Division of Applied Life Sciences (BK21plus), Graduate School of Gyeongsang National University, Jinju 660-701, Republic of Korea.
Department of Molecular, Cellular, and Developmental Biology, University of Michigan, Ann Arbor, Michigan 48109, USA.
Plant Physiol. 2021 Mar 15;185(2):405-423. doi: 10.1093/plphys/kiaa051.
In plants, root hairs undergo a highly polarized form of cell expansion called tip-growth, in which cell wall deposition is restricted to the root hair apex. In order to identify essential cellular components that might have been missed in earlier genetic screens, we identified conditional temperature-sensitive (ts) root hair mutants by ethyl methanesulfonate mutagenesis in Arabidopsis thaliana. Here, we describe one of these mutants, feronia-temperature sensitive (fer-ts). Mutant fer-ts seedlings were unaffected at normal temperatures (20°C), but failed to form root hairs at elevated temperatures (30°C). Map based-cloning and whole-genome sequencing revealed that fer-ts resulted from a G41S substitution in the extracellular domain of FERONIA (FER). A functional fluorescent fusion of FER containing the fer-ts mutation localized to plasma membranes, but was subject to enhanced protein turnover at elevated temperatures. While tip-growth was rapidly inhibited by addition of rapid alkalinization factor 1 (RALF1) peptides in both wild-type and fer-ts mutants at normal temperatures, root elongation of fer-ts seedlings was resistant to added RALF1 peptide at elevated temperatures. Additionally, at elevated temperatures fer-ts seedlings displayed altered reactive oxygen species (ROS) accumulation upon auxin treatment and phenocopied constitutive fer mutant responses to a variety of plant hormone treatments. Molecular modeling and sequence comparison with other Catharanthus roseus receptor-like kinase 1L (CrRLK1L) receptor family members revealed that the mutated glycine in fer-ts is highly conserved, but is not located within the recently characterized RALF23 and LORELI-LIKE-GLYCOPROTEIN 2 binding domains, perhaps suggesting that fer-ts phenotypes may not be directly due to loss of binding to RALF1 peptides.
在植物中,根毛经历一种高度极化的细胞扩展形式,称为尖端生长,其中细胞壁的沉积仅限于根毛的顶端。为了鉴定在早期遗传筛选中可能遗漏的必需细胞成分,我们通过在拟南芥中用乙基甲磺酸进行诱变,鉴定了条件性温度敏感(ts)根毛突变体。在这里,我们描述了其中的一个突变体,即 feronia-温度敏感(fer-ts)。在正常温度(20°C)下,突变体 fer-ts 幼苗不受影响,但在高温(30°C)下无法形成根毛。基于图谱的克隆和全基因组测序表明,fer-ts 是由于 FERONIA(FER)的细胞外结构域中的 G41S 取代所致。包含 fer-ts 突变的 FER 的功能荧光融合蛋白定位于质膜,但在高温下易发生蛋白质周转增强。虽然在正常温度下,RALF1 肽的添加迅速抑制了野生型和 fer-ts 突变体的尖端生长,但 fer-ts 幼苗的根伸长对添加的 RALF1 肽具有抗性。此外,在高温下,fer-ts 幼苗在生长素处理时表现出改变的活性氧(ROS)积累,并模拟了组成型 fer 突变体对各种植物激素处理的反应。分子建模和与其他长春花受体样激酶 1L(CrRLK1L)受体家族成员的序列比较表明,fer-ts 中的突变甘氨酸高度保守,但不在最近描述的 RALF23 和 LORELI-LIKE-GLYCOPROTEIN 2 结合结构域内,这可能表明 fer-ts 表型可能不是直接由于与 RALF1 肽结合的丧失所致。