Altered Root Growth, Auxin Metabolism and Distribution in Arabidopsis thaliana Exposed to Salt and Osmotic Stress

被引:32
|
作者
Smolko, Ana [1 ]
Bauer, Natasa [2 ]
Pavlovic, Iva [1 ,3 ,4 ]
Pencik, Ales [3 ,4 ]
Novak, Ondrej [3 ,4 ]
Salopek-Sondi, Branka [1 ]
机构
[1] Rudjer Boskovic Inst, Dept Mol Biol, Bijenicka Cesta 54, Zagreb 10000, Croatia
[2] Univ Zagreb, Fac Sci, Dept Mol Biol, Horvatovac 102, Zagreb 10000, Croatia
[3] Palacky Univ, Lab Growth Regulators, Fac Sci, Slechtitelu 27, CZ-78371 Olomouc, Czech Republic
[4] Czech Acad Sci, Inst Expt Bot, Slechtitelu 27, CZ-78371 Olomouc, Czech Republic
关键词
abiotic stress; Arabidopsis thaliana; auxin distribution; auxin metabolome; auxin transcriptome; root growth; BIOSYNTHESIS; HOMEOSTASIS; MODULATION; PHENOTYPES; TOLERANCE; CATALYZES; TRANSPORT; GRADIENTS; DROUGHT; GENES;
D O I
10.3390/ijms22157993
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Salt and osmotic stress are the main abiotic stress factors affecting plant root growth and architecture. We investigated the effect of salt (100 mM NaCl) and osmotic (200 mM mannitol) stress on the auxin metabolome by UHPLC-MS/MS, auxin distribution by confocal microscopy, and transcript levels of selected genes by qRT-PCR in Arabidopsis thaliana ecotype Columbia-0 (Col-0) and DR5rev::GFP (DR5) line. During long-term stress (13 days), a stability of the auxin metabolome and a tendency to increase indole-3-acetic acid (IAA) were observed, especially during salt stress. Short-term stress (3 h) caused significant changes in the auxin metabolome, especially NaCl treatment resulted in a significant reduction of IAA. The data derived from auxin profiling were consistent with gene expressions showing the most striking changes in the transcripts of YUC, GH3, and UGT transcripts, suggesting disruption of auxin biosynthesis, but especially in the processes of amide and ester conjugation. These data were consistent with the auxin distribution observed in the DR5 line. Moreover, NaCl treatment caused a redistribution of auxin signals from the quiescent center and the inner layers of the root cap to the epidermal and cortical cells of the root elongation zone. The distribution of PIN proteins was also disrupted by salt stress; in particular, PIN2 was suppressed, even after 5 min of treatment. Based on our results, the DR5 line was more sensitive to the applied stresses than Col-0, although both lines showed similar trends in root morphology, as well as transcriptome and metabolome parameters under stress conditions.
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页数:21
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