{"id":28,"date":"2015-02-23T16:46:51","date_gmt":"2015-02-23T07:46:51","guid":{"rendered":"http:\/\/www.sci.hokudai.ac.jp\/CSF2-web\/?page_id=28"},"modified":"2024-09-17T21:08:49","modified_gmt":"2024-09-17T12:08:49","slug":"research-outcome","status":"publish","type":"page","link":"https:\/\/c-mng.cwh.hokudai.ac.jp\/biol.sci\/Root\/research-outcome","title":{"rendered":"\u7814\u7a76\u767a\u8868\u30ea\u30b9\u30c8"},"content":{"rendered":"

\u4e3b\u8981\u8ad6\u6587\u30fb\u7dcf\u8aac<\/h1>\n

C\/N\u6804\u990a\u5fdc\u7b54<\/h2>\n
\n
C\/N\u30d0\u30e9\u30f3\u30b9\u8abf\u7bc0\u306b\u3088\u308b\u690d\u7269\u306e\u4ee3\u8b1d\u30fb\u6210\u9577\u6226\u7565<\/a>
\n\u4f50\u85e4\u9577\u7dd2\uff0c\u5c71\u53e3\u6df3\u4e8c
\n\u5316\u5b66\u3068\u751f\u7269\uff0c51, 763-772, 2013<\/li>\n
The TGN\/EE SNARE protein SYP61 and the ubiquitin ligase ATL31 cooperatively regulate plant responses to carbon\/nitrogen conditions in Arabidopsis<\/a>
\nHasegawa Y, Huarancca Reyes T, Uemura T, Baral A, Fujimaki A, Luo Y, Morita Y, Saeki Y, Maekawa S, Yasudaa S, Mukuta K, Fukao Y, Tanaka K, Nakano A, Takagi J, Bhalerao RP, Yamaguchi J and Sato T*
\nPlant Cell<\/em>, 34:1354-1374. 2022\u00a0 \u30d7\u30ec\u30b9\u30ea\u30ea\u30fc\u30b9\u8a18\u4e8b<\/a><\/li>\n
Low nitrogen conditions accelerate flowering by modulating the phosphorylation state of FLOWERING BHLH 4 in Arabidopsis<\/em><\/a>
\nSanagi M, Aoyama S, Kubo A, Lu Y, Sato Y, Ito S, Abe M, Mitsuda N, Ohme-Takagi M, Kiba T, Nakagami H, Rolland F, Yamaguchi J, Imaizumi T* and Sato T* Corresponding authors<\/em>
\nProc. Natl. Acad. Sci. U. S. A.<\/em>, 118: e2022942118. 2021\u3000\u30d7\u30ec\u30b9\u30ea\u30ea\u30fc\u30b9\u8a18\u4e8b<\/a><\/li>\n
Protein phosphorylation dynamics under carbon\/nitrogen-nutrient stress and identification of a cell death-related receptor-like kinase in Arabidopsis<\/a>
\nLi X, Sanagi M, Lu Y, Nomura Y, Stolze SC, Yasuda S, Saijo Y, Schulze WX, Regina F, Stitt M, Lunn JE, Nakagami H, Sato T, Yamaguchi J Corresponding authors<\/em>
\nFrontiers in Plant Science<\/em> 11: 377. 2020\u3000\u65e5\u672c\u8a9e\u89e3\u8aacPDF<\/a><\/li>\n<\/ul>\n
\n
Arabidopsis CBL-Interacting Protein Kinases Regulate Carbon\/Nitrogen-Nutrient Response by Phosphorylating Ubiquitin Ligase ATL31<\/a>.
\nYasuda S, Aoyama S, Hasegawa Y, Sato T* and Yamaguchi J
\nMol. Plant<\/em> 10: 605-618, 2017\u00a0 <\/span>\u65e5\u672c\u8a9e\u89e3\u8aacPDF<\/a><\/li>\n
Ubiquitin ligase ATL31 functions in leaf senescence in response to the balance between atmospheric CO2 and nitrogen availability in Arabidopsis.<\/a>
\nAoyama S, Huarancca Reyes T, Guglielminetti L, Yu L, Morita Y, Sato T, Yamaguchi J
\nPlant Cell Physiol.<\/em>\u00a055: 293-305, 2014\u3000\u65e5\u672c\u8a9e\u89e3\u8aacPDF<\/a><\/li>\n<\/ul>\n
\n
Phosphorylation of Arabidopsis ubiquitin ligase ATL31 is critical for plant C\/N-nutrient response under control of 14-3-3 stability.<\/a>
\nYasuda S, Sato T, Maekawa S, Aoyama S, Fukao Y, Yamaguchi J (2013)
\nJ. Biol. Chem.<\/em>\u00a0289: 15179-15193, 2014\u3000<\/span>\u65e5\u672c\u8a9e\u89e3\u8aacPDF<\/a><\/li>\n
Identification of 14-3-3 proteins as a target of ATL31 ubiquitin ligase, a regulator of the C\/N response in Arabidopsis thaliana.<\/a>
\nSato T, Maekawa S, Yasuda S, Domeki Y, Sueyoshi K, Fujiwara M, Fukao Y, Goto DB, Yamaguchi J
\nPlant J.<\/em>\u00a068: 137-146, 2011\u3000\u65e5\u672c\u8a9e\u89e3\u8aacPDF<\/a><\/li>\n<\/ul>\n
\u514d\u75ab\u5fdc\u7b54<\/h2>\n
\n
The C\/N regulator ATL31 controls papilla formation in response to powdery mildew fungi penetration by interacting with SNARE SYP121 in Arabidopsis.<\/a>
\nMaekawa S, Inada N, Yasuda S, Fukao Y, Fujiwara M, Sato T, Yamaguchi J
\nPlant Physiol.<\/em>\u00a0164: 879-887, 2014\u00a0 \u65e5\u672c\u8a9e\u89e3\u8aacPDF<\/a><\/li>\n<\/ul>\n
\u690d\u7269\u306e\u30e6\u30d3\u30ad\u30c1\u30f3\u30b7\u30b0\u30ca\u30eb\u30fb\u30d7\u30ed\u30c6\u30a2\u30bd\u30fc\u30e0\u6a5f\u80fd\u89e3\u6790<\/h2>\n
\n
\u690d\u7269\u306eRING\u578b\u30e6\u30d3\u30ad\u30c1\u30f3\u30ea\u30ac\u30fc\u30bc\u3068\u30d7\u30ed\u30c6\u30a2\u30bd\u30fc\u30e0\u30b7\u30b9\u30c6\u30e0\u306e\u6a5f\u80fd
\n\u524d\u5ddd\u4fee\u543e\uff0c\u4f50\u53e4\u9999\u7e54\uff0c\u4f50\u85e4\u9577\u7dd2
\n\u751f\u5316\u5b66 84: 416-42, 2012<\/li>\n
Proteomics analysis reveals a highly heterogenous proteasome composition and the post-translational regulation of peptidase activity under pathogen signaling in plants.<\/a>
\nSun HH, Fukao Y, Ishida S, Yamamoto H, Maekawa S, Fujiwara M, Sato T, Yamaguchi J
\nJ. Proteome Res.<\/em>\u00a012: 5084-5095, 2013\u00a0 \u65e5\u672c\u8a9e\u89e3\u8aacPDF<\/a><\/li>\n
Deubiquitinating enzymes UBP12 and UBP13 stabilize the brassinosteroid receptor BRI1<\/a>
\nYongming Luo\uff0cJunpei Takagi, Lucas Alves Neubus Claus, Chao Zhang, Shigetaka Yasuda, Yoko Hasegawa, Junji Yamaguchi, Libo Shan, Eugenia Russinova, Takeo Sato
\nEMBO reports<\/em>, e53354, 2022 (doi: 10.15252\/embr.202153354) \u30d7\u30ec\u30b9\u30ea\u30ea\u30fc\u30b9\u8a18\u4e8b<\/a><\/li>\n<\/ul>\n
2022<\/h1>\n
\n
Deubiquitinating enzymes UBP12 and UBP13 regulate carbon\/nitrogen-nutrient stress responses by interacting with the membrane-localized ubiquitin ligase ATL31 in Arabidopsis<\/a>
\nYongming Luo\uff0cShigetaka Yasuda, Junpei Takagi, Yoko Hasegawa, Yukako Chiba, Junji Yamaguchi, Takeo Sato
\nBiochemical and Biophysical Research Communications<\/em>, 636: 55-61, 2022<\/li>\n
The TGN\/EE SNARE protein SYP61 and the ubiquitin ligase ATL31 cooperatively regulate plant responses to carbon\/nitrogen conditions in Arabidopsis<\/a>
\nHasegawa Y, Huarancca Reyes T, Uemura T, Baral A, Fujimaki A, Luo Y, Morita Y, Saeki Y, Maekawa S, Yasudaa S, Mukuta K, Fukao Y, Tanaka K, Nakano A, Takagi J, Bhalerao RP, Yamaguchi J and Sato T
\nPlant Cell<\/em>, 34:1354-1374. 2022\u00a0 \u30d7\u30ec\u30b9\u30ea\u30ea\u30fc\u30b9\u8a18\u4e8b<\/a><\/li>\n
Deubiquitinating enzymes UBP12 and UBP13 stabilize the brassinosteroid receptor BRI1<\/a>
\nYongming Luo\uff0cJunpei Takagi, Lucas Alves Neubus Claus, Chao Zhang, Shigetaka Yasuda, Yoko Hasegawa, Junji Yamaguchi, Libo Shan, Eugenia Russinova, Takeo Sato
\nEMBO reports<\/em>, e53354, 2022 (doi: 10.15252\/embr.202153354) \u30d7\u30ec\u30b9\u30ea\u30ea\u30fc\u30b9\u8a18\u4e8b<\/a><\/li>\n
3-Phenyllactic acid is converted to phenylacetic acid and induces auxin-responsive root growth in Arabidopsis plants<\/a>
\nMaki Y, Soejima H, Sugiyama T, Watahiki MK, Sato T and Yamaguchi J
\nPlant Biotechnol.<\/em>, 39: 111-117, 2022<\/li>\n
Conjugates of 3-phenyllactic acid and tryptophan enhance root-promoting activity without adverse effects in Vigna angularis<\/a>
\nMaki Y, Soejima H, Sugiyama T, Sato T, Yamaguchi J, Watahiki MK
\nPlant Biotechnol.<\/em>, 39: 173-177, 2022<\/li>\n<\/ul>\n
2021<\/h1>\n
\n
Low nitrogen conditions accelerate flowering by modulating the phosphorylation state of FLOWERING BHLH 4 in Arabidopsis<\/em><\/a>
\nSanagi M, Aoyama S, Kubo A, Lu Y, Sato Y, Ito S, Abe M, Mitsuda N, Ohme-Takagi M, Kiba T, Nakagami H, Rolland F, Yamaguchi J, Imaizumi T* and Sato T* Corresponding authors<\/em>
\nProc. Natl. Acad. Sci. U. S. A.<\/em>, 118: e2022942118. 2021\u3000\u30d7\u30ec\u30b9\u30ea\u30ea\u30fc\u30b9\u8a18\u4e8b<\/a><\/li>\n
3-P henyllactic acid, a root-promoting substance isolated from Bokashi fertilizer, exhibits synergistic effects with tryptophan<\/a>
\nMaki Y, Soejima H, Kitamura T, Sugiyama T, Sato T, Watahiki MK and Junji Yamaguchi
\nPlant Biotechnol.<\/em>, 38:9-16. 2021<\/li>\n<\/ul>\n
2020<\/h1>\n
\n
Protein phosphorylation dynamics under carbon\/nitrogen-nutrient stress and identification of a cell death-related receptor-like kinase in Arabidopsis<\/a>
\nLi X, Sanagi M, Lu Y, Nomura Y, Stolze SC, Yasuda S, Saijo Y, Schulze WX, Regina F, Stitt M, Lunn JE, Nakagami H, Sato T, Yamaguchi J Corresponding authors<\/em>
\nFrontiers in Plant Science<\/em> 11: 377. 2020\u3000\u65e5\u672c\u8a9e\u89e3\u8aacPDF<\/a><\/li>\n
Proteomic analysis of 14-3-3 targets in tomato fruit tissues.<\/a>
\nLuo Y, Lu Y, Yamaguchi J and Sato T
\nMethod. Mol. Biol.<\/em> “Plant Proteomics Methods and Protocols” 3rd edition, 2139: 289-296. 2020<\/li>\n<\/ul>\n
2019<\/h1>\n
\n
Involvement of the membrane-localized ubiquitin ligase ATL8 in sugar starvation response in Arabidopsis<\/a>
\nLuo Y, Aoyama S, Fukao Y, Chiba Y, Sato T and Yamaguchi J*
\nPlant Biotechnol.<\/em> 37: 107-112, 2019<\/li>\n
Identification of Arabidopsis CCR4-NOT complexes with Pumilio RNA binding proteins, APUM5 and APUM2<\/a>
\nArae T, Morita K, Imahori R, Suzuki Y, Yasuda S, Sato T, Yamaguchi J and Chiba Y*
\nPlant Cell Physiol.<\/em>, 60: 2015-2025. 2019<\/li>\n<\/ul>\n
2018<\/h1>\n
\n
Methods for Elucidation of Plant Senescence in Response to C\/N-Nutrient Balance<\/a>
\nAoyama S, Yamaguchi J and Sato T*
\nMethod. Mol. Biol.<\/em> \u201cPlant Senescence\u201d 151-159, 2018<\/li>\n
Sugar-responsive transcription factor bZIP3 affects leaf shape in Arabidopsis plants<\/a>
\nSanagi M, Lu Y, Aoyama S, Morita Y, Mitsuda N, Ikeda M, Ohme-Takagi M, Sato T and Yamaguchi J*
\nPlant Biotechnol.<\/em> 35: 167-170, 2018\u3000\u65e5\u672c\u8a9e\u89e3\u8aacPDF<\/a><\/li>\n<\/ul>\n
2017<\/h1>\n
\n
Arabidopsis CBL-Interacting Protein Kinases Regulate Carbon\/Nitrogen-Nutrient Response by Phosphorylating Ubiquitin Ligase ATL31<\/a>.
\nYasuda S, Aoyama S, Hasegawa Y, Sato T* and Yamaguchi J
\nMol. Plant<\/em> 10: 605-618, 2017
\n<\/span>\u65e5\u672c\u8a9e\u89e3\u8aacPDF<\/a><\/li>\n
Direct Transcriptional Activation of BT Genes by NLP Transcription Factors Is a Key Component of the Nitrate Response in Arabidopsis<\/a>.
\nSato T, Maekawa S, Konishi M, Yoshioka M, Sasaki Y, Maeda H, Ishida T, Kato Y, Yamaguchi J and Yanagisawa S*
\nBiochem. Biophys. Res. Commun.<\/em> 483:380-386, 2017
\n\u65e5\u672c\u8a9e\u89e3\u8aacPDF<\/a><\/span><\/li>\n
Ubiquitin related enzymes and plant-specific ubiquitin ligase ATL family in tomato plants<\/a>.
\nLi X, Hasegawa Y, Lu Y and Sato T*
\nPlant Biotechnol.<\/em> 34: 71-78.
\n<\/span><\/li>\n
Membrane-localized ubiquitin ligase ATL15 functions in sugar-responsive growth regulation in Arabidopsis<\/a>
\nAoyama S, Terada S, Sanagi M, Hasegawa Y, Lu Y, Morita Y, Chiba Y, Sato T and Yamaguchi J^{<\/sup>
\nBiochem. Biophys. Res. Commun.<\/em> 2017, 491:33-39.
\n}\u65e5\u672c\u8a9e\u89e3\u8aacPDF<\/a>
\n<\/span><\/li>\n<\/ul>\n
2016<\/h1>\n
\n
Characterization of ubiquitin ligase SlATL31 and proteomic analysis of 14-3-3 targets in tomato fruit tissue (Solanum lycopersicum L.<\/em>).<\/a>
\nLu Y^{a<\/sup>, Yasuda S^{a<\/sup>, Li X, Fukao Y, Tohge T, Fernie AR, Matsukura C, Ezura H, Sato T and Yamaguchi J\u00a0 (^{a<\/sup>These authors contributed equally to this work)
\nJournal of Proteomics<\/em> 143: 254-264, 2016
\n<\/span>}}}\u65e5\u672c\u8a9e\u89e3\u8aacPDF<\/a><\/li>\n
Integration of C\/N-nutrient and multiple environmental signals into the ABA signaling cascade.<\/a>
\n Lu Y, Yamaguchi J, Sato T<\/a>
\nPlant Signaling & Behavior<\/em> e1048940, 2016<\/span><\/li>\n<\/ul>\n
2015<\/h1>\n
\n
ABI1 regulates carbon\/nitrogen-nutrient signal transduction independent of ABA biosynthesis and canonical ABA signaling pathways in Arabidopsis.<\/a>
\nLu Y, Sasaki Y, Li X, Mori C. Izumi, Matsuura T, Hirayama T, Sato T, Yamaguchi J
\nJ. Exp. Bot.<\/em> 66(9): 2763-2771, 2015
\n\u65e5\u672c\u8a9e\u89e3\u8aacPDF<\/a><\/li>\n<\/ul>\n
\n
Pale-green phenotype of atl31 atl6 double mutant leaves is caused by disruption of 5-aminolevulinic acid biosynthesis in Arabidopsis thaliana.<\/a>
\nMaekawa S, Takabayashi A, Huarancca Reyes T, Yamamoto H, Tanaka A, Sato T, Yamaguchi J
\nPLoS ONE<\/em>\u00a023;10(2): e0117662, 2015<\/li>\n<\/ul>\n
\n
The Arabidopsis<\/em>\u00a0ubiquitin ligase ATL31<\/em>\u00a0is transcriptionally controlled by WRKY33 transcription factor in response to pathogen attack.<\/a>
\nHuarancca Reyes T, Maekawa S, Sato T, Yamaguchi J
\nPlant Biotechnol.<\/em> 32:11-19, 2015<\/li>\n<\/ul>\n
2014<\/h1>\n
\n
Ubiquitin ligase ATL31 functions in leaf senescence in response to the balance between atmospheric CO2 and nitrogen availability in Arabidopsis.<\/a>
\nAoyama S, Huarancca Reyes T, Guglielminetti L, Yu L, Morita Y, Sato T, Yamaguchi J
\nPlant Cell Physiol.<\/em>\u00a055: 293-305, 2014
\n\u65e5\u672c\u8a9e\u89e3\u8aacPDF<\/a><\/li>\n<\/ul>\n
\n
Regulation of senescence under elevated atmospheric CO2 via ubiquitin modification.<\/a>
\nAoyama S, Lu Y, Sato T, Yamaguchi J
\nPlant Signaling & Behavior<\/em>\u00a0e28839, 2014<\/span><\/li>\n<\/ul>\n
\n
The C\/N regulator ATL31 controls papilla formation in response to powdery mildew fungi penetration by interacting with SNARE SYP121 in Arabidopsis.<\/a>
\nMaekawa S, Inada N, Yasuda S, Fukao Y, Fujiwara M, Sato T, Yamaguchi J
\nPlant Physiol.<\/em>\u00a0164: 879-887, 2014
\n\u65e5\u672c\u8a9e\u89e3\u8aacPDF<\/a><\/li>\n<\/ul>\n
\n
Phosphorylation of Arabidopsis ubiquitin ligase ATL31 is critical for plant C\/N-nutrient response under control of 14-3-3 stability.<\/a>
\nYasuda S, Sato T, Maekawa S, Aoyama S, Fukao Y, Yamaguchi J
\nJ. Biol. Chem.<\/em>\u00a0289: 15179-15193, 2014
\n<\/span>\u65e5\u672c\u8a9e\u89e3\u8aacPDF<\/a><\/li>\n<\/ul>\n
2013<\/h1>\n
\n
C\/N\u30d0\u30e9\u30f3\u30b9\u8abf\u7bc0\u306b\u3088\u308b\u690d\u7269\u306e\u4ee3\u8b1d\u30fb\u6210\u9577\u6226\u7565<\/a>
\n\u4f50\u85e4\u9577\u7dd2\uff0c\u5c71\u53e3\u6df3\u4e8c
\n\u5316\u5b66\u3068\u751f\u7269\uff0c51, 763-772.<\/li>\n<\/ul>\n
\n
Proteomics analysis reveals a highly heterogenous proteasome composition and the post-translational regulation of peptidase activity under pathogen signaling in plants.<\/a>
\nSun HH, Fukao Y, Ishida S, Yamamoto H, Maekawa S, Fujiwara M, Sato T, Yamaguchi J
\nJ. Proteome Res.<\/em>\u00a012: 5084-5095, 2013
\n\u65e5\u672c\u8a9e\u89e3\u8aacPDF<\/a><\/li>\n<\/ul>\n
\n
Assay for proteasome-dependent protein degradation and ubiquitinated proteins.
\nSato, T., Sako, K. and Yamaguchi J.
\nMethods. Mol. Biol.<\/em> \u201cPlant Proteomics: Methods and Protocols, 2nd edition”<\/em>, 655-663, 2013<\/li>\n<\/ul>\n
\n
Changes in mRNA stability associated with cold stress in Arabidopsis cells.
\nChiba Y, Mineta K, Hirai MY, Suzuki S, Kanaya S, Takahashi H, Onouchi H, Yamaguchi J, Naito S
\nPlant Cell Physiol.<\/em>\u00a054: 180-194, 2013<\/li>\n<\/ul>\n
\n
Arabidopsis transcriptional repressor ERF9 participates in resistance against necrotrophic fungi.
\nMaruyama Y, Yamoto N, Suzuki Y, Chiba Y, Yamazaki K, Sato T, Yamaguchi J
\nPlant Sci.<\/em> 213: 79-87, 2013<\/li>\n<\/ul>\n
2012<\/h1>\n
\n
Arabidopsis RPT2a, 19S proteasome subunit, regulates gene silencing via DNA methylation.
\nSako K, Maki Y, Kanai T, Kato E, Maekawa S, Yasuda S, Sato T, Watahiki MK, Yamaguchi J
\nPLoS ONE<\/em>\u00a07(5): e37086, 2012<\/li>\n<\/ul>\n
\n
The Arabidopsis ubiquitin ligases ATL31 and ATL6 control the defense response as well as the carbon\/nitrogen response.
\nMaekawa S, Sato T, Asada Y, Yasuda S, Yoshida M, Chiba Y, Yamaguchi J
\nPlant Mol. Biol.<\/em> 79: 217-227, 2012<\/li>\n<\/ul>\n
\n
Sugar-inducible RPT2a, a subunit of 26S proteasome, participates in sugar response in Arabidopsis.
\n<\/em>Sun H, Sako K, Suzuki Y, Maekawa S, Yasuda S, Chiba Y, Sato T and Yamaguchi J
\nPlant Biotechnol. <\/em>29: 279-284, 2012<\/li>\n<\/ul>\n
\n
Proteomics approach to study metabolic regulation mediated by ubiquitin-proteasome system in Arabidopsis.
\nYasuda S, Maekawa S, Sato T, Yamaguchi J
\nFrontiers in Agriculture Proteome Research<\/em>, 39-44, 2012<\/li>\n<\/ul>\n
\n
\u5e8f\u8ad6\uff1a\u9175\u6bcd\u304b\u3089\u52d5\u690d\u7269\u307e\u3067\u5305\u62ec\u3059\u308b\u30e6\u30d3\u30ad\u30c1\u30f3-\u30d7\u30ed\u30c6\u30a2\u30bd\u30fc\u30e0\u7cfb\u306e\u65b0\u5c55\u958b
\n\u5c71\u53e3\u6df3\u4e8c\uff0c\u7560\u5c71\u93ae\u6b21
\n\u751f\u5316\u5b66 84: 407-408, 2012<\/li>\n<\/ul>\n
\n
\u524d\u5ddd\u4fee\u543e\uff0c\u4f50\u53e4\u9999\u7e54\uff0c\u4f50\u85e4\u9577\u7dd2
\n\u690d\u7269\u306eRING\u578b\u30e6\u30d3\u30ad\u30c1\u30f3\u30ea\u30ac\u30fc\u30bc\u3068\u30d7\u30ed\u30c6\u30a2\u30bd\u30fc\u30e0\u30b7\u30b9\u30c6\u30e0\u306e\u6a5f\u80fd
\n\u751f\u5316\u5b66 84: 416-42, 2012<\/li>\n<\/ul>\n
\n
\u690d\u726926S\u30d7\u30ed\u30c6\u30a2\u30bd\u30fc\u30e0\u306e\u591a\u69d8\u306a\u6a5f\u80fd-\u300c\u54c1\u8cea\u7ba1\u7406\u300d\u306b\u3068\u3069\u307e\u3089\u305a\u5668\u5b98\u30b5\u30a4\u30ba\u3084\u907a\u4f1d\u5b50\u30b5\u30a4\u30ec\u30f3\u30b7\u30f3\u30b0\u306a\u3069\u69d8\u3005\u306a\u73fe\u8c61\u3092\u5236\u5fa1-
\n\u4f50\u53e4\u9999\u7e54
\n\u5316\u5b66\u3068\u751f\u7269\uff0c50: 232-234, 2012<\/span><\/li>\n<\/ul>\n
2011<\/h1>\n
\n
Identification of 14-3-3 proteins as a target of ATL31 ubiquitin ligase, a regulator of the C\/N response in Arabidopsis thaliana.
\n<\/em>Sato T, Maekawa S, Yasuda S, Domeki Y, Sueyoshi K, Fujiwara M, Fukao Y, Goto DB, Yamaguchi J
\nPlant J. <\/em>68: 137-146, 2011
\n\u65e5\u672c\u8a9e\u89e3\u8aacPDF<\/li>\n<\/ul>\n
\n
Carbon and nitrogen metabolism regulated by ubiquitin-proteasome system.
\nSato T, Maekawa S, Yasuda S, Yamaguchi J
\nPlant Signaling & Behavior<\/em> 6: 1465-1468, 2011
\n\u65e5\u672c\u8a9e\u89e3\u8aacPDF<\/li>\n<\/ul>\n
\n
The Arabidopsis NSL2 negatively controls systemic acquired resistance via hypersensitive response.
\nAsada Y, Yamamoto M, Tsutsui T, Yamaguchi J
\nPlant Biotechnol<\/em>. 28: 9-15, 2011<\/li>\n<\/ul>\n
\n
Arabidopsis thaliana 26S Proteasome Subunits RPT2a and RPT5a Are Crucial for Zinc Deficiency-Tolerance.
\nSakamoto T, Kamiya T, Sako K, Yamaguchi J, Yamagami M, Fujiwara T
\nBiosci. Biotech. Biochem.<\/em> 75: 561-567, 2011<\/span><\/li>\n<\/ul>\n
\n
Sucrose transporter NtSUT4 from tobacco BY-2 involved in plant cell shape during miniprotoplast culture.
\nOkubo-Kurihara E, Higaki T, Kurihara Y, Kutsuna N, Yamaguchi J, Hasezawa S
\nJ. Plant Res.<\/em> 123: 395-403, 2011<\/span><\/li>\n<\/ul>\n
2010<\/h1>\n
\n
Control of endoreduplication of trichome by RPT2a, a subunit of 19S proteasome in Arabidopsis.
\nSako K, Maki Y, Imai KK, Aoyama T, Goto DB, Yamaguchi J
\nJ Plant Res.<\/em> 123: 701-706, 2010<\/span><\/li>\n<\/ul>\n
\n
How does the plant proteasome control leaf size?
\nSako K, Yamaguchi J
\nPlant Signaling & Behavior <\/em>5(9):1119-20, 2010<\/li>\n<\/ul>\n
\n
In planta<\/em> observation of live fluorescent plant endoparasitic nematodes during early stages of infection.
\nGoto DK, Fosu-Nyarko J, Sakuma F, Sadler J, Flottman-Reid M, Uehara T, Kondo N, Yamaguchi J, Jones MGK
\nNematological Research<\/em>, 40: 15-19, 2010<\/span><\/li>\n<\/ul>\n
2009<\/h1>\n
\n
Regulation of leaf organ size by the Arabidopsis RPT2a 19S proteasome subunit.
\nSonoda Y, Sako K, Maki Y, Yamazaki N, Yamamoto H, Ikeda A, Yamaguchi J
\nPlant J. <\/em>60: 68-78, 2009<\/li>\n<\/ul>\n
\n
CNI1\/ATL31, a RING type ubiquitin ligase that functions in the Carbon\/Nitrogen response for growth phase transition in Arabidopsis seedlings.
\nSato T, Maekawa S, Yasuda S, Sonoda Y, Katoh E, Ichikawa T, Nakazawa M, Seki M, Shinozaki K, Matsui M, Goto DB, Ikeda A, Yamaguchi J
\nPlant J. <\/em>60: 852-864, 2009<\/li>\n<\/ul>\n
\n
DEAR1, a transcriptional repressor of DREB protein that mediates plant defense and freezing stress responses in Arabidopsis.
\nTsutsui T, Kato W, Asada Y, Sako K, Sato T, Sonoda Y, Kidokoro S, Yamaguchi-Shinozaki K, Tamaoki M, Arakawa K, Ichikawa T, Nakazawa M, Seki M, Shinozaki K, Matsui M, Ikeda A, Yamaguchi J
\nJ. Plant Res<\/em>. 122: 633-643, 2009<\/li>\n<\/ul>\n
\n
Arabidopsis MBF1s control Leaf Cell Cycle and its expansion.
\nTojo T, Tsuda K, Yoshizumi T, Ikeda A, Yamaguchi J, Matsui M and Yamazaki K
\nPlant Cell Physiol. <\/em>50: 254-264, 2009<\/span><\/li>\n<\/ul>\n
\n
\u30e6\u30d3\u30ad\u30c1\u30f3\u30ab\u30b9\u30b1\u30fc\u30c9-\u30d7\u30ed\u30c6\u30a2\u30bd\u30fc\u30e0\u30b7\u30b9\u30c6\u30e0\u306b\u3088\u308b\u690d\u7269\u306e\u6804\u990a\u5fdc\u7b54\u5236\u5fa1
\n\uff5eC\/N\u30d0\u30e9\u30f3\u30b9\u5fdc\u7b54\u6a5f\u69cb\u89e3\u660e\u306e\u65b0\u305f\u306a\u7cf8\u53e3\uff5e
\n\u4f50\u85e4\u9577\u7dd2
\n\u5316\u5b66\u3068\u751f\u7269 47: 2-4, 2009<\/li>\n<\/ul>\n
\n
\u7a2e\u5b50\u30c7\u30f3\u30d7\u30f3\u306e\u5206\u89e3
\n\u4f50\u85e4\u9577\u7dd2\uff0c\u5c71\u53e3\u6df3\u4e8c
\n\u7a2e\u5b50\u306e\u79d1\u5b66\u3068\u30d0\u30a4\u30aa\u30c6\u30af\u30ce\u30ed\u30b8\u30fc\uff08\u539f\u7530\u4e45\u4e5f\u76e3\u4fee\uff0c\u7a2e\u5b50\u751f\u7406\u751f\u5316\u5b66\u7814\u7a76\u4f1a\u7de8\uff09\uff0c\u5b66\u4f1a\u51fa\u7248\u30bb\u30f3\u30bf\u30fc\uff0c88-91\uff08ISBN978-4-7622-3059-2\uff09, 2009<\/li>\n<\/ul>\n
\n
\u70ad\u7d20\u4ee3\u8b1d
\n\u5c71\u53e3\u6df3\u4e8c
\n\u690d\u7269\u306e\u767e\u79d1\u4e8b\u5178\uff0e\u671d\u5009\u66f8\u5e97\u30009\uff08ISBN978-4-254-17137-2\uff09, 2009<\/span><\/li>\n<\/ul>\n
2008<\/h1>\n
\n
Promoter analysis of OsAMT1;2<\/em> and OsAMT1;3<\/em> implys their distinct roles of nitrogen utilization in rice.
\nYao S-G, Sonoda Y, Tsutsui T, Nakamura H, Ichikawa H, Ikeda A, Yamaguchi J
\nBreeding Sci. 58: 201-207, 2008<\/li>\n
Arabidopsis CAD1 negatively controls plant immunity mediated by both salicylic acid-dependent and -independent signalling pathways.
\nTsutsui T, Asada Y, Tamaoki M, Ikeda A, Yamaguchi J
\nPlant Sci.<\/em>175: 604-611, 2008<\/li>\n
\u30e6\u30d3\u30ad\u30c1\u30f3\u30ab\u30b9\u30b1\u30fc\u30c9\u3092\u8996\u70b9\u3068\u3057\u305f\u9ad8\u7b49\u690d\u7269\u306e\u201d\u7121\u9650\u6210\u9577\u201d
\n-\u830e\u9802\u5206\u88c2\u7d44\u7e54\u306e\u6a5f\u80fd\u7dad\u6301\u306b\u5fc5\u8981\u306a\u80fd\u52d5\u7684\u30bf\u30f3\u30d1\u30af\u8cea\u5206\u89e3\u30b7\u30b9\u30c6\u30e0\uff0d\uff0e
\n\u6c60\u7530\u4eae\uff0c\u4f50\u85e4\u9577\u7dd2
\n\u5316\u5b66\u3068\u751f\u7269 46(8): 516-517, 2008<\/li>\n<\/ul>\n
2007<\/h1>\n
\n
SHA1, a novel RING-finger protein functions in shoot apical meristem maintenance in Arabidopsis.
\nSonoda Y, Yao S-G, Sako K, Takeo Sato, Wataru Kato, Ohto M, Ichikawa T. Matsui M, Yamaguchi J and Ikeda A
\nPlant J. 50: 586-596, 2007<\/li>\n
alpha-Amylase production is induced by sulfuric acid in rice aleurone cells.
\nMitsunaga S, Kobayashi M, Fukui S, Fukuoka K, Kawakami O, Yamaguchi J, Ohshima M, Mitsui T
\nPlant Physiol. Biochem. 45: 922-925, 2007<\/li>\n
\u30d7\u30ed\u30c6\u30a2\u30bd\u30fc\u30e0\u3092\u4ecb\u3057\u305f\u7d30\u80de\u5236\u5fa1-\u9ad8\u7b49\u690d\u7269\u306e\u7d30\u80de\u30b5\u30a4\u30ba\u5236\u5fa1\u3092\u4e2d\u5fc3\u3068\u3057\u3066\uff0e
\n\u5712\u7530\u3000\u88d5\uff0c\u4f50\u85e4\u9577\u7dd2\uff0c\u5c71\u5d0e\u76f4\u5b50\uff0c\u4f50\u53e4\u9999\u7e54\uff0c\u6c60\u7530\u3000\u4eae\uff0c\u5c71\u53e3\u6df3\u4e8c
\n\u30d0\u30a4\u30aa\u3068\u30ca\u30ce\u306e\u878d\u5408\u2160\uff08\u5317\u6d77\u9053\u5927\u5b66COE\u7814\u7a76\u6210\u679c\u7de8\u96c6\u59d4\u54e1\u4f1a\u7de8\uff09\uff0c\u5317\u6d77\u9053\u5927\u5b66\u51fa\u7248\u4f1a\uff0c239-255, 2007<\/li>\n
\u690d\u7269\u30d7\u30ed\u30c6\u30a2\u30bd\u30fc\u30e0\u306e\u6a5f\u80fd-19S\u8907\u5408\u4f53\u3092\u4e2d\u5fc3\u3068\u3057\u3066\uff0e
\n\u4f50\u53e4\u9999\u7e54\uff0c\u5712\u7530\u3000\u88d5\uff0c\u6c60\u7530\u3000\u4eae\uff0c\u5c71\u53e3\u6df3\u4e8c
\n\u690d\u7269\u306e\u751f\u9577\u8abf\u7bc0\uff0c42: 54-60, 2007<\/li>\n<\/ul>\n
2006<\/h1>\n
\n
\u00a0Salicylic acid and a chitin elicitor both control expression of the CAD1 gene involved in plant immunity of Arabidopsis.
\nTsutsui T, Morita-Yamamuro C, Asada Y, Minami E, Shibuya N, Ikeda A, Yamaguchi J
\nBiosci. Biotech. Biochem. 70: 2042-2048, 2006<\/li>\n
Differential expression of two fructokinases in Oryza sativa seedlings grown under aerobic and anaerobic conditions.
\nGuglielminetti L, Morita A, Yamaguchi J, Loreti E, Perata P, Alpi A
\nJ Plant Res. 119: 351-356, 2006<\/li>\n<\/ul>\n
2005<\/h1>\n
\n
The Arabidopsis gene CAD1 controls programmed cell death in the plant innate immune system and encodes a protein containing a MACPF domain.
\nMorita-Yamamuro C, Tsutsui T, Sato M, Yoshioka H, Tamaoki M, Ogawa D, Matsuura H, Yoshihara T, Ikeda A, Uyeda I, Yamaguchi J
\nPlant Cell Physiol., 46: 902-912, 2005<\/li>\n
A transposon-induced spontaneous mutation results in low b-amylase content in rice.
\nSaika H, Nakazono M, Ikea A, Yamaguchi J, Masaki S, Kanekatsu M, Nemoto K
\nPlant Sci. 169: 239-244, 2005<\/li>\n
Measurement of the concentration of bioactive gibberellin in germinating rice seed using the alpha-amylase induction from aleurone cells.
\nMitsunaga S, Kawakami O, Yamaguchi J, Mitsui T
\nJ. Appl. Glycosci., 52: 399-402, 2005<\/li>\n<\/ul>\n
2004<\/h1>\n
\n
Low sugar status promotes endogenous ABA levels and ABA sensitivity in Arabidopsis.
\nMorita-Yamamuro C, Vernieri P, Yamaguchi J
\nPlant Biotechnol. 21: 9-14, 2004<\/li>\n
Knock-out of the plastid ribosomal protein S21 causes impaired photosynthesis and sugar-response during germination and seedling development in Arabidopsis thaliana.
\nMorita-Yamamuro C, Tsutsui T, Tanaka A, Yamaguchi J
\nPlant Cell Physiol. 45: 781-788, 2004<\/li>\n
Ammonium uptake and assimilation in rice.
\nYamaguchi J, Sonoda Y, Iwata A, Ikeda A, Tsutsui T, Morita-Yamamuro C, S.-G. Yao, Matsuhashi S, Fujimaki S, Sakamoto K, Arakawa K, Kume T
\nJAERI-Review 2004-025: 122-124, 2004<\/li>\n
Loss-of-function mutation of rice hexokinase OsHXK1 does not affect sugar regulation of alpha-amylase RAmy3D.
\nIwata A, Ikeda A, Miyao A, Hirochika H, Yamaguchi J
\nRice Genetics Newsletter, 21: 90-92<\/li>\n<\/ul>\n
2003<\/h1>\n
\n
Distinct expression and function of three ammonium transporter genes (OsAMT1;1-1;3) in rice.
\nSonoda Y, Ikeda, A, Saiki S, Von Wiren, N, Yamaya, T, Yamaguchi J
\nPlant Cell Physiol. 44: 726-734, 2003<\/li>\n
Feedback regulation of the ammonium transporter gene family AMT1 by glutamine in rice.
\nSonoda Y, Ikeda A, Saiki S, Yamaya T, Yamaguchi J
\nPlant Cell Physiol. 44: 1396-1402, 2003<\/li>\n
Constitutive expression of a novel-type ammonium transporter OsAMT2 in rice plants.
\nSuenaga A, Moriya K, Sonoda Y, Ikeda A, von Wiren N, Hayakawa T, Yamaguchi J, Yamaya T
\nPlant Cell Physiol. 44: 206-211, 2003<\/li>\n
Sugar transporters involved in flowering and grain development of rice.
\nNgampanya B, Takeda T, Naragajavana J, Ikeda A, Yamaguchi J
\nJ. Appli. Glycosci. 50: 237-240, 2003<\/li>\n
A novel gene encoding a Ca2+-binding protein is under hexokinase-dependent sugar regulation.
\nOhtsuki S, Ikeda A, Sunako T, Muto S, Yazaki J, Nakamura K, Fujii F, Kanako S, Otsuka Y, Yamamoto K , Sakata K, Sasaki T, Kishimoto N, Kikuchi S, Yamaguchi J
\nBiosci. Biotech. Biochem. 67: 347-353, 2003<\/li>\n
Characterization of new rice functional monosaccharide transporter, OsMST5, involved in Flower development.
\nNgampanya B, Sobolewska A, Takeda T, Toyofuku K, Naragajavana J, Ikeda A, Yamaguchi J
\nBiosci. Biotech. Biochem .67: 556-562, 2003<\/li>\n
Sugar modulation of a-amylase genes under anoxia.
\nLoret E, Yamaguchi J, Alpi A, Perata P
\nAnn. Bot. 91: 143-148, 2003<\/li>\n
Gibberellins are not required for rice germination under anoxia.
\nLoreti E, Yamaguchi J, Alpi A, Perata P
\nPlant and Soil 253: 137-143, 2003<\/li>\n
Negative-feedback regulation of ammonium uptake and translocation in rice under ambient and elevated CO2 conditions.
\nYamaguchi J, Ohtsuki S, Sonoda Y, Yamamuro C, Ikeda A, Fujimaki S, Ishioka N, Matsuhashi S, Sekine T and Kume T
\nJAERI-Review 2003-033: 126-128, 2003<\/li>\n
\u30b8\u30d9\u30ec\u30ea\u30f3\u30b7\u30b0\u30ca\u30eb\u4f1d\u9054\u56e0\u5b50\uff1bDELLA\u30d5\u30a1\u30df\u30ea\u30fc\u3092\u4e2d\u5fc3\u3068\u3057\u3066.
\n\u6c60\u7530\u3000\u4eae, \u5c71\u5ba4\u3000\u5343\u9db4\u5b50, \u5c71\u53e3\u6df3\u4e8c
\n\u690d\u7269\u306e\u5316\u5b66\u8abf\u7bc0, 38: 36-47, 2003<\/li>\n
\u70ad\u7d20\u6e90\u5206\u914d\u306e\u5236\u5fa1\u6a5f\u69cb\uff0dC\/N\u30d0\u30e9\u30f3\u30b9\u306b\u3088\u308b\u5236\u5fa1\u3092\u4e2d\u5fc3\u3068\u3057\u3066\uff0d
\n\u6c60\u7530\u3000\u4eae, \u5712\u7530\u3000\u88d5, \u5c71\u53e3\u6df3\u4e8c
\n\u86cb\u767d\u8cea\u6838\u9178\u9175\u7d20, 48: 2103-2112, 2003<\/li>\n
\u5149\u5408\u6210\u540c\u5316\u7523\u7269\u306e\u7d30\u80de\u9593\u8f38\u9001\u3068\u5668\u5b98\u9593\u8f38\u9001\uff0d\u7cd6\u30c8\u30e9\u30f3\u30b9\u30dd\u30fc\u30bf\u30fc\u3068\u7dad\u7ba1\u675f\u6a5f\u80fd\u3092\u4e2d\u5fc3\u3068\u3057\u3066\uff0d\uff0e
\n\u5c71\u53e3\u6df3\u4e8c
\nJ. Appl. Glycosci. 50: 91-92, 2003<\/li>\n<\/ul>\n
2002<\/h1>\n
\n
\u00a0The slender rice mutant, with constitutively activated gibberellin signal transduction, has enhanced capacity for abscisic acid level.
\nIkeda A, Sonoda Y, Vernieri P, Perata P, Hirochika H, Yamaguchi J
\nPlant Cell Physiol. 43: 974-979, 2002<\/li>\n
Characterization of OsSUT2 cDNA expressed before flowering stage of rice.
\nNgampanya B, Takeda T, Sonoda Y, Naragajavana J, Ikeda A, Yamaguchi J
\nRice Genetics Newsletter, 19: 49-52, 2002<\/li>\n
Positoron imaging analysis of assimilation and translocation of carbon and nitrogen sources in rice plant.
\nOtsuki S, Sonoda Y, Saiki S, Ikeda A, Matsuhashi S, Watanabe S, Ishioka N.S., Sekine T, Yamaguchi J
\nJAERI-Review 2002-035: 100-102, 2002<\/li>\n
\u6839\u306e\u30a2\u30f3\u30e2\u30cb\u30a6\u30e0\u30a4\u30aa\u30f3\u53d6\u308a\u8fbc\u307f\u306b\u95a2\u4e0e\u3059\u308b\u907a\u4f1d\u5b50\u7fa4
\n\u658e\u6728\u91cc\u6587\uff0c\u5712\u7530\u88d5\uff0c\u6c60\u7530\u4eae\uff0c\u5c71\u53e3\u6df3\u4e8c
\n\u8fb2\u696d\u304a\u3088\u3073\u5712\u82b8, 77: 39-47, 2002 [ISSN 0369-5247]<\/li>\n<\/ul>\n
2001<\/h1>\n
\n
Slender rice<\/i>, a constitutive gibberellin response mutant, is caused by a null mutation of the SLR1<\/i> gene, an ortholog of the height-regulating gene GAI\/RGA\/RHT\/D8.<\/i>
\nIkeda A, Ueguchi-Tanaka M, Sonoda Y, Kitano H, Koshioka M, Futsuhara Y, Matsuoka M, Yamaguchi J.
\nThe Plant Cell, 13: 99-110, 2001<\/li>\n
Sugar transporters in grain development of rice.
\nTakeda T, Toyofuku K, Matsukura C, Yamaguchi J
\nJ. Plant Physiol. 158: 465-470, 2001<\/li>\n
\u30c7\u30f3\u30d7\u30f3\u306e\u5408\u6210\u3068\u5206\u89e3\u3002
\n\u6b66\u7530\u6cf0\u6597, \u5c71\u53e3\u6df3\u4e8c
\n\u671d\u5009\u690d\u7269\u751f\u7406\u5b66\u8b1b\u5ea7\u7b2c\uff12\u5dfb\u4ee3\u8b1d(\u5c71\u8c37\u77e5\u884c\u7de8\u96c6), pp94-102, \u671d\u5009\u66f8\u5e97, \u6771\u4eac, 2001<\/li>\n
Polymorphism in rice amylases at an early stage of seed germination.
\nMitsunaga S, Kawakami O, Numata T, Yamaguchi J, Fukui K, Mitsui T
\nBiosci. Biotechnol. Biochem.65: 662-665, 2001<\/li>\n<\/ul>\n
2000<\/h1>\n
\n
Transverse vein differentiation associated with the gas space formation – fate of middle cell layer in leaf sheath development of rice
\nMatsukura C, Kawai M, Toyofuku K, Barrero RA, Uchimiya H and Yamaguchi J.
\nAnnals of Botany, 85: 19-27, 2000<\/li>\n
Isoform Characterization of Hexose Kinases in Rice Embryo
\nGuglielminetti L, Perata P, Morita A, Loreti E, Yamaguchi J, Alpi A.
\nPhytochemistry, 53: 195-200, 2000<\/li>\n
Glucose modulates the abscisic acid-inducible Rab16A<\/i> gene in cereal embryos.
\nToyofuku K, Loreti E, Vernieri P, Alpi A, Perata P, Yamaguchi J
\nPlant Mol. Biol. 42: 451-460, 2000<\/li>\n
Expression of alpha-amylase isoforms and the RAmy1A<\/i> gene in rice (Oryza sativa <\/i>L.<\/i>) during seed germination , and its relationship with coleoptile length in submerged soil.
\nHuang J, Toyofuku K , Yamaguchi J and Akita S.
\nPlant Prod. Sci. 3: 32-37, 2000<\/li>\n
Distribution and characterization of enzymes responsible causing starch degradation in rice (Oryza sativa cv. Koshihikari<\/i>).
\nAwazuhara M, Nakagawa A, Yamaguchi J, Fujiwara T, Hayashi H, Hatae K, Chino M, Shimada A
\nJ. Agr. Food Chem. 48: 245-252, 2000<\/li>\n
\u80a5\u80b2\u30a4\u30cd\u306e\u4f5c\u51fa\uff01-\u7cd6\u30bb\u30f3\u30b5\u30fc\u6539\u5909\u306b\u3088\u308b\u65b0\u3057\u3044\u690d\u7269\u4ee3\u8b1d\u5de5\u5b66-.
\n\u5927\u69fb\u8302\u7537, \u5c71\u53e3\u6df3\u4e8c
\n\u30d0\u30a4\u30aa\u30b5\u30a4\u30a8\u30f3\u30b9\u3068\u30a4\u30f3\u30c0\u30b9\u30c8\u30ea\u30fc, 58: 38-39, 2000<\/li>\n
Sugar represses alpha-amylase independently of GA-myb<\/i> transcription.
\nLoreti E, Matsukura C, Gubler F, Alpi A, Yamaguchi J, Perata P
\nPlant Mol. Biol. 44: 85-90, 2000<\/li>\n
Sugar uptake and transport in rice embryos. Expression of companion cell-specific sucrose transporter (OsSUT1<\/i>) induced by sugar as well as light.
\nMatsukura C, Saitoh T, Hirose T, Ohsugi R, Perata P, Yamaguchi J
\nPlant Physiol. 124: 85-94, 2000<\/li>\n
Characterization and expression of monosaccharide transporters (OsMSTs<\/i>) in rice.
\nToyofuku K, Kasahara M, Yamaguchi J
\nPlant Cell Physiol. 41: 940-947, 2000<\/li>\n
The expression of a gene encoding Ca2+-binding EF-hand motif is induced by sugars in rice embryos.
\nOtsuki S, Matsukura C, Yamaguchi J
\nRice Genetics Newsletter 17: 92-94, 2000<\/li>\n
Characterization of rice ammonium transporters, OsAMT1;1 and OsAMT1;2.
\nSonoda Y, Ikeda A, Yamaguchi J
\nRice Genetics Newsletter 17: 89-92, 2000<\/li>\n
\u6839\u306e\u5373\u6839\u5f62\u6210\u3068\u7a92\u7d20\u306e\u53d6\u308a\u8fbc\u307f\u306b\u95a2\u3059\u308b\u907a\u4f1d\u5b50\u7fa4-\u690d\u7269\u306e\u6839\u306b\u95a2\u3059\u308b\u8af8\u554f\u984c(79).
\n\u6c60\u7530\u3000\u4eae, \u5712\u7530\u3000\u88d5, \u5c71\u53e3\u6df3\u4e8c
\n\u8fb2\u696d\u304a\u3088\u3073\u5712\u82b8 75: 301-308, 2000<\/li>\n<\/ul>\n
1999<\/h1>\n
\n
Characterization of beta-amylase and its deficiency in various rice cultivars.
\nYamaguchi J, Itoh S, Saitoh T, Ikeda A, Tashiro T and Nagato Y
\nTheor. Appl. Genet., 98: 32-38, 1999<\/li>\n
Reducing agent-mediated solubilization and activation of debranching enzyme (pullulanase) in rice flour.
\nTakeuchi W, Masui H and Yamaguchi J
\nBiosci. Biotech. Biochem., 63: 510-514, 1999<\/li>\n
Differences in sugar regulation between two isoforms of alpha-amylase in suspension-cultured cells of rice.
\nGeshi N, Mitsui T, Akazawa T and Yamaguchi J
\nJ. Appl. Glycosci. 46: 111-119, 1999<\/li>\n
Changes in alpha-amylase isoforms during emergence of rice in submerged soil.
\nHuang J, Yamaguchi J and Akita S.
\nPlant Prod. Sci. 2: 12-13, 1999<\/li>\n
Sugar repression of alpha-amylase genes in rice embryos.
\nYamaguchi J, Toyofuku K, Morita A, Ikeda A, Matsukura C and Perata P.
\nEight International Symposium on Pre-harvest Sprouting in Cereals 1998, Ed Weipert, D., Association of Cereal Research, Detmold, pp 136-145, 1999<\/li>\n
\u30aa\u30fc\u30ad\u30b7\u30f3\u3068\u30a4\u30cd\u306e\u6839\u306e\u5f62\u614b\u5f62\u6210- GASR1\u907a\u4f1d\u5b50\u30fb\u30bf\u30f3\u30d1\u30af\u8cea\u306e\u89e3\u6790
\n\u6c60\u7530\u3000\u4eae, \u5c71\u53e3\u6df3\u4e8c
\n\u6839\u306e\u7814\u7a76 8(1): 9-12, 1999<\/li>\n
Subcellular localization of rice hexose kinase, OsHXK1
\nSunako T, Morita A and Yamaguchi J.
\nRice Genetics Newsletter , 16: 120-122, 1999<\/li>\n
\u690d\u7269\u306e\u7be9\u7ba1\u8f38\u9001-\u30b9\u30af\u30ed\u30fc\u30b9\u30c8\u30e9\u30f3\u30b9\u30dd\u30fc\u30bf\u30fc\u306e\u767a\u73fe\u3068\u6a5f\u80fd
\n\u677e\u5009\u5343\u662d, \u5c71\u53e3\u6df3\u4e8c
\n\u5316\u5b66\u3068\u751f\u7269, 37: 639-642, 1999<\/li>\n<\/ul>\n
1998<\/h1>\n
\n
Promoter elements required for sugar repression of the <\/b>RAmy3D <\/i>gene for alpha-amylase in rice.
\nToyofuku K, Umemura T and Yamaguchi J
\nFEBS Lett., 428:275-280, 1998<\/li>\n
Functional dissection of a sugar-repressed alpha-amylase gene (RAmy1A<\/i>) promoter in rice embryos.
\nMorita A, Umemura T, Kuroyanagi M, Futsuhara Y, Perata P, Yamaguchi J
\nFEBS Lett., 423: 81-85, 1998<\/li>\n
Sugar sensing and alpha-amylase gene repression in rice embryos
\nUmemura T, Perata P, Futsuhara Y, Yamaguchi J
\nPlanta, 204: 420-428, 1998<\/li>\n
Leaf sheath growth promoted by gibberellins in dwarf mutant of rice.
\nMatsukura C, Itoh S, Nemoto K, Tanimoto E, Yamaguchi J
\nPlanta, 205:145-152, 1998<\/li>\n
Temporal and spatial expression pattern of alpha-amylase gene during germination in rice and barley.
\nSugimoto N, Takeda G, Nagato Y, Yamaguchi J
\nPlant Cell Physiol., 39: 323-333, 1998<\/li>\n
Analysis of embryo-specific alpha-amylase using isolated mature rice embryos.
\nYamaguchi J
\nBreeding Sci., 48:365-370, 1998<\/li>\n
Detection of proteins binding to the promoter region DNA using a nonradioactive gel-retardation assay.
\nMitsunaga S, Fukui K, Ohyama H and and Yamaguchi J
\nBiosci. Biotech. Biochem., 62(9):1812-1814, 1998<\/li>\n
Effect of anoxia on gibberellic acid-induced protease and beta-amylase processing in barley seeds.
\nLoreti E, Guglielminetti L, Yamaguchi J, Gonzali S, Alpi A, Perata P.
\nJ. Plant Physiol., 152: 44-50, 1998<\/li>\n
Starch degradation during gibberellin-induced leaf sheath growth in rice.
\nMatsukura C and Yamaguchi J
\nRice Genetics Newsletter, 15: 114-117, 1998<\/li>\n
Abscisic acid does not affect sugar-repression of rice alpha-amylase gene, RAmy3D<\/i>.
\nToyofuku K and Yamaguchi J
\nRice Genetics Newsletter, 15: 173-175, 1998<\/li>\n
\u03b1-\u30a2\u30df\u30e9\u30fc\u30bc\u306e\u8a98\u5c0e. \u4eca\u95a2\u82f1\u96c5\u30fb\u67f4\u5ca1\u5f18\u90ce\u7de8,
\n\u5c71\u53e3\u6df3\u4e8c, \u677e\u5009\u5343\u662d
\n\u690d\u7269\u30db\u30eb\u30e2\u30f3\u3068\u7d30\u80de\u306e\u5f62, \u5b66\u4f1a\u51fa\u7248\u30bb\u30f3\u30bf\u30fc, \u5927\u962a, 43-52, 1998<\/li>\n<\/ul>\n
1997<\/h1>\n
\n
Sugar repression of gibberellin-dependent signaling pathway in barley embryos.
\nPerata P, Matsukura C, Vernieri P, Yamaguchi J
\nPlant Cell, 9: 2197-2208, 1997<\/li>\n
Effects of anoxia on sucrose degrading enzymes in cereal seeds.
\nGuglielminetti L, Wu J, Boschi E, Yamaguchi J, Favati A, Vergara MR, Perata P, Alpi A
\nJ. Plant Physiol., 150: 251-258, 1997<\/li>\n
Characterization and expression of GASR1<\/i>, a root-specific GAST1-like protein in rice.
\nIkeda A, Yamaguchi J, Futsuhara
\nRice Genet. Newslett., 14: 150-153, 1997<\/li>\n
Temporal and spatial expression pattern of rice alpha-amylase gene RAmy1A<\/i> during seed development.
\nSugimoto N, Takeda G, Nagato Y, Yamaguchi J
\nRice Genet. Newslett., 14: 148-150, 1997<\/li>\n
The first leaf sheath growth promoted by gibberellins in dwarf mutant of rice.
\nMatsukura C, Yamaguchi J
\nRice Genet. Newslett., 14: 153-155, 1997<\/li>\n
\u03b1-\u30a2\u30df\u30e9\u30fc\u30bc\u907a\u4f1d\u5b50\u306e\u767a\u73fe\u5236\u5fa1 -\u690d\u7269\u30db\u30eb\u30e2\u30f3\u3068\u7cd6\u306b\u3088\u308b\u30b7\u30b0\u30ca\u30eb\u4f1d\u9054\u904e\u7a0b\u3092\u89e3\u660e\u306e\u305f\u3081\u306e\u5206\u5b50\u6307\u6a19\u3068\u3057\u3066-,
\n\u8c4a\u798f\u606d\u5b50, \u5149\u6c38\u4f38\u4e00\u90ce, \u5c71\u53e3\u6df3\u4e8c
\n\u690d\u7269\u306e\u5316\u5b66\u8abf\u7bc0, 32: 132-143, 1997<\/li>\n
\u30a2\u30ea\u30e5\u30fc\u30ed\u30f3\u5c64\u7d30\u80de\u3092\u7528\u3044\u305f\u03b1-\u30a2\u30df\u30e9\u30fc\u30bc\u8a98\u5c0e\u691c\u5b9a\u6cd5.
\n\u5c71\u53e3\u6df3\u4e8c
\n\u690d\u7269\u5316\u5b66\u8abf\u7bc0\u5b9f\u9a13\u30de\u30cb\u30e5\u30a2\u30eb, [\u690d\u7269\u5316\u5b66\u8abf\u7bc0\u5b66\u4f1a], pp.2-7, \u5168\u56fd\u8fb2\u6751\u6559\u80b2\u5354\u4f1a, \u6771\u4eac, 1997<\/li>\n
\u30a2\u30d6\u30b7\u30b8\u30f3\u9178\u306b\u3088\u308b\u03b1-\u30a2\u30df\u30e9\u30fc\u30bc\u8a98\u5c0e\u306e\u963b\u5bb3.
\n\u5c71\u53e3\u6df3\u4e8c, \u4f0a\u85e4\u4f38\u4e00
\n\u690d\u7269\u5316\u5b66\u8abf\u7bc0\u5b9f\u9a13\u30de\u30cb\u30e5\u30a2\u30eb, [\u690d\u7269\u5316\u5b66\u8abf\u7bc0\u5b66\u4f1a], pp.11-13, \u5168\u56fd\u8fb2\u6751\u6559\u80b2\u5354\u4f1a. \u6771\u4eac, 1997<\/li>\n
\u30ec\u30dd\u30fc\u30bf\u30fc\u907a\u4f1d\u5b50\u306e\u5c0e\u5165\u3068\u305d\u306e\u5fdc\u7528.
\n\u5c71\u53e3\u6df3\u4e8c, \u4f0a\u85e4\u7d00\u7f8e\u5b50, \u5cf6\u672c\u529f
\n\u690d\u7269\u5316\u5b66\u8abf\u7bc0\u5b9f\u9a13\u30de\u30cb\u30e5\u30a2\u30eb, [\u690d\u7269\u5316\u5b66\u8abf\u7bc0\u5b66\u4f1a], pp.139-143, \u5168\u56fd\u8fb2\u6751\u6559\u80b2\u5354\u4f1a. \u6771\u4eac, 1997<\/li>\n<\/ul>\n
1996<\/h1>\n
\n
Expression of <\/b>RAmy3D<\/i>-protein (isoform H) in rice seedlings. In K. Noda and Mares, D.J., eds,
\nYamaguchi J, Geshi N, Mitsunaga S, Itoh S, Umemura T, Masui H, Mitsui T
\nSeventh International Symposium on Pre-harvest Sprouting in Cereals 1995, Center for Academic Societies Japan, Osaka, 405-410, 1996<\/li>\n
Physicochemical and serological characterization of rice alpha-amylase isoforms and identification of their corresponding genes.
\nMitsui T, Yamaguchi J, Akazawa T
\nPlant Physiol., 110: 1395-1404, 1996<\/li>\n
Changes in alpha-amylase activity during plant regeneration from rice calli.
\nAbe T, Kudo M, Oka Y, Yamaguchi J, Sasahara T
\nJ. Plant Physiol., 149: 592-598, 1996<\/li>\n
The same nuclear proteins bind to the 5′-flanking regions of the rice seed storage protein, 16 kDa albumin, 13 kDa prolamin and type II glutelin genes.
\nNakase M, Yamada T, Kira T, Yamaguchi J, Aoki N, Nakamura R, Matsuda T, Adachi T
\nPlant Mol. Biol., 32: 621-630, 1996<\/li>\n<\/ul>\n
1995-1992<\/h1>\n
\n
Developmental and Hormonal Regulation of Rice alpha-Amylase (RAmy1A<\/i>)-gusA<\/i> Fusion Genes in Transgenic Rice Seeds.
\nItoh K, Yamaguchi J, Huang N, Rodriguez RL, Akazawa T, Shimamoto\u3000K
\nPlant Physiol., 107: 25-31, 1995<\/li>\n
Amylolytic Activities in Cereal Seeds under Aerobic and Anaerobic Conditions.
\nGuglielminetti L, Yamaguchi J, Perata P, Alpi A
\nPlant Physiol., 109: 1069-1076, 1995<\/li>\n
Sequence-specific interactions of a nulear protein factor with the promoter region of a rice gene for alpha-amylase, RAmy3D<\/i>.
\nMitsunaga S, Rodriguez RL, Yamaguchi J
\nNucleic Acids Res., 22: 1948-1953, 1994<\/li>\n
Identification and characterization of gibberellin-insensitive mutants selected from among dwarf mutants of rice.
\nMitsunaga S, Tashiro T, Yamaguchi J
\nTheor. Appl. Genet., 87<\/b>: 705-712, 1994<\/li>\n
Induction of alpha-Amylase is Repressed by Uniconazole, an Inhibitor of the Biosynthesis of Gibberellin, in a Dwarf Mutant of Rice, Waito-C.
\nMitsunaga S, Yamaguchi J
\nPlant Cell Physiol., 34: 243-249, 1993<\/li>\n
Effect of anoxia on the induction of alpha-amylase in cereal seeds.
\nPerata P, Geshi N, Yamaguchi J, Akazawa T
\nPlanta, 191: 402-408, 1993<\/li>\n
Effect of anoxia on starch breakdown in rice and wheat seeds.
\nPerata P, Pozueta-Romero J, Akazawa T, Yamaguchi J
\nPlanta, 188: 611-618, 1992<\/li>\n<\/ul>\n
\u8ad6\u6587\u767a\u8868<\/a><\/p>\n
\u5b66\u4f1a\u767a\u8868<\/a><\/p>\n","protected":false},"excerpt":{"rendered":"
\u4e3b\u8981\u8ad6\u6587\u30fb\u7dcf\u8aac C\/N\u6804\u990a\u5fdc\u7b54 C\/N\u30d0\u30e9\u30f3\u30b9\u8abf\u7bc0\u306b\u3088\u308b\u690d\u7269\u306e\u4ee3\u8b1d\u30fb\u6210\u9577\u6226\u7565 \u4f50\u85e4\u9577\u7dd2\uff0c\u5c71\u53e3\u6df3\u4e8c \u5316\u5b66\u3068\u751f\u7269\uff0c51, 763-772, 2013 The TGN\/EE SNARE protein SYP61 and th […]<\/p>\n","protected":false},"author":2,"featured_media":0,"parent":0,"menu_order":6,"comment_status":"closed","ping_status":"closed","template":"","meta":{"footnotes":""},"_links":{"self":[{"href":"https:\/\/c-mng.cwh.hokudai.ac.jp\/biol.sci\/Root\/wp-json\/wp\/v2\/pages\/28"}],"collection":[{"href":"https:\/\/c-mng.cwh.hokudai.ac.jp\/biol.sci\/Root\/wp-json\/wp\/v2\/pages"}],"about":[{"href":"https:\/\/c-mng.cwh.hokudai.ac.jp\/biol.sci\/Root\/wp-json\/wp\/v2\/types\/page"}],"author":[{"embeddable":true,"href":"https:\/\/c-mng.cwh.hokudai.ac.jp\/biol.sci\/Root\/wp-json\/wp\/v2\/users\/2"}],"replies":[{"embeddable":true,"href":"https:\/\/c-mng.cwh.hokudai.ac.jp\/biol.sci\/Root\/wp-json\/wp\/v2\/comments?post=28"}],"version-history":[{"count":4,"href":"https:\/\/c-mng.cwh.hokudai.ac.jp\/biol.sci\/Root\/wp-json\/wp\/v2\/pages\/28\/revisions"}],"predecessor-version":[{"id":3694,"href":"https:\/\/c-mng.cwh.hokudai.ac.jp\/biol.sci\/Root\/wp-json\/wp\/v2\/pages\/28\/revisions\/3694"}],"wp:attachment":[{"href":"https:\/\/c-mng.cwh.hokudai.ac.jp\/biol.sci\/Root\/wp-json\/wp\/v2\/media?parent=28"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}