Department of Genetics, University of Silesia, Jagiellonska 28, 40-032 Katowice, Poland.
Plant Mol Biol. 2013 Jan;81(1-2):189-209. doi: 10.1007/s11103-012-9991-1. Epub 2012 Nov 30.
Although the importance of abscisic acid (ABA) in plant development and response to abiotic and biotic stresses is well recognized, the molecular basis of the signaling pathway has not been fully elucidated. Mutants in genes related to ABA are widely used as a tool for gaining insight into the mechanisms of ABA signal transduction and ABA-dependent stress response. We used a genetic approach of a suppressor screening in order to decipher the interaction between ABH1 (CBP80) and other components of ABA signaling. ABH1 (CBP80) encodes a large subunit of CBC (CAP BINDING COMPLEX) and the abh1 mutant is drought-tolerant and hypersensitive to ABA during seed germination. The suppressor mutants of abh1 were generated after chemical mutagenesis. The mutant named soa1 (suppressor of abh1 hypersensitivity to ABA 1) displayed an ABA-insensitive phenotype during seed germination. The genetic analysis showed that the soa1 phenotype is dominant in relation to abh1 and segregates as a single locus. Based on soa1's response to a wide spectrum of physiological assays during different stages of development, we used the candidate-genes approach in order to identify a suppressor gene. The molecular analysis revealed that mutation causing the phenotype of soa1 occurred in the ABI4 (ABA insensitive 4) gene. Analysis of pre-miR159 expression, whose processing depends on CBC, as well as targets of miR159: MYB33 and MYB101, which are positive regulators of ABA signaling, revealed a possible link between CBP80 (ABH1) and ABI4 presented here.
尽管脱落酸 (ABA) 在植物发育和对非生物和生物胁迫的响应中的重要性已得到广泛认可,但信号转导途径的分子基础尚未完全阐明。与 ABA 相关的基因的突变体被广泛用作深入了解 ABA 信号转导和 ABA 依赖的应激反应机制的工具。我们使用了一种抑制子筛选的遗传方法,以揭示 ABH1(CBP80)与 ABA 信号转导的其他成分之间的相互作用。ABH1(CBP80)编码 CBC(CAP 结合复合物)的大亚基,abh1 突变体在种子萌发过程中耐旱且对 ABA 敏感。通过化学诱变产生了 abh1 的抑制子突变体。名为 soa1(ABA 不敏感突变体 1 的抑制子)的突变体在种子萌发过程中表现出 ABA 不敏感表型。遗传分析表明,soa1 表型相对于 abh1 是显性的,并作为一个单基因座分离。基于 soa1 在发育的不同阶段对广泛的生理测定的反应,我们使用候选基因方法来鉴定抑制子基因。分子分析表明,导致 soa1 表型的突变发生在 ABI4(ABA 不敏感 4)基因中。分析依赖于 CBC 的 pre-miR159 的表达及其靶标 miR159:MYB33 和 MYB101,它们是 ABA 信号的正调节剂,揭示了这里提出的 CBP80(ABH1)和 ABI4 之间的可能联系。