Inhibitors and the Dependence of Kinetin-induced Expansion on RNA Synthesis in Fenugreek Cotyledons: ETHIONINE AS AN INHIBITOR

The effect of a range of inhibitors on kinetin-induced increasein fresh weight (expansion) and in RNA content of isolated cotyledonsof fenugreek (Trigonella foenum-graecum L.) has been measuredover incubation periods of up to 48 h in darkness. Some compounds inhibited both expansion and net RNA increase:2, 4-dinitrophenol, cycloheximide, L-azetidine-2-carboxylicacid, 6-methylpurine, thiouracil, and actinomycin D. Other compoundsinhibited net RNA increase but not expansion: 5-fluorouracil,2, 6-diamino-purine, 5-azacytidine, and L-ethionine. Ethionine stimulated the induction of nitrate reductase. Effectsby ethionine on RNA content were reversed by methionine, butnot by adenosine. Inhibitory interactions between ethionineand guanosine, hypoxanthine and especially some 6-substitutedadenines were observed. Ethionine, apart from inhibiting uptakeof labelled uridine, also inhibited its incorporation into rRNAbut not that into tRNA. Results confirm that kinetin-induced expansion in cotyledonsis dependent on mRNA synthesis and suggest that the inhibitoryeffect of ethionine on kinetin-induced RNA increase is not dueto ATP trapping or inhibition of protein synthesis or reducedmethylation of tRNA, but to interference with the metabolismof rRNA.     

Effect of 5-fluorouracil and cycloheximide on the early development of Phycomyces blakesleeanus spores and the activity of N-acetylglucosamine synthesizing enzymes

The development of germinating Phycomyces spores was not inhibited by 5-fluorouracil (1 mM) until the emergence of the germination tube. Fluorouracil was incorporated into RNA as efficiently as uracil; it did not inhibit the synthesis of proteins and the increase in respiratory activity during early develpment. Cycloheximide inhibited development as well as the increase in respiration and protein synthesis. This suggested that protein synthesis or some other cycloheximide dependent process, but no mRNA synthesis, was needed for the first developmental stages. The activity of two enzymes involved in the synthesis of N-acetylglucosamine increased markedly during germination. This increase was inhibited by both 5-fluorouracil and cycloheximide; this suggested that those enzymes were synthesized on mRNA formed during germination.     

Effects of enzymatically digested microsome fractions on red-light-enhanced pelletability of pea phytochrome in vitro in the presence of calcium ion

The 130,000 ?g supernatant of Sephadex G-50 filtrate and a 78,000?g microsomal fraction were prepared separately from homogenatesof etiolated pea (Pisum sativum L. cv. Alaska) shoots. The pelletabilityof phytochrome increased ca. 10-fold by exposure of the filtrateto red light and mixing the filtrate with the microsomal fractionin the dark at ca. 0?C. The increase of pelletable phytochromewas inhibited by 84% when the microsomal fraction digested withtrypsin was used. Phospholipase C (Clostridium welchii) digestionof the microsome inhibited no more than 13% of the pelletability.Although phospholipase A₂ (Crotalus terrificus terrificus) digestioninhibited 43% of the pelletability, addition of defatted albuminduring the enzymatic digestion completely restored the levelof the pelletability. The decrease of RNA content of the microsomalfractions by ribonuclease A digestion did not result in a proportionalinhibition of the pelletability. These results indicate thatproteinaceous component in the microsomal fraction is essentialfor phytochrome pelletability in vitro, that RNA and polar headsof phospholipids are unlikely to be the partner for the binding,and that products of phospholipase A₂ digestion inhibit thepelletability partially. (Received September 12, 1979; )     

Stereological Analysis of Floral Development and Quantitative Histochemistry of Nucleic Acids in Fertile and Base-sterile Varieties of Wheat

The speltoid series of mutations provides a genetic tool forinvestigating the control of flower development. In fertileGabo wheat and in St₂ and St₃ basal sterile speltoids, the changesin RNA staining patterns have been followed histochemicallyas a marker of cellular activity. Sterile floret sites are characterizedby a reduced RNA content. Use of dual-wavelength microspectrophotometryhas provided evidence that RNA content is similar in lemma primordiasubtending presumptive fertile and sterile primordia, but isstrikingly different in the floral meristems in the two types.The total nucleic acid content of the floral primordia has beenrelated to the number of epidermal cells in the subtending lemmaprimordium as a marker of development, using a linear modelanalysis of covariance. There is a linear increase in nucleicacid content during fertile floret development, but no significantincrease in RNA content in sterile St₃ primordia. The rate constantis only 1/10th to 1/20th of that of Gabo. A stereological analysisshows that cell number in the floral meristems of Gabo increasesexponentially during development. In contrast, in St₃, whilethere is a significant increase in cell number, it is at a drasticallyreduced rate. The intercept values are close to zero, indicatingthat only one or two cells initiate floral meristem development.The fertility-controlling alleles exert their effect prior tothe appearance of a visible floral primordium, and probablyafter initiation of the lemma. Triticum aestivum, wheat, floral development, histochemistry, nucleic acids, speltoids     

Influence of IBA and Cordycepin on Rooting and RNA Synthesis in Stem Cuttings of Phaseolus aureus Roxb

Adventitious roots are initiated on stem cuttings of Phaseolusaureus Roxb. by treatment with IBA for 24 h, although subsequenttransfer to boric acid is essential for their development. Cordycepinenhances auxin-induced rooting when supplied for 4 h withinthe first twenty hours of IBA treatment, but not thereafter.Cordycepin alone does not enhance rooting. IBA treatment ofcuttings for 12 h results in a marked inhibition of RNA synthesis,including poly(A)-rich RNA, in the hypocotyl. After 24 h treatmentRNA synthesis is seen to increase, with a more marked recoveryin the synthesis of poly(A)+RNA relative to other RNAs. Subsequenttransfer to boric acid maintains this recovery. Cordycepin doesnot inhibit RNA synthesis below the level induced by IBA althoughon subsequent transfer to boric acid is seen to enhance synthesisand turnover of both polyadenylated and non-polyadenylated RNA. (Received August 28, 1982; Accepted November 25, 1982)     

Effects of Benzyladenine on Chlorophyll, DNA, RNA and Protein Content of Attached Young Bean (Phaseolus vulgaris L.) Leaves

N⁶-Benzyladenine (BA) was applied to intact bean (Phaseolusvulgaris L.) primary leaves at 2 and 6 days after imbibition,when they were in the cell division and post-cell division stages,respectively. BA treatment at day 2 temporarily inhibited an increase in chlorophyllcontent in the following day, but stimulated it in later days.No such inhibition by BA was observed for changes with timein DNA, RNA, and protein content and f. wt. On the other hand,BA treatment at day 6 enhanced RNA and protein content, withoutsignificant influence on DNA and chlorophyll content and f.wt. The mode of cytokinin action on greening in leaves during cell-divisiongrowth seems to be different from that in etiolated cotyledons. Phaseolus vulgaris L., bean, greening, benzyladenine, DNA, RNA, protein     

Involvement of Water Channels in the Hydration-Induced Calcium Release in Nitella flexilis

An internodal cell of Nitella flexilis treated with 10 mM KC1was vacuole-perfused with an isotonic solution containing ethyleneglycol-bis-(rß-aminoethylether)N,N,N,N-tetraaceticacid (EGTA) and its content including cytoplasm was squeezedout into a vessel and covered with silicone oil. When the hypotonicsolution was added into the cytoplasmic drop which had beenmixed with aequorin, a significant increase in the light emissionfrom aequorin was detected with the photomultiplier, indicatinga release of Ca²⁺ from some cell organdies storing Ca²⁺. Thisincrease in the light emission was strongly inhibited by treatingcells with 0.1 mM HgCl₂ which is known to inhibit water channelsin the plasma membrane. The inhibition was completely recoveredby washing HgCl₂ with 2-mer-captoethanol. This suggests thatwater channels may exist in the membrane of Ca²⁺ stores andplay an essential role in the hydration-induced Ca²⁺ release. (Received February 12, 1998; Accepted May 21, 1998)     

Inhibition of Flowering in the Long-Day Plant Lemna gibba G3 by Hutner's Medium and its Reversal by Medium Modification

The long-day plant Lemna gibba G3 flowers normally in E medium(Hoagland-type medium plus 30 µM EDTA) but in 0.5 H mediumthere is no flowering. Ammonium is present in 0.5 H medium andis known to inhibit flowering in L. gibba G3, but even in NH₄⁺-free0.5 H medium there is virtually no flowering under continuouslight. Increasing the phosphate concentration of the NH₄⁺-free0.5 H medium from 1.15 ITIM to 12 or 16 mM results in substantialflowering. Decreasing the EDTA concentration from 850 µIMto 250 µM, or raising the nitrate concentration from 4mM to 12 mM, results in only a small increase in flowering.If the decrease in EDTA and increase in nitrate are combinedwith the increase in phosphate, however, the flowering responseis nearly as good as that obtained using E medium. Thus, withthese three changes the inhibitory effect of NH₄⁺free 0.5 Hmedium for flowering in L. gibba G3 is almost completely reversed In the above studies flowering was not limited by daylength.When plants were grown on E medium under an 11 hour daylengthwhere flowering is limited by daylength, decreasing the phosphateconcentration in the medium reduced flowering, but increasingthe phosphate concentration in the medium did not stimulateflowering. Thus, when flowering is limited by daylength, highphosphate will not cause flowering, but a certain level of phosphateappears to be necessary for the expression of photoinductionunder long days. (Received January 14, 1986; Accepted June 24, 1986)     

Effects of lipophilic and water-soluble membrane probes on ethylene synthesis in apple and Penicillium digitatum

Several chemicals were used to probe the in situ ethylene formingenzyme systems in apple tissue and Penicillium digilatum. 2,4-Dinitrofluorobenzene,a membrane permeant probe, inhibited ethylene production effectivelyin apples but far less effectively in P. digitatum. In contrast,salicylaldehyde, another membrane permeant probe, effectivelyinhibited the P. digitatum system but, except at 0.1 mM concentration,little influenced the apple system. l,5-Difluoro-2,4-dinitrobenzene(DFDNB), a membrane permeant probe which cross-links proteinswith proteins and with phospholipids, strongly inhibited ethylenebiosynthesis in both apple and P. digitatum, whereas dimethylsuberimidate, the protein cross-linking reagent, inhibited slightlythe apple system but not P. digitatum system. Picrylsulfonate(TNBS), a non-permeant membrane probe, up to 0.1 mM, did notinhibit any of the two systems studied. However, in the presenceof exogenous methionine in the apple system and glutamate inP. digitatum, TNBS at 0.1 and 1 mM caused inhibition of ethylenesynthesis. These probes did not affect respiration of appleslices under similar incubating conditions, excepting for DFDNBwhich on longer incubation did inhibit respiration, but theeffect on ethylene synthesis was 15 times greater. Divalentcation ionophores, A23187 [GenBank] and X537 A, had no effect on ethylenesynthesis in both the systems. The water soluble iron chelatingagent, o-phenanthroline, was a more potent inhibitor of theapple system but minimally affected P. digitatum. In contrast,the lipophilic chelator, bathophenanthroline, was a more potentinhibitor of the P. digitatum system. Assay of the fatty acidcomposition of polar lipids from crude membrane fractions showedconsiderably greater linoleic to linolenic ratio in P. digitatumthan in apple. We suggest that the ethylene formations in appleand P. digitatum are sensitive to a modification of membranestructure and that specific chelator-sensitive metals (perhapsiron and copper) are involved in ethylene synthesis in boththese systems. ¹ On leave from the M.S. University of Baroda (India); presentaddress: Department of Plant Genetics, The Weizmann Instituteof Science, Rehovot, Israel. ²Present address: Agricultural Research Organization, The VolcaniCenter, Bet-Dagan, Israel. (Received February 23, 1979; )     

Adrenocorticotropic hormone stimulation of adrenal RNA polymerase I and III activities. Nucleotide incorporation into internal positions and 3' chain termini.

In the presence of 50 mM (NH4)2SO4 and low concentrations of alpha-amanitin (7.7 mug/ml), adrenal nuclei synthesize predominately rRNA as characterized by size and base composition. Approximately 10% of the RNA synthesized under these conditions sediments at 4-5 S; this RNA synthesizing activity is inhibited by high concentrations of alpha-amanitin (231 mug/ml) indicating the presence of RNA polymerase III activity. ACTH administration to guinea pigs results in a twofold increase in adrenal nuclear RNA polymerase I and III activities at 14 hr of hormone treatment. Analysis of the amount of radiolabeled nucleoside triphosphate incorporated in vitro into 3' chain termini and into internal nucleotide positions has been utilized to measure the number of RNA chains and the average chain length synthesized in vitro. Incorporation into 3' chain termini is not changed by ACTH; incorporation into internal nucleotides is doubled in parallel with the increase in RNA polymerase I activity. These results are not due to an altered Km of RNA polymerase I for the four nucleoside triphosphates, nor to differential R Nase or phosphatase activity. These studies suggest that the regulation of RNA polymerase I by ACTH is accomplished in part through an increase in the rate of RNA chain elongation.     

Effects of extracellular calcium on the proliferation and differentiation of porcine osteoblasts in vitro

We examined the effects of various extracellular calcium concentrations on DNA content, procollagen type I carboxy-terminal propeptide (PICP) release (reflects type I collagen synthesis), and alkaline phosphatase activity of porcine osteoblasts. Osteoblasts seeded in control medium (2.2 mM calcium) were transferred to low (0.5 or 1 mM) calcium medium or to high (3, 5, 7, or 10 mM) calcium medium at different stages of the culture period and for different incubation times. When osteoblasts were transferred to low or high (3 or 5 mM) calcium medium 1 or 2 days after plating and kept in that medium until the end of the culture period, PICP release was inhibited, but DNA content and alkaline phosphatase activity were unchanged, except in 5 mM calcium, which inhibited alkaline phosphatase activity. Short-term culture of subconfluent and near-confluent osteoblasts in 7 or 10 mM calcium for 48 h inhibited DNA content. DNA content returned to normal levels when cells were transferred back to control medium, whereas alkaline phosphatase inhibition induced by 5, 7, or 10 mM calcium was not reversible. Short-term culture in high calcium media did not affect PICP release. Thus, in porcine osteoblasts, low and high extracellular calcium concentrations affect DNA content, PICP release, and the expression of osteoblastic phenotype markers (alkaline phosphatase activity). These effects are dependent on the duration of calcium treatment and the state of differentiation of the osteoblasts.     

Specific inhibition by cyclodextrins of raw starch digestion by fungal glucoamylase.

alpha-, beta-, and gamma-cyclodextrins (CDs) completely inhibited raw starch digestion by glucoamylase I (GA I, MW 90,000) from Aspergillus awamori var. kawachi, and inhibited by 85% the raw starch adsorption of GA I at the CD concentrations of 1-5 mM. CDs at 1-5 mM did not inhibit gelatinized starch hydrolysis by GA I, but at the concentration of 50 mM, they inhibited such hydrolysis slightly. GA I was specifically adsorbed onto CD-Sepharose 6B, but glucoamylase I' (GA I', MW 73,000), which does not adsorb onto or digest raw starch, from the same strain was not adsorbed onto that gel. The adsorption of the glucoamylases onto raw starch and CD-Sepharose 6B was correlated to their digestion of raw starch. The hydrophobic adsorption of GA I onto CDs and raw starch occurred competitively at the Cp region, which is on the C-terminal side of Gp-I in the site for raw starch affinity of GA I, and inclusion complexes were formed.     

ROLE OF NUCLEIC ACID AND PROTEIN METABOLISM IN THE INITIATION OF GROWTH AT GERMINATION

When dry decotyledonized embryos of Raphanus are supplied withwater, a brief period of water absorption (phase A) is followedby a period of no fresh weight increase (phase B) which lastsfor 8 hr at 30°. In this period, embryos become ready toadvance into the period of fresh weight increase (phase C). When embryos were exposed to various concentrations of thiouracilor actinomycin D solution from 0 hr of water supply, increasesin fresh weight and in RNA content measured at 13 hr were inhibitedin parallel with each other. Chloramphenicol and puromycin inhibitedthe fresh weight increase without affecting the RNA increase.When embryos were exposed to thiouracil or puromycin for 2,4 and 6 hr, beginning at 0 hr of water supply, the start ofphase C delayed 2, 4 and 6 hr, respectively. When these drugswere given after phase B had progressed at least for 2 hr, thedelay of the start of phase C was shorter than the period ofthe drug treatment. If given at the end of phase B, thiouraciland actinomycin D inhibited the incorporation of ¹⁴C-uracilbut not the fresh weight increase, while chloramphenicol andpuromycin inhibited the latter without inhibiting the former. During phase B, protein content per dry weight of embryo didnot increase, but the rate of ¹⁴C-leucine incorporation increasedremarkably to reach the level in phase C. Incorporation of labeledleucine was inhibited if embryos were subjected to thiouracilor actinomycin D action during phase B, but not if the drugswere given when phase B had been completed. Puromycin and chloramphenicolinhibited the incorporation whenever they were given. The increase in respiratory activity during phase B was inhibitedrelatively little by the above mentioned four drugs. In conclusion syntheses of RNA and protein seem to be essentialfor the progress of phases B and C, protein synthesis havinga more direct effect. (Received September 17, 1965; )     

Inhibition of RNA synthesis in embryo of Xenopus laevis by protease inhibitor

We have studied the role of proteases during the development of Xenopus laevis embryos with the aid of protease inhibitors. The activity of proteases was found to be only minimal in the unfertilized egg and during the initiation of development, but activity began to increase at the morula stage. When the activity of proteases was inhibited by antipain, an inhibitor of endopeptidase activity, RNA synthesis in the embryo was inhibited. To examine the relationship between the inhibitory effect of antipain on protease activity and its effect on RNA synthesis, antipain was reduced with NaBH4 to inactivate its protease inhibitory activity. The reduced antipain did not inhibit RNA synthesis in the embryo. Antipain effectively inhibited synthesis of both rRNA and poly(A)+RNA but not 4S RNA. We therefore suggest that protease activity plays an important role in the initiation and/or continuation of RNA synthesis.     

Sink-stimulated photosynthesis, increased transpiration and increased demand-dependent stimulation of nitrate uptake: nitrogen and carbon relations in the parasitic association Cuscuta reflexa-Coleus blumei

When parasitizing Coleus blumei Benth., grown in quartz sandculture and fed with 0.2, 1 or 5 mM nitrate, the biomass productionof Cuscuta reflexa Roxb. was inhibited to a similar extent asthat of the host supplied limiting concentrations of nitrate.In the presence of Cuscuta the growth and dry matter increaseof the host plant was severely inhibited. However, dry matterproduction of host plus parasite was only slightly less thanor at 0.2 mM nitrate almost the same as that of uninfected Coleusplants. Under all conditions of nitrate nutrition, parasitismby Cuscuta led to a substantial increase in photosynthesis inhost leaves under light-saturating conditions and in transpiration.Particularly with 0.2 mM and mM     

Salt Tolerance in Suaeda maritima (L.) Dum: THE EFFECT OF SODIUM CHLORIDE ON GROWTH, RESPIRATION, AND SOLUBLE ENZYMES IN A COMPARATIVE STUDY WITH PISUM SATIVUM L

The effect of sodium, chloride on the growth of a halophyte,Suaeda maritima (L.) Dum., was compared with its effect on Pisumsativum L. cv. Alaska under controlled environmental conditions.The salt stimulated the growth of Suaeda maximally at concentrationsof 170 to 340 mM while the growth of Pisum was inhibited evenby 100 mM. Both species accumulated ions in the tops and themaximum concentrations of Na⁺ and Cl^– rose in Suaeda to860 mM (based on the water content) and 730 mM and in Pisumto 170 mM and 300 mM respectively. Respiration in both specieswas inhibited as the NaCl level in the culture solution wasraised. Four supernatant enzymes (malic dehydrogenase, glucose-6-phosphatedehydrogenase, peroxidase, and acid phosphatase) prepared fromPisum and from Suaeda (grown either in the absence of addedNaCl or in the presence of 340 mM NaCl) were assayed in variouslevels of sodium chloride. The dehydrogenases were markedlyinhibited by increasing salt concentrations while there wasa smaller effect on the peroxidase and acid phosphatase. Therewas no difference in the effect of salt on the enzymes preparedfrom the two species although one is halophilic and the otherhalophobic.     

Diurnal rhythm of nuclear RNA polymerase I activity in a duckweed, Lemna gibba G3, under continuous light conditions

The diurnal change of nuclear RNA polymerases I and II was examinedin a longday duckweed, Lemna gibba G3, under continuous lightconditions. RNA synthesis in crude nuclei was dramatically stimulatedby addition of the exogenous RNA polymerase of Escherichia coli,but not by the addition of calf thymus DNA. Treatment of crudenuclei with the supernatant fractions after precipitation ofthe nuclei decreased the RNA synthetic activity of the nucleiirrespective of the preparation time of both fractions. RNApolymerase I activity in crude nuclei, which was determinedin the presence of -amanitin at a low concentration of KCl,exhibited a diurnal rhythm but RNA polymerase II activity, whichwas presumed to be a portion of RNA synthesis inhibited by -amanitinin the presence of a high concentration of KCl, remained constantthroughout the day. Identical results were obtained when bothenzymes were solubilized widi ammonium sulfate and chromatographedon DEAE-Sephadex column. Both activities in the supernatantfraction obtained after precipitation of the nuclei did notchange diurnally. It was concluded, therefore, that the diurnalrhythm of RNA synthetic activity in the crude nuclei is dueto the RNA polymerase I activity and not the RNA polymeraseII activity. (Received August 29, 1978; )     

Transport pathways in canine lingual epithelium involved in sweet taste

The responses of canine lingual epithelium to D-glucose weremeasured in an Ussing chamber to determine the possible contributionof the osmotic changes of taste cells to the response of saccharides.With the mucosal solution containing 50 mM NaCl, 2 mM HEPES,pH 7.4 (solution A) and the serosal solution containing Krebs—Henseleit(KH) buffer the addition of up to 0.5 M D-glucose in the mucosalsolution increased the short circuit current (I_sc) in a sigmoidalmanner. The D-glucose-stimulated I_sc was inhibited by 0.1 mMamiloride or 1 mM ouabain added to either the mucosal or theserosal solution, and partially inhibited by 5 mM BaCl₂ addedto the serosal solution. The inhibition by these three compoundswas also observed in the presence of 0.5 M NaCl. Ouabain alsoinhibited transport when added to solution A. These experimentssuggest that in canine lingual epithelium the paracellular pathwaypermits molecules as large as ouabain (mol. wt 586) to diffusefrom the mucosal to the serosal solution and vice versa underall osmotic conditions. These results may explain the phenomenonof intravascular taste. Such is not the case in rat tongue whereouabain only inhibited transport when added to the serosal solution.Increasing the osmolality of the serosal KH buffer by additionof relatively membrane-impermeable saccharides such as sucroseor L-glucose did not significantly alter the I_sc, whereas makingthe serosal KH solution hypo-osmotic resulted in a transientdecrease in I_sc. These data suggest that the increase in I_scinduced by saccharides, such as D-glucose, is not simply anosmotic response of the epithelium but more likely the consequenceof saccharides binding weakly to receptors. That the responseto both salts by themselves and in the presence of saccharidesexhibits the same cation selectivity, and that both are inhibitedby amiloride, ouabain, BaCl₂ and LaCl₃ suggest that in caninelingual epithelia, in contrast to rat epithelium, the responsesto hyperosmotic concentrations of salts and saccharides mightoccur via the same transcellular pathways.