State Key Laboratory of Crop Genetics & Germplasm Enhancement and Utilization, College of Resources and Environmental Sciences, Nanjing Agricultural University, Nanjing, 210095, China.
School of Molecular Science and ARC Centre of Excellence in Plant Energy Biology, The University of Western Australia, Crawley, Western Australia 6009, Australia.
J Exp Bot. 2024 Jan 1;75(1):438-453. doi: 10.1093/jxb/erad366.
Cadmium (Cd) is highly toxic to plants, but the targets and modes of toxicity remain unclear. We isolated a Cd-hypersensitive mutant of Arabidopsis thaliana, Cd-induced short root 2 (cdsr2), in the background of the phytochelatin synthase-defective mutant cad1-3. Both cdsr2 and cdsr2 cad1-3 displayed shorter roots and were more sensitive to Cd than their respective wild type. Using genomic resequencing and complementation, IAR4 was identified as the causal gene, which encodes a putative mitochondrial pyruvate dehydrogenase E1α subunit. cdsr2 showed decreased pyruvate dehydrogenase activity and NADH content, but markedly increased concentrations of pyruvate and alanine in roots. Both Cd stress and IAR4 mutation decreased auxin level in the root tips, and the effect was additive. A higher growth temperature rescued the phenotypes in cdsr2. Exogenous alanine inhibited root growth and decreased auxin level in the wild type. Cadmium stress suppressed the expression of genes involved in auxin biosynthesis, hydrolysis of auxin-conjugates and auxin polar transport. Our results suggest that auxin homeostasis is a key target of Cd toxicity, which is aggravated by IAR4 mutation due to decreased pyruvate dehydrogenase activity. Decreased auxin level in cdsr2 is likely caused by increased auxin-alanine conjugation and decreased energy status in roots.
镉(Cd)对植物具有高度毒性,但靶标和毒性模式仍不清楚。我们在植物螯合肽合酶缺陷突变体 cad1-3 的背景下,分离出拟南芥 Cd 超敏突变体 Cd 诱导短根 2(cdsr2)。cdsr2 和 cdsr2 cad1-3 的根都比其各自的野生型更短,对 Cd 更敏感。通过基因组重测序和互补,确定 IAR4 为致病基因,该基因编码一个假定的线粒体丙酮酸脱氢酶 E1α 亚基。cdsr2 表现出较低的丙酮酸脱氢酶活性和 NADH 含量,但根中丙酮酸和丙氨酸的浓度明显增加。Cd 胁迫和 IAR4 突变均降低根尖生长素水平,且具有加性效应。较高的生长温度可挽救 cdsr2 中的表型。外源性丙氨酸抑制野生型根的生长并降低生长素水平。Cd 胁迫抑制了生长素生物合成、生长素结合物水解和生长素极性运输相关基因的表达。我们的结果表明,生长素稳态是 Cd 毒性的关键靶标,由于丙酮酸脱氢酶活性降低,IAR4 突变会加重这种毒性。cdsr2 中生长素水平降低可能是由于生长素-丙氨酸结合物增加和根中能量状态降低所致。