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Cited 28 time in webofscience Cited 32 time in scopus
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A temperature-sensitive <i>FERONIA</i> mutant allele that alters root hair growthopen access

Authors
Kim, DaewonYang, JiyuanGu, FangweiPark, SungjinCombs, JonathonAdams, AlexanderMayes, Heather B.Jeon, Su JeongBahk, Jeong DongNielsen, Erik
Issue Date
Feb-2021
Publisher
OXFORD UNIV PRESS INC
Citation
PLANT PHYSIOLOGY, v.185, no.2, pp 405 - 423
Pages
19
Indexed
SCIE
SCOPUS
Journal Title
PLANT PHYSIOLOGY
Volume
185
Number
2
Start Page
405
End Page
423
URI
https://scholarworks.gnu.ac.kr/handle/sw.gnu/72825
DOI
10.1093/plphys/kiaa051
ISSN
0032-0889
1532-2548
Abstract
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 degrees C), but failed to form root hairs at elevated temperatures (30 degrees 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.
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