Brassinazole (BioDeep_00000791556)
代谢物信息卡片
(Rac)-Brassinazole
化学式: C18H18ClN3O (327.1138)
中文名称: 芸苔素唑
谱图信息:
最多检出来源 () 0%
分子结构信息
SMILES: CC(C1=CC=CC=C1)(C(CC2=CC=C(C=C2)Cl)N3C=NC=N3)O
InChI: InChI=1S/C18H18ClN3O/c1-18(23,15-5-3-2-4-6-15)17(22-13-20-12-21-22)11-14-7-9-16(19)10-8-14/h2-10,12-13,17,23H,11H2,1H3
数据库引用编号
分类词条
相关代谢途径
Reactome(0)
BioCyc(0)
PlantCyc(0)
代谢反应
0 个相关的代谢反应过程信息。
Reactome(0)
BioCyc(0)
WikiPathways(0)
Plant Reactome(0)
INOH(0)
PlantCyc(0)
COVID-19 Disease Map(0)
PathBank(0)
PharmGKB(0)
0 个相关的物种来源信息
在这里通过桑基图来展示出与当前的这个代谢物在我们的BioDeep知识库中具有相关联信息的其他代谢物。在这里进行关联的信息来源主要有：
- PubMed: 来源于PubMed文献库中的文献信息，我们通过自然语言数据挖掘得到的在同一篇文献中被同时提及的相关代谢物列表，这个列表按照代谢物同时出现的文献数量降序排序，取前10个代谢物作为相关研究中关联性很高的代谢物集合展示在桑基图中。
- NCBI Taxonomy: 通过文献数据挖掘，得到的代谢物物种来源信息关联。这个关联信息同样按照出现的次数降序排序，取前10个代谢物作为高关联度的代谢物集合展示在桑吉图上。
- Chemical Taxonomy: 在物质分类上处于同一个分类集合中的其他代谢物
- Chemical Reaction: 在化学反应过程中，存在为当前代谢物相关联的生化反应过程中的反应底物或者反应产物的关联代谢物信息。
点击图上的相关代谢物的名称，可以跳转到相关代谢物的信息页面。
| 亚细胞结构定位 | 关联基因列表 |
|---|
文献列表
- Linna Wang, Miao Lin, Lina Zou, Shunran Zhang, Yangang Lan, Hanwei Yan, Yan Xiang. Comprehensive investigation of BZR gene family in four dicots and the function of PtBZR9 and PtBZR12 under drought stress.
Plant physiology and biochemistry : PPB.
2024 Jan; 207(?):108360. doi:
10.1016/j.plaphy.2024.108360. [PMID: 38266559] - Yu-Tong Jiang, Lu-Han Yang, Ji-Xuan Zheng, Xian-Chen Geng, Yu-Xuan Bai, Yu-Chen Wang, Hong-Wei Xue, Wen-Hui Lin. Vacuolar H+-ATPase and BZR1 form a feedback loop to regulate the homeostasis of BR signaling in Arabidopsis.
Molecular plant.
2023 12; 16(12):1976-1989. doi:
10.1016/j.molp.2023.10.007. [PMID: 37837193] - Runjie Diao, Mengru Zhao, Yannan Liu, Zhenhua Zhang, Bojian Zhong. The advantages of crosstalk during the evolution of the BZR1-ARF6-PIF4 (BAP) module.
Journal of integrative plant biology.
2023 Dec; 65(12):2631-2644. doi:
10.1111/jipb.13554. [PMID: 37552560] - Wenqi Feng, Hongwanjun Zhang, Yang Cao, Yuan Liu, Yiran Zhao, Fuai Sun, Qingqing Yang, Xuecai Zhang, Yuanyuan Zhang, Yingge Wang, Wanchen Li, Yanli Lu, Fengling Fu, Haoqiang Yu. Maize ZmBES1/BZR1-1 transcription factor negatively regulates drought tolerance.
Plant physiology and biochemistry : PPB.
2023 Dec; 205(?):108188. doi:
10.1016/j.plaphy.2023.108188. [PMID: 37979574] - Xuxu Wang, Jia Wei, Jiahao Wu, Baojing Shi, Peihui Wang, Ahmed Alabd, Duanni Wang, Yuhao Gao, Junbei Ni, Songling Bai, Yuanwen Teng. Transcription factors BZR2/MYC2 modulate brassinosteroid and jasmonic acid crosstalk during pear dormancy.
Plant physiology.
2023 Nov; ?(?):. doi:
10.1093/plphys/kiad633. [PMID: 38036294] - So-Hee Kim, Se-Hwa Lee, Tae-Ki Park, Yanchen Tian, Kyoungjae Yu, Byeong-Ha Lee, Ming-Yi Bai, Sung-Jin Cho, Tae-Wuk Kim. Comparative analysis of BZR1/BES1 family transcription factors in Arabidopsis.
The Plant journal : for cell and molecular biology.
2023 Nov; ?(?):. doi:
10.1111/tpj.16527. [PMID: 37926922] - Ruizhen Yang, Ziyi Yang, Meng Xing, Yexing Jing, Yunwei Zhang, Kewei Zhang, Yun Zhou, Huixian Zhao, Weihua Qiao, Jiaqiang Sun. TaBZR1 enhances wheat salt tolerance via promoting ABA biosynthesis and ROS scavenging.
Journal of genetics and genomics = Yi chuan xue bao.
2023 Nov; 50(11):861-871. doi:
10.1016/j.jgg.2023.09.006. [PMID: 37734712] - Ruizhen Yang, Pan Liu, Tianren Zhang, Huixue Dong, Yexing Jing, Ziyi Yang, Sha Tang, Yu Zhang, Mingjie Lv, Jun Liu, Yunwei Zhang, Weihua Qiao, Jie Liu, Jiaqiang Sun. Plant-specific BLISTER interacts with kinase BIN2 and BRASSINAZOLE RESISTANT1 during skotomorphogenesis.
Plant physiology.
2023 09; 193(2):1580-1596. doi:
10.1093/plphys/kiad353. [PMID: 37335918] - Yicheng Wang, Yansong Zhu, Huiyan Jiang, Zuolin Mao, Junkang Zhang, Hongcheng Fang, Wenjun Liu, Zongying Zhang, Xuesen Chen, Nan Wang. The regulatory module MdBZR1-MdCOL6 mediates brassinosteroid- and light-regulated anthocyanin synthesis in apple.
The New phytologist.
2023 05; 238(4):1516-1533. doi:
10.1111/nph.18779. [PMID: 36710519] - Shilei Luo, Guobin Zhang, Zeyu Zhang, Zilong Wan, Zeci Liu, Jian Lv, Jihua Yu. Genome-wide identification and expression analysis of BZR gene family and associated responses to abiotic stresses in cucumber (Cucumis sativus L.).
BMC plant biology.
2023 Apr; 23(1):214. doi:
10.1186/s12870-023-04216-9. [PMID: 37095428] - Fanliang Meng, Haoran Liu, Songshen Hu, Chengguo Jia, Min Zhang, Songwen Li, Yuanyuan Li, Jiayao Lin, Yue Jian, Mengyu Wang, Zhiyong Shao, Yuanyu Mao, Lihong Liu, Qiaomei Wang. The brassinosteroid signaling component SlBZR1 promotes tomato fruit ripening and carotenoid accumulation.
Journal of integrative plant biology.
2023 Apr; ?(?):. doi:
10.1111/jipb.13491. [PMID: 37009849] - De Peng Yuan, Shuo Yang, Lu Feng, Jin Chu, Hai Dong, Jian Sun, Huan Chen, Zhuo Li, Naoki Yamamoto, Aiping Zheng, Shuang Li, Hong Chan Yoon, Jingsheng Chen, Dianrong Ma, Yuan Hu Xuan. Red-light receptor phytochrome B inhibits BZR1-NAC028-CAD8B signaling to negatively regulate rice resistance to sheath blight.
Plant, cell & environment.
2023 04; 46(4):1249-1263. doi:
10.1111/pce.14502. [PMID: 36457051] - Yui Otani, Mika Kawanishi, Miyu Kamimura, Azusa Sasaki, Yasushi Nakamura, Takako Nakamura, Shigehisa Okamoto. Behavior and possible function of Arabidopsis BES1/BZR1 homolog 2 in brassinosteroid signaling.
Plant signaling & behavior.
2022 12; 17(1):2084277. doi:
10.1080/15592324.2022.2084277. [PMID: 35695417] - Mengyu Wang, Congxi Cai, Yubo Li, Han Tao, Fanliang Meng, Bo Sun, Huiying Miao, Qiaomei Wang. Brassinosteroids fine-tune secondary and primary sulfur metabolism through BZR1-mediated transcriptional regulation.
Journal of integrative plant biology.
2022 Dec; ?(?):. doi:
10.1111/jipb.13442. [PMID: 36573424] - Shohei Nosaki, Nobutaka Mitsuda, Shingo Sakamoto, Kazuki Kusubayashi, Ayumi Yamagami, Yuqun Xu, Thi Bao Chau Bui, Tohru Terada, Kenji Miura, Takeshi Nakano, Masaru Tanokura, Takuya Miyakawa. Brassinosteroid-induced gene repression requires specific and tight promoter binding of BIL1/BZR1 via DNA shape readout.
Nature plants.
2022 12; 8(12):1440-1452. doi:
10.1038/s41477-022-01289-6. [PMID: 36522451] - Kangqi Sang, Junjie Li, Xiangjie Qian, Jingquan Yu, Yanhong Zhou, Xiaojian Xia. The APETALA2a/DWARF/BRASSINAZOLE-RESISTANT 1 module contributes to carotenoid synthesis in tomato fruits.
The Plant journal : for cell and molecular biology.
2022 12; 112(5):1238-1251. doi:
10.1111/tpj.16009. [PMID: 36271694] - Uzair Ullah, Abdullah Shalmani, Mohammad Ilyas, Ali Raza, Sheraz Ahmad, Amir Zaman Shah, Fahim Ullah Khan, AzizUd-Din, Ayesha Bibi, Shafee Ur Rehman, Zaheer Abbas, Zeeshan Ali Buttar. BZR proteins: identification, evolutionary and expression analysis under various exogenous growth regulators in plants.
Molecular biology reports.
2022 Dec; 49(12):12039-12053. doi:
10.1007/s11033-022-07814-2. [PMID: 36309612] - Chunliu Zuo, Lan Zhang, Xinyue Yan, Xinyue Guo, Qing Zhang, Songyang Li, Yanling Li, Wen Xu, Xiaoming Song, Jinpeng Wang, Min Yuan. Evolutionary analysis and functional characterization of BZR1 gene family in celery revealed their conserved roles in brassinosteroid signaling.
BMC genomics.
2022 Aug; 23(1):568. doi:
10.1186/s12864-022-08810-3. [PMID: 35941544] - Jiaqi Hou, Xueke Zheng, Ruifei Ren, Qipeng Shi, Huangzhuo Xiao, Zhenfei Chen, Mengxia Yue, Yequn Wu, Haoli Hou, Lijia Li. The histone deacetylase 1/GSK3/SHAGGY-like kinase 2/BRASSINAZOLE-RESISTANT 1 module controls lateral root formation in rice.
Plant physiology.
2022 06; 189(2):858-873. doi:
10.1093/plphys/kiac015. [PMID: 35078247] - Min Xiong, Jiawen Yu, Jindong Wang, Qiang Gao, Lichun Huang, Chen Chen, Changquan Zhang, Xiaolei Fan, Dongsheng Zhao, Qiao-Quan Liu, Qian-Feng Li. Brassinosteroids regulate rice seed germination through the BZR1-RAmy3D transcriptional module.
Plant physiology.
2022 05; 189(1):402-418. doi:
10.1093/plphys/kiac043. [PMID: 35139229] - Yanchen Tian, Na Zhao, Minmin Wang, Wenying Zhou, Jieqiong Guo, Chao Han, Chuanen Zhou, Wenfei Wang, Shuang Wu, Wenqiang Tang, Min Fan, Ming-Yi Bai. Integrated regulation of periclinal cell division by transcriptional module of BZR1-SHR in Arabidopsis roots.
The New phytologist.
2022 01; 233(2):795-808. doi:
10.1111/nph.17824. [PMID: 34693527] - Mahipal Singh Kesawat, Bhagwat Singh Kherawat, Anupama Singh, Prajjal Dey, Mandakini Kabi, Debanjana Debnath, Debanjana Saha, Ansuman Khandual, Sandeep Rout, Manorama, Asjad Ali, Ramasubba Reddy Palem, Ravi Gupta, Avinash Ashok Kadam, Hyun-Uk Kim, Sang-Min Chung, Manu Kumar. Genome-Wide Identification and Characterization of the Brassinazole-resistant (BZR) Gene Family and Its Expression in the Various Developmental Stage and Stress Conditions in Wheat (Triticum aestivum L.).
International journal of molecular sciences.
2021 Aug; 22(16):. doi:
10.3390/ijms22168743. [PMID: 34445448] - Xuehuan Dai, Qing Lu, Jing Wang, Lili Wang, Fengning Xiang, Zhenhua Liu. MiR160 and its target genes ARF10, ARF16 and ARF17 modulate hypocotyl elongation in a light, BRZ, or PAC-dependent manner in Arabidopsis: miR160 promotes hypocotyl elongation.
Plant science : an international journal of experimental plant biology.
2021 Feb; 303(?):110686. doi:
10.1016/j.plantsci.2020.110686. [PMID: 33487334] - Huixue Dong, Jie Liu, Guanhua He, Pan Liu, Jiaqiang Sun. Photoexcited phytochrome B interacts with brassinazole resistant 1 to repress brassinosteroid signaling in Arabidopsis.
Journal of integrative plant biology.
2020 May; 62(5):652-667. doi:
10.1111/jipb.12822. [PMID: 31081597] - Jae Hoon Lee, Geunhwa Kwak, Yong Pyo Lim, Man-Ho Oh. 14-3-3 proteins contribute to leaf and root development via brassinosteroid insensitive 1 in Arabidopsis thaliana.
Genes & genomics.
2020 03; 42(3):347-354. doi:
10.1007/s13258-019-00909-4. [PMID: 31902106] - Wilfried Rozhon, Sonia Akter, Atiara Fernandez, Brigitte Poppenberger. Inhibitors of Brassinosteroid Biosynthesis and Signal Transduction.
Molecules (Basel, Switzerland).
2019 Nov; 24(23):. doi:
10.3390/molecules24234372. [PMID: 31795392] - Michael Derevyanchuk, Sergii Kretynin, Yaroslav Kolesnikov, Raisa Litvinovskaya, Jan Martinec, Vladimir Khripach, Volodymyr Kravets. Seed germination, respiratory processes and phosphatidic acid accumulation in Arabidopsis diacylglycerol kinase knockouts - The effect of brassinosteroid, brassinazole and salinity.
Steroids.
2019 07; 147(?):28-36. doi:
10.1016/j.steroids.2019.04.002. [PMID: 30981682] - Keisuke Fujiyama, Tomoya Hino, Masahiro Kanadani, Bunta Watanabe, Hyoung Jae Lee, Masaharu Mizutani, Shingo Nagano. Structural insights into a key step of brassinosteroid biosynthesis and its inhibition.
Nature plants.
2019 06; 5(6):589-594. doi:
10.1038/s41477-019-0436-6. [PMID: 31182839] - Ning Cao, Binhui Zhan, Xueping Zhou. Nitric Oxide as a Downstream Signaling Molecule in Brassinosteroid-Mediated Virus Susceptibility to Maize Chlorotic Mottle Virus in Maize.
Viruses.
2019 04; 11(4):. doi:
10.3390/v11040368. [PMID: 31013593] - Andrzej Bajguz, Wacław Orczyk, Agnieszka Gołębiewska, Magdalena Chmur, Alicja Piotrowska-Niczyporuk. Occurrence of brassinosteroids and influence of 24-epibrassinolide with brassinazole on their content in the leaves and roots of Hordeum vulgare L. cv. Golden Promise.
Planta.
2019 Jan; 249(1):123-137. doi:
10.1007/s00425-018-03081-3. [PMID: 30594955] - Qiqi Yan, Lixiang Wang, Xia Li. GmBEHL1, a BES1/BZR1 family protein, negatively regulates soybean nodulation.
Scientific reports.
2018 05; 8(1):7614. doi:
10.1038/s41598-018-25910-x. [PMID: 29769571] - Jutiporn Thussagunpanit, Kanapol Jutamanee, Sureeporn Homvisasevongsa, Apichart Suksamrarn, Ayumi Yamagami, Takeshi Nakano, Tadao Asami. Characterization of synthetic ecdysteroid analogues as functional mimics of brassinosteroids in plant growth.
The Journal of steroid biochemistry and molecular biology.
2017 09; 172(?):1-8. doi:
10.1016/j.jsbmb.2017.05.003. [PMID: 28479230] - Xing-Guang Deng, Tong Zhu, Da-Wei Zhang, Hong-Hui Lin. The alternative respiratory pathway is involved in brassinosteroid-induced environmental stress tolerance in Nicotiana benthamiana.
Journal of experimental botany.
2015 Oct; 66(20):6219-32. doi:
10.1093/jxb/erv328. [PMID: 26175355] - Hak-Soo Lee, Yoon Kim, Giang Pham, Ju Won Kim, Ji-Hye Song, Yew Lee, Yong-Sic Hwang, Stanley J Roux, Soo-Hwan Kim. Brassinazole resistant 1 (BZR1)-dependent brassinosteroid signalling pathway leads to ectopic activation of quiescent cell division and suppresses columella stem cell differentiation.
Journal of experimental botany.
2015 Aug; 66(15):4835-49. doi:
10.1093/jxb/erv316. [PMID: 26136267] - Anna Janeczko, Jana Oklestkova, Ondrej Novak, Katarzyna Śniegowska-Świerk, Zuzanna Snaczke, Ewa Pociecha. Disturbances in production of progesterone and their implications in plant studies.
Steroids.
2015 Apr; 96(?):153-63. doi:
10.1016/j.steroids.2015.01.025. [PMID: 25676788] - Setsuko Shimada, Tomoyuki Komatsu, Ayumi Yamagami, Miki Nakazawa, Minami Matsui, Hiroshi Kawaide, Masahiro Natsume, Hiroyuki Osada, Tadao Asami, Takeshi Nakano. Formation and dissociation of the BSS1 protein complex regulates plant development via brassinosteroid signaling.
The Plant cell.
2015 Feb; 27(2):375-90. doi:
10.1105/tpc.114.131508. [PMID: 25663622] - Florian Schröder, Janina Lisso, Toshihiro Obata, Alexander Erban, Eugenia Maximova, Patrick Giavalisco, Joachim Kopka, Alisdair R Fernie, Lothar Willmitzer, Carsten Müssig. Consequences of induced brassinosteroid deficiency in Arabidopsis leaves.
BMC plant biology.
2014 Nov; 14(?):309. doi:
10.1186/s12870-014-0309-0. [PMID: 25403461] - Christoph A Bücherl, G Wilma van Esse, Alex Kruis, Jeroen Luchtenberg, Adrie H Westphal, José Aker, Arie van Hoek, Catherine Albrecht, Jan Willem Borst, Sacco C de Vries. Visualization of BRI1 and BAK1(SERK3) membrane receptor heterooligomers during brassinosteroid signaling.
Plant physiology.
2013 Aug; 162(4):1911-25. doi:
10.1104/pp.113.220152. [PMID: 23796795] - Jens Hartmann, Nils Stührwohldt, Renate I Dahlke, Margret Sauter. Phytosulfokine control of growth occurs in the epidermis, is likely to be non-cell autonomous and is dependent on brassinosteroids.
The Plant journal : for cell and molecular biology.
2013 Feb; 73(4):579-90. doi:
10.1111/tpj.12056. [PMID: 23083315] - Qian-Feng Li, Chunming Wang, Lei Jiang, Shuo Li, Samuel S M Sun, Jun-Xian He. An interaction between BZR1 and DELLAs mediates direct signaling crosstalk between brassinosteroids and gibberellins in Arabidopsis.
Science signaling.
2012 Oct; 5(244):ra72. doi:
10.1126/scisignal.2002908. [PMID: 23033541] - G Wilma van Esse, Simon van Mourik, Hans Stigter, Colette A ten Hove, Jaap Molenaar, Sacco C de Vries. A mathematical model for BRASSINOSTEROID INSENSITIVE1-mediated signaling in root growth and hypocotyl elongation.
Plant physiology.
2012 Sep; 160(1):523-32. doi:
10.1104/pp.112.200105. [PMID: 22802611] - Thomas Hartwig, Claudia Corvalan, Norman B Best, Joshua S Budka, Jia-Ying Zhu, Sunghwa Choe, Burkhard Schulz. Propiconazole is a specific and accessible brassinosteroid (BR) biosynthesis inhibitor for Arabidopsis and maize.
PloS one.
2012; 7(5):e36625. doi:
10.1371/journal.pone.0036625. [PMID: 22590578] - Tomoaki Shigeta, Yuya Yoshimitsu, Yasushi Nakamura, Shigehisa Okamoto, Tomoaki Matsuo. Does brassinosteroid function require chromatin remodeling?.
Plant signaling & behavior.
2011 Nov; 6(11):1824-7. doi:
10.4161/psb.6.11.17478. [PMID: 22057321] - Zhihong Peng, Chengyun Han, Libing Yuan, Kun Zhang, Hongman Huang, Chunmei Ren. Brassinosteroid enhances jasmonate-induced anthocyanin accumulation in Arabidopsis seedlings.
Journal of integrative plant biology.
2011 Aug; 53(8):632-40. doi:
10.1111/j.1744-7909.2011.01042.x. [PMID: 21545406] - Jin-Xia Cui, Yan-Hong Zhou, Jian-Gang Ding, Xiao-Jian Xia, Kai Shi, Shuang-Chen Chen, Tadao Asami, Zhixiang Chen, Jing-Quan Yu. Role of nitric oxide in hydrogen peroxide-dependent induction of abiotic stress tolerance by brassinosteroids in cucumber.
Plant, cell & environment.
2011 Feb; 34(2):347-58. doi:
10.1111/j.1365-3040.2010.02248.x. [PMID: 21054437] - Wenqiang Tang, Min Yuan, Ruiju Wang, Yihong Yang, Chunming Wang, Juan A Oses-Prieto, Tae-Wuk Kim, Hong-Wei Zhou, Zhiping Deng, Srinivas S Gampala, Joshua M Gendron, Else M Jonassen, Cathrine Lillo, Alison DeLong, Alma L Burlingame, Ying Sun, Zhi-Yong Wang. PP2A activates brassinosteroid-responsive gene expression and plant growth by dephosphorylating BZR1.
Nature cell biology.
2011 Feb; 13(2):124-31. doi:
10.1038/ncb2151. [PMID: 21258370] - Mark Belmonte, Mohamed Elhiti, Blaine Waldner, Claudio Stasolla. Depletion of cellular brassinolide decreases embryo production and disrupts the architecture of the apical meristems in Brassica napus microspore-derived embryos.
Journal of experimental botany.
2010 Jun; 61(10):2779-94. doi:
10.1093/jxb/erq110. [PMID: 20435696] - Jae-Hoon Jung, Minsun Lee, Chung-Mo Park. A transcriptional feedback loop modulating signaling crosstalks between auxin and brassinosteroid in Arabidopsis.
Molecules and cells.
2010 May; 29(5):449-56. doi:
10.1007/s10059-010-0055-6. [PMID: 20396969] - Xiao-Jian Xia, Li-Feng Huang, Yan-Hong Zhou, Wei-Hua Mao, Kai Shi, Jian-Xiang Wu, Tadao Asami, Zhixiang Chen, Jing-Quan Yu. Brassinosteroids promote photosynthesis and growth by enhancing activation of Rubisco and expression of photosynthetic genes in Cucumis sativus.
Planta.
2009 Nov; 230(6):1185-96. doi:
10.1007/s00425-009-1016-1. [PMID: 19760261] - Adaucto B Pereira-Netto, Ute Roessner, Shozo Fujioka, Antony Bacic, Tadao Asami, Shigeo Yoshida, Steven D Clouse. Shooting control by brassinosteroids: metabolomic analysis and effect of brassinazole on Malus prunifolia, the Marubakaido apple rootstock.
Tree physiology.
2009 Apr; 29(4):607-20. doi:
10.1093/treephys/tpn052. [PMID: 19203977] - Farnusch Kaschani, Renier van der Hoorn. Small molecule approaches in plants.
Current opinion in chemical biology.
2007 Feb; 11(1):88-98. doi:
10.1016/j.cbpa.2006.11.038. [PMID: 17208036] - Yong-Hui Shi, Sheng-Wei Zhu, Xi-Zeng Mao, Jian-Xun Feng, Yong-Mei Qin, Liang Zhang, Jing Cheng, Li-Ping Wei, Zhi-Yong Wang, Yu-Xian Zhu. Transcriptome profiling, molecular biological, and physiological studies reveal a major role for ethylene in cotton fiber cell elongation.
The Plant cell.
2006 Mar; 18(3):651-64. doi:
10.1105/tpc.105.040303. [PMID: 16461577] - Gregory M Symons, Christopher Davies, Yuri Shavrukov, Ian B Dry, James B Reid, Mark R Thomas. Grapes on steroids. Brassinosteroids are involved in grape berry ripening.
Plant physiology.
2006 Jan; 140(1):150-8. doi:
10.1104/pp.105.070706. [PMID: 16361521] - Yan Sun, Randy D Allen. Functional analysis of the BIN 2 genes of cotton.
Molecular genetics and genomics : MGG.
2005 Aug; 274(1):51-9. doi:
10.1007/s00438-005-1122-0. [PMID: 15973517] - Ryuuichi D Itoh, Noriyuki Nakahara, Tadao Asami, Tetsuo Denda. The leaf morphologies of the subtropical rheophyte Solenogyne mikadoi and its temperate relative S. bellioides (Asteraceae) are affected differently by plant hormones and their biosynthesis inhibitors.
Journal of plant research.
2005 Jun; 118(3):181-6. doi:
10.1007/s10265-005-0208-4. [PMID: 15917989] - Kiwamu Tanaka, Tadao Asami, Shigeo Yoshida, Yasushi Nakamura, Tomoaki Matsuo, Shigehisa Okamoto. Brassinosteroid homeostasis in Arabidopsis is ensured by feedback expressions of multiple genes involved in its metabolism.
Plant physiology.
2005 Jun; 138(2):1117-25. doi:
10.1104/pp.104.058040. [PMID: 15908602] - Yan Sun, Mohamed Fokar, Tadao Asami, Shigeo Yoshida, Randy D Allen. Characterization of the brassinosteroid insensitive 1 genes of cotton.
Plant molecular biology.
2004 Jan; 54(2):221-32. doi:
10.1023/b:plan.0000028788.96381.47. [PMID: 15159624] - Kyoko Ohashi-Ito, Hiroo Fukuda. HD-zip III homeobox genes that include a novel member, ZeHB-13 (Zinnia)/ATHB-15 (Arabidopsis), are involved in procambium and xylem cell differentiation.
Plant & cell physiology.
2003 Dec; 44(12):1350-8. doi:
10.1093/pcp/pcg164. [PMID: 14701930] - Hideo Nakashita, Michiko Yasuda, Takako Nitta, Tadao Asami, Shozo Fujioka, Yuko Arai, Katsuhiko Sekimata, Suguru Takatsuto, Isamu Yamaguchi, Shigeo Yoshida. Brassinosteroid functions in a broad range of disease resistance in tobacco and rice.
The Plant journal : for cell and molecular biology.
2003 Mar; 33(5):887-98. doi:
10.1046/j.1365-313x.2003.01675.x. [PMID: 12609030] - Hideki Goda, Yukihisa Shimada, Tadao Asami, Shozo Fujioka, Shigeo Yoshida. Microarray analysis of brassinosteroid-regulated genes in Arabidopsis.
Plant physiology.
2002 Nov; 130(3):1319-34. doi:
10.1104/pp.011254. [PMID: 12427998] - Francine M Carland, Shozo Fujioka, Suguru Takatsuto, Shigeo Yoshida, Timothy Nelson. The identification of CVP1 reveals a role for sterols in vascular patterning.
The Plant cell.
2002 Sep; 14(9):2045-58. doi:
10.1105/tpc.003939. [PMID: 12215504] - K Sekimata, T Kimura, I Kaneko, T Nakano, K Yoneyama, Y Takeuchi, S Yoshida, T Asami. A specific brassinosteroid biosynthesis inhibitor, Brz2001: evaluation of its effects on Arabidopsis, cress, tobacco, and rice.
Planta.
2001 Sep; 213(5):716-21. doi:
10.1007/s004250100546. [PMID: 11678275] - N Nagata, T Asami, S Yoshida. Brassinazole, an inhibitor of brassinosteroid biosynthesis, inhibits development of secondary xylem in cress plants (Lepidium sativum).
Plant & cell physiology.
2001 Sep; 42(9):1006-11. doi:
10.1093/pcp/pce122. [PMID: 11577196] - T Asami, M Mizutani, S Fujioka, H Goda, Y K Min, Y Shimada, T Nakano, S Takatsuto, T Matsuyama, N Nagata, K Sakata, S Yoshida. Selective interaction of triazole derivatives with DWF4, a cytochrome P450 monooxygenase of the brassinosteroid biosynthetic pathway, correlates with brassinosteroid deficiency in planta.
The Journal of biological chemistry.
2001 Jul; 276(28):25687-91. doi:
10.1074/jbc.m103524200. [PMID: 11319239] - N Nagata, Y K Min, T Nakano, T Asami, S Yoshida. Treatment of dark-grown Arabidopsis thaliana with a brassinosteroid-biosynthesis inhibitor, brassinazole, induces some characteristics of light-grown plants.
Planta.
2000 Nov; 211(6):781-90. doi:
10.1007/s004250000351. [PMID: 11144262] - T Asami, Y K Min, N Nagata, K Yamagishi, S Takatsuto, S Fujioka, N Murofushi, I Yamaguchi, S Yoshida. Characterization of brassinazole, a triazole-type brassinosteroid biosynthesis inhibitor.
Plant physiology.
2000 May; 123(1):93-100. doi:
10.1104/pp.123.1.93. [PMID: 10806228] - Y K Min, T Asami, S Fujioka, N Murofushi, I Yamaguchi, S Yoshida. New lead compounds for brassinosteroid biosynthesis inhibitors.
Bioorganic & medicinal chemistry letters.
1999 Feb; 9(3):425-30. doi:
10.1016/s0960-894x(99)00008-6. [PMID: 10091696]
