Genetic and Structural Analysis of Five Arabidopsis Mutants with Abnormal Root Morphology Generated by the Seed Transformation Method

A number of Arabidopsis thaliana mutants with abnormal rootmorphology have been isolated from a population of Agrobacterium-mediated seed transformants. Five of these mutants identifiedby their abnormal root morphology have been genetically andmorphologically characterised. Two mutants, 5905 and 1767 havedefective cellular elongation, mutant 7203 lacks an endodermalcell layer and mutants 4792 and 7133 exhibit abnormal radialcellular expansion. It is apparent from detailed analysis thatabnormal root morphology is accompanied by abnormal hypocotylphenotype. Genetic analysis has revealed that only one of thesemutants is tagged with a T-DNA insert.Copyright 1994, 1999 AcademicPress Arabidopsis thaliana, root, development, T-DNA insertion mutagenesis, endodermis, elongation     

Induction of Oligosporogeneous and Asporogeneous Mutants of Blue-green Alga, Anabaena doliolum by Acriflavine and Acridine Orange

Acriflavine and acridine orange were highly effective in producingmutants defective in spore differentiation in the blue-greenalga, Anabaena doliolum. Acridine orange produced both oligosporogeneous(Osp) and asporogeneous (Sp^–) mutants in high yield withthe frequency ranging from 2.4 to 21 per 10⁴ survivors, whereaswith acriflavine no oligosporogeneous mutants were detected,although it produced non-sporulating (Sp^–) mutants withthe frequency of 1.4 per 10⁴ survivors. Mutants isolated throughthese dyes were stable and showed no tendency towards spontaneousor induced reversion. Behaviour of various mutants indicatedtheir being blocked at different stages of sporulation withdifferent mutagenic sites. Induction of high numbers of Ospand Sp^– mutants after acridine dye treatment indicatesthe involvement of an extrachromosomal determinant in sporulationin Anabaena doliolum. Ohgosporogeneous mutants, asporogeneous mutants, Anabaena doliolum, blue-green algae, mutagenesis, acriflavine, acridine orange     

Two Ineffective-Nodulating Mutants of Lotus japonicus--Different Phenotypes Caused by the Blockage of Endocytotic Bacterial Release and Nodule Maturation

Mutants defective in nodule development and nitrogen fixationof Lotus japonicus B-129 ‘Gifu’ were obtained byinduced mutagenesis with EMS (ethylmethane sulfonate) treatment.Using a symbiont of L. japonicus, Rhizobium loti JRLS01, 17,000M2 seeds were screened for plants affected in their symbioticphenotype, resulting in the successful isolation of eleven stablemutants. In this paper, we report two ineffective nodulatingmutants among them. Reciprocal crossing between wild type 'Gifu'and these mutants indicated that their phenotypes are undermono-genic and recessive control. Furthermore, tests for alle-lismwith these mutants showed that the mutated genes are non-allelic.Ultrastructural analysis revealed that these mutants were inhibitedat different stages of nodule development and maturation. Basedon histological characteristics of the nodules, two ineffectivenodulating mutants were named albl (aberrant localization ofbacteria inside nodule) and fenl (fail in enlargement of infectedcells), respectively. In the nodules of albl, most of the bacteriafailed to invade the cytoplasm of cortical cells and were tightlyconfined inside infection threads or localized in intercellularspaces of nodules. Following prolonged inoculation, albl mutantalso formed pale-pink colored nodules with a low frequency,in which bacteria differentiated into bacteroid and fixed nitrogennormally. Although the infected cells in the nodules of fenlmutant contained numerous differentiated bacteroids, they failedto enlarge by cell expansion and showed a low activity of nitrogenfixation. (Received March 18, 1997; Accepted May 8, 1997)     

An analysis of seed development in Pisum sativum XIX. Effect of mutant alleles at the r and rb loci on starch grain size and on the content and composition of starch in developing pea seeds

The effects of mutant alleles at the r and rb loci on starchgrain size and the levels of starch and amylose in developingpea (Pisum sativum L.) seeds have been examined. Four lines,near-isogenic except for genes at these loci, have been usedto show that both mutations reduce levels of starch throughoutembryo development and reduce levels still further when combinedin the ‘double mutant’. The reduction in starchcontent was due, at least in part, to a reduction in starchgranule size. Although the proportion of starch in mature embryoswas similar in the rrRbRb and RRrbrb lines, the starch contentdiffered between these two lines during development, as a percentageof embryo dry weight. This difference was due to a reductionin the absolute growth of the embryo caused by the rb mutation.Lines homozygous for the mutant r allele with either wild-type(RbRb) or mutant (rbrb) alleles at the rb locus contained increasedproportions of amylose in their starch throughout development,due to a reduced production of amylopectin. The presence ofthe rb mutation, however, also reduced the amount of amylosein relation to the reduction in total starch levels. Mutantalleles at both loci also reduced starch levels in the testaduring development, the reduction due to rb being more extreme.Reciprocal crosses showed a maternal effect of the rb mutationon final seed size and on the absolute amount of starch in theembryo. Key words: Pisum sativum L., seed, starch, development, mutant     

The Herbicide-Resistant Species of the Cyanobacterial Dl Protein Obtained by Thorough and Random in vitro Mutagenesis

Random mutations were introduced into the DNA fragment of thepsbA2 gene of Synechocystis sp. PCC 6803, which encodes thecarboxyl-terminal 178 amino acid region of the Dl protein ofthe PSII reaction center, by in vitro random mutagenesis toobtain Dl species resistant to herbicides and to understandthe protein-herbicide interactions. The mutants were screenedon the criterion of resistance to either 1 µM DCMU or10 µM atrazine. In these mutants, amino acid substitutionswere distributed throughout the entire area of the targetedregion in the Dl protein. However, in every mutant, except forone case, the substitution was present in the region describedas the "herbicide-binding niche", i.e., between Phe211 and Leu275,although some amino acid substitutions which were not previouslydescribed were found at residues known to be involved with herbicideaffinity. Thus, the result of random mutagenesis basically supportsthe validity of the proposed structural model for the Dl protein,as well as of the herbicide-binding niche. Preliminary characterizationof the herbicide-resistant mutants obtained in this study hasalso been conducted. (Received December 8, 1997; )     

A Transgenic Mutant Defective in Cell Elongation and Cellular Organization during Both Root and Shoot Development in Lettuce, Lactuca sativa

A recessive mutation affecting both root and shoot developmentwas isolated from transformants of lettuce cv. Diana co-transformedwith maize Ac transposase and Ds. Mutant phenotype in the progenywas co-segregated with the T-DNA containing Ac transposase indicatingthat the mutation was caused by insertional mutagenesis. Mutationin this novel genetic locus, designated as ANORMAL ROOT ANDSHOOT (ARS), showed a dwarf phenotype with short thick roots,short hypocotyl and abnormal filamentous leaves without anyfurther reproductive development. The anatomical analysis revealedthat the ars mutant root phenotype is primarily due to the lackof cell elongation and to the abnormal increase in cell numberin the cortex region in the roots. ars mutants are able to initiatenormal leaf primodia, but, the cell elongation and cellularorganization of the developing leaf primodia is impaired andresults in sequentially abnormal development of the leaf. arsmutants also display photomorphogenic development in darknessby producing open cotyledons, developing vegetative leaves,and short hypocotyls. This suggests that the ARS gene may alsobe involved in the regulation of cell elongation in the hypocotylin the absence of light. Abnormal development in ars mutationscan not be normalized by exogenous application of phytohormonessuch as gibberellin and brassinosteroids, indicating that themutant is not impaired in the biosynthesis of these two hormones. (Received January 5, 1999; Accepted August 19, 1999)     

Pseudomonas aeruginosa attachment and biofilm development in dynamic environments

Biofilm formation by Pseudomonas aeruginosa is hypothesized to follow a developmental pattern initiated by attachment to a surface followed by microcolony formation and mature biofilm development. Swimming and twitching motility are important for attachment and biofilm development in P. aeruginosa. However, it is clear that many P. aeruginosa strains lacking swimming motility exist as biofilms in the lungs of cystic fibrosis patients. Consequently, we have developed a dynamic attachment assay to identify motility-independent attachment-defective mutants. Using transposon mutagenesis, we identified 14 novel dynamic attachment-deficient (dad) mutants including four mutants specific to dynamic assay conditions (dad specific). Two of the dad-specific mutants contain insertions in genes involved in sensing and responding to external stimuli, implying a significant impact of external factors on the biofilm developmental pathway. Observations of initial attachment and long-term biofilm formation characterized our dad mutants into two distinct classes: biofilm delayed and biofilm impaired. Biofilm-delayed mutants form wild-type biofilms but are delayed at least 24 h compared with the wild type, whereas biofilm-impaired mutants never form wild-type biofilms in our assays. We propose a dynamic model for attachment and biofilm formation in P. aeruginosa including these two classes.     

Light Quality and Vernalization Interact in Controlling Late Flowering in Arabidopsis Ecotypes and Mutants

The late flowering ecotypes of Arabidopsis thaliana L. (Heyn.)Eifel, Pitztal and Innsbruck responded to 10 d vernalization(cold treatment) by flowering earlier with less with less thanhalf the number of leaves of non-induced plants. The vernalizationresponse was cumulative: increased numbers of days of vernalizationinduced earlier flowering up to an apparent saturation in responseafter 30 to 40 d. The ratio of red:far-red (R:FR) light alsoaffected non-vernalized time-to-flower. When grown under fluorescentplus incandescent lamps (R:FR = 1·0), time-to-flowerwas approximately half that required by plants grown under fluorescentlamps (R:FR = 5·8) at the same photon flux density andphotoperiod. Leaf production rate was unaffected by either vernalizationor light quality changes and time-to-flower and leaf numberwere highly correlated (r² = 0·973). The late flowering mutants of Landsberg erecta were grown underlighting which displayed a gradient of R:FR. Some mutants likeco, flowered at the same time in all R:FR treatment, while otherlike fca took nearly twice as long to flower, with double thenumber of leaves at R:FR ratio of 5·8 compared with theR:FR = 1 treatment. The ranking of the response from least tomost responsive was co, fe, gi, WT, fd, fwa, ft, fha, fpa, fy,fve and fca. Vernalization of these Landsberg mutants always resulted inearlier flowering, although only fca, fve, fy and fpa were significantlymore sensitive to thermoinduction than the wild type parent.There was a high correlation (r² = 0·89 between the responseto thermoinduction and to R:FR ratio. Vernalization of fca for24 d largely eliminated the R:FR time-to-flower response. Vernalizationand photoinduction similarly affect late flowering and can substitutefor each another.Copyright 1993, 1999 Academic Press Light quality, vernalization, flowering, Arabidopsis thaliana, phytochrome, thermoinduction, photoperiod, photoinduction, growth conditions, photon flux density, daylength, spectral quality, far-red light     

Induced albina mutations as a tool for genetic analysis and cell biology in flax (Linum usitatissimum)

In order to obtain nuclear recessive albina mutants, seeds ofLinum usitatissimum ‘Antares’ were treated withethyl methanesulphonate (EMS) for 4 h at a concentration of0.5% (v/v). After the mutagenic treatment, the M₁ seeds weresown in the greenhouse, selfed and the resulting M₂ seeds ofeach M₁ plant were harvested separately. Observation of albinamutants in the M₂ generation facilitated the estimation of thegenetically effective cell number (GECN). In flax, four cellscontribute to the formation of the inflorescence. The transmissionof the albinism trait was further analysed in the progeny derivedfrom the albina mutants. In four of these mutants, the albinismcharacter was found to be encoded by recessive nuclear genes.The utility of these mutants as a source of regenerating explantsor of protoplasts was tested. These features are critical tothe development of interspecific hybrids in flax by creatinga universal hybridizer which carries a positive and dominanttrait (e.g. resistance to an antibiotic) and a recessive trait(e.g. nuclear recessive albinism). Key words: Albinism, ethyl methanesulphonate mutagenesis, genetically effective cell number, Linum usitatissimum     

Protein-O-glycosylation in yeast: protein-specific mannosyltransferases

S.cerevisiae contains at least six genes (PMT1–6) fordolicholphosphate-D-mannose: protein-O-D-mannosyltransferases.The in vivo mannosylation of seven O-mannosylated yeast proteinshas been analyzed in a number of pmt mutants. The results clearlyindicate that the various protein O-mannosyltransferases havedifferent specificities for protein substrates. Five of theproteins tested (chitinase, a-agglutinin, Kre9p, Bar1p, Pir2p/hsp150)are mainly underglycosylated in pmt1 and pmt2 mutants, wherebyqualitative differences exist among the various proteins. Twoof the O-mannosylated proteins (Ggp1p and Kex2p) are not atall affected in pmt1 and pmt2 mutants but are clearly underglycosylatedwhen PMT4 is mutated. Although the PMT4 gene product is shownto be responsible for O-mannosylating a Ser-rich region of Ggp1pin vivo, a penta-seryl-peptide is not an in vitro substratefor this transferase. A PMT3 mutation does affect O-manno-sylationof chitinase only in the genetic background of a pmt1pmt2 doublemutation, indicating that PMT1 and PMT2 can compensate for adeleted PMT3 gene. dolichol-phosphate PMT gene family protein glycosylation S. cerevisiae     

The Chloroplast and Leaf Developmental Mutant, pale cress, Exhibits Light-conditional Severity and Symptoms Characteristic of its ABA Deficiency

The PALE CRESS gene (PAC) is essential for proper chloroplastand leaf development in Arabidopsis thaliana. The ability ofpac mutants to accumulate significantly more chlorophyll whengrown in low light conditions than in high light conditionssuggests that carotenoid deficiency is at least partly responsiblefor premature cessation of chloroplast development. In additionto accumulation of low levels of chlorophyll and carotenoidpigments,pac mutants are abscisic acid (ABA) deficient and havecharacteristics which may be explained by this deficiency. Theseinclude reduced seed viability and, in enclosed growth conditions,increased leaf growth. Plants transformed with an antisensePAC construct often bear viviparous embryos which may be symptomaticof a deficiency in ABA. Since carotenoids are precursors ofABA, a role for PAC in carotenoid biosynthesis is further supported.The nuclear-encoded, chloroplast-localized PAC protein has beenimplicated in the maturation of plastid-encoded mRNAs. Thus,PAC may affect the abundance of one or more chloroplast proteinswhich function in the synthesis or stability of carotenoids.Using thePROLIFERA gene as a marker for cell division, it isshown that cell division profiles in the pac shoot apex aredisrupted. pac leaves are relatively normal in size and shapedespite the light intensity-induced variability of leaf celldefects. Copyright 2000 Annals of Botany Company Abscisic acid, carotenoid, chloroplast development, leaf development, organismal theory, PALE CRESS,PROLIFERA , vivipary     

ABA insensitivity and low ABA levels during seed development of non-dormant wheat mutants

Three wheat (Triticum aestivum L.) mutants that lacked dormancyat maturity were isolated from an ethylmethane sulphonate-treatedpopulation of a dormant red-grained line, Kitakei-1354 (Kitakei).The three mutants (EH47-1, EH47-2-5 and EH47-2-6) were selectedin segregating generations derived from one M₂ plant. They differin morphological and physiological characteristics, showingthat these mutants contained several mutations besides non-dormancy.Despite these differences, embryos of all the mutants rapidlylost sensitivity to abscisic acid (ABA) during the later halfof seed maturation while Kitakei embryos maintained the sensitivityeven after maturity. These results suggest that embryo sensitivityto ABA plays a key role in seed dormancy. The profile of ABAcontent of EH47-1 embryos during seed development was similarto that of Kitakei, except for a significantly lower level at30 d after pollination (DAP). This reduced level of ABA at DAP30is discussed in relation to the development of seed dormancyand ABA sensitivity of the embryos. Segregation ratios for non-dormancyin progeny of EH47-1Kitakei crosses suggest that the non-dormancyof EH47-1 is a single dominant mutation. Key words: Abscisic acid, wheat, seed dormancy, inheritance, mutant     

Isolation and Characterization of Sex-Linked Female-Sterile Mutants in DROSOPHILA MELANOGASTER

The purpose of the experiments described was to identify X chromosome genes functioning mainly or exclusively during oogenesis. Two mutagenesis experiments were carried out with ethyl methane sulfonate. Following treatment inducing 60% lethals, 9% of the treated X chromosomes carried a female sterility mutation which did not otherwise seriously affect viability. Among —95 isolated mutants, 19 were heat-sensitive and 5 cold-sensitive. The mutants have been classified as follows: I (16 mutants; 12 complementation groups): the females laid few or no eggs; the defect concerned either ovulation or oogenesis. II (37 mutants; 18 complementation groups): the female laid morphologically abnormal eggs, often with increased membrane permeability. III A (13 mutants; at least 8 complementation groups): the homozygous females were sterile if mated to mutant males; their progeny (homo- and hemizygous) died at a late embryonic stage (11 mutants), at the larval stage (1 mutant) or at the pupal stage (1 mutant). However fertility was partly restored by breeding to wild-type males as shown by survival of some heterozygous descendants. III B (29 mutants; 22 complementation groups): the fertility of the females was not restored by breeding to a wild-type male. Most of the eggs of 13 of the mutants died at a late stage of embryogenesis. The eggs of the others ceased development earlier or, perhaps, remained unfertilized. The distribution of the number of mutants per complementation group led to an estimation of a total of about 150 X-linked genes involved in female fertility. The females of three mutants, heat-sensitive and totally sterile at 29°, produced at a lower temperature descendants morphologically abnormal or deprived of germ cells. Three other mutants not described in detail showed a reduction in female fertility with many descendants lacking germ cells. A desirable mutant which was not recovered was one with normal fertile females producing descendants which, regardless of their genotype, bore specific morphological abnormalities. The value of the mutants isolated for analysis of the complex processes leading to egg formation and initiation of development is discussed.     

Mutations in the Arabidopsis SWC6 gene, encoding a component of the SWR1 chromatin remodelling complex, accelerate flowering time and alter leaf and flower development

Mutations affecting the Arabidopsis SWC6 gene encoding a putativeorthologue of a component of the SWR1 chromatin remodellingcomplex in plants have been characterized. swc6 mutations causeearly flowering, shortened inflorescence internodes, and alteredleaf and flower development. These phenotypic defects resemblethose of the photoperiod independent early flowering 1 (pie1)and early in short days 1 (esd1) mutants, also affected in homologuesof the SWR1 complex subunits. SWC6 is a ubiquitously expressednuclear HIT-Zn finger-containing protein, with the highest levelsfound in pollen. Double mutant analyses suggest that swc6 abolishesthe FLC-mediated late-flowering phenotype of plants carryingactive alleles of FRI and of mutants of the autonomous pathway.It was found that SWC6 is required for the expression of theFLC repressor to levels that inhibit flowering. However, theeffect of swc6 in an flc null background and the down-regulationof other FLC-like/MAF genes in swc6 mutants suggest that floweringinhibition mediated by SWC6 occurs through both FLC- and FLC-likegene-dependent pathways. Both genetic and physical interactionsbetween SWC6 and ESD1 have been demonstrated, suggesting thatboth proteins act in the same complex. Using chromatin immunoprecipitation,it has been determined that SWC6, as previously shown for ESD1,is required for both histone H3 acetylation and H3K4 trimethylationof the FLC chromatin. Altogether, these results suggest thatSWC6 and ESD1 are part of an Arabidopsis SWR1 chromatin remodellingcomplex involved in the regulation of diverse aspects of plantdevelopment, including floral repression through the activationof FLC and FLC-like genes. Key words: Arabidopsis, chromatin remodelling, floral repression, HIT-Zn finger, phase transition, SWR1 complex     

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     

Tagged Mutagenesis and Gene-trap in the Moss, Physcomitrella patens by Shuttle Mutagenesis

The moss, Physcomitrella patens has been used as a useful materialin many fields, because of its simple body plan, ease of genetargeting, and other reasons. Although many mutants have beenreported, no method to isolate the corresponding genes was reported.We developed a gene tagging and gene-trap system in P. patensby using the shuttle mutagenesis technique, which has been usedin the budding yeast. In 5264 tagged lines, 203 mutants withaltered developmental or morphological phenotypes were obtained.In 129 of 4757 gene-trap lines, ß-glucuronidase (GUS)activity was detected in some tissue. Although multiple copiesof a tag were detected in many tagged lines by Southern analyses,most copies are likely integrated at the same locus accordingto PCR analyses.     

Identification of phytochrome B amino acid residues mutated in three new phyB mutants of Arabidopsis thaliana

The growth and development of plants is regulated by light viathe action of photoreceptors which are responsive to the red/far-red,blue and UV regions of the spectrum. Phytochrome B (the apoproteinof which is encoded by the PHYB gene) is one of the red/far-redabsorbing photoreceptors active in this process. In this paper,the isolation and characterization of three new EMS-inducedmutations of Arabidopsis which confer phytochrome B deficiencyare described. Complementation analysis showed that these mutations(phyB-101, phyB-102 and phyB-104) were allelic with PHYB. DNAsequence analysis showed that all three mutants contain nucleotidesubstitutions in the PHYB-101 gene sequence. phyB-101 carriesa nucleotide substitution within the second exon of the PHYBgene. This G-to-A substitution is a missense mutation that convertsa glutamate residue at position 812 of the phytochrome B apoproteinto a lysine residue. phyB-102, another missense mutant, carriesa C-to-T substitution which converts a serine residue at position349 of the phytochrome B apoprotein to a phenylalanine residue.phyB-104 carries a premature stop codon as a result of a G-to-Amutation 1190 bp down-stream of the ATG start codon of the PHYBsequence. The missense mutations in phyB-101 and phyB-102 causesignificant alterations in the predicted second ary structureof their respective mutant polypeptides, and identify aminoacid residues playing crucial roles in phytochrome B function,assembly or stability. Key words: Arabidopsis thaliana, phytochromet, phyB mutants, missense mutations     

Carbon Dioxide Photoassimilation in Normal-leaved and Mutant Forms of Pisum sativum L.

The reproducible steady-state carbon dioxide (CO₂) photoassimilationpotentials of three mutants and a normal form of pea (Pisumsativum L.) have been compared. The three mutants studied differed markedly in foliar morphology:genotype af af Tl Tl had leaflets converted to tendrils; AfAf tl tl had tendrils converted to leaflets; af af tl tl hadrelatively minute leaflets on a branched petiole. Interest layprimarily in the phenotype with only tendrils since it provideda potential means of reducing the volume of haulm that has tobe rapidly processed in the case of vining peas, and dried inthe case of harvest peas. These mutants had been derived from relatively unimproved cultivars.Before completion of the lengthy backcrossing required to makea full assessment of the value of such mutants an interim studyusing infra red gas analysis indicated that, in terms of CO₂ photoassimilation perunit area of youngest expanded attached leaf of glasshouse-grownplants, the mutants were comparable to normal. The phenotypewith only tendrils was the least efficient of those assayedat utilizing light of an intensity below 100 J m² sec¹ (400–700nm), and on a unit dry-weight basis it was only 18 per centas efficient as a normal-leaved pea. The other mutants werecomparable to normal in this respect. Comparison of CO₂ photoassimilation of glasshouse-grown andfield-grown plants showed them to be similar though they differedin dry weight, transpiration, and dark respiration.     

Effects of food quality on individual growth and development in the freshwater copepod Boeckella triarticulata

To quantify the demographic effects of food quality, and specificallyof the ‘poorquality’ cyanobecterium Anabaena flos-aquae,we reared individual Boeckella triarticulata (Copepoda, Calanoida)on two diets (monospecific Cryptomom sp. versus mixed Cryptomonas-Anabanmadiets) and quantified individual growth and developmental trajectoriesby examining exuviae produced at each molt, from hatching tomaturity. Size at molting was less variable among individuals,within and between diets, than age. Food quality had significanteffects on male sizes at molting and on stage-specific dailygrowth rates of both sexes; these effects were strongest duringlate naupliar and all copepodite stages Tke med Cryptomonas-Anabaenadiet significantly slowed development, particularly of copepoditestages. As a consequence of these effects, individuals raisedon the mixed diet were smaller and older at maturity. Withina given diet, individual differences explained much, if notmost, of the variation exhibited in growth and development.By following growth and development of a large number of individualsthroughout their Life cycles, we show that individual femalesproduce variable offspring, indicative of a bet-hedging life-historystrategy, and that B.triarticulata (like other calanoids) cangrow, develop and survive on diets that include ‘poorquality’ cyanobacteria. ¹Present address: Department of Biological Sciences, Universityof Rhode Island, Kingston, RI 02881, USA     

Isolation and characterization of perithecial development mutants in neurospora

The isolation and characterization of mutants that block perithecial development in Neurospora crassa are described. Several classes of mutants have been isolated after UV mutagenesis, and those that block perithecial development when used as the female (protoperithecial) component of a cross have been further characterized. These mutants fall into 29 complementation groups. Twelve of the 33 mutants block development at the protoperithecial stage; no other clustering of block points is observed. Many of the mutants show an altered vegetative growth rate as well; in several mutants this lower growth rate cosegregates with the female sterile phenotype. Only one mutant also blocks development of the perithecium when used as the conidial parent. None of the mutants are temperature sensitive; two can be suppressed by growth on a complete crossing medium. There is no indication that the mutants are at or in the mating-type locus, nor are any of the mutants mating-type specific. Genetic mosaics have been formed using mixtures of mutant and marked wild-type nuclei; no mutants are cell autonomous by this criterion. The significance of these results in terms of "developmental" mutants isolated in other organisms and in relation to models of eukaryotic development is discussed.