Search results for "METAMORPHOSIS"
showing 10 items of 93 documents
The ultrastructure of the thread-hairs on the cerci of the cockroach Periplaneta americana L.: The intermoult phase
1976
The structure of the thread-hairs on the cerci of the cockroach Periplaneta american during the intermoult phase has been investigated by scanning and transmission electron microscopy. The present study demonstrates that to each thread-hair belong one sensory cell, two glial cells, and three enveloping cells. The data indicate that: (a) the inner glial cells, which may have a trophic function, sends fingerlike processes into the cytoplasm of the senory cell body; (b) the internal enveloping cell forms the dendritic sheath; (c) the middle enveloping cell corresponds to the trichogen cell and the external enveloping cell to the tormogen cell; (d) the outer dendritic segment terminates in a ca…
Brains in metamorphosis: reprogramming cell identity within the central nervous system
2014
During embryonic development, uncommitted pluripotent cells undergo progressive epigenetic changes that lock them into a final differentiated state. Can mammalian cells change identity within the living organism? Direct lineage reprogramming of cells has attracted attention as a means to achieve organ regeneration. However, it is unclear whether cells in the CNS are endowed with the plasticity to reprogram. Neurons in particular are considered among the most immutable cell types, able to retain their class-specific traits for the lifespan of the organism. Here we focus on two experimental paradigms, glia-to-neuron and neuron-to-neuron conversion, to consider how lineage reprogramming has ch…
GAL4-responsive UAS- tau as a tool for studying the anatomy and development of the Drosophila central nervous system
1997
To improve the quality of cytoplasmic labelling of GAL4-expressing cells in Drosophila enhancer-trap and transgenic strains, a new GAL4-responsive reporter UAS-tau, which features a bovine tau cDNA under control of a yeast upstream activation sequence (UAS), was tested. Tau, a microtubule-associated protein, is distributed actively and evenly into all cellular processes. Monoclonal anti-bovine Tau antibody reveals the axonal structure of the labelled cells with detail similar to that of Golgi impregnation. We demonstrate that the UAS-tau system is especially useful for studying processes of differentiation and reorganisation of identified neurones during postembryonic development.
Cloning and characterization of new orphan nuclear receptors and their developmental profiles duringTenebriometamorphosis
1999
Five PCR fragments corresponding to a part of the DNA-binding domain of different hormone nuclear receptors were isolated from Tenebrio molitor mRNAs. The sequence identity of three of them with known Drosophila nuclear receptors strongly suggests that they are the Tenebrio orthologs of seven-up, DHR3 and β-FTZ-F1, and thus named Tmsvp, TmHR3 and TmFTZ-F1. The full-length sequences of the other two were established. TmHR78 is either a new receptor of the DHR78 family or the same gene which has evolved rapidly, particularly in the E domain. TmGRF belongs to the GCNF1 family and its in vitro translated product binds to the extended half site TCAAGGTCA with high affinity. The periods of expres…
Salinity effects on asexual reproduction of Carybdea sp. (Cnidaria: Cubozoa)
2014
6 pages, 2 figures, 1 table, supplementary data http://plankt.oxfordjournals.org/content/36/2/585/suppl/DC1
Ultrafast Metamorphosis of a Complex Charge Density Wave in Tantalumdiselenite
2016
Using ultrafast electron diffraction, we record the transformation between a nearly-commensurate and an incommensurate charge-density-wave in 1T-TaS2, which takes place orders of magnitude faster than previously observed for commensurate-to-incommensurate transitions.
Identification, sequence and mRNA expression pattern during metamorphosis of a cDNA encoding a glycine-rich cuticular protein in Tenebrio molitor
1995
The study of insect cuticular proteins and their sequences is of interest because they are involved in protein-protein and protein-chitin interactions which confer the mechanical properties and fine architecture of the cuticle. Moreover, in the coleopteran Tenebrio molitor there is a dramatic change in cuticular architecture between pre- and postecdysial secretion. We report the isolation, by differential screening, and the sequence characterization of a cDNA clone encoding a cuticular protein of T. molitor, ACP17. After insertion in the expression vector pEX1, the recognition of the fusion protein by an anti-cuticular monoclonal antibody confirmed the cuticular nature of ACP17. Northern hy…
Molecular cloning and expression of Tenebrio molitor ultraspiracle during metamorphosis and in vivo induction of its phosphorylation by 20-hydroxyecd…
2000
Using a RT-PCR approach, the Tenebrio molitor homologue of Drosophila Ultraspiracle (TmUSP) was characterized. Its DNA binding domain shows a degree of identity with those of the other insect USPs. However, the ligand binding domain is closer to those of retinoid X receptors. Using an antibody raised against DmUSP, Western blot analysis of proteins from epidermis and other tissues revealed five immunoreactive bands, corresponding to different phosphorylated forms of a unique polypeptide, as shown by lambda-phosphatase treatment. The nuclear form of TmUSP seems unphosphorylated. An in vivo 20-hydroxyecdysone treatment increases considerably and rapidly the phosphorylated forms of TmUSP. This…
Cloning and Sequencing of a cDNA Encoding a Larval-Pupal-Specific Cuticular Protein in Tenebrio Molitor (Insecta, Coleoptera). Developmental Expressi…
1996
A cDNA clone encoding a larval-pupal cuticular protein, named TMLPCP-22, has been isolated by screening a library in expression vector with a monoclonal antibody made against pupal cuticular proteins of Tenebrio molitor. Northern-blot and in situ hybridization analyses showed that the expression of TMLPCP-22 is regulated in a stage-specific and tissue-specific manner; the transcript was present during the secretion of preecdysial larval and pupal cuticles and was restricted to epidermal cells. No expression was observed during adult cuticle deposition. In supernumerary pupae obtained after application of a juvenile hormone analogue, which is known to inhibit the adult programme, TMLPCP-22 m…
Ultrastructural changes of the oenocytes of Gryllus bimaculatus DEG (Saltatoria, Insecta) during the moulting cycle
1974
1. The oenocytes of Gryllus bimaculatus are characterized by an abundant smooth-surfaced ER (ATER). In spite of the great cell size the plasma membrane never shows extensive infoldings during the moulting cycle. In addition to mitochondria there are very large numbers of microbodies containing peroxidase but apparently not uricase. Within the second part of the instar the microbodies lie along the clefts which run through the whole cell. 2. The following changes are observed in the course of a moulting cycle: Immediately after hatching the ATER is scarcely developed, some liposomes are located within areas of ATER disappearing some hours later. 20 hours after emergence glycogen deposits app…