Reduced levels of cadinane sesquiterpenoids in cotton plants expressing antisense (+)-delta-cadinene synthase

Cotton plants were transformed with an antisense construct of cdn1-Cl, a member of a complex gene family of delta-(+)cadinene (CDN) synthase. This synthase catalyzes the cyclization of (E,E)-farnesyl diphosphate to form CDN, and in cotton, it occupies the committed step in the biosynthesis of cadinane sesquiterpenoids and heliocides (sesterterpenoids). Southern analyses of the digestion of leaf DNA from R(o), T(o), and T(1) plants with Hind III, Pst I and Kpn I restriction enzymes show the integration of antisense cdn1-C1 cDNA driven by the CaMV 35S promoter into the cotton genome. Northern blots demonstrate the appearance of cdn synthase mRNA preceding CDN synthase activity and the formation of gossypol in developing cottonseed. T(2) cottonseed show a reduced CDN synthase activity and up to a 70% reduction in gossypol. In T(1) leaves the accumulated amounts of gossypol, hemigossypolone and heliocides are reduced 92.4, 83.3 and 68.4%, respectively. These data demonstrate that the integration of antisense cdn1-C1 cDNA into the cotton genome leads to a reduction of CDN synthase activity and negatively impacts on the biosynthesis of cadinane sesquiterpenoids and heliocides in cotton plants.     

棉叶中棉酚的快速提取与测定方法研究

棉酚(G)及其相关物甲氧基半棉酚(DHG)、半棉酚酮(HGQ)、半棉酚(HG)、杀实夜蛾素(H1-4)等是棉花中重要的抗虫性萜烯类次生物质.利用高效液相色谱法(HPLC)对棉酚及其相关物进行了分离,测定了棉叶中的棉酚含量,讨论了不同的提取方法和测定条件对结果的影响,给出了一套简便、快速的分析测试方法,同时与紫外-可见分光光度法(苯胺法)的结果进行了对比,认为对于棉花的抗虫性的研究来说,HPLC是比较适宜的方法.     

Sesquiterpenoid aldehyde quinones and derivatives in pigment glands of Gossypium

The resistance of Gossypium species to insects is enhanced by compounds in their lysigenous pigment glands. In cultivated cottons, glands in achlorophyllous plant parts contained predominately the terpenoid aldehyde gossypol in G. hirsutum, and gossypol and its methyl and dimethyl ethers in G. barbadense. Glands in young green tissues, however, contained hemigossypolone as the predominant terpenoid aldehyde in G. hirsutum, and a new quinone, hemigossypolone-7-methyl ether, in G. barbadense. As glands aged in green tissues, the sesquiterpenoid quinones were replaced by several C₂₅-terpenoids formed by the Diels-Alder reaction of the quinones with myrcene or trans-β-ocimene. Two C₂₅-terpenoids isolated from G. barbadense, but not G. hirsutum, were the methyl ethers of heliocides H₁ and H₄ and were designated heliocides B₁ and B₄, respectively. A dark red pigment, gossyrubilone, from glands of young leaves of both species is the isopentylimine of hemigossypolone. Similar red imines, formed from sesquiterpenoid quinones and amino acids, resembled the red coloration of the envelope cells surrounding the gland sac. The terpenoid quinones of Gossypium had physical characteristics different from quinones in Bombax which apparently were incorrectly identified as being the same. A survey of the terpenoid quinones and their heliocide derivates in wild Gossypium species and related genera in the Gossypieae showed considerable diversity which may be used for establishing biochemical and phylogenetic relationships.     

Ultra-low gossypol cottonseed: generational stability of the seed-specific, RNAi-mediated phenotype and resumption of terpenoid profile following seed germination

Cottonseed, containing 22.5% protein, remains an under-utilized and under-valued resource because of the presence of toxic gossypol. RNAi-knockdown of δ-cadinene synthase gene(s) was used to engineer plants that produced ultra-low gossypol cottonseed (ULGCS). In the original study, we observed that RNAi plants, a month or older, maintain normal complement of gossypol and related terpenoids in the roots, foliage, floral organs, and young bolls. However, the terpenoid levels and profile of the RNAi lines during the early stages of germination, under normal conditions and in response to pathogen exposure, had not been examined. Results obtained in this study show that during the early stages of seed germination/seedling growth, in both non-transgenic and RNAi lines, the tissues derived directly from bulk of the seed kernel (cotyledon and hypocotyl) synthesize little, if any new terpenoids. However, the growing root tissue and the emerging true leaves of RNAi seedlings showed normal, wild-type terpenoid levels. Biochemical and molecular analyses showed that pathogen-challenged parts of RNAi seedlings are capable of launching a terpenoid-based defence response. Nine different RNAi lines were monitored for five generations. The results show that, unlike the unstable nature of antisense-mediated low seed-gossypol phenotype, the RNAi-mediated ULGCS trait exhibited multi-generational stability.     

Stereoselective coupling of hemigossypol to form (+)-gossypol in moco cotton is mediated by a dirigent protein

The terpenoid gossypol, a secondary metabolite found in the cotton plant, is synthesized by a free radical dimerization of hemigossypol. Gossypol exists as an atropisomeric mixture because of restricted rotation around the central binaphthyl bond. The dimerization of hemigossypol is regiospecific in cotton. In the case of some moco cotton, the dimerization also exhibits a high level of stereoselectivity. The mechanism that controls this stereoselective dimerization is poorly understood. In this paper, we demonstrate that a dirigent protein controls this stereoselective dimerization process. A partially purified protein preparation from cotton flower petals, which by itself is unable to convert hemigossypol to gossypol, converts hemigossypol with a 30% atropisomeric excess into (+)-gossypol when combined with an exogenous laccase, which by itself produces racemic gossypol.     

Specificity of constitutive and induced resistance: pigment glands influence mites and caterpillars on cotton plants

Cotton plants contain suites of phytochemicals thought to be important in defense against herbivores, some of which are localized in pigment glands which contain gossypol and other terpenoid aldehydes. The simple genetic basis for the expression of these glands has led to the development of near-isogenic glanded and glandless genotypes. Glands may also be phenotypically induced by herbivory. We determined the consequences of constitutive and induced gland expression on two types of herbivores, spider mites (cell content feeders) and noctuid caterpillars (leaf chewers).Induction of glands was strongly dependent on the density of attackers. Spider mite herbivory on cotyledons (1) increased the density (but not total number) of glands on cotyledons linearly, (2) increased the density and total number of glands on the first true leaf linearly, and (3) affected the density and total number of glands on the second true leaf non-linearly, compared to controls. Neither constitutive nor induced expression of glands affected mite population growth. An equal reduction of mite population size on induced glanded and glandless plants (50%) relative to uninduced controls indicated that factors other than glands were associated with induced resistance to mites. Constitutive gland expression had a strong negative impact on caterpillar performance, reducing growth by 45%. Induced resistance to caterpillars was three times stronger in glanded genotypes than in glandless genotypes, indicating that factors associated with induced resistance to caterpillars are strongly associated with glands. Three cotton varieties were highly variable in their constitutive and induced resistance to mites and caterpillars.Thus, defense of cotton plants against herbivores can be roughly categorized as constitutive and inducible factors associated with terpenoid aldehyde containing pigment glands that are effective against caterpillars, and factors not associated with glands that are effective against mites.     

Cadmium-Induced Structure Change of Pigment Glands and the Reduction of the Gossypol Content in Cottonseed Kernels

The risk of cotton production on arable land contaminated with heavy metals has increased in recent years. Cotton shows stronger and more extensive resistance to heavy metals, such as cadmium (Cd) than that of other major crops. Here, a potted plant experiment was performed to study Cd-induced alterations in the cottonseed kernel gossypol content and pigment gland structure at maturity in two transgenic cotton cultivars (ZD-90 and SGK3) and an upland cotton standard genotype (TM-1). The results showed that Cd accumulation in cottonseed kernels increased with increasing Cd levels in the soil. The seed kernel Cd content in plants grown on Cd-treated soils was 10-20 times greater than the amount in the corresponding controls. There was a significant difference in Cd accumulation in cottonseed kernels at the 400 and 600 μM Cd levels. Cd accumulation was higher in SGK3 and ZD-90 than in TM-1. However, the gossypol content in cottonseed kernels was lower in SGK3 and ZD-90 than in TM-1. There was a negative correlation (r = 0.550) between Cd accumulation and the gossypol content in cottonseed kernels. The density of cottonseed kernel pigment glands decreased under Cd stress. This is consistent with the change in gossypol content, which decreased under Cd stress. The damage of the cultivars ZD-90 and SGK3 from Cd poisoning was relatively low under Cd stress, while TM-1 was seriously affected and exhibited Cd sensitivity. Further studies are necessary to understand the cause of the reduced gossypol content in cotton seeds under Cd stress.     

Antisense suppression of a (+)-delta-cadinene synthase gene in cotton prevents the induction of this defense response gene during bacterial blight infection but not its constitutive expression

In cotton (Gossypium hirsutum) the enzyme (+)-delta-cadinene synthase (CDNS) catalyzes the first committed step in the biosynthesis of cadinane-type sesquiterpenes, such as gossypol, that provide constitutive and inducible protection against pests and diseases. A cotton cDNA clone encoding CDNS (cdn1-C4) was isolated from developing embryos and functionally characterized. Southern analysis showed that CDNS genes belong to a large multigene family, of which five genomic clones were studied, including three pseudogenes and one gene that may represent another subfamily of CDNS. CDNS expression was shown to be induced in cotton infected with either the bacterial blight or verticillium wilt pathogens. Constructs for the constitutive or seed-specific antisense suppression of cdn1-C4 were introduced into cotton by Agrobacterium-mediated transformation. Gossypol levels were not reduced in the seeds of transformants with either construct, nor was the induction of CDNS expression affected in stems of the constitutive antisense plants infected with Verticillium dahliae Kleb. However, the induction of CDNS mRNA and protein in response to bacterial blight infection of cotyledons was completely blocked in the constitutive antisense plants. These results suggest that cdn1-C4 may be involved specifically in the bacterial blight response and that the CDNS multigene family comprises a complex set of genes differing in their temporal and spatial regulation and responsible for different branches of the cotton sesquiterpene pathway.     

Chlorophyll reduction in the seed of Brassica napus with a glutamate 1-semialdehyde aminotransferase antisense gene*

Chlorophyll reduction in the seed of Brassica can be achieved by downregulating its synthesis. To reduce chlorophyll synthesis, we have used a cDNA clone of Brassica napus encoding glutamate 1-semialdehyde aminotransferase (GSA-AT) to make an antisense construct for gene manipulation. Antisense glutamate 1-semialdehyde aminotransferase gene (Gsa) expression, directed by a Brassica napin promoter, was targeted specifically to the embryo of the developing seed. Transformants expressing antisense Gsa showed varying degrees of inhibition resulting in a range of chlorophyll reduction in the seeds. Seed growth and development were not affected by reduction of chlorophyll. Seeds from selfed transgenic plants germinated with high efficiency and growth of seedlings was vigorous. Seedlings from T₂ transgenic lines segregated into three distinctive phenotypes: dark green, light green and yellow, indicating the dominant inheritance of Gsa antisense gene. These transgenic lines have provided useful materials for the development of a low chlorophyll seed variety of B. napus.     

HPLC preparation of the chiral forms of 6-methoxy-gossypol and 6,6'-dimethoxy-gossypol

A concentrated mixture of gossypol, 6-methoxy-gossypol, and 6,6'-dimethoxy-gossypol was extracted from the root bark of St. Vincent Sea Island cotton with acetone. This extract was derivatized with R-(-)-2-amino-1-propanol to form diastereomeric gossypol Schiff's bases. Analytical-scale reverse-phase chromatography of these Schiff's bases produced six peaks, indicating separation of the enantiomeric forms of the three gossypol compounds. The elution order of the peaks was found to vary with the polarity of the mobile phase. The chromatography was scaled to a preparative level and was used to isolate each compound. After hydrolysis of the separated Schiff's bases, the original compounds were recovered by precipitation from solutions of diethyl ether, acetic acid, and water. Fifty injections yielded approximately 500 mg of each methoxy-gossypol enantiomer and 300 mg of each dimethoxy-gossypol enantiomer. Each compound was characterized for carbon and hydrogen content, optical rotation, UV-vis light absorption, and melting point. Standard curves were developed and were used to measure the concentration of each gossypol form in the root bark and dehulled seed of St. Vincent Sea Island cotton. In seed tissue, 48% of the gossypol compounds were methylated, and the (-)-optical form was found to be in a slight excess to the (+)-optical form (53-54%) for all three compounds. In root bark, 71% of the gossypol compounds were methylated, and the (+)-optical form was in excess to the (-)-optical form for all three compounds. However, in this tissue the extent of enantiomeric excess decreased with the degree of methylation, with 77% of the gossypol existing in the (+)-optical form and 59% of the 6,6'-dimethoxy-gossypol existing in the (+)-optical form.     

Resistance Mechanisms Against Arthropod Herbivores in Cotton and Their Interactions with Natural Enemies

Cotton plants (genus Gossypium) are grown on more than 30 million hectares worldwide and are a major source of fiber. The plants possess a wide range of direct and indirect resistance mechanisms against herbivorous arthropods. Direct resistance mechanisms include morphological traits such as trichomes and a range of secondary metabolites. The best known insecticidal compounds are the terpenoid gossypol and its precursors and related compounds. Indirect resistance mechanisms include herbivore-induced volatiles and extrafloral nectaries that allow plants to attract and sustain natural enemy populations. We discuss these resistance traits of cotton, their induction by herbivores, and their impact on herbivores and natural enemies. In addition, we discuss the use of genetically engineered cotton plants to control pest Lepidoptera and the influence of environmental factors on the resistance traits.     

RNAi suppression of CYP82D P450 hydroxylase,an enzyme involved in gossypol biosynthesis,enhances resistance to Fusarium wilt in cotton

Cotton plants produce two classes of terpenoid defence compounds against pathogens and other pests. Both classes are derived from a common sesquiterpenoid precursor, δ-cadinen-2-one, which enters either the gossypol pathway or the lacinilene pathway. Blocking the gossypol pathway by RNAi suppression of the early pathway biosynthetic enzyme CYP82D hydroxylase resulted in enhanced resistance to the Fusarium wilt pathogen. Analyses of root terpenoids revealed no overall increases in the products of the gossypol pathway in the roots infected by the wilt pathogen. However, the lacinilene pathway was elicited by the pathogen and the lacinilene levels were 19-fold higher in the RNAi plants than in wild-type plants. In the pathogen inoculated RNAi 73R plants, the concentrations of DHC and HMC were 231 μg and 886 μg/g dry roots, respectively, which may have contributed to the inhibition of fungal invasion. In comparison, the concentrations of DHC and HMC in the pathogen inoculated control wild-type 73W plants were only 0.7 μg and 58 μg/g dry roots, respectively. Fungitoxicity testing showed that DHC at 100 μg/ml inhibited growth of the Fusarium wilt pathogen by >93%. Treatment with the phytohormone jasmonic acid failed to elicit production of lacinilene pathway terpenoids in roots of either RNAi plants or their wild-type sibling lines, but increased production of gossypol pathway terpenoids with concentrations in RNAi plants 80%–97% less than those in wild-type plants. This indicates that induction of the lacinilene pathway is not directly mediated by jasmonic acid signalling and requires other signalling to activate the pathway. These results illustrate possible mechanisms of wilt disease resistance in cotton and provide a new approach to increase host resistance by manipulating these two major cotton chemical defence pathways.     

Phenotypic changes in transgenic tobacco plants with an antisense form of the hmg1 gene

Tobacco plants were genetically transformed with the Arabidopsis thaliana heterologous hmg1 gene encoding 3-hydroxy-3-methylglutaryl-CoA reductase, a key enzyme involved in the metabolism of terpenoid compounds. The hmg1 gene was inserted under the control of the 35S RNA double promoter from the cauliflower mosaic virus (CaMV 35S) both in direct and reverse orientation relative to the promoter. DNA analysis by polymerase chain reaction (PCR) and Southern blotting confirmed the transgenic nature of the tobacco plants obtained. DNA-RNA hybridization revealed expression of the hmg1 gene in these tobacco plants. The plants transformed with the antisense copy of the hmg1 gene differed from the control plants in delayed development and in flower color and shape.     

棉酚对棉铃虫生长及其寄生物齿唇姬蜂发育的影响(英文)

以中国北方棉区的主要害虫棉铃虫Helicoverpaarmigera（Hbner）及其内寄生蜂棉铃虫齿唇姬蜂Campoletischlorideae（Uchida）为试虫,研究了棉花重要抗虫次生性物质棉酚对棉铃虫生长和齿唇姬蜂发育的影响。0．1％的棉酚对棉铃虫幼虫有生长刺激作用,0．5％的棉酚则对棉铃虫幼虫生长有抑制作用。齿唇姬蜂成虫在寄生时对寄主大小有较严格的选择性,92％的被寄生幼虫体重小于18mg。0．1％的棉酚使寄主适合寄生期缩短10．75％;0．5％棉酚使寄主适合寄生期延长28．15％。棉酚对齿唇姬蜂发育有负效应。0．1％棉酚对寄主的生长刺激作用,不能使蜂成虫体重显著增加,但可显著延长蜂卵和幼虫期,缩短蛹期;高浓度的生长抑制作用,导致蜂成虫体重显著减轻,蛹期缩短,蜂卵和幼虫期亦显著延长。据此,对棉花抗虫性与生物防治在害虫综合防治实践中应用的协调性进行了讨论。     

通过共转化和花药培养快速获得直链淀粉含量降低且无抗性标记的转基因水稻

用根癌农杆菌共转化的方法将p13W8质粒(含反义蜡质基因)和pCAMBIA1300质粒(含潮霉素抗性基因)导入水稻.经PCR检测,发现在29个T1群体中发生抗潮霉素抗性基因和反义蜡质基因的分离;从1 264个T1单株中筛选到183个只带反义蜡质基因片段的转基因植株.选择了4个直链淀粉含量降低的T1单株进行花药培养,获得正常结实的花培苗34株;经PCR检测,有23株为只含反义蜡质基因而无潮霉素抗性基因的植株.从转化到获得直链淀粉含量降低、遗传稳定的转基因植株仅用了一年半时间.     

Gossypol mediated DNA degradation

Gossypol, a polyphenolic compound isolated from cotton plant was found to degrade pBR322 DNA in vitro in a reaction which required the presence of a metal ion, a reducing agent (2-mercaptoethanol) and oxygen as revealed after agarose gel electrophoresis. Fe3+ and Co2+ showed maximum degradation whereas addition of Ca2+ and Mg2+ prevented the gossypol mediated DNA damage. Gossypol caused degradation of rat liver DNA incubated in vitro even in the absence of added metal ions and 2-mercaptoethanol. Incubation of intact rat liver nuclei with gossypol revealed DNA degradation and nuclei isolated from rats treated with gossypol in vivo showed higher susceptibility to DNA fragmentation when incubated with gossypol in vitro than control nuclei. EcoR1 and AIuI digestion of DNA isolated from gossypol treated rats gave clear cut evidence for DNA degradation. These observations indicate that gossypol is genotoxic and considerable care has to be exercised in its use.     

Host plant effects on activity of the mitosporic fungi Beauveria bassiana and Paecilomyces fumosoroseus against two populations of Bemisia whiteflies (Homoptera: Aleyrodidae)

Laboratory bioassays were conducted to determine the effect of host plant on mycosis in two geographically distinct populations of early 2nd-instar nymphs of Bemisia argentifolii Bellows & Perring from the entomopathogenic fungi Beauveria bassiana (Balsamo) Vuillemin and Paecilomyces fumosoroseus (Wize) Brown & Smith. Mycosis in B. argentifolii nymphs varied according to the host plant on which the nymphs were reared but not according to the population. Both populations of whiteflies reared on cotton were consistently significantly less susceptible to infection by either fungus than when reared on melon. We hypothesized that the cotton plant produced a fungal inhibitor that may confer protection on whiteflies feeding (and possibly sequestering) upon it. Germination of conidia of both fungi was strongly inhibited (below 12% germination) on the cuticle of nymphs reared on cotton but was over 95% on the cuticle of nymphs reared on melon. We further hypothesized that the terpenoid gossypol, produced by many cultivars of cotton, might have been involved in antibiosis. Gossypol mixed with Noble agar at five concentrations was tested for its effects on germination of conidia of both fungi. P. fumosoroseus was highly tolerant of gossypol, even at the relatively high concentration of 1000 ppm, while B. bassiana tolerated gossypol at concentrations up to 500 ppm and strong inhibition only occurred in presence of gossypol at 1000 ppm. Our in vivo findings on cotton and on the insect's cuticle pointed at a potential host plant-mediated antibiosis. The in vitro tolerance of P. fumosoroseus and partial tolerance of B. bassiana to gossypol disagreed with our in vivo data. Gossypol concentrations higher than 1000 ppm might have increased the sensitivity of the fungi in our in vitro tests. Sequestered gossypol (and/or other cotton plant allelochemicals) by B. argentifolii nymphs would explain, at least partially, the insect's defense against the pathogens.This revised version was published online in October 2005 with corrections to the Cover Date.     

The effect of gossypol on the frequency of DNA-strand breaks in human leukocytes in vitro

Gossypol, a human antifertility agent isolated from the cotton plant, was found to induce a dose-dependent increase in the frequency of DNA-strand breaks in human leukocytes exposed to 2-40 micrograms/ml of the drug for 1 h in serum-free medium in vitro. DNA-strand breaks were studied by alkaline elution or alkaline unwinding of DNA followed by hydroxylapatite-chromatography. No decrease of gossypol-induced DNA-strand breaks was observed after post-treatment incubation times up to 24 h, whereas X-ray-induced DNA breaks disappeared within 2 h under the same incubation conditions. Cells exposed to gossypol in the presence of 10% fetal calf serum showed no or little increase of DNA breaks, suggesting that serum proteins inhibit the DNA-damaging activity of the drug. Both optical isomers of gossypol induced DNA-strand breaks. However, the effect of (-)-gossypol was only about half of that of (+)-gossypol and the racemic form. The induction and persistence of DNA-strand breaks by gossypol, as well as the reduction of this effect in the presence of serum should be considered in the evaluation of the potential in vivo genotoxicity of the drug.     

Potential detoxification of gossypol by UDP-glycosyltransferases in the two Heliothine moth species Helicoverpa armigera and Heliothis virescens

The cotton bollworm Helicoverpa armigera and the tobacco budworm Heliothis virescens are closely related generalist insect herbivores and serious pest species on a number of economically important crop plants including cotton. Even though cotton is well defended by its major defensive compound gossypol, a toxic sesquiterpene dimer, larvae of both species are capable of developing on cotton plants. In spite of severe damage larvae cause on cotton plants, little is known about gossypol detoxification mechanisms in cotton-feeding insects. Here, we detected three monoglycosylated and up to five diglycosylated gossypol isomers in the feces of H. armigera and H. virescens larvae fed on gossypol-supplemented diet. Candidate UDP-glycosyltransferase (UGT) genes of H. armigera were selected by microarray studies and in silico analyses and were functionally expressed in insect cells. In enzymatic assays, we show that UGT41B3 and UGT40D1 are capable of glycosylating gossypol mainly to the diglycosylated gossypol isomer 5 that is characteristic for H. armigera and is absent in H. virescens feces. In conclusion, our results demonstrate that gossypol is partially metabolized by UGTs via glycosylation, which might be a crucial step in gossypol detoxification in generalist herbivores utilizing cotton as host plant.