https://www.ahs.ac.cn/images/0513-353X/images/top-banner1.jpg|#|苹果
https://www.ahs.ac.cn/images/0513-353X/images/top-banner2.jpg|#|甘蓝
https://www.ahs.ac.cn/images/0513-353X/images/top-banner3.jpg|#|菊花
https://www.ahs.ac.cn/images/0513-353X/images/top-banner4.jpg|#|灵芝
https://www.ahs.ac.cn/images/0513-353X/images/top-banner5.jpg|#|桃
https://www.ahs.ac.cn/images/0513-353X/images/top-banner6.jpg|#|黄瓜
https://www.ahs.ac.cn/images/0513-353X/images/top-banner7.jpg|#|蝴蝶兰
https://www.ahs.ac.cn/images/0513-353X/images/top-banner8.jpg|#|樱桃
https://www.ahs.ac.cn/images/0513-353X/images/top-banner9.jpg|#|观赏荷花
https://www.ahs.ac.cn/images/0513-353X/images/top-banner10.jpg|#|菊花
https://www.ahs.ac.cn/images/0513-353X/images/top-banner11.jpg|#|月季
https://www.ahs.ac.cn/images/0513-353X/images/top-banner12.jpg|#|菊花

园艺学报 ›› 2019, Vol. 46 ›› Issue (4): 714-722.doi: 10.16420/j.issn.0513-353x.2018-0663

• 研究论文 • 上一篇    下一篇

基于家族基因分析的甘蓝MLPK互作PUB蛋白的筛选

高启国1,*,雷镇泽1,*,梁云飞1,*,姜宇鹏1,朱利泉2   

  1. 1西南大学园艺园林学院,南方山地园艺学教育部重点实验室,重庆 400716;2西南大学农学与生物科技学院,重庆 400716
  • 出版日期:2019-04-25 发布日期:2019-04-25
  • 基金资助:
    国家自然科学基金项目(31572127)

Screening of Brassica oleracea MLPK-interacting PUB Proteins Based on Gene Family Analysis

GAO Qiguo1,*,LEI Zhenze1,*,LIANG Yunfei1,*,JIANG Yupeng1,and ZHU Liquan2   

  1. 1College of Horticulture and Landscape Architecture,Southwest University,Key Laboratory of Horticulture Science for Southern Mountainous Regions Ministry of Education,Chongqing 400716,China;2College of Agronomy and Biotechnology,Southwest University,Chongqing 400716,China
  • Online:2019-04-25 Published:2019-04-25

摘要: MLPK(M–位点受体激酶)是芸薹属自交不亲和正向调控关键元件,其参与自交不亲和信号传导的分子机制尚不明确,同时自交不亲和下游信号元件也有待于进一步分离。为了探索分离MLPK互作蛋白的思路和方法,构建了不含核定位信号的MLPK短截蛋白(MLPK-T),并利用酵母双杂交检测到MLPK与臂重复蛋白1(ARC1)作用,通过全基因组鉴定分别获得了96个甘蓝、101个白菜、70个琴叶拟南芥和62个拟南芥PUB蛋白,其中含有臂重复序列的PUB蛋白共为127个。通过系统进化分析,筛选到8个含臂重复序列的甘蓝BoPUB蛋白,其8个基因全部在柱头内表达,且成功利用酵母双杂交检测到MLPK与3个含臂重复序列的BoPUB蛋白Bol008579、Bol016165和Bol023511相互作用。

关键词: 甘蓝, 自交不亲和, M–位点受体激酶, PUB蛋白, 家族基因, 相互作用, 番茄, SELF-PRUNING, 基因, 株形, 调控, 生长习性

Abstract: MLPK(M-locus protein kinase)is a positive key mediator of Brassica self-incompatibility signaling,however,the molecular mechanism of MLPK in mediating Brassica self-incompatibility response is still unknown. Meanwhile,the downstream factors of Brassica self-incompatibility signaling still need to be isolated. Aim to explore the idea and methods to isolate MLPK-interacting proteins,here,the MLPK truncated protein MLPK-T lack of the plasma membrane localization motif was constructed,the interaction of MLPK with ARC1 was proved via conventional yeast two-hybrid system. Then,we obtained 96,101,70 and 62 PUB proteins from B. olercea,B. rapa,Arabidopsis lyrata and A. thaliana through genome-wide identification,amount to 127 PUB proteins containing ARM repeat domains. Based on phylogenetic analysis,we selected 8 PUB proteins,and RT-PCR showed that all these 8 genes expressed in B. oleracea stigmas. Finally,the interaction of MLPK with Bol008579,Bol016165 and Bol023511 were proved through yeast two-hybrid system.

Key words: Brassica oleracea, self-incompatibility, M-locus protein kinase, plant U-box protein, gene family, interaction, tomato, SELF-PRUNING, gene, shoot architecture, regulatory, growth habit

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