Mechanisms of inhibition of cadmium uptake and translocation by
selenite: roles of root morphology, endogenous phytohormones, and root
exudates via non–invasive micro–test technique and a combined analysis
of transcriptome and metabolome
Abstract
Selenium (Se) can reduce the uptake and translocation of cadmium (Cd) in
plants in a number of ways, including the regulation of root morphology.
However, the actual mechanisms underlying the regulation of root
morphology and root exudates by Se are unknown. To explore the action of
Se in root systems, we investigated the effect of Se on root exudates,
root morphology, root endogenous hormones, and Cd uptake using a
non–invasive micro–test technique and a conjunction analysis of the
transcriptome and metabolome in a hydroponically grown rice variety
(Yong you No.9). The results showed that selenite (Se(IV)) significantly
reduced Cd concentrations in the shoots and roots, and reduced Cd uptake
efficiency in rice root hair. Additionally, compared to the 1 mg L
–1 Cd treatment (Cd1), treatment with 0.5 mg L
–1 Se(IV) and 1 mg L –1 Cd
(Se0.5Cd1) significantly reduced root surface area and root tip numbers,
non–significantly reduced root length, and enhanced concentrations of
auxin (IAA) and jasmonic acid (JA) in the roots. The results of
metabolomic analysis showed that Se(IV) significantly increased the
expression of differential metabolites correlated with the synthesis of
IAA, JA, gibberellin (GA), and salicylic acid, such as GA53, M–SA,
(+/–)7–epi–JA, and derivatives of tryptophan and indole. Analysis of
the transcriptome indicated that no upregulated differentially expressed
genes (DEGs) were enriched in IAA synthesis; however, some upregulated
DEGs were found to be enriched in JA and GA53 synthesis pathways. In
summary, although Se(IV) stimulated the synthesis of IAA, JA, and GA53,
it significantly inhibited root growth mainly by 1) affecting the signal
transduction of IAA and GA; 2) altering IAA polar transport and
homeostasis; and 3) regulating the expression of the genes
SAUR32, SAUR36, SAUR76, OsSub33,
OsEXPA8, OsEXPA18, and Os6bglu24.