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OsNAC120 balances plant growth and drought tolerance by integrating GA and ABA signaling in rice
Friday, 2024/09/13 | 08:32:31

Zizhao XieLiang JinYing SunChenghang ZhanSiqi TangTian QinNian LiuJunli Huang

Plant Commun.; 2024 Mar 11; 5(3):100782. doi: 10.1016/j.xplc.2023.100782. 

Abstract

The crosstalk between gibberellin (GA) and abscisic acid (ABA) signaling is crucial for balancing plant growth and adaption to environmental stress. Nevertheless, the molecular mechanism of their mutual antagonism still remains to be fully clarified. In this study, we found that knockout of the rice NAC (NAM, ATAF1/2, CUC2) transcription factor gene OsNAC120 inhibits plant growth but enhances drought tolerance, whereas OsNAC120 overexpression produces the opposite results. Exogenous GA can rescue the semi-dwarf phenotype of osnac120 mutants, and further study showed that OsNAC120 promotes GA biosynthesis by transcriptionally activating the GA biosynthetic genes OsGA20ox1 and OsGA20ox3. The DELLA protein SLENDER RICE1 (SLR1) interacts with OsNAC120 and impedes its transactivation ability, and GA treatment can remove the inhibition of transactivation activity caused by SLR1. On the other hand, OsNAC120 negatively regulates rice drought tolerance by repressing ABA-induced stomatal closure. Mechanistic investigation revealed that OsNAC120 inhibits ABA biosynthesis via transcriptional repression of the ABA biosynthetic genes OsNCED3 and OsNCED4. Rice OSMOTIC STRESS/ABA-ACTIVATED PROTEIN KINASE 9 (OsSAPK9) physically interacts with OsNAC120 and mediates its phosphorylation, which results in OsNAC120 degradation. ABA treatment accelerates OsNAC120 degradation and reduces its transactivation activity. Together, our findings provide evidence that OsNAC120 plays critical roles in balancing GA-mediated growth and ABA-induced drought tolerance in rice. This research will help us to understand the mechanisms underlying the trade-off between plant growth and stress tolerance and to engineer stress-resistant, high-yielding crops.

 

See https://pubmed.ncbi.nlm.nih.gov/38148603/

 

Figure 1:

OsNAC120 regulates plant growth by promoting GA biosynthesis

(A) Schematic diagram showing the T-DNA insertion sites in genomic regions of osnac120 mutants. Black boxes represent exons, and lines between black boxes represent introns. The arrow indicates the transcription orientation.

(B and C) Growth of 3-month-old T-DNA insertion mutants (osnac120-1 and osnac120-2). Scale bars correspond to 20 cm (B)(C) Values are means ± SD (n = 10).

(D) Schematic diagram of OsNAC120 gene structure and single-guide RNA (sgRNA)-targeted sites. Target site position is indicated on the gene structure.

(E and F) Growth of 3-month-old CRISPR/Cas9 mutants (osnac120-cr1 and osnac120-cr2). Scale bars correspond to 20 cm (E)(F) Values are means ± SD (n = 10).

(G and H) Growth of 3-month-old OsNAC120-overexpressing lines (OE11 and OE20). Scale bars correspond to 25 cm (G)(H) Values are means ± SD (n = 10).

(I and J) Exogenous GA rescued the growth of osnac120 mutants. Scale bars correspond to 2 cm (I)(J) Three independent experiments were performed with similar results, and values are means ± SD (n = 10) from one experiment.

(K) Bioactive GA3 content in plants of different OsNAC120 genotypes. Three independent experiments were performed with similar results, and values are means ± SD (n = 4) from one experiment.

(L) Expression of the GA biosynthetic genes OsGA20ox1OsGA20ox2, and OsGA20ox3 in leaves of 2-week-old wild-type and osnac120-2 mutant plants. OsActin and OsEF1a were used as the internal references to calculate the relative expression of target genes. Values are means ± SD (n = 3). (C and L) Significant differences were determined by Student’s t-test (∗p < 0.05, ∗∗p < 0.01; ns, not significant). (F, H, and K) Different lowercase letters indicate significant differences (p < 0.05, one-way ANOVA with Bonferroni post hoc test). (J) Significant differences were determined by two-way ANOVA with post hoc Tukey’s HSD test (p < 0.05).

 

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