共查询到20条相似文献,搜索用时 15 毫秒
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Huapeng Zhou Huixin Lin She Chen Katia Becker Yongqing Yang Jinfeng Zhao J?rg Kudla Karen S. Schumaker Yan Guo 《The Plant cell》2014,26(3):1166-1182
The Salt Overly Sensitive (SOS) pathway regulates intracellular sodium ion (Na+) homeostasis and salt tolerance in plants. Until recently, little was known about the mechanisms that inhibit the SOS pathway when plants are grown in the absence of salt stress. In this study, we report that the Arabidopsis thaliana 14-3-3 proteins λ and κ interact with SOS2 and repress its kinase activity. Growth in the presence of salt decreases the interaction between SOS2 and the 14-3-3 proteins, leading to kinase activation in planta. 14-3-3 λ interacts with the SOS2 junction domain, which is important for its kinase activity. A phosphorylation site (Ser-294) is identified within this domain by mass spectrometry. Mutation of Ser-294 to Ala or Asp does not affect SOS2 kinase activity in the absence of the 14-3-3 proteins. However, in the presence of 14-3-3 proteins, the inhibition of SOS2 activity is decreased by the Ser-to-Ala mutation and enhanced by the Ser-to-Asp exchange. These results identify 14-3-3 λ and κ as important regulators of salt tolerance. The inhibition of SOS2 mediated by the binding of 14-3-3 proteins represents a novel mechanism that confers basal repression of the SOS pathway in the absence of salt stress. 相似文献
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E. A. Belousova M. M. Kutuzov P. A. Ivankina A. A. Ishchenko O. I. Lavrik 《Doklady. Biochemistry and biophysics》2018,482(1):233-237
Poly(ADP-ribosyl)ation, which is catalyzed by PARP family proteins, is one of the main reactions in the cell response to genomic DNA damage. Massive impact of DNA-damaging agents (such as oxidative stress and ionizing radiation) causes numerous breaks in DNA. In this case, the development of a fast cell response, which allows the genomic DNA integrity to be retained, may be more important than the repair by more accurate but long-term restoration of the DNA structure. This is the first study to show the possibility of eliminating DNA breaks through their PARP3-dependent mono(ADP-ribosyl)ation followed by ligation and repair of the formed ribo-AP sites by the base excision repair (BER) enzyme complex. Taken together, the results of the studies on ADP-ribosylation of DNA and the data obtained in this study suggest that PARP3 may be a component of the DNA break repair system involving the BER enzyme complex. 相似文献
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The proteins of the 14-3-3 family are universal adapters participating in multiple processes running in the cell. We describe
the structure, isoform composition, and distribution of 14-3-3 proteins in different tissues. Different elements of 14-3-3
structure important for dimer formation and recognition of protein targets are analyzed in detail. Special attention is paid
to analysis of posttranslational modifications playing important roles in regulation of 14-3-3 function. The data of the literature
concerning participation of 14-3-3 in regulation of intercellular contacts and different elements of cytoskeleton formed by
microfilaments are analyzed. We also describe participation of 14-3-3 in regulation of small G-proteins and protein kinases
important for proper functioning of cytoskeleton. The data on the interaction of 14-3-3 with different components of microtubules
are presented, and the probable role of 14-3-3 in developing of certain neurodegenerative diseases is discussed. The data
of the literature concerning the role of 14-3-3 in formation and normal functioning of intermediate filaments are also reviewed.
It is concluded that due to its adapter properties 14-3-3 plays an important role in cytoskeleton regulation. The cytoskeletal
proteins that are abundant in the cell might compete with the other protein targets of 14-3-3 and therefore can indirectly
regulate many intracellular processes that are dependent on 14-3-3. 相似文献
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The 14-3-3 Proteins: Gene,Gene Expression,and Function 总被引:6,自引:0,他引:6
Takahashi Y 《Neurochemical research》2003,28(8):1265-1273
14-3-3 Proteins were discovered by Moore and Perez in the soluble extract of bovine brain. These proteins are highly abundant in the brain. In this review 14-3-3 cDNA cloning, nucleotide sequence of 14-3-3 cDNA, the structure of 14-3-3 gene and 14-3-3 gene expression, in situ hybridization of 14-3-3 mRNA in the brain, the function and regulation of 14-3-3 protein, the binding of 14-3-3 protein to other proteins, the effects of 14-3-3 protein on the binding of a protein to other proteins, and the effect on protein kinase, etc., are concisely described. From the recent rapid development of proteom technology, markedly more target proteins of 14-3-3 protein should be discovered. 相似文献
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14-3-3蛋白与植物细胞信号转导 总被引:2,自引:0,他引:2
14-3-3蛋白通过直接蛋白质-蛋白质相互作用对植物代谢关键酶、质膜H^+ -ATP酶等发挥广泛调节作用。越来越多证据显示14-3-3蛋白通过与转录因子和其他信号分子结合参与调控植物细胞信号转导。对植物细胞中14-3-3蛋白调控信号转导途径,尤其是植物细胞对胁迫响应的调控机制进行了综述。 相似文献
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Ruihua Li Xiaotong Jiang Donghao Jin Sangeeta Dhaubhadel Shaomin Bian Xuyan Li 《PloS one》2015,10(11)
14-3-3s are a class of conserved regulatory proteins ubiquitously found in eukaryotes, which play important roles in a variety of cellular processes including response to diverse stresses. Although much has been learned about 14-3-3s in several plant species, it remains unknown in common bean. In this study, 9 common bean 14-3-3s (PvGF14s) were identified by exhaustive data mining against the publicly available common bean genomic database. A phylogenetic analysis revealed that each predicted PvGF14 was clustered with two GmSGF14 paralogs from soybean. Both epsilon-like and non-epsilon classes of PvGF14s were found in common bean, and the PvGF14s belonging to each class exhibited similar gene structure. Among 9 PvGF14s, only 8 are transcribed in common bean. Expression patterns of PvGF14s varied depending on tissue type, developmental stage and exposure of plants to stress. A protein-protein interaction study revealed that PvGF14a forms dimer with itself and with other PvGF14 isoforms. This study provides a first comprehensive look at common bean 14-3-3 proteins, a family of proteins with diverse functions in many cellular processes, especially in response to stresses. 相似文献
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Weifeng Xu Liguo Jia Weiming Shi Franti?ek Balu?ka Herbert J. Kronzucker Jiansheng Liang Jianhua Zhang 《Plant physiology》2013,163(4):1817-1828
Alkaline stress is a common environmental stress, in particular in salinized soils. Plant roots respond to a variety of soil stresses by regulating their growth, but the nature of the regulatory pathways engaged in the alkaline stress response (ASR) is not yet understood. Previous studies show that PIN-FORMED2, an auxin (indole-3-acetic acid [IAA]) efflux transporter, PKS5, a protein kinase, and DNAJ HOMOLOG3 (J3), a chaperone, play key roles in root H+ secretion by regulating plasma membrane (PM) H+-ATPases directly or by targeting 14-3-3 proteins. Here, we investigated the expression of all 14-3-3 gene family members (TOMATO 14-3-3 PROTEIN1 [TFT1]–TFT12) in tomato (Solanum lycopersicum) under ASR, showing the involvement of four of them, TFT1, TFT4, TFT6, and TFT7. When these genes were separately introduced into Arabidopsis (Arabidopsis thaliana) and overexpressed, only the growth of TFT4 overexpressors was significantly enhanced when compared with the wild type under stress. H+ efflux and the activity of PM H+-ATPase were significantly enhanced in the root tips of TFT4 overexpressors. Microarray analysis and pharmacological examination of the overexpressor and mutant plants revealed that overexpression of TFT4 maintains primary root elongation by modulating PM H+-ATPase-mediated H+ efflux and basipetal IAA transport in root tips under alkaline stress. TFT4 further plays important roles in the PKS5-J3 signaling pathway. Our study demonstrates that TFT4 acts as a regulator in the integration of H+ efflux, basipetal IAA transport, and the PKS5-J3 pathway in the ASR of roots and coordinates root apex responses to alkaline stress for the maintenance of primary root elongation.Alkaline soils occur commonly in terrestrial ecology, in particular in areas affected by salinity, thus contributing to one of the most widespread environmental challenges that limit agricultural productivity globally (Kawanabe and Zhu, 1991; Ge et al., 2010; Xu et al., 2012a). Worldwide, it is estimated that up to 831 × 106 ha of land is saline, and more than half of this area is alkalinized. High-pH stress limits the survival of most plants under these conditions and can be a more significant factor in reducing plant growth than the stress resulting from salinity (Guo et al., 2010). Improved understanding of the basic mechanisms of plant responses to alkaline stress is urgently needed and will aid biotechnological efforts focused on breeding suitable crops for fodder and human food on these unproductive lands.Primary root elongation regulated by a sensory zone in the root tip plays a pivotal role in the plastic acclimation response to fluctuating soil environments (Baluška et al., 2010). The root functions simultaneously as an organ for the uptake and transport of water and nutrients and as the primary site for the perception of soil stresses. Thus, roots must be the obvious first focus in any examination of the adaptive and acclimation mechanisms underpinning the alkaline stress response. However, currently, only limited information is available on this particular form of stress (Degenhardt et al., 2000; Zhu, 2001; Yang et al., 2008).Acidification of the aqueous fraction of the cell wall apoplast by H+ excretion via the plasma membrane (PM) H+-ATPase is a critical component of the growth-promoting effect and a key factor determining the elongation of the primary root (Moloney et al., 1981; Palmgren, 2001). Optimal primary root elongation requires the fine regulation of H+-ATPase-mediated H+ efflux, particularly at the root tip (Staal et al., 2011; Haruta and Sussman, 2012). Under alkaline stress, in Arabidopsis (Arabidopsis thaliana), PROTEIN KINASE5 (PKS5) and the chaperone DNAJ HOMOLOG3 (J3) play important roles in H+ efflux by regulating the interaction between PM H+-ATPase and 14-3-3 proteins (Fuglsang et al., 2007; Yang et al., 2010). Furthermore, PIN-FORMED2 (PIN2), an auxin (indole-3-acetic acid [IAA]) efflux transporter, is required for the acclimation of roots to alkaline stress through the modulation of H+ secretion in the root tip, maintaining primary root elongation (Xu et al., 2012a). However, these mechanisms, and other physiologically relevant processes that may fine-tune root-apical responses to alkaline stress, have not been investigated in depth.The 14-3-3 proteins are highly conserved, and nearly ubiquitous, phosphoserine-binding proteins that regulate the activities of a wide array of targets via direct protein-protein interactions (Moore and Perez, 1967; Comparot et al., 2003). In higher plants, 14-3-3 proteins are encoded by a multigene family and play important roles in regulating plant development and stress responses (Mayfield et al., 2012). Although 14-3-3 proteins in plants possess a highly conserved target-binding domain, several studies indicate that various 14-3-3 isoforms may regulate different targets or act in distinct locations under variable abiotic stresses (Sehnke et al., 2002; Xu et al., 2012b). At least 12 genes predicted to encode 14-3-3 proteins (TOMATO 14-3-3 PROTEIN1 [TFT1]–TFT12) have been identified in tomato (Solanum lycopersicum; Roberts, 2003; Xu and Shi, 2006). However, little is known about the detailed actions of tomato 14-3-3 proteins in response to alkaline stress in relation to H+ secretion, auxin modulation, or specific signaling pathways. Thus, in this study, we investigated the roles of tomato 14-3-3 proteins, incorporated into Arabidopsis, in root acclimation to alkaline stress and the involvement of PKS5 and J3 in modulating H+ secretion and basipetal (shoot-ward) IAA transport for maintaining primary root elongation. 相似文献
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CDPKs and 14-3-3 Proteins: Emerging Duo in Signaling 总被引:1,自引:0,他引:1
Mélanie Ormancey Patrice Thuleau Christian Mazars Valérie Cotelle 《Trends in plant science》2017,22(3):263-272
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Chelysheva V. V. Zorinyants S. E. Smolenskaya I. N. Babakov A. V. 《Russian Journal of Plant Physiology》2001,48(3):273-280
All higher plants have high-specific sites for binding fusicoccin (FCBS), a metabolite of the fungus Fusicoccum amygdaliDel. These sites are localized on the plasmalemma and produced by the association of the dimers of 14-3-3 proteins with the C-terminal autoinhibitory domain of H+-ATPase. Considering the fusicoccin binding to the plasmalemma as an index characterizing the formation of this complex, we studied the influence of osmotic stress on the interaction between 14-3-3 proteins and H+-ATPase in the suspension-cultured sugar beet cells and protoplasts obtained from them. An increase in the osmolarity of the extracellular medium up to 0.3 Osm was shown to enhance proton efflux from the cells by several times. The number of FCBS in isolated plasma membranes increased in parallel, whereas 14-3-3 proteins accumulated in this membrane to a lesser degree. The amount of H+-ATPase molecules did not change, and the ATP-hydrolase activity changed insignificantly. The data obtained indicate that osmotic stress affects H+-ATPase pumping in the plasmalemma through its influence on the coupling between H+-transport and ATP hydrolysis; 14-3-3 proteins are involved in this coupling. The interaction between the plasmalemma and the cell wall is suggested to be very important in this process. 相似文献
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Marina Shenkman Bella Groisman Efrat Ron Edward Avezov Linda M. Hendershot Gerardo Z. Lederkremer 《The Journal of biological chemistry》2013,288(4):2167-2178
Studies of misfolded protein targeting to endoplasmic reticulum-associated degradation (ERAD) have largely focused on glycoproteins, which include the bulk of the secretory proteins. Mechanisms of targeting of nonglycosylated proteins are less clear. Here, we studied three nonglycosylated proteins and analyzed their use of known glycoprotein quality control and ERAD components. Similar to an established glycosylated ERAD substrate, the uncleaved precursor of asialoglycoprotein receptor H2a, its nonglycosylated mutant, makes use of calnexin, EDEM1, and HRD1, but only glycosylated H2a is a substrate for the cytosolic SCFFbs2 E3 ubiquitin ligase with lectin activity. Two nonglycosylated BiP substrates, NS-1κ light chain and truncated Igγ heavy chain, interact with the ERAD complex lectins OS-9 and XTP3-B and require EDEM1 for degradation. EDEM1 associates through a region outside of its mannosidase-like domain with the nonglycosylated proteins. Similar to glycosylated substrates, proteasomal inhibition induced accumulation of the nonglycosylated proteins and ERAD machinery in the endoplasmic reticulum-derived quality control compartment. Our results suggest a shared ERAD pathway for glycosylated and nonglycosylated proteins composed of luminal lectin machinery components also capable of protein-protein interactions. 相似文献
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Although an increasing body of evidence indicates that plant MAP kinases are involved in a number of cellular processes, such
as cell cycle regulation and cellular response to abiotic stresses, hormones and pathogen attack, very little is known about
their biochemical properties and regulation mechanism. In this paper we report on the identification and characterization
of a novel member of the MAP kinase family from maize, ZmMPK6. The amino acid sequence reveals a high degree of identity with
group D plant MAP kinases. Recombinant ZmMPK6, expressed in Escherichia coli, is an active enzyme able to autophosphorylate. Remarkably, ZmMPK6 interacts in vitro with GF14-6, a maize 14-3-3 protein and the interaction is dependent on autophosphorylation. The interacting domain of ZmMPK6
is on the C-terminus and is comprised between amino acid 337 and amino acid 467. Our results represent the first evidence
of an interaction between a plant MAP kinase and a 14-3-3 protein. Possible functional roles of this association in vivo are discussed. 相似文献