1、植物学及园艺学英文版_botany_and_horticulture_(28)1.Introduction Hormones act as chemical messengers in the control of the molecular,biochemical,and physiological events underlying growth and development.Hormones also serve as essential integrators of developmental programs with the environmental signals.A bas
2、ic challenge in biology is,therefore,to understand the molecular mechanisms that underlie hormone action,in other words,how those chemical signals are sensed by and communicated within the cells to trigger the relevant responses.This process can be divided into three main steps:(1)signal perception,
3、(2)signal transduction or a cascade of biochemical events that ultimately leads to the induction of the final step,(3)the response.Among the plant hormones,ethylene distinguishes itself by its simple hydrocarbon chemical structure(C2H4)and its gaseous nature.This simple molecule,however,plays a majo
4、r role in plant growth and development by influencing a wide range of complex physiological processes throughout the entire plant life cycle,from seed germination to flowering,fruitripening,and senescence One of the most dramatic effects of ethylene on plant morphogenesis is the classical triple res
5、ponse exhibited by dark-grown seedlings exposed to ethylene.The triple response in Arabidopsis is characterized by(1)exaggerated curvature of the apical hook,(2)radial swelling of the hypocotyl,and(3)inhibition of hypocotyl and root growthFig.1 Phenotypes of dark-grown three-day-old seedlings ofArab
6、idopsis thaliana.The plant on the left was grown without hormonal supplementation,whereas the plant on the right was exposed to 10 mM ethylene precursor ACC and thus shows a typical triple response.A series of elegant genetic,molecular,and biochemical studies are uncovering a largelylinear pathway t
7、hat transduces the ethylene signal from the endoplasmic reticulum membrane to the nucleusFig.2 The ethylene signaling pathway and its genetically characterized components.The signaling pathway components are shown in their sequential order of action.Components drawn in white represent active forms,w
8、hereas gray ovals represent their inactive versions.Binding of ethylene to the receptors,represented by ETR1,leads to activation of ethylene responses.Dotted oval represents EIN3 degradation by the 26S proteasome pathway due to action of EBF1 and EBF2.Arrows indicate activation steps,whereas a block
9、ed arrow depicts repression of downstream elements by CTR1.This review aims to summarize the current state of knowledge in the ethylene field.We will start with the description of the main experimental breakthroughs that resulted in the discovery of the known ethylene signaling components to then de
10、scribe the genomic approaches employed to characterize the molecular aspects of the ethylene response.2.Ethylene perception is mediated by a small family of receptors The development of modern molecular genetic approaches and the selection of Arabidopsis as a plantmodel system opened a new door not
11、only for the identification of the ethylene receptors,but for the elucidation of the entire signal transduction pathway.The new quest for the molecular components of the ethylene signal transduction machinery first led to the isolation of ethylene response1,etr1,a dominant mutation that confers ethy
12、lene insensitivity.ETR1 encodes a histidine kinase with similarity to the classical bacterial two-component histidine kinases.The novel hydrophobic amino-terminal domain of ETR1 heterologously expressed in yeast was shown to possess high-affinity binding properties to the gas ethylene.ETR1 was found
13、 to act as a dimer that localizes to a cellular membrane system.A series of elegant studies performed in the nineties revealed that ethylene receptors are encoded by a small gene family that in Arabidopsis consists of five members:ETR1,ethylene response2(etr2),ethylene insensitive4(ein4),ethylene re
14、sistant1(ers1),and ethylene resistant2(ers2).Their sequence similarity and structural organization,the five receptors are categorized into two subfamilies.Subfamily I members(ETR1 and ERS1)harbor three hydrophobic transmembrane domains in the amino-terminus followed by a conserved histidine kinase d
15、omain.Subfamily II members(ETR2,ERS2,and EIN4)possess four predicted amino-terminal hydrophobic transmembrane regions followedby a less conserved kinase domain that lacks several of the canonical features required for histidine-kinase activity.Furthermore,three of the five receptors,ETR1,ETR2,and EI
16、N4,also possess a carboxyl-terminal receiver domain.A major breakthrough came with the isolation of loss-offunction(LOF)alleles of the receptors.Each of the single LOF alleles was still able to respond to ethylene,indicating a high degree of functional redundancy among the receptors.Furthermore,trip
17、le and quadruple LOF mutants displayed a constitutive ethylene response in the absence of the hormone.Both receptor subfamilies appear to be able to sense ethylene,as double etr1;ers1 and triple etr2;ers2;ein4 LOF mutants are still able to respond to ethylene in the triple response assay.However,a p
18、articular role for subfamily I receptors in light-grown plants has been recently suggested.Double etr1;ers1 LOF mutants displayed severe phenotypes,including miniature rosettes,fertility defects,and altered flower morphology.All of these effects were dependent on a functional ethylene signaling path
19、way,implying that the observed growth defects arose from a misregulation of ethylene responses.Overexpression of the subfamily II members was unable to rescue the observed phenotypes,whereas ectopic expression of either wild-type ETR1 or ERS1 restored normal development,further supporting the notion
20、 of a unique role for the subfamily I receptors.Ethylene was found to bind to the receptors through a transition metal cofactor,copper.Moreover,the copper cofactor was shown to be essential for ethylene binding,and thus,proper receptor function.The current structural model for the ethylene binding d
21、omain suggests that the copper(I)cofactor is located in the electron-rich hydrophobic pocket formed by the N-terminal transmembrane domains of the receptors.In particular,residues Cys65 and His69 are thought to play a fundamental role in this protein-metal-hormone interaction.In planta,the relevance
22、 of this interaction was further confirmed with the identification of RESPONSIVE TO ANTAGONIST1(RAN1).RAN1 was isolated using a screening for mutants with altered specificity in hormone binding by employing the ethylene antagonist trans-cyclooctene(TCO).ran1 plants are defective in a copper transpor
23、ter similar to P-type ATPases.The lack of the metal cofactor impairs receptor function in ran1 mutants by causing altered ligand specificity and thus rendering the plants responsive to the antagonist TCO.Furthermore,a strong LOF ran1 allele results in a constitutive ethylene response phenotype in th
24、e absence of the gaseous hormone.Autophosphorylation activity has been demonstrated for ETR1 and all other members of the receptor family.However,while ETR1 autophosphorylates in the predicted conserved histidine residue,ERS1 and all of the subfamily II members display a serine-kinase activity in vi
25、tro.ERS1 also possesses a histidine-kinase activity,whereas its serine autophosphorylation is thought not to be significant in vivo.Another interesting study addressed the roles of the kinase activity and of the carboxyl-terminal receiver domain of ETR1,ETR2,and EIN4 in ethylene signaling by looking
26、 at the effect of expressing truncated versions of ETR1 in a triple LOF etr1;etr2;ein4 mutant background.Transformation of the triple mutant with a truncated version of ETR1 that lacks both the histidine-kinase and the receiver domain failed to restore ethylene responsiveness to the triple mutant.Co
27、nversely,a second truncated ETR1 construct in which only the receiver domain was missing did rescue the partial constitutive triple response phenotype of the triple knockout line.Moreover,transgenic plants harboring this particularconstruct displayed hypersensitivity to ethylene.These observations i
28、mplied that the kinase domain was necessary for signal transmission by the receptors and that the receiver domain was not essential for restoring ethylene responsiveness.Modulation of the ethylene responses by the receiver domain could be achieved,for instance,through its reported interaction with a
29、nother negative regulator of the pathway,CONSTITUTIVE TRIPLE RESPONSE1(CTR1)(see below),assuming that in the absence of the receiver domain the function of CTR1 is impaired.Interestingly,a detailed kinetic analysis of seedling growth response in the presence of exogenous ethylene and of the consecut
30、ive recovery after ethylene withdrawal also indicated the importance of both the kinase and receiver domains in specific aspects of the ethylene response.These results suggest that both the kinase and the receiver domain are important for the hypocotyl recovery from short ethylene treatment and indi
31、cate that,despite the large functional overlap,some specificity can be attributed to the different receptors.The accumulated data have provided a model for the role of the receptors in ethylene signaling.(1)In the absence of the hormone,the receptors actively repress downstream components of the pat
32、hway and inhibit ethylene responses.(2)Ethylene gas binds to all five receptors,causing the receptors to become inactive and releasing the pathway from their repression.Although still controversial,(3)receptor kinase activity possibly plays an important role in signaling.3.A Raf-like kinase acts dow
33、nstream of the receptors repressing ethylene responses A subset of those was further characterized as defective in ethylene biosynthesis,namely ethylene overproducer(eto).Conversely,the ctr1 mutant did not respond to inhibitors of ethylene biosynthesis indicative of an alteration in signal transduct
34、ion.CTR1 encodes a serine/threonine kinase whose carboxyl-terminus shares sequence similarity with the Raf family of protein kinases.The constitutive response phenotype exhibited by LOF mutants indicates that CTR1 negatively regulates the ethylene signaling pathway.Interestingly,CTR1 was shown to ph
35、ysically interact with the receptors.Subsequently,CTR1 was shown to co-localize with the receptors at the ER membranes.Moreover,co-purification of an affinity-tagged CTR1 and endogenous ETR1 in transgenic Arabidopsis lines strongly supported the in vivo interaction of these proteins.The significance
36、 of this interaction in signal transmission is corroborated by the observation that double and triple LOF receptor mutants result in a loss of ER-localization of CTR1.Taken together,these data suggested that the receptors and CTR1 function as part of an ER-localized complex that actively represses e
37、thylene responses.The serine/threonine kinase activity of CTR1 was demonstrated in vitro and shown to be essential for proper functioning of the receptors/CTR1 signaling complex.It has been established that ethylene binding to the receptors affects neither the interaction between the receptors and C
38、TR1 nor their sub-cellular localization.The current proposed model predicts that upon ethylene binding,the receptors/CTR1 signaling complexes are turned off.4.A unique plant protein is a central component of the signaling pathway and positively regulates ethylene responses Downstream of the receptor
39、s/CTR1 complexes there acts a positive regulator of the pathway,ETHYLENEINSENSITIVE2(EIN2).EIN2 is required for all ethylene responses studied and constitutes a critical step in the signal transduction.The hydrophobic amino-terminus is predicted to form twelve transmembrane domains and shares sequen
40、ce similarity with the family of NRAMP metal ion transporters.The long EIN2 carboxyl-terminus contains a coiled-coil structure(a motif typically involved in proteinprotein interactions)but otherwise displays no similarity to known protein.Conversely,the NRAMP-like amino-terminal domain of EIN2 is be
41、lieved to sense the upstream signaling events.5.A transcriptional cascade mediates ethylene responses at the gene expression level ETHYLENE INSENSITIVE3,EIN3,is a nuclear-localized protein required for ethylene signaling that genetically works downstream of EIN2.EIN3 belongs to a small gene family t
42、hat in Arabidopsis also includes five EIN3-LIKE(EIL)proteins.These observations suggested that EIN3 and at least some of the EILs may act as transcriptional regulators of ethylene responses.In Arabidopsis,EIN3,EIL1,and EIL2 were demonstrated to bind to a short palindromic region,known as the EIN3-bi
43、nding site,or EBS,in the promoter of the EREBP family member ETHYLENE RESPONSE FACTOR1(ERF1).ERF1,in turn,is a GCC box-binding transcription factor that acts downstream of EIN3 and EILs and is responsible for the modulation of a set of secondary ethylene responsive genes.Consistent with these result
44、s,transgenic lines overexpressing EIN3 show a constitutive triple response,whereas in ERF1-overexpressing plants only some of the ethylene responses are activated.ERF1 is also required for the activation of defense-related responses by the plant hormone jasmonicacid.Moreover,both ethylene and jasmon
45、ate pathways must be intact for proper ERF1 expression.Ethylene and jasmonate interact synergistically to achieve maximal expression of ERF1.This transcription factor,therefore,represents a critical element in the interaction between these two important hormones.6.The ubiquitin/26S proteasome pathwa
46、y regulates EIN3 activity A recently emerging picture positions the SCF-E3 ligases in the center of many plant hormone signaling pathways,including those of auxin,gibberellins,and jasmonic acid.The ethylene signaling pathway also employs the SCF/26S proteasome to regulate the levels of at least one
47、of its components,EIN3.Recently,two F-box proteins,EIN3 BINDING FACTOR1(EBF1)and EBF2,were shown to act as part of an E3-ligase and to bind and target the constitutively produced EIN3 for degradation in the absence of ethylene.In the presence of exogenous ethylene,EIN3 protein levels were found to i
48、ncrease.In addition to the negative regulation by EBF1 and EBF2,a stimulatory mechanism that activates the stabilized EIN3 protein is also expected to participate in the regulation of the activity of this critical transcription factor.This observation is supported by the ethylene responsiveness of E
49、IN3-overexpression lines and ebf1;ebf2 double LOF mutants.These plants respond to exogenous ethylene in spite of having elevated levels of EIN3,suggesting that regulation of the protein levels is not the only mechanism that governs the EIN3 activity.7.Ethylene triggers genome-wide changes in gene ex
50、pression EIN3 is the initial factor in the transcriptional cascade responsible for inducing ethylene responses at the molecular level.The importance of this transcriptional regulation in ethylene responses is emphasized by the observation that ein3;eil1 double mutants display almost complete insensi
