origin. The chromosomal breakpoints of the homoeologous translocations 2A/2B and 7A/7B were successfully localized using the genomic in situ hybridization (GISH) technique. The breakpoints for translocation 2A/2B were at or close to the centromere region while those of 7A/7B were noncentromeric types. This is the first application of GISH to locating translocation breakpoints between homoeologous chromosomes. Probable mechanisms of origin for homoeologous translocations are discussed.
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Chromosome science 10(3) 75-81 2007年Four spontaneous chromosomal translocations were previously detected in tetraploid (Triticum turgidum L., 2n=4x=28) wheat landraces from Ethiopia. We identified here the chromosomes involved in the translocations through the application of meiotic analysis using the double-ditelosomic series of the durum wheat variety LD222. The landrace wheat lines, K-1-1, B-3-11 and CD-7 carried 2A/2B, 7A/7B and 4A/4B (?) translocations, respectively. The landrace variety DZ-04-118 carried a cyclic translocation involving three chromosomes, 2A/2B/4B. Translocation 2A/2B in K-1-1 and in DZ-04-118 has the same origin. The chromosomal breakpoints of the homoeologous translocations 2A/2B and 7A/7B were successfully localized using the genomic in situ hybridization (GISH) technique. The breakpoints for translocation 2A/2B were at or close to the centromere region while those of 7A/7B were noncentromeric types. This is the first application of GISH to locating translocation breakpoints between homoeologous chromosomes. Probable mechanisms of origin for homoeologous translocations are discussed.
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Daeheung Press Inc.Advances in Chromosome Science 2 117-120 2006年
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Daeheung Press Inc.Advances in Chromosome Sciences 2 95-100 2006年
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Daeheung Press Inc.Advances in Chromosome Sciences 2 45-51 2006年
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Deaheung Press Inc.Advance in Chromosome Sciences 2 31-37 2006年
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Daeheung Press Inc.Advances in Chromosome Science 2 117-120 2006年
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Daeheung Press Inc.Advances in Chromosome Sciences 2 95-100 2006年
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Daeheung Press Inc.Advances in Chromosome Sciences 2 45-51 2006年
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Deaheung Press Inc.Advance in Chromosome Sciences 2 31-37 2006年
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JOURNAL OF THE JAPANESE SOCIETY FOR HORTICULTURAL SCIENCE 74(4) 275-280 2005年7月
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GENES & GENETIC SYSTEMS 80(3) 199-212 2005年6月
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MOLECULAR GENETICS AND GENOMICS 273(2) 123-129 2005年4月
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JOURNAL OF HEREDITY 96(2) 155-160 2005年3月
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Wheat Information Service 100: 17-31. 100 17-31 2005年
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Wheat Information Service 100: 17-31. 100 17-31 2005年
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Cytogenetic and Genome Research 109(1-3) 79-82 2005年
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CHROMOSOME RESEARCH 12(5) 475-481 2004年
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GENOME 46(2) 330-338 2003年4月
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Functional & Integrative Genomics 3(1-2) 76-85 2003年
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The Journal of Histochemistry & Cytochemistry (51) 1249-1254 2003年
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The Journal of Histochemistry & Cytochemistry (51) 1249-1254 2003年
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Functional and Integrative Genomics 3(1-2) 76-85 2003年
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Functional and Integrative Genomics 3(1-2) 69-75 2003年
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PLANT SYSTEMATICS AND EVOLUTION 233(3-4) 243-258 2002年
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THEORETICAL AND APPLIED GENETICS 103(6-7) 839-845 2001年11月
書籍等出版物
26共同研究・競争的資金等の研究課題
27-
日本学術振興会 科学研究費助成事業 基盤研究(B) 2018年4月 - 2021年3月
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日本学術振興会 科学研究費助成事業 基盤研究(C) 2013年4月 - 2017年3月
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日本学術振興会 科学研究費助成事業 特別研究員奨励費 2014年4月 - 2016年3月
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日本学術振興会 科学研究費助成事業 挑戦的萌芽研究 2011年 - 2013年
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日本学術振興会 科学研究費助成事業 基盤研究(C) 2010年 - 2012年