Biotechnology Bulletin ›› 2018, Vol. 34 ›› Issue (6): 66-72.doi: 10.13560/j.cnki.biotech.bull.1985.2017-0978
Previous Articles Next Articles
SHI Jia YANG Dan-dan GE Hui-wen DU Jing-yao LIANG Wei-hong
Received:
2017-11-13
Online:
2018-06-26
Published:
2018-07-03
SHI Jia YANG Dan-dan GE Hui-wen DU Jing-yao LIANG Wei-hong. cDNA Cloning and Transcriptional Expression Analysis of OsMPK15 in Rice[J]. Biotechnology Bulletin, 2018, 34(6): 66-72.
[1] Nam-Soo J. The rice MAPKK-MAPK interactome:the biological significance of MAPK components in hormone signal transduction[J] . Plant Cell, 2013, 32:923-931. [2] Huang HJ, Fu SF, Tai YH, et al. Expression of Oryza sativa MAP kinase gene is developmentally regulated and stress-responsive[J] . Physiology Plant, 2002, 114:572-580. [3] Krishna M, Narang H. The complexity of mitogen-activated protein kinases(MAPKs)made simple[J] . Cellular and Molecular Life Science, 2008, 65(22):3525-3544. [4] De Smet I, Voss U, Jürgens G et al. Receptor-like kinases shape the plant[J] . Cell Biology, 2009, 11:1166-1173. . [5] Li J, Tax FE. Receptor-like kinases:key regulators of plant development and defense[J] . Plant Biol, 2013, 55:1184-1187. [6] Gish LA, Clark SE. The RLK/Pelle family of kinases[J] . Plant J, 2011, 66:117-127. [7] Nishihama R, Ishikawa M, et al. The NPK1 mitogen-activated protein kinase kinase kinase is a regulator of cell-plate formation in plant cytokinesis[J] . Genes Dev, 2001, 3:352-363. [8] Soyano T, Nishihama R, et al. NQK1/NtMEK1 is a MAPKK that acts in the NPK1 MAPKKK-mediated MAPK cascade and is required for plant cytokinesis[J] . Genes Dev, 2003, 17:1055-1067. [9] Wen JQ, Oono K, Imai R. Two novel mitogen-activated protein signaling componets, OsMEK1 and OsMAP1, are involved in a moderate low-temperature signaling pathway in rice[J] . Plant Physiology, 2002, 129(4):1880-1891. [10] Hadiarto T, Nanmori T, Matsuoka D, et al. Activation of Arabidopsis MAPK kinase(AtMEKK1)and induction of AtMEKK1-AtMEK1 pathway by wounding[J] . Planta, 2006, 223(4):708-713. [11] Teige M, et al. The MKK2 pathway mediates cold and salt stress signaling in Arabidopsis[J] . Mol Cell, 2004, 1:141-152. [12] Pitzschke A, Djamei A, Bitton F, et al. A major role of the MEKK1-MKK1/2-MPK4 pathway in ROS signaling[J] . Molecular Plant, 2009, 2(1):120-137. [13] Yuan B, Shen X, Li X, et al. Mitogen-activated protein kinase OsMPK6 negatively regulates rice disease resistance to bacterial pathogens[J] . Planta, 2007, 226(4):953-960. [14] Shen X, Yuan B, Liu H, et al. Opposite functions of a rice mitogen-activated protein kinase during the process of resistance against Xanthomonas oryzae[J] . Plant J, 2010, 64(1):86-99. [15] Xiong L, Yang Y. Disease resistance and abiotic stress tolerance in rice are inversely modulated by an abscisic acid-inducible mitogen-activated protein kinase[J] . Plant Cell, 2003(3):745-759. [16] Agrawal GK, et al. Isolation of novel rice(Oryza sativa L.)multi-ple stress responsive MAP kinase gene, OsMSRMK2, whose mRNA accumulates rapidly in response to environmental cues[J] . Biochem Biophys Res Commun, 2002, 5:1009-1016. [17] Wen JQ, Oono K, Imai R. Two novel mitogen-activated protein signaling components, OsMEK1 and OsMAP1, are involved in a moderate low-temperature signaling pathway in rice[J] . Plant Physiology, 2002, 129(4):1880-1891. [18] 梁卫红, 等. 水稻促分裂原活化蛋白激酶基因OsMPK14的克隆及表达分析[J] . 中国水稻科学, 2010(2):125-130. [19] Yoshida S, Forno DA, Cock JH, et al. Laboratory manual for physiological studies of rice[M] . Manila:International Rice Research Institute, 1976. [20] 张静, 梁卫红. 2种非生物胁迫和7种激素对水稻OsAQP基因表达的影响[J] . 河南师范大学学报:自然科学版, 2016, 44(1):105-109. [21] Jiang M, Wen F, Cao JM, et al. Genome-wide exploration of the molecular evolution and regulatory network of mitogen-activated protein kinase cascades upon multiple stresses in Brachypodium distachyon[J] . BMC Genomics, 2015, 16:228. [22] Reyna NS, Yang Y. Molecular analysis of the rice MAP kinase gene family in relation to Magnaporthe grisea infection[J] . Molecular Plant-Microbe Interactions, 2006, 19(5):530-540. [23] Song D, et al. A novel rice MAPK gene, OsBIMK2, is involved in disease-resistance responses[J] . Plant Biol, 2006, 5:587-596. [24] Mizoguchi T, Irie K, et al. A gene encoding a mitogen-activated protein kinase kinase kinase is induced simultaneously with genes for a mitogen-activated protein kinase and an S6 ribosomal protein kinase by touch, cold, and water stress in Arabidopsis thaliana[J] . Proc Natl Acad Sci USA, 1996, 93:765-769. [25] Ichimura K, Mizoguchi T, Yoshida R, et al. Various abiotic stresses rapidly activate Arabidopsis MAP kinases ATMPK4 and ATMPK6[J] . Plant J, 2000, 24:655-665. [26] Jeong M, Park S, Lee S, et al. A rice(Oryza sativa L.)MAP kinase gene, OsMAPK44, is involved in response to abiotic stresses[J] . Plant Cell Tissue Organ Cult, 2006, 85(2):151-160. [27] Agrawal GK, Agrawal SK, Shibato J, et al. Novel rice MAP kinases OsMSRMK3 and OsWJUMK1 involved in encountering diverse environmental stresses and developmental regulation[J] . Biochem Biophys Res Commun, 2003, 300(3):775-783. [28] Agrawal GK, Tamogami S, Iwahashi H, et al. Transient regulation of jasmonic acid-inducible rice MAP kinase gene(OsBWMK1)by diverse biotic and abiotic stresses[J] . Plant Physiology and Biochemistry, 2003, 41(4):355-361. [29] Jammes F, Song C, Shin D, et al. MAP kinases MPK9 and MPK12 are preferentially expressed in guard cells and positively regulate ROS-mediated ABA signaling[J] . Proc Natl Acad Sci USA, 2009, 106:20520-20525. [30] Xing Y, Jia W, Zhang J. AtMKK1 mediates ABA-induced CAT1 expression and H2O2 production via AtMPK6-coupled signaling in Arabidopsis[J] . Plant J, 2008, 54:440-451. [31] Zhang A, Zhang J, Ye N, et al. ZmMPK5 is required for the NADPH oxidase-mediated self-propagation of apoplastic H2O2 in brassinosteroid-induced antioxidant defence in leaves of maize[J] . J Exp Bot, 2010, 61:4399-4411. [32] Zong XJ, Li DP, Gu LK, et al. Abscisic acid and hydrogen peroxide induce a novel maize group C MAP kinase gene, ZmMPK7, which is responsible for the removal of reactive oxygen species[J] . Planta, 2009, 229:485-495. [33] Zhang S, Klessig DF. Salicylic acid activates a 48-kD MAP kinase in tobacco[J] . Plant Cell, 1997, 9(5):809-824. [34] Seo S, Katou S, Seto H, et al. The mitogen-activated protein kinases WIPK and SIPK regulate the levels of jasmonic and salicylic acids in wounded tobacco plants[J] . Plant J, 2007, 49(5):899-909. |
[1] | WANG Zi-ying, LONG Chen-jie, FAN Zhao-yu, ZHANG Lei. Screening of OsCRK5-interacted Proteins in Rice Using Yeast Two-hybrid System [J]. Biotechnology Bulletin, 2023, 39(9): 117-125. |
[2] | WU Yuan-ming, LIN Jia-yi, LIU Yu-xi, LI Dan-ting, ZHANG Zong-qiong, ZHENG Xiao-ming, PANG Hong-bo. Identification of Rice Plant Height-associated QTL Using BSA-seq and RNA-seq [J]. Biotechnology Bulletin, 2023, 39(8): 173-184. |
[3] | YAO Sha-sha, WANG Jing-jing, WANG Jun-jie, LIANG Wei-hong. Molecular Mechanisms of Rice Grain Size Regulation Related to Plant Hormone Signaling Pathways [J]. Biotechnology Bulletin, 2023, 39(8): 80-90. |
[4] | LI Yu, LI Su-zhen, CHEN Ru-mei, LU Hai-qiang. Advances in the Regulation of Iron Homeostasis by bHLH Transcription Factors in Plant [J]. Biotechnology Bulletin, 2023, 39(7): 26-36. |
[5] | ZHAO Xue-ting, GAO Li-yan, WANG Jun-gang, SHEN Qing-qing, ZHANG Shu-zhen, LI Fu-sheng. Cloning and Expression of AP2/ERF Transcription Factor Gene ShERF3 in Sugarcane and Subcellular Localization of Its Encoded Protein [J]. Biotechnology Bulletin, 2023, 39(6): 208-216. |
[6] | LI Yuan-hong, GUO Yu-hao, CAO Yan, ZHU Zhen-zhou, WANG Fei-fei. Research Progress in the Microalgal Growth and Accumulation of Target Products Regulated by Exogenous Phytohormone [J]. Biotechnology Bulletin, 2023, 39(6): 61-72. |
[7] | FENG Shan-shan, WANG Lu, ZHOU Yi, WANG You-ping, FANG Yu-jie. Research Progresses on WOX Family Genes in Regulating Plant Development and Abiotic Stress Response [J]. Biotechnology Bulletin, 2023, 39(5): 1-13. |
[8] | LIANG Cheng-gang, WANG Yan, LI Tian, OHSUGI Ryu, AOKI Naohiro. Effect of SP1 on Panicle Architecture by Regulating Carbohydrate Remobilization [J]. Biotechnology Bulletin, 2023, 39(5): 152-159. |
[9] | ZHAI Ying, LI Ming-yang, ZHANG Jun, ZHAO Xu, YU Hai-wei, LI Shan-shan, ZHAO Yan, ZHANG Mei-juan, SUN Tian-guo. Heterologous Expression of Soybean Transcription Factor GmNF-YA19 Improves Drought Resistance of Transgenic Tobacco [J]. Biotechnology Bulletin, 2023, 39(5): 224-232. |
[10] | ZHOU Ding-ding, LI Hui-hu, TANG Xing-yong, YU Fa-xin, KONG Dan-yu, LIU Yi. Research Progress in the Biosynthesis and Regulation of Glycyrrhizic Acid and Liquiritin [J]. Biotechnology Bulletin, 2023, 39(5): 44-53. |
[11] | YANG Chun-hong, DONG Lu, CHEN Lin, SONG Li. Characterization of Soybean VAS1 Gene Family and Its Involvement in Lateral Root Development [J]. Biotechnology Bulletin, 2023, 39(3): 133-142. |
[12] | YU Shi-xia, JIANG Yu-tong, LIN Wen-hui. Research Progress in Signals and Molecular Mechanisms of Ovule Primordia Initiation [J]. Biotechnology Bulletin, 2023, 39(2): 1-9. |
[13] | YANG Mao, LIN Yu-feng, DAI Yang-shuo, PAN Su-jun, PENG Wei-ye, YAN Ming-xiong, LI Wei, WANG Bing, DAI Liang-ying. OsDIS1 Negatively Regulates Rice Drought Tolerance Through Antioxidant Pathways [J]. Biotechnology Bulletin, 2023, 39(2): 88-95. |
[14] | MIAO Shu-nan, GAO Yu, LI Xin-ru, CAI Gui-ping, ZHANG Fei, XUE Jin-ai, JI Chun-li, LI Run-zhi. Functional Analysis of Soybean GmPDAT1 Genes in the Oil Biosynthesis and Response to Abiotic Stresses [J]. Biotechnology Bulletin, 2023, 39(2): 96-106. |
[15] | JIANG Min-xuan, LI Kang, LUO Liang, LIU Jian-xiang, LU Hai-ping. Advances on the Expressions of Foreign Proteins in Plants [J]. Biotechnology Bulletin, 2023, 39(11): 110-122. |
Viewed | ||||||
Full text |
|
|||||
Abstract |
|
|||||