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作物学报 ›› 2011, Vol. 37 ›› Issue (12): 2136-2144.doi: 10.3724/SP.J.1006.2011.02136

• 作物遗传育种·种质资源·分子遗传学 • 上一篇    下一篇

甘蓝自交不亲和信号转导元件ARC1与EXO70A1的相互作用

杨昆1,张贺翠1,**,Richard CONVERSE2,朱利泉1,*,杨永军1,薛丽琰1,罗兵1,常登龙1,高启国2,王小佳2   

  1. 1 西南大学农学与生物科技学院, 重庆 400716; 2 Department of Biology, University of Cincinnati, Cincinnati OH 45267-0524; 3 西南大学重庆市蔬菜重点实验室, 重庆 400716
  • 收稿日期:2011-04-23 修回日期:2011-07-25 出版日期:2011-12-12 网络出版日期:2011-09-29
  • 通讯作者: 朱利泉, E-mail: zhuliquan@swu.edu.cn, Tel: 023-68250794
  • 基金资助:

    本研究由中央高校基本科研业务费专项资金(XDJK2009C109)和国家自然科学基金项目(30971849)资助。

Interaction between Two Self-incompatible Signal Elements, EXO70A1 and ARC1

YANG Kun1, ZHANG He-Cui1, Richard CONVERSE2, ZHU Li-Quan1,*, YANG Yong-Jun1, XUE Li-Yan1, LUO Bing1,CHANG Deng-Long1,GAO Qi-Guo2,WANG Xiao-Jia2   

  1. 1 College of Agronomy and Biotechnology, Southwest University, Chongqing 400716, China; 2 Department of Biology, University of Cincinnati, Cincinnati OH 45267-0524, USA; 3 Key Laboratory in Olericulture of Chongqing, Southwest University, Chongqing 400716, China
  • Received:2011-04-23 Revised:2011-07-25 Published:2011-12-12 Published online:2011-09-29
  • Contact: 朱利泉, E-mail: zhuliquan@swu.edu.cn, Tel: 023-68250794

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被引次数

7

摘要： 从甘蓝型油菜与羽衣甘蓝柱头中克隆出ARC1与EXO70A1基因的编码区, 序列分析显示推导的甘蓝型油菜ARC1比羽衣甘蓝ARC1少编码2个氨基酸, ARC1蛋白在羽衣甘蓝与甘蓝型油菜中存在45个氨基酸的差异, 其序列相似度与一致性分别达到95.9%和93.9%; 推导的EXO70A1在两种植物中仅有6个氨基酸的差异, 其序列相似度与一致性分别达到99.4%和98.9%; EXO70A1蛋白在种内和物种间都保持着高度的保守性, 其保守的程度高于ARC1。应用酵母双杂交系统检测两种蛋白质的相互作用, 发现: 在二倍体酵母细胞中, 全长的ARC1与EXO70A1之间存在较强的相互作用, 能激活4个报告基因(ADE2、HIS3、AUR1-C和MEL1)的表达; 去除C-端(包括臂重复区) 316个氨基酸残基后的ARC1N与EXO70A1之间表现出较弱的相互作用, 只能激活3个报告基因(ADE2、AUR1-C和MEL1)的表达, 表明ARC1的臂重复区可能并不位于ARC1与EXO70A1的互作界面的核心区段, ARC1的N-端结构域对ARC1-EXO70A1互作起关键作用; 同时发现不同ARC1-EXO70A1组合的互作强度相当, 其可能原因是ARC1和EXO70A1在甘蓝与甘蓝型油菜中存在的这些序列差异并未影响ARC1- EXO70A1互作界面的构象。

关键词: 自交不亲和, 信号元件, 蛋白质相互作用, 酵母双杂交

Abstract: ARC1 and EXO70A1 are important signal elements of self-incompatibility in Brassica. To identify the interaction of ARC1-EXO70A1 during the course of SI, we cloned the coding sequences of ARC1 and EXO70A1 from Brassica napus L.and Brassica oleracea L. var. acephala. Sequence analysis showed that ARC1 consisted of 663 amino acids in Brassica oleracea and 661amino acids in Brassica napus, and there existed 45 amino acids difference between them. Sequence alignment showed that similarity positions and identity positions reached 95.9% and 93.9% between BoARC1 and BnARC1, whereas there existed only six-amino-acid difference between BoEXO70A1 and BnEXO70A1. The Similarity positions and identity positions reached 99.4% and 98.9% between BoEXO70A1 and BnEXO70A1 respectively. The homology of EXO70A1 was higher than that of ARC1. Yeast two-hybrid results indicated that the strong interaction existed between ARC1 and EXO70A1, and it could activate the expression of four reporter genes (ADE2, HIS3, AUR1-C,and MEL1) in diploid yeasts. However, low interaction existed between EXO70A1 and ARC1N with 316 amino acids deleted from C-terminal, and it only activated the expression of three reporter genes (ADE2, AUR1-C, and MEL1). This provides an insight that the interface of interaction between ARC1 and EXO70A1 may not consist of the domains of arm repeats in ARC1. N-terminal domains of ARC1 play an essential role in the interaction of ARC1-EXO70A1. The influences of the differences in amino-acid composition between BoARC1 and BnARC1 on the interaction of ARC1-EXO70A1 couldn’t be detected by means of yeast two-hybrid system, which probably resulted from that the binding interface between ARC1 and EXO70A1 was not altered by sequence difference of two proteins in two Brassica species.

Key words: Self-incompatibility, Signal element, Protein interaction, Yeast two-hybrid

[1]McCubbin A G, Kao T H. Molecular recognition and response in pollen and pistil interactions. Annu Rev Cell DevBiol, 2000, 16: 333–364
[2]Wheeler M J, Vatovec S, Franklin-Tong V E. The pollen S-determinant in Papaver: comparisons with known plant receptors and protein ligand partners. J Exp Bot, 2010, 61: 2015–2025
[3]Mattison O, Knox R B, Heslopha J, Heslopha Y. Protein pellicle of stigmatic papillae as a probable recognition site in incompatible reactions. Nature, 1974, 247: 298–300
[4]Stead A D, Roberts I N, Dickinson H G. Pollen-stigma interaction in Brassica oleracea: the role of stigmatic proteins in pollen grain adhesion. J Cell Sci, 1980, 42: 417–423
[5]Didier C, Mark C J, Christian D, Thierry G. The S-locus receptor kinase inhibited by thioredoxins and activated by pollen coat proteins. Nature, 2001, 4l0: 220–223
[6]Rea A C, Nasrallah J B. Self-incompatibility systems: barriers to self-fertilization in flowering plants. Intl J Dev Biol, 2008, 52: 627–636
[7]Murase K, Shiba H, Iwano M, Che F S, Watanabe M, Isogal A, Takayama S. A Membrane-anchored protein kinase involved in Brassica self- incompatibility signaling. Science, 2004, 303: 1516–1519
[8]Goring D R, Walker J C. Self-rejection—a new kinase connection. Science, 2004, 303: 1474–1475
[9]Kakita M, Shimosato H, Murasea K, Isogai A, Takayama S. Direct interaction between S-locus receptor kinase and M-locus protein kinase involved in Brassica self-incompatibility signaling. Plant Biotechnol, 2007, 24: 185–190
[10]Kakita M, Murase K, Iwano M, Matsumoto T, Watanabe M, Shiba H, Isogai A, Takayama S. Two distinct forms of M-locus protein kinase localize to the plasma membrane and interact directly with S-locus receptor kinase to transduce self-incompatibility signaling in Brassica rapa. Plant Cell, 2007, 19: 3961–3973
[11]Stone S L, Anderson E M, Mullen R T, Goring D R. ARC1 is an E3 ubiquitin ligase and promotes the ubiquitination of proteins during the rejection of self-incompatible Brassica pollen. Plant Cell, 2003, 15: 885–898
[12]Samuel M A, Yee D, Haasen K E, Goring D R. ‘Self’ pollen rejection through the intersection of two cellular pathways in the Brassicaceae: self-incompatibility and the compatible pollen response. Self-incompatibility Flower Plants, 2008, 173–191
[13]Liu P, Sherman-Broyles S, Nasralllah M E, Nasrallah J B, A cryptic modifier causing transient self-incompatibility in Arabidopsis thaliana. Curr Biol, 2007, 17: 734–740
[14]Samuel M A, Chong Y T, Haasen K E, Aldea-Brydges M G, Stone S L, Goring D R. Cellular pathways regulating responses to compatible and self-incompatible pollen in Brassica and Arabidopsis stigmas intersect at Exo70A1, a putative component of the exocyst complex. Plant Cell, 2009, 21: 2655–2671
[15]Azevedo C, Santos-Rosa M J, Shirasu K. The U-box protein family in plants. Trends Plant Sci, 2001, 6: 354–358
[16]Yee D, Goring D R. The diversity of plant U-box E3 ubiquitin ligases: from upstream activators to downstream target substrates. J Exp Bot, 2009, 60: 1109–1121
[17]Gu T, Mazzurco M, Sulaman W, Matias D D, Goring D R. Binding of an arm repeat protein to the kinase domain of the S-locus receptor kinase. Proc Natl Acad Sci, 1998, 95: 382–387
[18]Mazzurco M, Sulaman W, Elina H, Cock J M, Goring D R. Further analysis of the interactions between the Brassica S receptor kinase and three interacting proteins (ARC1, THL1 and THL2) in the yeast two-hybrid system. Plant Mol Biol, 2001, 45: 365–376
[19]Shimosato H, Yokota N, Shiba H, Iwano M, Entani T, Che Fang-Sik, Watanabe M, Isogai A, Takayama S. Characterization of the SP11/SCR high-affinity binding site involved in self/nonself recognition in Brassica self-incompatibility. Plant Cell, 2007, 19: 107–117
[20]Fields S, Song O. A novel genetic system to detect protein-protein interactions. Nature, 1989, 340: 245–246
[21]Aravind L, Koonin E V. The U box is a modified RING finger: a common domain in ubiquitination. Curr Biol, 2000, 10: R132–R134
[22]Patterson C. A new gun in town: the U box is a ubiquitin ligase domain. Sci STKE, 2002, 116: PE4
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