Abstract:Nitrate is a major nitrogen resource for plant growth and development and acts as both a crucial nutrient and a signaling molecule for plants; hence, understanding nitrate signaling is important for crop production. Abscisic acid (ABA) has been demonstrated to be involved in nitrate signaling, but the underlying mechanism is largely unknown in apple. In this study, we found that exogenous ABA inhibited the transport of nitrate from roots to shoots in apple, and the transcription of the nitrate transporter MdNR… Show more
“…For example, in a very recent study, two bZIP TFs, including bZIP29 and Opaque2, were phosphorylated by SnRK2.2 to transactivate downstream target genes for endosperm filling in maize (Yang et al, 2022). In addition, either SnRK2s or ABFs have been separately shown to act as the pivotal regulators of various physiological and biological processes, such as root growth (Liu et al, 2021), stomatal development (Ding et al, 2020), sugar metabolism (Ma et al, 2017a), flower senescence (J. Z.…”
Section: Introductionmentioning
confidence: 99%
“…For example, in a very recent study, two bZIP TFs, including bZIP29 and Opaque2, were phosphorylated by SnRK2.2 to transactivate downstream target genes for endosperm filling in maize (Yang et al ., 2022). In addition, either SnRK2s or ABFs have been separately shown to act as the pivotal regulators of various physiological and biological processes, such as root growth (Liu et al ., 2021), stomatal development (Ding et al ., 2020), sugar metabolism (Ma et al ., 2017a), flower senescence (J. Liu et al ., 2017; Z. Liu et al ., 2017), and abiotic stress response (Chen et al ., 2020; Takahashi et al ., 2020; Li et al ., 2021), among others. As increasing evidence showed that activation of ABFs requires SnRK2‐mediated phosphorylation (Kobayashi et al ., 2005; Wang et al ., 2012; Umezawa et al ., 2013; W. Wang et al ., 2019; X. Wang et al ., 2019), it is reasonable to assume that SnRK2s and ABFs in various combinations might function in synergy to play crucial roles in the regulation of plant development and responses to environmental stresses.…”
Summary
Arginine decarboxylase (ADC)‐mediated putrescine (Put) biosynthesis plays an important role in plant abiotic stress response. SNF1‐related protein kinases 2s (SnRK2s) and abscisic acid (ABA)‐response element (ABRE)‐binding factors (ABFs), are core components of the ABA signaling pathway involved in drought stress response. We previously reported that ADC of Poncirus trifoliata (PtrADC) functions in drought tolerance. However, whether and how SnRK2 and ABF regulate PtrADC to modulate putrescine accumulation under drought stress remains largely unclear.
Herein, we employed a set of physiological, biochemical, and molecular approaches to reveal that a protein complex composed of PtrSnRK2.4 and PtrABF2 modulates putrescine biosynthesis and drought tolerance by directly regulating PtrADC.
PtrABF2 was upregulated by dehydration in an ABA‐dependent manner. PtrABF2 activated PtrADC expression by directly and specifically binding to the ABRE core sequence within its promoter and positively regulated drought tolerance via modulating putrescine accumulation. PtrSnRK2.4 interacts with and phosphorylates PtrABF2 at Ser93. PtrSnRK2.4‐mediated PtrABF2 phosphorylation is essential for the transcriptional regulation of PtrADC. Besides, PtrSnRK2.4 was shown to play a positive role in drought tolerance by facilitating putrescine synthesis.
Taken together, this study sheds new light on the regulatory module SnRK2.4‐ABF2‐ADC responsible for fine‐tuning putrescine accumulation under drought stress, which advances our understanding on transcriptional regulation of putrescine synthesis.
“…For example, in a very recent study, two bZIP TFs, including bZIP29 and Opaque2, were phosphorylated by SnRK2.2 to transactivate downstream target genes for endosperm filling in maize (Yang et al, 2022). In addition, either SnRK2s or ABFs have been separately shown to act as the pivotal regulators of various physiological and biological processes, such as root growth (Liu et al, 2021), stomatal development (Ding et al, 2020), sugar metabolism (Ma et al, 2017a), flower senescence (J. Z.…”
Section: Introductionmentioning
confidence: 99%
“…For example, in a very recent study, two bZIP TFs, including bZIP29 and Opaque2, were phosphorylated by SnRK2.2 to transactivate downstream target genes for endosperm filling in maize (Yang et al ., 2022). In addition, either SnRK2s or ABFs have been separately shown to act as the pivotal regulators of various physiological and biological processes, such as root growth (Liu et al ., 2021), stomatal development (Ding et al ., 2020), sugar metabolism (Ma et al ., 2017a), flower senescence (J. Liu et al ., 2017; Z. Liu et al ., 2017), and abiotic stress response (Chen et al ., 2020; Takahashi et al ., 2020; Li et al ., 2021), among others. As increasing evidence showed that activation of ABFs requires SnRK2‐mediated phosphorylation (Kobayashi et al ., 2005; Wang et al ., 2012; Umezawa et al ., 2013; W. Wang et al ., 2019; X. Wang et al ., 2019), it is reasonable to assume that SnRK2s and ABFs in various combinations might function in synergy to play crucial roles in the regulation of plant development and responses to environmental stresses.…”
Summary
Arginine decarboxylase (ADC)‐mediated putrescine (Put) biosynthesis plays an important role in plant abiotic stress response. SNF1‐related protein kinases 2s (SnRK2s) and abscisic acid (ABA)‐response element (ABRE)‐binding factors (ABFs), are core components of the ABA signaling pathway involved in drought stress response. We previously reported that ADC of Poncirus trifoliata (PtrADC) functions in drought tolerance. However, whether and how SnRK2 and ABF regulate PtrADC to modulate putrescine accumulation under drought stress remains largely unclear.
Herein, we employed a set of physiological, biochemical, and molecular approaches to reveal that a protein complex composed of PtrSnRK2.4 and PtrABF2 modulates putrescine biosynthesis and drought tolerance by directly regulating PtrADC.
PtrABF2 was upregulated by dehydration in an ABA‐dependent manner. PtrABF2 activated PtrADC expression by directly and specifically binding to the ABRE core sequence within its promoter and positively regulated drought tolerance via modulating putrescine accumulation. PtrSnRK2.4 interacts with and phosphorylates PtrABF2 at Ser93. PtrSnRK2.4‐mediated PtrABF2 phosphorylation is essential for the transcriptional regulation of PtrADC. Besides, PtrSnRK2.4 was shown to play a positive role in drought tolerance by facilitating putrescine synthesis.
Taken together, this study sheds new light on the regulatory module SnRK2.4‐ABF2‐ADC responsible for fine‐tuning putrescine accumulation under drought stress, which advances our understanding on transcriptional regulation of putrescine synthesis.
“…AtNRT2.7 is induced by nitrate and hormones, enhances the growth of the root system, and improves the absorption and utilization of nitrogen [ 47 ]. In apples, the expression of MdNRT1.5 / MdNPF7.3 inhibits the transport of nitrate from root to branch [ 48 ]. Nitrate has been reported to mediate phosphorus absorption and starvation signals by activating the NIGT1-SPX-PHR cascade signaling pathway [ 49 ].…”
The mitogen-activated protein kinase (MAPK) signaling cascade is a widely existing signal transduction system in eukaryotes, and plays an important role in the signal transduction processes of plant cells in response to environmental stress. In this study, we screened MdMKK9, a gene in the MAPK family. This gene is directly related to changes in anthocyanin synthesis in the ‘Daihong’ variety of red-fleshed apple (Malus sieversii f neidzwetzkyana (Dieck) Langenf). MdMKK9 expression was up-regulated in ‘Daihong’ tissue culture seedlings cultured at low levels of nitrogen. This change in gene expression up-regulated the expression of genes related to anthocyanin synthesis and nitrogen transport, thus promoting anthocyanin synthesis and causing the tissue culture seedlings to appear red in color. To elucidate the function of MdMKK9, we used the CRISPR/Cas9 system to construct a gene editing vector for MdMKK9 and successfully introduced it into the calli of the ‘Orin’ apple. The MdMKK9 deletion mutants (MUT) calli could not respond to the low level of nitrogen signal, the expression level of anthocyanin synthesis-related genes was down-regulated, and the anthocyanin content was lower than that of the wild type (WT). In contrast, the MdMKK9-overexpressed calli up-regulated the expression level of anthocyanin synthesis-related genes and increased anthocyanin content, and appeared red in conditions of low level of nitrogen or nitrogen deficiency. These results show that MdMKK9 plays a role in the adaptation of red-fleshed apple to low levels of nitrogen by regulating the nitrogen status and anthocyanin accumulation.
“…The apple calli was transiently transformed by Agrobacterium carrying ProMdERF113::GUS as previously described (Hu et al, 2017; Y. J. Liu et al, 2021). They were cultured on a solid medium containing NaCl (120 mM), PEG 6000 (4%), temperature (4°C), and ABA (100 μM) for 24 h, respectively.…”
The AP2/ERF family is an important class of transcription factors involved in plant growth and various biological processes. One of the AP2/ERF transcription factors, RAP2.6L, participates in various stresses responses. However, the function of RAP2.6L is largely unknown in apples (Malus domestica). In this study, an apple gene homologous to Arabidopsis AtRAP2.6L, MdERF113, was analyzed by bioinformatic characterization, gene expression analysis and subcellular localization assessment. MdERF113 was highly expressed in the sarcocarp and was responsive to hormonal signals and abiotic stresses. MdERF113‐overexpression apple calli were less sensitive to low temperature, drought, salinity, and abscisic acid than wild‐type. Subcellular localization revealed that MdERF113 was a nuclear‐localized transcription factor, and yeast experiments confirmed that MdERF113 has no autonomous activation activity. Overall, this study indicated that MdERF113 plays a role in regulating plant growth under abiotic conditions.
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