Yeh Chuan-Ming, Kobayashi Koichi, Fujii Sho, Fukaki Hidehiro, Mitsuda Nobutaka, Ohme-Takagi Masaru
Graduate School of Science and Engineering, Saitama University, Saitama, Japan.
Bioproduction Research Institute, National Institute of Advanced Industrial Science and Technology (AIST), Tsukuba, Japan.
Front Plant Sci. 2020 Jan 31;10:1803. doi: 10.3389/fpls.2019.01803. eCollection 2019.
Plants have evolved mechanisms to improve utilization efficiency or acquisition of inorganic phosphate (Pi) in response to Pi deficiency, such as altering root architecture, secreting acid phosphatases, and activating the expression of genes related to Pi uptake and recycling. Although many genes responsive to Pi starvation have been identified, transcription factors that affect tolerance to Pi deficiency have not been well characterized. We show here that the ectopic expression of () and the mutation of (), whose transcriptional activity is negatively regulated by BBX32, resulted in the tolerance to Pi deficiency in Arabidopsis. The primary root lengths of and plants were only slightly inhibited under Pi deficient condition and the fresh weights were significantly higher than those of wild type. The Pi deficiency-tolerant root phenotype of was similarly observed when grown on the medium without Pi. In addition, a double mutant, , without lateral roots, also showed a long primary root phenotype under phosphate deficiency, indicating that the root phenotype of does not result from an increase of external Pi uptake. Moreover, we found that blue light may regulate Pi deficiency-dependent primary root growth inhibition through activating peroxidase gene expression, suggesting the Pi-deficiency tolerant root phenotype of may be due to blockage of blue light responses. Altogether, this study points out light quality may play an important role in the regulation of Pi deficiency responses. It may contribute to regulate plant growth under Pi deficiency through proper illumination.
植物已经进化出机制来提高无机磷(Pi)的利用效率或获取量,以应对Pi缺乏,例如改变根系结构、分泌酸性磷酸酶以及激活与Pi吸收和循环相关的基因表达。尽管已经鉴定出许多对Pi饥饿有反应的基因,但影响对Pi缺乏耐受性的转录因子尚未得到很好的表征。我们在此表明,()的异位表达和()的突变,其转录活性受BBX32负调控,导致拟南芥对Pi缺乏具有耐受性。在Pi缺乏条件下,和植物的主根长度仅受到轻微抑制,鲜重显著高于野生型。在无Pi的培养基上生长时,同样观察到的耐Pi缺乏根表型。此外,一个没有侧根的双突变体,在磷缺乏条件下也表现出主根长的表型,表明的根表型不是由于外部Pi吸收增加所致。此外,我们发现蓝光可能通过激活过氧化物酶基因表达来调节Pi缺乏依赖的主根生长抑制,这表明的耐Pi缺乏根表型可能是由于蓝光反应受阻。总之,这项研究指出光质可能在Pi缺乏反应的调节中起重要作用。通过适当的光照,它可能有助于调节Pi缺乏条件下的植物生长。