|本期目录/Table of Contents|

[1]邹禹,刘园园,张培江,等.水稻富亮氨酸重复类受体蛋白激酶OsRPK1响应外源生长素的作用研究[J].江苏农业科学,2019,47(08):46-51.
 Zou Yu,et al.Study on role of a rice leucine-rich repeat receptor protein kinase OsRPK1 in response to exogenous auxin[J].Jiangsu Agricultural Sciences,2019,47(08):46-51.
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水稻富亮氨酸重复类受体蛋白激酶OsRPK1响应
外源生长素的作用研究
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《江苏农业科学》[ISSN:1002-1302/CN:32-1214/S]

卷:
第47卷
期数:
2019年第08期
页码:
46-51
栏目:
生物技术
出版日期:
2019-05-19

文章信息/Info

Title:
Study on role of a rice leucine-rich repeat receptor protein kinase OsRPK1 in response to exogenous auxin
作者:
邹禹1 刘园园2 张培江1 钱宝云1 张炜2
1.安徽省农业科学院水稻研究所,安徽合肥 210031; 2.南京农业大学生命科学学院,江苏南京 210095
Author(s):
Zou Yuet al
关键词:
水稻富亮氨酸重复类受体蛋白激酶OsRPK1原核表达外源生长素融合蛋白GST-LRRs
Keywords:
-
分类号:
S511.01;Q55
DOI:
-
文献标志码:
A
摘要:
为明确水稻富亮氨酸重复类受体蛋白激酶OsRPK1响应外源生长素的作用机制,首先分析外源生长素2,4-D 对OsRPK1转基因水稻根部表型的影响;其次,异源表达OsRPK1胞外富亮氨酸重复LRRs,检测H3-IAA竞争结合融合蛋白GST-LRRs后的放射性活度以及利用等温滴定量热(ITC)法分析IAA与融合蛋白GST-LRRs相互作用的微热量变化。结果表明,在正常生长条件下,OsRPK1过表达能够抑制水稻侧根的生长;0.01 μmol/L 2,4-D处理 4 d 后发现,OsRPK1抑制表达植株侧根的数量比野生型多112%(P<0.01),而OsRPK1过表达植株侧根生长受到极显著抑制(P<0.001);0.1 μmol/L 2,4-D处理10 d后,抑制表达植株不定根的数量相对于野生型多18.2%(P<005),而过表达植株不定根的生长受到显著抑制(P<0.01);大肠杆菌BL21(DE3)诱导表达获得了包涵体形式的GST-LRRs融合蛋白,通过复性、纯化获得可溶性融合蛋白;H3-IAA竞争结合融合蛋白GST-LRRs以及IAA溶液滴定融合蛋白的微热量分析都表明OsRPK1与外源生长素未发生直接作用。
Abstract:
-

参考文献/References:

[1]查笑君,马伯军,潘建伟,等. 植物富亮氨酸重复类受体蛋白激酶的研究进展[J]. 浙江师范大学学报(自然科学版),2010,33(1):7-12.
[2]Liu P L,Du L,Huang Y,et al. Origin and diversification of leucine-rich repeat receptor-like protein kinase (LRR-RLK) genes in plants[J]. BMC Evolutionary Biology,2017,17(1):47.
[3]Hohmann U,Lau K,Hothorn M. The structural basis of ligand perception and signal activation by receptor kinases[J]. Annual Review of Plant Biology,2017,68(1):109-137.
[4]Song W,Han Z F,Wang J Z,et al. Structural insights into ligand recognition and activation of plant receptor kinases[J]. Current Opinion in Structural Biology,2017,43:18-27.
[5]Lee S W,Han S W,Sririyanum M,et al. A typeⅠ-secreted,sulfated peptide triggers XA21-mediated innate immunity[J]. Science,2013,342(6155):850-853.
[6]Song W Y,Wang G L,Chen L L,et al. A receptor kinase-like protein encoded by the rice disease resistance gene,Xa21[J]. Science,1995,270(5243):1804-1806.
[7]Nam K H,Li J M. BRI1/BAK1,a receptor kinase pair mediating brassinosteroid signaling[J]. Cell,2002,110(2):203-212.
[8]Oh M H,Clouse S D,Huber S C. Tyrosine phosphorylation of the BRI1 receptor kinase occurs via a post-translational modification and is activated by the juxtamembrane domain[J]. Frontiers in Plant Science,2012,3:175.
[9]Oh M H,Wang X F,Kota U,et al. Tyrosine phosphorylation of the BRI1 receptor kinase emerges as a component of brassinosteroid signaling in Arabidopsis[J]. Proceedings of the National Academy of Sciences of the United States of America,2009,106(2):658-663.
[10]Gomez-Gomez L,Bauer Z,Boller T. Both the extracellular leucine-rich repeat domain and the kinase activity of FSL2 are required for flagellin binding and signaling in Arabidopsis[J]. Plant Cell,2001,13(5):1155-1163.
[11]Sun Y D,Li L,Macho A P,et al. Structural basis for flg22-induced activation of the Arabidopsis FLS2-BAK1 immune complex[J]. Science,2013,342(6158):624-628.
[12]Gish L A,Clark S E. The RLK/pelle family of kinases[J]. Plant Journal,2011,66(1):117-127.
[13]Kinoshita A,Betsuyaku S,Osakabe Y,et al. RPK2 is an essential receptor-like kinase that transmits the CLV3 signal in Arabidopsis[J]. Development,2010,137(22):3911-3920.
[14]Song W,Liu L,Wang J Z,et al. Signature motif-guided identification of receptors for peptide hormones essential for root meristem growth[J]. Cell Research,2016,26(6):674-685.
[15]Lavy M,Estelle M. Mechanisms of auxin signaling[J]. Development,2016,143(18):3226-3229.
[16]Ruegger M,Dewey E,Hobbie L,et al. Reduced naphthylphthalamic acid binding in the tir3 mutant of Arabidopsis is associated with a reduction in polar auxin transport and diverse morphological defects[J]. Plant Cell,1997,9(5):745-757.
[17]Dharmasiri N,Dharmasiri S,Estelle M. The F-box protein TIR1 is an auxin receptor[J]. Nature,2005,435(7041):441-445.
[18]Kepinski S,Leyser O. The Arabidopsis F-box protein TIR1 is an auxin receptor[J]. Nature,2005,435(7041):446-451.
[19]Gao Y B,Zhang Y,Zhang D,et al. Auxin binding protein 1 (ABP1) is not required for either auxin signaling or Arabidopsis development[J]. Proceedings of the National Academy of Sciences of the United States of America,2015,112(7):2275-2280.
[20]Zou Y,Liu X Y,Wang Q,et al. OsRPK1,a novel leucine-rich repeat receptor-like kinase,negatively regulates polar auxin transport and root development in rice[J]. Biochimica et Biophysica Acta (BBA) - General Subjects,2014,1840(6):1676-1685.
[21]Zhang J,Peng Y C,Guo Z. Constitutive expression of pathogen-inducible OsWRKY31 enhances disease resistance and affects root growth and auxin response in transgenic rice plants[J]. Cell Research,2008,18(4):508-521.
[22]Inukai Y,Sakamoto T,Ueguchi-Tanaka M,et al. Crown rootless1,which is essential for crown root formation in rice,is a target of an auxin response factor in auxin signaling[J]. Plant Cell,2005,17(5):1387-1396.
[23]Wang X F,He F F,Ma X X,et al. OsCAND1 is required for crown root emergence in rice[J]. Molecular Plant,2010,4(2):289-299.
[24]Lewis E A,Murphy K P. Isothermal titration calorimetry[J]. Methods in Molecular Biology,2005,305(3):1-16.
[25]Frazier R A,Papadopoulou A,Green R J. Isothermal titration calorimetry study of epicatechin binding to serum albumin[J]. Journal of Pharmaceutical and Biomedical Analysis,2006,41(5):1602-1605.
[26]Singh S K,Kishore N. Thermodynamic insights into the binding of Triton X-100 to globular proteins:a calorimetric and spectroscopic investigation[J]. The Journal of Physical Chemistry B,2006,110(19):9728-9737.
[27]齐心洁,王玥,王彦晟,等. 等温滴定量热法在蛋白质-配体相互作用中的应用[J]. 生物技术通报,2017,33(5):40-49.
[28]Peret B,De Rybel B,Casimiro I,et al. Arabidopsis lateral root development:an emerging story[J]. Trends in Plant Science,2009,14(7):399-408.
[29]Peret B,Li G W,Zhao J,et al. Auxin regulates aquaporin function to facilitate lateral root emergence[J]. Nature Cell Biology,2012,14(10):991-998.
[30]Kant S,Bi Y M,Zhu T,et al. SAUR[STBX]39[STBZ],a small auxin-up RNA gene,acts as a negative regulator of auxin synthesis and transport in rice[J]. Plant Signaling & Behavior,2009,151(2):691-701.
[31]Zhuang X L,Jiang J F,Li J H,et al. Over-expression of OsAGAP,an ARF-GAP,interferes with auxin influx,vesicle trafficking and root development[J]. Plant Journal,2006,48(4):581-591.
[32]Kitomi Y,Inahashi H,Takehisa H,et al. OsIAA13-mediated auxin signaling is involved in lateral root initiation in rice[J]. Plant Science,2012,190(3):116-122.
[33]王继纵,李红菊,韩志富,等. 植物肽激素受体激活的新机制[J]. 中国细胞生物学学报,2016(2):123-126.
[34]Hohmann U,Santiago J,Nicolet J,et al. Mechanistic basis for the activation of plant membrane receptor kinases by SERK-family coreceptors[J]. Proceedings of the National Academy of Sciences,2018,115(13):3488-3493.
[35]Smakowska-Luzan E,Mott G A,Parys K A,et al. An extracellular network of Arabidopsis leucine-rich repeat receptor kinases[J]. Nature,2018,553(7688):342-346.

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备注/Memo

备注/Memo:
收稿日期:2018-12-05
基金项目:国家重点研发计划(编号:2016YFD0101801);国家自然科学基金(编号:31701409);安徽省自然科学基金(编号:1408085MKL63);安徽省农业科学院学科建设项目(编号:17A0101)。
作者简介:邹禹(1986—),男,安徽安庆人,博士,助理研究员,主要从事水稻基因功能解析及分子育种。Tel:(0551)62160151;E-mail:zouyu0308@126.com。
通信作者:张炜,博士,教授,主要从事植
更新日期/Last Update: 2019-04-20