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甘蓝中含犰狳重复序列1(ARC1)与外泌体70 A1(Exo70A1)蛋白之间相互作用基序的鉴定

Identification of Interacting Motifs Between Armadillo Repeat Containing 1 (ARC1) and Exocyst 70 A1 (Exo70A1) Proteins in Brassica oleracea.

作者信息

Liu Jing, Zhang Hecui, Lian Xiaoping, Converse Richard, Zhu Liquan

机构信息

College of Agronomy and Biotechnology, Southwest University, Chongqing, 400716, China.

College of Horticulture and Landscape Architecture, Southwest University, Chongqing, 400716, China.

出版信息

Protein J. 2016 Feb;35(1):34-43. doi: 10.1007/s10930-015-9644-8.

Abstract

In order to identify the functional domains which regulate the interaction between the self-incompatibility proteins armadillo repeat containing 1 (ARC1) and exocyst 70 A1 (Exo70A1) in Brassica oleracea, fragments containing selected motifs of ARC1 (ARC1210, ARC1246, ARC1279, ARC1354) and site-specific mutants with substitutions at possible interaction sites (ARC1354m, ARC1664m) were PCR amplified and inserted into pGADT7, while coding sequences from Exo70A1 (Exo70A185, Exo70A1) were subcloned into pGBKT7. The interactions between the protein products produced by these constructs were then analyzed utilizing a yeast two-hybrid system. Our data indicate that both ARC1210 and ARC1246 interact strongly with Exo70A185 and Exo70A1, while ARC1279, ARC1354, ARC1354m and ARC1664m exhibited a weak interaction, indicating that the recognition sites are located within the 210 N-terminal amino acids of ARC1 and the 85 N-terminal amino acids of Exo70A1. This was further verified by GST pull-down analysis. This supports a model in which the N-terminal leucine zipper of ARC1 and the first 85 N-terminal amino acids of Exo70A1 mediate the interaction between these two proteins. Bioinformatic and phylogenetic analysis demonstrated that these motifs were highly conserved across different species, indicating that the interaction characterized in B. oleracea may operate in a wide array of cultivars.

摘要

为了鉴定调控甘蓝中自交不亲和蛋白犰狳重复序列包含蛋白1(ARC1)和外泌体70 A1(Exo70A1)之间相互作用的功能结构域,对包含ARC1选定基序的片段(ARC1210、ARC1246、ARC1279、ARC1354)以及在可能的相互作用位点发生取代的位点特异性突变体(ARC1354m、ARC1664m)进行PCR扩增,并插入到pGADT7中,同时将Exo70A1的编码序列(Exo70A185、Exo70A1)亚克隆到pGBKT7中。然后利用酵母双杂交系统分析这些构建体产生的蛋白质产物之间的相互作用。我们的数据表明,ARC1210和ARC1246都与Exo70A185和Exo70A1强烈相互作用,而ARC1279、ARC1354、ARC1354m和ARC1664m表现出较弱的相互作用,这表明识别位点位于ARC1的210个N端氨基酸和Exo70A1的85个N端氨基酸内。这通过GST下拉分析得到了进一步验证。这支持了一个模型,即ARC1的N端亮氨酸拉链和Exo70A1的前85个N端氨基酸介导了这两种蛋白质之间的相互作用。生物信息学和系统发育分析表明,这些基序在不同物种中高度保守,表明在甘蓝中鉴定的这种相互作用可能在多种品种中起作用。

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