Jiang Fei, Wang Tao, Wang Yuqi, Kochian Leon V, Chen Fang, Liu Jiping
Robert W. Holley Center, US Department of Agriculture-Agricultural Research Service, Ithaca, NY, 14853, USA.
College of Life Science, Sichuan University, Chengdu, Sichuan, China.
BMC Plant Biol. 2017 Jul 24;17(1):128. doi: 10.1186/s12870-017-1079-2.
Proton stress and aluminum (Al) toxicity are major constraints limiting crop growth and yields on acid soils (pH < 5). In Arabidopsis, STOP1 is a master transcription factor that controls the expression of a set of well-characterized Al tolerance genes and unknown processes involved in low pH resistance. As a result, loss-of-function stop1 mutants are extremely sensitive to low pH and Al stresses.
Here, we report on screens of an ethyl-methane sulphonate (EMS)-mutagenized stop1 population and isolation of nine strong stop1 suppressor mutants, i.e., the tolerant to proton stress (tps) mutants, with significantly enhanced root growth at low pH (4.3). Genetic analyses indicated these dominant and partial gain-of-function mutants are caused by mutations in single nuclear genes outside the STOP1 locus. Physiological characterization of the responses of these tps mutants to excess levels of Al and other metal ions further classified them into five groups. Three tps mutants also displayed enhanced resistance to Al stress, indicating that these tps mutations partially rescue the hypersensitive phenotypes of stop1 to both low pH stress and Al stress. The other six tps mutants showed enhanced resistance only to low pH stress but not to Al stress. We carried out further physiologic and mapping-by-sequencing analyses for two tps mutants with enhanced resistance to both low pH and Al stresses and identified the genomic regions and candidate loci in chromosomes 1 and 2 that harbor these two TPS genes.
We have identified and characterized nine strong stop1 suppressor mutants. Candidate loci for two tps mutations that partially rescue the hypersensitive phenotypes of stop1 to low pH and Al stresses were identified by mapping-by-sequencing approaches. Further studies could provide insights into the structure and function of TPSs and the regulatory networks underlying the STOP1-mediated processes that lead to resistance to low pH and Al stresses in Arabidopsis.
质子胁迫和铝(Al)毒性是限制酸性土壤(pH < 5)上作物生长和产量的主要因素。在拟南芥中,STOP1是一个主要的转录因子,它控制一组已充分表征的耐铝基因的表达以及参与低pH抗性的未知过程。因此,功能缺失的stop1突变体对低pH和Al胁迫极其敏感。
在此,我们报告了对经甲基磺酸乙酯(EMS)诱变的stop1群体的筛选,并分离出9个强stop1抑制突变体,即耐质子胁迫(tps)突变体,它们在低pH(4.3)条件下根生长显著增强。遗传分析表明,这些显性和部分功能获得性突变体是由STOP1基因座外的单核基因中的突变引起的。这些tps突变体对过量Al和其他金属离子反应的生理特征进一步将它们分为五组。三个tps突变体也表现出对Al胁迫的抗性增强,表明这些tps突变部分挽救了stop1对低pH胁迫和Al胁迫的超敏表型。其他六个tps突变体仅表现出对低pH胁迫的抗性增强,而对Al胁迫没有抗性增强。我们对两个对低pH和Al胁迫均具有增强抗性的tps突变体进行了进一步生理和测序定位分析,并确定了1号和2号染色体上携带这两个TPS基因的基因组区域和候选基因座。
我们已经鉴定并表征了9个强stop1抑制突变体。通过测序定位方法确定了两个tps突变的候选基因座,它们部分挽救了stop1对低pH和Al胁迫的超敏表型。进一步的研究可以深入了解TPS的结构和功能,以及拟南芥中导致对低pH和Al胁迫抗性的STOP1介导过程的调控网络。