Expression of the Drosophila optomotor-blind gene transcript in neuronal and glial cells of the developing nervous system

Development ◽  
1993 ◽  
Vol 117 (3) ◽  
pp. 1017-1029 ◽  
Author(s):  
B. Poeck ◽  
A. Hofbauer ◽  
G.O. Pflugfelder

Mutations in the complex gene locus optomotor-blind (omb) can lead to defects in the development of both the optic lobes and external features of the adult fly. We describe here the expression of omb in the developing and adult nervous system using in situ hybridization. During embryogenesis, omb expression is first observed in the optic lobe anlagen. It later expands to a larger part of the developing larval brain and to the gnathal lobes. Cells in the ventral and peripheral nervous systems begin to express omb after completion of germ band extension. Later in embryonic development, expression declines and only persists in the antennomaxillary complex and in part of the brain hemispheres. During the larval and pupal stages, omb expression in the brain is confined to the developing optic lobes and contiguous regions of the central brain. At these stages, only a few cells show expression in the ventral ganglion. In the eye imaginal disc, transcript accumulation is most conspicuous in a group of presumptive glia precursor cells posterior to the morphogenetic furrow and in the optic stalk. In the adult brain, expression is prominent in several regions of the optic lobe cortex and along the border between central brain and optic lobes. In the mutation In(1)ombH31, 40 kb of regulatory DNA, downstream from the transcription unit, are removed from the omb gene. In(1)ombH31 is characterized by the lack of a set of giant interneurons from the lobula plate of the adult optic lobes. We find that, already during embryogenesis, there is a drastic difference between wild type and In(1)ombH31 in the level of the omb transcript in the optic lobe primordia. The adult mutant phenotype may thus be caused by omb misexpression during embryonic development.

Author(s):  
Shiori Kobayashi ◽  
Chitoshi Takayama ◽  
Yuzuru Ikeda

Among invertebrates, cephalopods have one of the most well-organized nervous systems. However, with respect to the ontogeny of the nervous system, the post-embryonic development of the cephalopod brain has only been documented for a few species. Here, we investigated the development of the brain of captive oval squid Sepioteuthis lessoniana during the post-hatching phase. The central part of the brain of the oval squid is divided into four main regions, namely, the supraoesophageal, anterior suboesophageal, middle suboesophageal, and posterior suboesophageal masses, each consisting of several lobes. At various ages in juvenile squid, the total volume of the central part of the brain (except the optic lobe) is significantly correlated with its body size, indicated by mantle length and wet body weight. The vertical lobe, superior frontal lobe, and anterior subesophageal mass drastically increase in relative volume as the squid grows. In contrast, the middle suboesophageal mass and posterior suboesophageal mass do not increase in volume with increasing squid age and body size. The effects of these results have been discussed in relation to the onset of squid behaviours during post-hatching.


2001 ◽  
Vol 204 (2) ◽  
pp. 305-314 ◽  
Author(s):  
A. Nighorn ◽  
P.J. Simpson ◽  
D.B. Morton

Guanylyl cyclases are usually characterized as being either soluble (sGCs) or receptor (rGCs). We have recently cloned a novel guanylyl cyclase, MsGC-I, from the developing nervous system of the hawkmoth Manduca sexta that cannot be classified as either an sGC or an rGC. MsGC-I shows highest sequence identity with receptor guanylyl cyclases throughout its catalytic and dimerization domains, but does not contain the ligand-binding, transmembrane or kinase-like domains characteristic of receptor guanylyl cyclases. In addition, MsGC-I contains a C-terminal extension of 149 amino acid residues. In this paper, we report the expression of MsGC-I in the adult. Northern blots show that it is expressed preferentially in the nervous system, with high levels in the pharate adult brain and antennae. In the antennae, immunohistochemical analyses show that it is expressed in the cell bodies and dendrites, but not axons, of olfactory receptor neurons. In the brain, it is expressed in a variety of sensory neuropils including the antennal and optic lobes. It is also expressed in structures involved in higher-order processing including the mushroom bodies and central complex. This complicated expression pattern suggests that this novel guanylyl cyclase plays an important role in mediating cyclic GMP levels in the nervous system of Manduca sexta.


Author(s):  
Karl Zilles ◽  
Nicola Palomero-Gallagher

The pre- and post-natal development of the human nervous system is briefly described, with special emphasis on the brain, particularly the cerebral and cerebellar cortices. The central nervous system originates from a specialized region of the ectoderm—the neural plate—which develops into the neural tube. The rostral part of the neural tube forms the adult brain, whereas the caudal part (behind the fifth somite) differentiates into the spinal cord. The embryonic brain has three vesicular enlargements: the forebrain, the midbrain, and the hindbrain. The histogenesis of the spinal cord, hindbrain, cerebellum, and cerebral cortex, including myelination, is discussed. The chapter closes with a description of the development of the hemispheric shape and the formation of gyri.


1995 ◽  
Vol 347 (1320) ◽  
pp. 139-154 ◽  

Neuropeptide-immunoreactive neurons have been mapped by immunocytochemistry in whole-mount preparations and sections of the central nervous system of Oniscus asellus . We tested rabbit antisera against decapod crustacean hyperglycemic hormone (CHH), moult inhibiting hormone (MIH ), pigment dispersing hormone (PDH) and red pigment concentrating hormone (RPCH). four CHH- and three PDH-immunoreactive neurons localized in the superior median protocerebrum of the brain constitute neurosecretory pathways to the neurohaemal sinus gland. No immunoreactive structures have been detected with an antiserum against MIH of Carcinus maenus . Another, newly identified neurosecretory pathway is formed by a group of RPCH-immunoreactive neurons in the mandibular ganglion. These neurons project to the neurohaemal lateral cephalic nerve plexus, further PDH- and RPCH-immunoreactive neurons and fibres occur in the brain and the ventral nerve cord (VNC). Two groups of PDH-immunoreactive neurons supply brain and optic lobe neuropils, the bases of the ommatidia, and probably give rise to descending fibres innervating all VNC-neuropils. Two groups and five individuals of RPCH-immunoreactive neurons that innervate several brain neuropils or occur as ascending neurons in the VNC have been reconstructed. The CHH-immunoreactive neurons, and distinct types of PDH- and RPCH-immunoreactive neurons obviously belong to classical hormone-producing neurosecretory pathways. At least the CHH-immunoreactive cells seem to be part of an isopod homologue of the decapod X-organ. The existence of other PDH- and RPCH-immunoreactive interneurons suggests additional functions of these peptides as neurotransmitters or neuromodulators, which is in agreement with similar observations in the decapod central nervous system.


Development ◽  
2001 ◽  
Vol 128 (10) ◽  
pp. 1757-1769 ◽  
Author(s):  
C. Olivier ◽  
I. Cobos ◽  
E.M. Perez Villegas ◽  
N. Spassky ◽  
B. Zalc ◽  
...  

Oligodendrocytes are the myelin-forming cells in the central nervous system. In the brain, oligodendrocyte precursors arise in multiple restricted foci, distributed along the caudorostral axis of the ventricular neuroepithelium. In chick embryonic hind-, mid- and caudal forebrain, oligodendrocytes have a basoventral origin, while in the rostral fore-brain oligodendrocytes emerge from alar territories (Perez Villegas, E. M., Olivier, C., Spassky, N., Poncet, C., Cochard, P., Zalc, B., Thomas, J. L. and Martinez, S. (1999) Dev. Biol. 216, 98–113). To investigate the respective territories colonized by oligodendrocyte progenitor cells that originate from either the basoventral or alar foci, we have created a series of quail-chick chimeras. Homotopic chimeras demonstrate clearly that, during embryonic development, oligodendrocyte progenitors that emerge from the alar anterior entopeduncular area migrate tangentially to invade the entire telencephalon, whereas those from the basal rhombomeric foci show a restricted rostrocaudal distribution and colonize only their rhombomere of origin. Heterotopic chimeras indicate that differences in the migratory properties of oligodendroglial cells do not depend on their basoventral or alar ventricular origin. Irrespective of their origin (basal or alar), oligodendrocytes migrate only short distances in the hindbrain and long distances in the prosencephalon. Furthermore, we provide evidence that, in the developing chick brain, all telencephalic oligodendrocytes originate from the anterior entopeduncular area and that the prominent role of anterior entopeduncular area in telencephalic oligodendrogenesis is conserved between birds and mammals.


The tracheal supply to the central nervous system of the locust has been revealed by staining with cobalt sulphide. Air that enters through the first pair of thoracic spiracles is carried first to the brain and then to the rest of the central nervous system. The air is expelled through the abdominal spiracles, so that there is a one-way circulation with diffusional exchange only in the blindly ending tracheae that enter the brain or ganglia. Once inside a ganglion, the tracheae branch profusely to end in a mass of fine tracheoles through which gaseous exchange takes place. The densest tracheation is in the neuropile areas, where the spacing between tracheoles is about 17 μm. In the optic lobes, where there is order to the synaptic arrangement of a neuropile, there is a matching orderliness of the tracheation. Cortical areas, which contain the cell bodies of neurons, have only a sparse tracheation. It may be concluded that it is the processes associated with synaptic transmission that require the most immediate access to the sites of gaseous exchange.


2004 ◽  
Vol 47 (4) ◽  
pp. 635-641 ◽  
Author(s):  
Paula Andréa Oliveira Soares ◽  
Jacques Hubert Charles Delabie ◽  
José Eduardo Serrão

Neuropile is the region of the central nervous system where the synapses and neurons branching occur. During the development of an holometabolous insect can occurs break of the neurons fibers forming new axon and dendrites and their distribution in brain neuropile is organized so as to reflect specific nervous functions of adult insects. The components of this organization were observed and discussed in this study in the ant Acromyrmex octospinosus, evidencing similar features to those described for A. subterraneus subterraneus, among other insects for the which ones this information is available.


Hereditas ◽  
2021 ◽  
Vol 158 (1) ◽  
Author(s):  
Christine Klöppel ◽  
Kirsten Hildebrandt ◽  
Dieter Kolb ◽  
Nora Fürst ◽  
Isabelle Bley ◽  
...  

Abstract Background The Drosophila brain is an ideal model system to study stem cells, here called neuroblasts, and the generation of neural lineages. Many transcriptional activators are involved in formation of the brain during the development of Drosophila melanogaster. The transcription factor Drosophila Retinal homeobox (DRx), a member of the 57B homeobox gene cluster, is also one of these factors for brain development. Results In this study a detailed expression analysis of DRx in different developmental stages was conducted. We show that DRx is expressed in the embryonic brain in the protocerebrum, in the larval brain in the DM and DL lineages, the medulla and the lobula complex and in the central complex of the adult brain. We generated a DRx enhancer trap strain by gene targeting and reintegration of Gal4, which mimics the endogenous expression of DRx. With the help of eight existing enhancer-Gal4 strains and one made by our group, we mapped various enhancers necessary for the expression of DRx during all stages of brain development from the embryo to the adult. We made an analysis of some larger enhancer regions by gene targeting. Deletion of three of these enhancers showing the most prominent expression patterns in the brain resulted in specific temporal and spatial loss of DRx expression in defined brain structures. Conclusion Our data show that DRx is expressed in specific neuroblasts and defined neural lineages and suggest that DRx is another important factor for Drosophila brain development.


1957 ◽  
Vol 34 (3) ◽  
pp. 378-393
Author(s):  
M. J. WELLS ◽  
J. WELLS

1. Blind octopuses were trained to make tactile discriminations between the members of pairs of objects and their performance was compared with that of other blind animals having. parts of the brain removed. 2. It was found that removal of the optic lobes, together constituting more than half of the total mass of the brain, did not affect the performance of animals in these discrimination 3. Removal of the vertical lode, on the other hand, produced deficiencies proportiante to the amount d tissue removed; these deficiencies were mat marked in the cose of the more difIicult of the two discrimination problems used in the tests. 4. It was possible to compensate for loss of the vertical lobe to a considerable extent by arranging trials at more frequent intervals. Animals unable to learn a tactile discrimination when trained at rate of 8 trials per day did so when trained at 40 trials per day. 5. When animals trained at the latter rate were subjected to reversed training, thoselacking the vertical lobe re-learned in fewer trials than controls, indicating shorter persistence of the effects of pre-reversal training. 6. It is concluded that the vertical lobe is concerned with the persistence of conditions set up in the nervous system as a result of sensory experience. It is not known whether the vertical lobe serves to increase the initial intensity of these conditions, or to delay their decay.


Endocrinology ◽  
2010 ◽  
Vol 151 (11) ◽  
pp. 5550-5558 ◽  
Author(s):  
Arturo Hernandez ◽  
Laure Quignodon ◽  
M. Elena Martinez ◽  
Frederic Flamant ◽  
Donald L. St. Germain

The type 3 deiodinase (D3) is an enzyme that inactivates thyroid hormones (TH) and is highly expressed during development and in the central nervous system. D3-deficient (D3KO) mice develop markedly elevated serum T3 level in the perinatal period. In adulthood, circulating T4 and T3 levels are reduced due to functional deficits in the thyroid axis and peripheral tissues (i.e. liver) show evidence of decreased TH action. Given the importance of TH for brain development, we aimed to assess TH action in the brain of D3KO mice at different developmental stages and determine to what extent it correlates with serum TH parameters. We used a transgenic mouse model (FINDT3) that expresses the reporter gene β-galactosidase (β-gal) in the central nervous system as a readout of local TH availability. Together with experiments determining expression levels of TH-regulated genes, our results show that after a state of thyrotoxicosis in early development, most regions of the D3KO brain show evidence of decreased TH action at weaning age. However, later in adulthood and in old age, the brain again manifests a thyrotoxic state, despite reduced serum TH levels. These region-specific changes in brain TH status during the life span of the animal provide novel insight into the important role of the D3 in the developing and adult brain. Our results suggest that, even if serum concentrations of TH are normal or low, impaired D3 activity may result in excessive TH action in multiple brain regions, with potential consequences of altered neural function that may be of clinical relevance to neurological and neuroendocrine disorders.


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