Larval and early post-larval stages in the abbreviated development of Heterosquilla tricarinata (Claus, 1871) (Crustacea, Stomatopoda)

Heterosquilla tricarinata was laboratory-cultured through itscomplete larval development and found to have one propelagicand two pelagic larval stages prior to metamorphosis to thejuvenile. These larval stages, the first juvenile, and relevantportions of the second juvenile stage, are described and figured.Individual larvae do not change in size during intermoult periods.Larvae occurring in the plankton show a progressive decreasein mean size between early (September) and late (November) springtime.Reasons for this are suggested. The first pelagic stage of H.tricarinata is anatomically very advanced in development, andthe number of pelagic stages very few, in comparison with otherknown stomatopod life-histories. Ecological implications ofthis are discussed in relation to the high-latitude distributionof the species. Comparison is made between the final pelagicstage of H. tricarinata and that of its congenor H. brazieri. ^*Permanent address: Zoology Department, University of Queensland,Brisbane, Australia     

Altered pH(i) regulation and Na(+)/HCO3(-) transporter activity in choroid plexus of cilia-defective Tg737(orpk) mutant mouse

Tg737^orpk mice have defects in cilia assembly and develop hydrocephalus in the perinatal period of life. Hydrocephalus is progressive and is thought to be initiated by abnormal ion and water transport across the choroid plexus epithelium. The pathology is further aggravated by the slow and disorganized beating of motile cilia on ependymal cells that contribute to decreased cerebrospinal fluid movement through the ventricles. Previously, we demonstrated that the hydrocephalus phenotype is associated with a marked increase in intracellular cAMP levels in choroid plexus epithelium, which is known to have regulatory effects on ion and fluid movement in many secretory epithelia. To evaluate whether the hydrocephalus in Tg737^orpk mutants is associated with defects in ion transport, we compared the steady-state pH_i and Na⁺-dependent transport activities of isolated choroid plexus epithelium tissue from Tg737^orpk mutant and wild-type mice. The data indicate that Tg737^orpk mutant choroid plexus epithelium have lower pH_i and higher Na⁺-dependent HCO₃^– transport activity compared with wild-type choroid plexus epithelium. In addition, wild-type choroid plexus epithelium could be converted to a mutant phenotype with regard to the activity of Na⁺-dependent HCO₃^– transport by addition of dibutyryl-cAMP and mutant choroid plexus epithelium toward the wild-type phenotype by inhibiting PKA activity with H-89. Together, these data suggest that cilia have an important role in regulating normal physiology of choroid plexus epithelium and that ciliary dysfunction in Tg737^orpk mutants disrupts a signaling pathway leading to elevated intracellular cAMP levels and aberrant regulation of pH_i and ion transport activity. cAMP; ion transport     

Ontogeny of the Immune System in Amphibians

SYNOPSIS. Experiments with amphibians have revealed that tissuesallografted in embryonic and early larval life may later succumbto a host immunological attack. In Xenopus, the ontogeny ofthis alloimmune response is correlated with the lymphoid maturationof the thymus. This article describes experiments primarilydesigned to ascertain if such a correlation exists in Rana pipiens. Initially, a histological study of the differentiation of thelymphomyeloid complex of the leopard frog was undertaken. At18–21°C lymphoid histogenesis is well under way inthe thymus and is beginning in many other organs during thethird week of larval life. Extensive growth and differentiationof these organs follow. Observations are also presented on thestructure, function and development of the lymphoid and Iymphomyeloidorgans from late larval life throughmetamorphosis to adulthood. Experiments were then performed to determine the onset of thealloimmune response to embryonically transplanted neural foldmaterial. At 18–21°C incompatibility phenomena, albeitslight, are first detected in these grafts as early as 17 daysafter fertilization, i.e. 15 days after transplantation. Thus,in the leopard frog, the alloimmune response develops soon afterlymphoid maturation of the thymus. At later stages of development,a more vigorous response is witnessed, concomitant with a rapidphase of lymphoid organ differentiation.     

Characterization of a wilty sunflower (Helianthus annuus L.) mutant: I. Abscisic acid content, light-dark changes in the stomatal conductance and genetic analysis

The present study was conducted to characterize geneticallyand physiologically a spontaneous mutation in sunflower whichconfers a wilty phenotype. The wilting condition of the mutantis due to abnormal stomatal behaviour. The mutant stomata resistclosure in darkness. This abnormality is associated with lowlevels of endogenous abscisic acid (ABA). By artificially elevatingthe ABA content of the mutant plants by spray treatments with10^– and 10^– M solutions it proved possible to effecta phenotypic reversion of the mutant. It has, therefore, beenproposed that the primary effect of this spontaneous mutationis to reduce the level of ABA. The genetic analysis has shownthat the willy phenotype is due to recessive nuclear mutationat a single locus. Key words: ABA, Helianthus annuus L, stomatal conductance, wilty mutant     

The proprotein convertase amontillado (amon) is required during Drosophila pupal development

Peptide hormones governing many developmental processes are generated via endoproteolysis of inactive precursor molecules by a family of subtilisin-like proprotein convertases (SPCs). We previously identified mutations in the Drosophila amontillado (amon) gene, a homolog of the vertebrate neuroendocrine-specific Prohormone Convertase 2 (PC2) gene, and showed that amon is required during embryogenesis, early larval development, and larval molting. Here, we define amon requirements during later developmental stages using a conditional rescue system and find that amon is required during pupal development for head eversion, leg and wing disc extension, and abdominal differentiation. Immuno-localization experiments show that amon protein is expressed in a subset of central nervous system cells but does not co-localize with peptide hormones known to elicit molting behavior, suggesting the involvement of novel regulatory peptides in this process. The amon protein is expressed in neuronal cells that innervate the corpus allatum and corpora cardiaca of the ring gland, an endocrine organ which is the release site for many key hormonal signals. Expression of amon in a subset of these cell types using the GAL4/UAS system in an amon mutant background partially rescues larval molting and growth. Our results show that amon is required for pupal development and identify a subset of neuronal cell types in which amon function is sufficient to rescue developmental progression and growth defects shown by amon mutants. The results are consistent with a model that the amon protein acts to proteolytically process a diverse suite of peptide hormones that coordinate larval and pupal growth and development.     

The Development of Fast-Start Performance in Fishes: Escape Kinematics of the Chinook Salmon (Oncorhynchus tshawytscha)

C-starts are high acceleration swimming movements critical forpredator avoidance by fishes. Since larval fishes are particularlyvulnerable to predation, C-start behavior is likely to be especiallyimportant during early life history stages. This paper examinesthe developmental changes in C-start performance with kinematicdata on immature chinook salmon (Oncorhynchus tshawytscha) (eleuthroembryostage, sensu Balon, 1975). The scaling of C-start kinematicsof immature fishes differs from that of adults. Adult C-startdurations increase with increasing body length while C-startdurations of immature fishes decrease (e.g., adult stage 1 duration[sec] = 0.0019.length [L] [cm] $ 0.026 [R² = 0.77] [Webb, 1978];eleuthroembryos stage 1 duration [sec] = –0.026L [cm]$ 0.100 [R² = 0.81]). Distance traveled during stage 2 alsodiffers between adult and immature fishes. Adult distance traveledscales directly with length (distance [cm] = 0.38L^1.01 [cm],R² = 0.96 [Webb, 1978]) while chinook eleuthroembryo distancetraveled is positively allometric with length (distance [cm]=0.37L¹³¹ [cm], R² = 0.83). There are similarities in the developmentof C-starts and burst swimming. For example, mean velocity scalessimilarly between the two locomotor modes (For burst swimming:U_mean [cm/sec] = 8.1 ± 1.1L [cm] $ 4.89 [R² = 0.86] [Webband Corolla, 1981]. For C-start stage 2: U_mean [cm/sec] = 10.96L[cm] - 14.09 [R² = 0.70]). This study demonstrates that C-startescape performance improves during early post-hatching development.Comparisons of immature chinook salmon fast-starts with dataon larval burst swimming and on adult C-starts suggest thatchanges specific to developing fish affect the scaling of kinematicparameters.     

Analysis of the conserved neurotrophic factor MANF in the Drosophila adult brain

Mesencephalic astrocyte-derived neurotrophic factor (MANF) is an evolutionarily conserved neurotrophic factor that supports and protects dopaminergic neurons. The Drosophila MANF (DmMANF) null mutant animals die during early development, and DmMANF is required for the maintenance of dopamine positive neurites. The aim of this study was to investigate the role of DmMANF during later developmental stages. Here we report that DmMANF expression in the adult brain is much wider than in the embryonic and larval stages. It is expressed in both glia and neurons including dopaminergic neurons. Clonal analysis showed that DmMANF is not required cell-autonomously for the differentiation of either glia or dopaminergic neurons. In addition, DmMANF overexpression resulted in no apparent abnormal dopaminergic phenotype while DmMANF silencing in glia resulted in prolonged larval stage.     

REVIEW ARTICLE: Zygotic embryogenesis versus somatic embryogenesis

This review will summarize molecular and genetic analyses aimedat identifying the mechanisms underlying the sequence of eventsduring plant zygotic embryogenesis. These events are being studiedin parallel with the histotogical and morphological analysesof somatic embryogenesis. The strength and limitations of somaticembryogenesis as a model system will be discussed briefly. Theformation of the zygotic embryo has been described in some detail,but the molecular mechanisms controlling the differentiationof the various cell types are not understood. In recent yearsplant molecular and genetic studies have led to the identificationand characterization of genes controlling the establishmentof polarity, tissue differentiation and elaboration of patternsduring embryo development. An investigation of the developmentalbasis of a number of mutant phenotypes has enabled the identificationof gene activities promoting (1) asymmetric cell division andpolarization leading to heterogeneous partitioning of the cytoplasmicdeterminants necessary for the initiation of embryogenesis (e.g.GNOM),(2) the determination of the apical-basal organization whichis established independently of the differentiation of the tissuesof the radial pattern elements (e.g.KNOLLE, FACKEL, ZWILLE),(3) the differentiation of meristems (e.g.SHOOT-MERISTEMLESS),and (4) the formation of a mature embryo characterized by theaccumulation of LEA and storage proteins. The accumulation ofthese two types of proteins is controlled by ABA-dependent regulatorymechanisms as shown using both ABA-deficient and ABA-insensitivemutants (e.g.ABA, ABI3). Both types of embryogenesis have beenstudied by different techniques and common features have beenidentified between them. In spite of the relative difficultyof identifying the original cells involved in the developmentalprocesses of somatic embryogenesis, common regulatory mechanismsare probably involved in the first stages up to the globularform. Signal molecules, such as growth regulators, have beenshown to play a role during development of both types of embryos.The most promising method for identifying regulatory mechanismsresponsible for the key events of embryogenesis willcome frommolecular and genetic analyses. The mutations already identifiedwill shed light on the nature of the genes that affect developmentalprocesses as well as elucidating the role of the various regulatorygenes that control plant embryogenesis. Key words: Development, marker, mutant, somatic embryogenesis, zygotic embryogenesis     

Direct Somatic Embryogenesis in Roots of Cichorium: Is Callose an Early Marker?

Direct somatic embryogenesis can be obtained from epidermaland cortical cells in roots from in vitro Cichorium plantlets.The first embryogenic cells are seen after six days of culturein darkness, at 35 °C, in a liquid medium supplemented withNAA (1 x 10^–7 M), 6-dimethylallyl-amino-purine (2·5x 10^–6 M), sucrose (0.03 M) and glutamine (1·7x 10^–3 M). Embryogenic cells undergo first a linear andthen a globular segmentation, with increasing cytoplasmic density.These cells and young embryoids show aniline blue fluorescence.SEM allows the same microglobular pattern to be seen on thesurface of young embryoids and on young microspores of Cichoriumused as controls. In this root system, callose deposition seemsto be an early marker in somatic embryogenesis. Somatic embryogenesis, callose, Cichorium     

Somatic Embryogenesis and Its Hormonal Regulation in Tissue Cultures of Freesia refracta

Somatic embryogenesis can be induced in tissue cultures of Freesiarefracta either directly from the epidermal cells of explants,or indirectly via intervening callus. These two pathways ofsomatic embryogenesis can be controlled and regulated by varyingthe combinations and levels of exogenous hormones. When younginflorescence segments were cultured in vitro on modified N₄(MN₄) medium supplemented with 2 mg l^–1 indoleacetic acid(IAA) and 3 mg l^–1 6-benzylaminopurine (BAP), some ofthe epidermal cells began to exhibit the features of embryogeniccells. These cells produced embryoids and developed into newplants through direct somatic embryogenesis. If the same explantswere placed on Murashige and Skoog's (MS) medium containing2 mg l^–1 IAA, 05 mg l^–1 BAP and 05 mg l^–1naphthaleneacetic acid (NAA), pale-yellow translucent nodularcalluses appeared on the surface of the explants. When thiskind of callus was transferred to MN6 medium with 2 mg l^–1IAA and 3 mg l^–1 BAP, embryoids formed which further developedinto plantlets. The regenerated plants were morphologicallynormal and possessed the normal diploid chromosome number of2n = 22. A similar result has also been obtained with youngleaf explants of this plant. The early segmentations of embryogeniccells and the development of embryoids were studied using histologicaland scanning electron microscopic techniques, and the resultshave been discussed in association with the ontogeny and originof the embryoids. Freesia refracta Klatt, somatic embryogenesis, plant regeneration, exogenous hormones     

Kit无义突变致W-3Bao小鼠生殖腺异常及纯合子贫血死亡

W-^3Bao是本研究组通过诱变获得、Kit无义突变的白斑小鼠。突变基因杂合子小鼠腹部、四肢肢端及尾尖白化,其部分精曲小管内无精原细胞。突变纯合子小鼠在胚胎后期色泽苍白、个体矮小,于出生前后死亡;血液学检查发现纯合子小鼠血色素极低且红细胞变大;18.5天胚胎的连续切片可见精曲小管轮廓欠清晰,精原细胞分散分布于睾丸间质,未迁入精曲小管;卵巢结构紊乱,无明显的原始卵泡结构;骨髓等器官组织未见显著异常。结论：Kit无义突变不仅导致了W-3Bao杂合子小鼠白斑形成及纯合子小鼠贫血死亡,同时影响生殖腺发育。     

A Maize Mutant with an Altered Vascular Pattern

A recessive maize mutant with disrupted seedling developmentwas isolated following transpositional mutagenesis with Mutator.This mutant, initially identified during germination on thebasis of abnormal growth of the scutellar node, was designatedlsn1 (l arge s cutellar n ode). The mutant seedling exhibitsan enlarged primary root with a longitudinal groove and multipleseparate root tips. The mutant root is shorter than normal,because of defective cell elongation, and lacks lateral roots.The mutant plant shows defective leaves and reduced internodeelongation. Histological analyses on primary root, shoot, scutellarnode and juvenile leaves revealed a series of defects, all relatedto an irregular differentiation of vascular elements. In addition,in situ hybridization of mutant leaves demonstrates an abnormalpattern of expression of Knotted-1, a marker of meristem function.The presence of multiple roots fused together can be interpretedas suppression of the negative control responsible for the differentiationof only one root primordium. Therefore, the data obtained onseedlings of lsn1 point to a relationship between meristem activity,vascular differentiation and auxin polar transport, and mayallow the identification of a gene which is active during embryogenesis.Copyright2000 Annals of Botany Company Auxin, defective seedling, maize, meristem activity, vascular differentiation, Zea mays.     

Sources of seasonal variability in mesozooplankton aspartate transcarbamylase activity in coastal waters off Plymouth, UK

Some investigators have proposed aspartate transcarbamylase(ATCase) activity as an overall index of mesozooplankton productivity.However, seasonal changes in mesozooplankton species compositionhave never been investigated as a possible source of variationin ATCase activity. In this study, we investigate mesozooplanktoncomposition in terms of (i) developmental stages, (ii) speciesand developmental stages body mass and (iii) species composition,and their relationship to ATCase activity. In controlled laboratoryconditions, ATCase activity variability was closely relatedto changes in somatic growth rate of the copepod Calanus helgolandicus,but was not related to changes in nucleic acid concentrations.It can be argued, however, that the activity of this enzymeis partially involved in copepod somatic productivity, and shouldbe a good index of embryogenesis. In addition, changes in ATCaseactivity were not significantly influenced by variability inmesozooplankton biomass, when investigated both on inter- andintraspecific levels. Finally, when a complete seasonal cyclewas investigated at a fixed station off Plymouth (English Channel),ATCase activity was not correlated with the abundance of anymesozooplankton species apart from copepodites and adult C.helgolandicus.Furthermore, ATCase activity measured both on mesozooplanktonand female C.helgolandicus was significantly correlated (R²= 0.72, n = 33, P < 0.001) throughout the year, apart fromApril. At that particular time of the year, ATCase activitywas in phase with the peak of abundance of copepod eggs andnauplii. It is suggested that mesozooplankton peaks of ATCaseactivity reflect two periods in the life history of the copepod:embryogenesis and terminal moult. We propose further experimentsto test this hypothesis and to promote the development of molecularbiomarkers in order to characterize specific zooplankton metabolicprocesses.     

The zebrafish mutant bumper shows a hyperproliferation of lens epithelial cells and fibre cell degeneration leading to functional blindness

The development of the eye lens is one of the classical paradigms of induction during embryonic development in vertebrates. But while there have been numerous studies aimed at discovering the genetic networks controlling early lens development, comparatively little is known about later stages, including the differentiation of secondary lens fibre cells. The analysis of mutant zebrafish isolated in forward genetic screens is an important way to investigate the roles of genes in embryogenesis. In this study we describe the zebrafish mutant bumper (bum), which shows a transient, tumour-like hyperproliferation of the lens epithelium as well as a progressively stronger defect in secondary fibre cell differentiation, which results in a significantly reduced lens size and ectopic location of the lens within the neural retina. Interestingly, the initial hyperproliferation of the lens epithelium in bum spontaneously regresses, suggesting this mutant as a valuable model to study the molecular control of tumour progression/suppression. Behavioural analyses demonstrate that, despite a morphologically normal retina, larval and adult bum^?/? zebrafish are functionally blind. We further show that these fish have defects in their craniofacial skeleton with normal but delayed formation of the scleral ossicles within the eye, several reduced craniofacial bones resulting in an abnormal skull shape, and asymmetric ectopic bone formation within the mandible. Genetic mapping located the mutation in bum to a 4 cM interval on chromosome 7 with the closest markers located at 0.2 and 0 cM, respectively.     

Phenotypic Characterization and Molecular Mapping of an acaulis2 Mutant of Arabidopsis thaliana with Flower Stalks of Much Reduced Length

An acaulis2-1 (acl2-1) mutant of Arabidopsis thaliana (L.) Heynh.was isolated and characterized. The mutant had inflorescencesof much reduced length. The defect was severer in lower internodesand was visible preferentially in type 2 metamers. The defectin the elongation of internodal cells of inflorescences wasattributable to a defect in the mechanism for elongation ofthese cells. The cortical microtubules (MTs) were analyzed inthe acl2 mutant, in a comparison with those of an acl1 mutantwhich was described earlier, but no changes were detected inamounts of MTs. In the type 2 and type 3 metamers, the defectin elongation in acl mutants was loosely correlated with a changein the orientation of MTs. Thus, the abnormal arrangement ofMTs appears to be one of the pleiotropic effects of acaulismutations. Genetic mapping was performed using molecular markers and theACL2 gene was located at 100 map units on chromosome 1. ¹Present address: Institute of Molecular and Cellular Biosciences,The University of Tokyo, Yayoi, Bunkyo-ku, Tokyo, 113 Japan ²Present address: Division of Biological Sciences, GraduateSchool of Science, Hokkaido University, Kita-ku, Sapporo, 060Japan     

Mutation in<Emphasis Type="Italic"> slowmo</Emphasis> causes defects in<Emphasis Type="Italic"> Drosophila</Emphasis> larval locomotor behaviour

We have identified a mutant slowmotion phenotype in first instar larval peristaltic behaviour of Drosophila. By the end of embryogenesis and during early first instar phases, slowmo mutant animals show a marked decrease in locomotory behaviour, resulting from both a reduction in number and rate of peristaltic contractions. Inhibition of neurotransmitter release, using targeted expression of tetanus toxin light chain (TeTxLC), in the slowmo neurons marked by an enhancer-trap results in a similar phenotype of largely absent or uncoordinated contractions. Cloning of the slowmo gene identifies a product related to a family of proteins of unknown function. We show that Slowmo is associated with mitochondria, indicative of it being a mitochondrial protein, and that during embryogenesis and early larval development is restricted to the nervous system in a subset of cells. The enhancer-trap marks a cellular component of the CNS that is seemingly required to regulate peristaltic movement.     

Auxin and heat shock activation of a novel member of the calmodulin like domain protein kinase gene family in cultured alfalfa cells

A calmodulin like domain protein kinase (CPK) homologue wasidentified in alfalfa and termed MsCPK3. The full-length sequenceof cDNA encoded a 535 amino acid polypeptide with a molecularweight of 60.2 kDa. The deduced amino acid sequence showed allthe conserved motifs that define other members of this kinasefamily, such as serine-threonine kinase domain, a junction regionand four potential Ca²⁺-binding EF sites. The recombinant MsCPK3protein purified from E. coli was activated by Ca²⁺and inhibitedby calmodulin antagonist (W-7) in in vitro phosphorylation assays.The expression of MsCPK3 gene increased in the early phase ofthe 2,4-D induced alfalfa somatic embryogenesis. Heat shockalso activated this gene while kinetin, ABA and NaCl treatmentdid not result in MsCPK3 mRNA accumulation. The data presentedsuggest that the new alfalfa CPK differs in stress responsesfrom the previously described homologues and in its potentialinvolvement in hormone and stress-activated reprogramming ofdevelopmental pathways during somatic embryogenesis. Key words: Medicago sativa, CPK, stress, 2,4-D, phosphorylation, somatic embryogenesis.     

Early Cellular Events During Direct Somatic Embryogenesis in Cotyledon Explants of Solanum aviculare Forst.

A detailed light and electron microscope study of early cellularevents at the onset of somatic embryogenesis in cotyledon explantsof Solanum aviculare Forst., cultured on MS medium supplementedwith 1 mg l^–1 2,4-dichloro-phenoxyacetic acid (2,4-D)for periods of 0–12 d in darkness, is described. Examinationsof longitudinal sections in a plane offset from the centralveins indicated that the earliest embryogenic events in explantstook place within the first 3–4 d of culture in the parenchymacells associated with the vascular traces closest to the cutbasal ends of cotyledons. Thereafter, parenchyma associatedwith more distal vascular traces became active in an apparentlysequential manner such that, by the second week of culture,progressive stages of embryogenesis could be observed alongthe lengths of cotyledon sections. Despite the fact that epidermalcells and palisade tissues were exposed directly to the 2,4-Dmedium, initiation of embryogenic development was never observedin cells other than those directly associated with vasculartraces. None of the embryogenic events characterized at theultrastructural level were observed in cotyledons cultured onMS medium in the absence of 2,4-D with the exception that starchaccumulated in decreasing amounts from the wounded basal endto the distal end of each cotyledon. This system provides a valuable model with which to study earlybiochemical and molecular events occurring in explants duringthe onset of somatic embryogenesis because they occur in a predictablefashion at sequentially situated sites along the explant tissues. Somatic embryogenesis, Solanum aviculare, cotyledon explants, cellular changes     

Amylolytic Activity and Carbohydrate Levels During the Stamen Ontogeny of a Male Fertile, and a 'Gibberellin-Sensitive' Male Sterile Mutant of Tomato (Lycopersicon esculentum)

The activity of amylases, and the level of starch and solublesugar content were analysed in the normal (+/+), a ‘gibberellin-sensitive’male sterile stamenless-2 (sl-2/sl-2) mutant, and GA³-revertedsl-2/sl-2 mutant stamens of tomato (Lycopersicon esculentumMill.), at various stages of development. In the mutant stamens,amylolytic activity did not differ from that of the normal untilthe tetrad stage, but thereafter it was significantly lowerthan that of normal stamens. The starch content also did notdiffer in the two lines at early stages of development. However,at later stages it decreased in normal stamens, whereas it remainedunchanged in the mutant. The soluble sugar content graduallyincreased during the development of normal stamens. But in mutantstamens, it remained the same throughout development and wassignificantly lower than the normal. In GA₃-reverted mutantstamens, the amylolytic activity and the level of starch andsoluble sugars were comparable to normal stamens. It is proposedthat the sl-2/sl-2 mutation, through its effects on endogenousgibberellins, affects the activity of amylases which, in turn,result in lower sugar levels leading ultimately to abnormalpollen development. Key words: Amylases, male-sterility, tomato     

Mutations that affect flightin expression in Drosophila alter the viscoelastic properties of flight muscle fibers

Striated muscles across phyla share a highly conserved sarcomere design yet exhibit broad diversity in contractile velocity, force, power output, and efficiency. Insect asynchronous flight muscles are characterized by high-frequency contraction, endurance, and high-power output. These muscles have evolved an enhanced delayed force response to stretch that is largely responsible for their enhanced oscillatory work and power production. In this study we investigated the contribution of flightin to oscillatory work using sinusoidal analysis of fibers from three flightless mutants affecting flightin expression: 1) fln⁰, a flightin null mutant, 2) Mhc¹³, a myosin rod point mutant with reduced levels of flightin, and 3) Mhc⁶, a second myosin rod point mutant with reduced levels of phosphorylated flightin. Fibers from the three mutants show deficits in their passive and dynamic viscoelastic properties that are commensurate with their effect on flightin expression and result in a significant loss of oscillatory work and power. Passive tension and passive stiffness were significantly reduced in fln⁰ and Mhc¹³ but not in Mhc⁶. The dynamic viscous modulus was significantly reduced in the three mutants, whereas the dynamic elastic modulus was reduced in fln⁰ and Mhc¹³ but not in Mhc⁶. Tension generation under isometric conditions was not impaired in fln⁰. However, when subjected to sinusoidal length perturbations, work-absorbing processes dominated over work-producing processes, resulting in no net positive work output. We propose that flightin is a major contributor to myofilament stiffness and a key determinant of the enhanced delayed force response to stretch in Drosophila flight muscles. flight muscles; muscle mutants; myosin