Bai Yili, Zhu Wenbo, Hu Xiaochen, Sun Congcong, Li Yanlin, Wang Dandan, Wang Qinhu, Pei Guoliang, Zhang Yanfeng, Guo Aiguang, Zhao Huixian, Lu Haibin, Mu Xiaoqian, Hu Jingjiang, Zhou Xiaona, Xie Chang Gen
State Key Laboratory of Crop Stress Biology for Arid Areas, College of Life Science, Northwest A&F University, Yangling, Shaanxi, 712100, China.
Hybrid Rapeseed Research Centre of Shaanxi Province, Yangling, Shaanxi, 712100, China.
PLoS One. 2016 Jul 14;11(7):e0158966. doi: 10.1371/journal.pone.0158966. eCollection 2016.
bZIP (basic leucine zipper) transcription factors coordinate plant growth and development and control responses to environmental stimuli. The genome of Chinese cabbage (Brassica rapa) encodes 136 putative bZIP transcription factors. The bZIP transcription factors in Brassica rapa (BrbZIP) are classified into 10 subfamilies. Phylogenetic relationship analysis reveals that subfamily A consists of 23 BrbZIPs. Two BrbZIPs within subfamily A, Bra005287 and Bra017251, display high similarity to ABI5 (ABA Insensitive 5). Expression of subfamily A BrbZIPs, like BrABI5a (Bra005287/BrbZIP14) and BrABI5b (Bra017251/BrbZIP13), are significantly induced by the plant hormone ABA. Subcellular localization assay reveal that both BrABI5a and BrABI5b have a nuclear localization. BrABI5a and BrABI5b could directly stimulate ABA Responsive Element-driven HIS (a HIS3 reporter gene, which confers His prototrophy) or LUC (LUCIFERASE) expression in yeast and Arabidopsis protoplast. Deletion of the bZIP motif abolished BrABI5a and BrABI5b transcriptional activity. The ABA insensitive phenotype of Arabidopsis abi5-1 is completely suppressed in transgenic lines expressing BrABI5a or BrABI5b. Overall, these results suggest that ABI5 orthologs, BrABI5a and BrABI5b, have key roles in ABA signalling in Chinese cabbage.
碱性亮氨酸拉链(bZIP)转录因子协调植物的生长发育,并控制对环境刺激的反应。大白菜(Brassica rapa)基因组编码136个假定的bZIP转录因子。甘蓝型油菜中的bZIP转录因子(BrbZIP)被分为10个亚家族。系统发育关系分析表明,A亚家族由23个BrbZIP组成。A亚家族中的两个BrbZIP,即Bra005287和Bra017251,与ABI5(脱落酸不敏感5)具有高度相似性。A亚家族BrbZIP的表达,如BrABI5a(Bra005287/BrbZIP14)和BrABI5b(Bra017251/BrbZIP13),受到植物激素脱落酸的显著诱导。亚细胞定位分析表明,BrABI5a和BrABI5b都具有核定位。BrABI5a和BrABI5b可以直接刺激酵母和拟南芥原生质体中脱落酸反应元件驱动的HIS(一种赋予组氨酸原养型的HIS3报告基因)或LUC(荧光素酶)的表达。bZIP基序的缺失消除了BrABI5a和BrABI5b的转录活性。在表达BrABI5a或BrABI5b的转基因系中,拟南芥abi5-1的脱落酸不敏感表型被完全抑制。总体而言,这些结果表明,ABI5直系同源基因BrABI5a和BrABI5b在大白菜的脱落酸信号传导中起关键作用。