The Promoter of the Gene for Plastidic Glutamine Synthetase (GS2) fromRice Is Developmentally Regulated and Exhibits Substrate-Induced Expression in Transgenic Tobacco Plants

A 1.3-kb fragment from the 5'-flanking region of the RGS-38gene, which encodes the plastidic glutamine synthetase in Oryzasativa L., was fused to a ß-glucuronidase (GUS) reportergene and introduced into Nicotiana tabacum by Agrobacterium-mediatedtransformation. The promoter directed GUS expression, both inleaves and in roots, and the expression of GUS was regulatedby light. The GUS activity was high in the mature leaves ofthe transgenic tobacco plants, in marked contrast to the activityof the GS1 promoter. The GS2 promoter also responded to externallyapplied ammonia, as is the case for the GS1 promoter. Theseresults suggest that the cis-acting regulatory elements thatcontrol the response to ammonia, a substrate for glutamine synthetase,are located within a 1.3-kb region of the promoter. (Received October 1, 1991; Accepted January 20, 1992)     

Evidence for sugar signalling in the regulation of asparagine synthetase gene expressed in Phaseolus vulgaris roots and nodules

A cDNA clone, designated as PvNAS2, encoding asparagine amidotransferase(asparagine synthetase) was isolated from nodule tissue of commonbean (Phaseolus vulgaris cv. Negro Jamapa). Southern blot analysisindicated that asparagine synthetase in bean is encoded by asmall gene family. Northern analysis of RNAs from various plantorgans demonstrated that PvNAS2 is highly expressed in roots,followed by nodules in which it is mainly induced during theearly days of nitrogen fixation. Investigations with the PvNAS2promoter gusA fusion revealed that the expression of PvNAS2in roots is confined to vascular bundles and meristematic tissues,while in root nodules its expression is solely localized tovascular traces and outer cortical cells encompassing the centralnitrogen-fixing zone, but never detected in either infectedor non-infected cells located in the central region of the nodule.PvNAS2 is down-regulated when carbon availability is reducedin nodules, and the addition of sugars to the plants, mainlyglucose, boosted its induction, leading to the increased asparagineproduction. In contrast to PvNAS2 expression and the concomitantasparagine synthesis, glucose supplement resulted in the reductionof ureide content in nodules. Studies with glucose analoguesas well as hexokinase inhibitors suggested a role for hexokinasein the sugar-sensing mechanism that regulates PvNAS2 expressionin roots. In light of the above results, it is proposed that,in bean, low carbon availability in nodules prompts the down-regulationof the asparagine synthetase enzyme and concomitantly asparagineproduction. Thereby a favourable environment is created forthe efficient transfer of the amido group of glutamine for thesynthesis of purines, and then ureide generation. Key words: Asparagine and ureide synthesis, asparagine synthetase, nodules, Phaseolus vulgaris, sugar signalling     

Glutamine Synthetase Isoenzymes of Striga hermonthica and other Angiosperm Root Parasites

The occurrence of multiple forms of glutamine synthetase inStriga hermonthica and other angiosperm root parasites was investigated.The facultative chlorophyllous parasite Melampyrum arvense exhibitedtwo isoenzymes in leaf tissue, the cytosolic component (GS₁)comprised less than 30% of total glutamine synthetase. In contrastGS₁ was the major component (<70%) in photosynthetic tissueof Striga hermonthica and S. gesnerioides. Only a single isoenzyme(GS₁) was detectable in the achlorophyllous root parasites Orobancheand Lathraea and in non-photosynthetic tissue of S. gesnerioides.The kinetic and physical properties of GS₁ and GS₂ of theseangiosperm parasites were similar to those of the isoenzymesin other non-parasitic angiosperms. Key words: Glutamine synthetase, Angiosperms, Root parasites     

Cloning and Sequencing of a 23-kb Region of the Bacillus subtilis Genome between the iol and hut Operons

Within the framework of an international project for the sequencingof the entire Bacillus subtilis genome, a 23-kb chromosomalsegment, which covers the region between the iol and hut operons,has been cloned and sequenced, creating a 99-kb contig fromthe gnt operon to the wapA locus. This region (23351 bp) contains25 complete open reading frames (ORFs; genes) including deoR,dra, nupC and pdp and two partial ones. The region (5140 bp)containing these four genes, being also sequenced by H. H. Saxildet al., was sequenced by subjecting a long polymerase chainreaction product to random sequencing using phage M13mp19. However,we could detect no conflict, between two independently determinedsequences, which could be attributed to our sequencing method.A homology search for the 24 newly identified gene productsrevealed significant homology to known proteins in 14 of them.It was notable that three proteins, encoded by the successivegenes (yxeMNO), exhibited meaningful homology to the E. coliGlnHPQ products constituting a periplasmic ATP-dependent transportsystem for glutamine.     

Effect of Ammonia on Dark CO2 Fixation by Anabaena Cells Treated with Methionine Sulfoximine

Dark CO₂ fixation by Anabaena cylindrica was stimulated aboutthree-fold by the addition of NH₄Cl to the cells. The ¹⁴CO₂incorporation experiments showed that ¹⁴C is most rapidly incorporatedinto aspartate and then glutamine by adding NH4CI. Glutamineaccumulated predominantly after the addition of NH₄Cl showingthat NH₄ is incorporated into glutamine by glutamine synthetase.The stimulating effect of NH4Cl on CO₂ fixation and amino acidsynthesis was suppressed by methionine sulfoximine, an inhibitorof glutamine synthetase. It was suggested that dark CO₂ fixationwas stimulated by the action of glutamine synthesis which isenhanced by ammonia. (Received February 10, 1981; Accepted April 2, 1981)     

Two glutamine synthetase genes from Phaseolus vulgaris L. display contrasting developmental and spatial patterns of expression in transgenic Lotus corniculatus plants.

The gln-gamma gene, which specifies the gamma subunit of glutamine synthetase in Phaseolus vulgaris L., has been isolated and the regulatory properties of its promoter region analyzed in transgenic Lotus corniculatus plants. A 2-kilobase fragment from the 5'-flanking region of gln-gamma conferred a strongly nodule-enhanced pattern of expression on the beta-glucuronidase reporter gene. Parallel studies on the promoter of another glutamine synthetase gene (gln-beta) showed that a 1.7-kilobase fragment directed 20-fold to 140-fold higher levels of beta-glucuronidase expression in roots than in shoots. Histochemical localization of beta-glucuronidase activity in nodules of the transgenic plants indicated that the chimeric gln-gamma gene was expressed specifically in the rhizobially infected cells; expression of the gln-beta construct was detected in both cortical and infected regions of young nodules, and became restricted to the vascular tissue as the nodule matured. We conclude that gln-beta and gln-gamma genes are differentially expressed both temporally and spatially in plant development and that the cis-acting regulatory elements responsible for conferring these contrasting expression patterns are located within a 2-kilobase region upstream of their coding sequences.     

Assimilation of Nitrogen in Mutants Lacking Enzymes of the Glutamate Synthase Cycle

¹⁵N labelling was used to investigate the pathway of nitrogenassimilation in photorespiratory mutants of barley (Hordeumvulgare cv. Maris Mink), in which the leaves have low levelsof glutamine synthetase (GS) or glutamate synthase, key enzymesof ammonia assimilation. These plants grew normally when maintainedin high CO₂, but the deletions were lethal when photorespirationwas initiated by transfer to air. Enzyme levels in roots weremuch less affected, compared to leaves, and assimilation oflabelled nitrate into amino acids of the root showed very littledifference between wild type and mutants. Organic nitrogen wasexported from roots in the xylem sap mainly as glutamine, levelsof which were somewhat reduced in the GS-deficient mutant andenhanced in the glutamate synthase deficient mutant. In theleaf, the major effect was seen in the glutamatesynthase mutant,which had an extremely limited capacity to utilize the importedglutamine and amino acid synthesis was greatlyrestricted. Thiswas confirmed by the supply of [¹⁵N]-glutamine directly to leaves.Leaves of the GS-deficient mutant assimilatedammonia at about75% the rate found for the wild type, and this was almost completelyeliminated by addition of the inhibitormethionine sulphoximine.Root enzymes, together with residual levels of the deleted enzymesin the leaves, have sufficient capacityfor ammonia assimilation,through the glutamate synthase cycle, to provide adequate inputof nitrogen for normal growth of themutants, if photorespiratoryammonia production is suppressed. Key words: Hordeum vulgare, ¹⁵N, glutamine synthetase, glutamate synthase, ammonia assimilation     

Tissue-Specific Distribution of Glutamine Synthetase in Potato Tubers

Cytosolic isoforms of the enzyme glutamine synthetase (GS) locatedin the phloem have been implicated in the mobilization of nitrogenfor intracellular transport in higher plants. The potato tuberrepresents an important reservoir of nitrogen and an approachwas made to the characterization of GS in this organ, particularlyat the stages of sprouting and of new tuber formation. By immunoblottingafter SDS-PAGE, and by immunological tissue printing, it waspossible to conclude that a cytosolic GS is present in tubersand sprouts, and that it is mainly expressed in the internalphloem, in a very precise tissue-specific pattern of distribution.These data provide additional clues to the interpretation ofthe functional role of GS in the mobilization of nitrogen andits utilization in growing parts of the plant. The importanceof morphological data and localization studies in complementingmolecular and biochemical work is emphasized. The proposed functionalimportance of the internal phloem inSolanum tuberosum organsis also reinforced. Solanum tuberosum L. cv. Desirée; potato; tubers; plant glutamine synthetase; tissue-specific distribution; phloem; nitrogen mobilization; in situlocalization; tissue printing     

Ammonia emission from young barley plants: influence of N source, light/dark cycles and inhibition of glutamine synthetase

Barley (Hordeum vulgare L. cv. Golf) plants were grown at twodifferent relative addition rates; 0.1 and 0.2 d^–1 ofnitrate. Three to five days before measurements started theplants were transferred to a nutrient solution with 2 mM nitrateor ammonium. The ammonium-grown plants showed increased ammoniumlevels in both shoots and roots and also increased ammoniumconcentrations in xylem sap. Ammonia emission measured in cuvettes connected to an automaticNH₃ monitor was close to zero for nitrate-grown plants but increasedto 0.59 and 0.88 nmol NH₃ m^–2 S^–1 for plants transferredto ammonium after growing at RA=0.2 and 0.1 d^–1, respectively.In darkness, NH₃ emission decreased together with photosynthesisand transpiration, but increased rapidly when the light wasturned on again. Addition of 0.5 mM methionine sulphoximine (MSO) to the plantscaused an almost complete inhibition of both root and shootglutamine synthetase (GS) activity after 24 h. Ammonia emissionincreased dramatically and photosynthesis and transpirationdecreased in both nitrate- and ammonium-grown plants as a resultof the GS inhibition. At the same time plant tissue and xylemsap ammonium concentrations increased, indicating the importanceof GS in controlling plant ammonium levels and thereby NH₃ emissionfrom the leaves. Key words: Hordeum vulgare, ammonia emission, ammonium, glutamine synthetase, nitrogen nutrition, photosynthesis, transpiration     

Glutamine Synthetase Activity and Foliar Nitrogen Volatilization in Response to Temperature and Inhibitor Chemicals

In soyabeans (Glycine max (L.) Merr.), glutamine synthetase(GS) activity was greater at 28 °C than at 35 °C. Thereverse was true for foliar-N loss. In field-grown plants at29 °C, the GS activity was higher and foliar-N loss waslower in soyabeans than in Amaranthus palmeri (S.) Wats. Methioninesulphoximine, a GS inhibitor, and 6-diazo-5-oxo-L-norleucine,a glutamate synthase inhibitor, significantly increased foliar-Nloss from soyabeans. The data suggest that conditions conduciveto decreased GS or glutamate synthase activity may result inincreased foliar-N loss. Palmer amaranth, Amaranthus palmeri, soyabean, Glycine max, methionine sulphoximine, 6-diazo-5-oxo-L-norleucine     

The Effects of Compatible Solutes on the Heat Stability of Glutamine Synthetase from Chickpeas Grown under Different Nitrogen and Temperature Regimes

The activity of glutamine synthetase (GS) extracted from chickpeasgrown under different nitrogen and temperature regimes was examined.Cytosolic GS (GS₁) was much less temperature sensitive thanchloroplastic GS (GS₂). There was no change in the ratio ofthe two isoforms from plants with different growth temperatures.Specific activity of GS appeared to be independent of growthtemperature and was little affected by nitrogen supply. In vitro studies were performed on the heat stability of GS₂in the presence of glycine betaine, proline, and myoinositol.The latter was most effective in preventing loss of enzyme activityat high temperatures. Glycine betaine was also effective asa heat protectant but enzyme activity in the presence of prolinewas lower than the control at temperatures above 30 ?C. Theimportance of myo-inositol protection of metabolism is discussedin relation to the accumulation in chickpeas of another cyclitol,pinitol. Key words: Chickpeas, high temperature stress, glutamine synthetase     

The Maize Glutamine Synthetase GS1- Gene is Preferentially Expressed in Kernel Pedicels and is Developmentally-Regulated

The pedicel region of Zea mays kernels contains a unique formof maize glutamine synthetase (GS), GS_pl. RNA blot analysisusing GS gene-specific probes revealed that the expression ofthe GS.₂ gene was specific to the pedicel and that it increasedin the kernels during development. This pattern of the maizeGS.₂ gene expression is consistent with the tissue specificityof the GS_pl protein and suggests that it encodes the GS_pl isoformof maize GS. (Received September 16, 1997; Accepted January 19, 1998)     

Cloning and Sequencing of a 36-kb Region of the Bacillus subtilis Genome between the gnt and iol Operons

Within the framework of an international project for the sequencingof the entire Bacillus subtilis genome, a 36-kb chromosome segment,which covers the region between the gnt and iol operons, hasbeen cloned and sequenced. This region (36447 bp) contains 33complete open reading frames (ORFs; genes) including the fourgnt genes and one partial gene. A homology search for the productsof the 33 complete ORFs revealed significant homology to knownproteins in 16 of them such as tetracycline resistance protein(Clostridium perfringens), asparagine synthetase (Arabidopsisthaliana), aldehyde dehydrogenase (Pseudomonas oleovorans),2,5-dichloro-2,5-cyclohexadiene-1,4-diol dehydrogenase (P. paucimobilis),heat shock protein HtpG (Escherichia coli), galactose-protonsymporter (E. coli), auxin-induced protein (common tobacco),glucitol operon repressor (E. coli) and methylmalonate-semialdehydedehydrogenase (P. aeruginosa). Unlike the regions we sequencedso far, this region contained two short sequence multiplications:one was a tandem sequence duplication (409 and 410 bp), andthe other a triplication consisting of two highly conserved118-bp tandem sequences preceded by a less conserved similarsequence (129 bp). The reasons for the presence of these sequencemultiplications in the gnt to iol region were deduced.     

Use of the rice sucrose synthase-1 promoter to direct phloem-specific expression of {beta}-glucuronidase and snowdrop lectin genes in transgenic tobacco plants

The promoter region from the rice sucrose synthase-1 gene (RSs1)was fused with coding sequences for ß-glucuronidase(GUS) and snowdrop (Galanthus nivalis) lectin (GNA). Tobaccoplants were transformed with these chimaenc genes in order todetermine the expression pattern directed by the RSs1 promoter.Histochemical and immunochemical assays demonstrated that theexpression of both GUS and GNA was restricted to phloem tissue,and was not observed in any other tissues. This phloem-specificexpression pattern was consistent in stem, leaf and root, andin different transgenic plants. Chimaeric genes of RSs 1-GUSand RSs1 GNA were stably inherited in T1 plants. In addition,GNA was detected by immunological assay in the honeydew producedby peach potato aphids (Myzus persicae) feeding on RSs1-GNAtransgenic tobacco plants. This provided direct evidence thatGNA was not only expressed in the phloem tissue, but was alsopresent in the phloem sap of transgenic tobacco plants. TheRSs1 promoter can thus be used to direct expression of an insecticidalprotein, such as GNA, in transgenic plants to control phloemsap-feeding insect pests. Key words: Rice sucrose synthase-1 promoter, phloemspecific, transgenic plants, ß-glucuronidase, Galanthus nivalis agglutinin, gene expression     

Growth and nitrogen assimilation in nodules in response to nitrate levels in Vicia faba under salt stress

This study analyses the effects of salt on the effective symbiosisof faba bean (Vicia faba L. var. minor cv. Alborea) and salt-tolerantRhizobium leguminosarum biovar. viciae strain GRA19 grown withtwo KNO₃ levels (2 and 8 mM). The addition of 8 mM KNO₃ to thegrowth medium increases plant tolerance to salinity even witha concentration of 100 mM NaCl. This KNO₃ level in control plantsreduced the N₂ fixation. For 2 and 8 mM KNO₃ the plants treatedwith NaCl reduced N₂ fixation to identical values. The activityof the enzymes mediating ammonium assimilation in nodules (GS,NADH-GOGAT and NADH-GDH) was decreased by high KNO₃ levels.The results show that NADH-GOGAT activity was more markedlyinhibited than was GS activity by salinity, therefore NADH-GOGATlimits the ammonium assimilation by nodules in V. faba undersalt stress. The total proline content in the nodule was notrelated to salt tolerance and thus does not serve as a salttoleranceindex for V. faba. Key words: Glutamate synthase, glutamine synthetase, N₂ fixation, nitrate, salinity     

Oats Tolerant of Pseudomonas syringae pv. tabaci Contain Tabtoxinine-beta-Lactam-Insensitive Leaf Glutamine Synthetases

Pseudomonas syringae pv. tabaci, a commonly recognized leaf pathogen of tobacco, can infest the rhizosphere of many plants, including oats. Normal oat plants do not survive this infestation as a consequence of the complete and irreversible inactivation of all of their glutamine synthetases by tabtoxinine-β-lactam (TβL), a toxin released by pv. tabaci. We have identified a population of oat (Avena sativa L. var Lodi) plants that are tolerant of pv. tabaci. The tolerant plants had no detectable TβL-detoxification mechanisms. Pathogen growth on these plant roots was not inhibited. These plants contain leaf glutamine synthetases (GS₁ and GS₂) that were less sensitive to inactivation by TβL in vitro; these GSs have normal K_m values for glutamate and ATP when compared with those of GS in control plants. Root glutamine synthetase of the tolerant plants was inactivated in vivo during infestation by the pathogen or by TβL in vitro. When growing without pv. tabaci, the tolerant plants contained normal levels of glutamine synthetase in their roots and leaves and normal levels of protein, ammonia, glutamate, and glutamine in their leaves. However, when the tolerant plants' rhizosphere was infested with pv. tabaci, the plant leaves contained elevated levels of glutamine synthetase activity, protein, ammonia, glutamate, and glutamine. No changes in glutamate dehydrogenase activity were detected in leaves and roots of pathogen-infested tolerant plants.     

Nodulin gene expression in effective root nodules of white sweetclover (Melilotus alba Desr.) and in ineffective nodules elicited by mutant strains of Rhizobium meliloti

Fifteen nodulins and several nodule-stimulated gene productswere expressed in effective, nitrogen-fixing root nodules ofwhite sweetclover (Melilotus alba Desr. cv. U389), as determinedby two-dimensional gel electrophoresis of in vitro translationproducts. The number and gel position of eight leghaemoglobin(Lb) products, as well as a product tentatively identified asnodule-stimulated glutamine synthetase (GS), was similar toprevious reports of alfalfa (Medicago sativa L. cv. Iroquois)nodulins. Three mutants of Rhizobium meliloti, including anexoH mutant, a lipopolysaccharide mutant, and a nifH mutant,elicited ineffective sweetclover nodules blocked at empty (bacteria-free),partially infected, or fully infected stages of nodule development,respectively. In these ineffective nodules, the nodulin Nma30and nodule-stimulated NSTma42 were expressed early in development,while a group of four nodulins and two nodule-stimulated productswere intermediate in order of expression. Lb, GS and the latenodulin Nmal2a were expressed later, following infection. TheexoH mutant, Rm7154, appeared to be a leaky mutant, as a smallpercentage of the plants developed nitrogen-fixing nodules about4 weeks after inoculation. The sequential expression of a largenumber of nodulins and nodule-stimulated products, as well asthe availability of sweetclover nodulation mutants indicatesthat sweetclover is a useful diploid system for analysis ofhost genes essential to the Rhizobium/legume symbiosis. Key words: Nitrogen fixation, nodulation mutants, nodulins     

Glutamine synthesis in germinating seeds of Cucurbita moschata

During germination, an increase in glutamine and glutamine synthetase[L-glutamate: ammonia ligase (ADP), EC 6.3.1.2 [EC] ] occurred inthe cotyledons reaching a maximum at 4 to 6 days. The enzymehad a Km of 4.5 nun for L-glutamate, and 0.67 mu for hydroxylamine.Hydroxylamine exhibited substrate inhibition kinetics. The enzymewas inhibited by calcium ion, fluoride ion and p-hydroxymercuribenzoatebut not by EDTA, sodium ion or chloride ion. The sulf hydrylinhibition was reversed by dithiothreitol. In vivo synthesisof glutamine-¹⁴C from glutamate-¹⁴C was found to parallel theincrease in glutamine content and the in vitro glutamine synthetaseactivity during germination. ¹ Present address: Department of Biology, Mercyhurst College,Erie, Pennsylvania 16501, U.S.A. (Received June 12, 1971; )     

Nucleotide Sequence of a 28-kb Mouse Genomic Region Comprising the Imprinted Igf2 Gene

The mouse insulin-like growth factor II gene (Igf2) is physicallylinked to the insulin II gene (Ins2) and both are subject totissue-specific genomic imprinting. The paternal-specific expressionof Igf2 has been associated with hypermethylation of some CpGsites in the 5' flanking region and in the body of the gene.As a first step in analyzing the structural features of thisimprinted locus, we here report the complete nucleotide sequenceof Igf2, including all introns and the intergenic region adjacentto Ins2. This 28-kb segment of mouse chromosome 7 exhibits 80%overall identity with the corresponding rat sequence and hasa high GC content of 52%. In addition to the known CpG islandwithin the second Igf2 promoter, another island was identifiedapproximately 2 kb 5' to the first exon. Other features of thislocus include a 35-fold tandem repeat of an 11-bp sequence thatoverlaps Igf2 pseudo-exon 2, and a B2 repeat element in theintergenic region between Ins2 and Igf2. The GC-richness andthe presence of CpG islands associated with tandem repeats arecommon features of imprinted genes and thus may play a rolein the imprinting mechanism.