CONTENT - International Society of Zoological Sciences
CONTENT - International Society of Zoological Sciences
CONTENT - International Society of Zoological Sciences
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S10 ICZ2008 - Abstracts<br />
Myogenesis in the articulate brachiopods Argyrotheca cordata<br />
(Risso, 1826), Argyrotheca cistellula (searles-wood, 1841) and<br />
Terebratalia transversa (Sowerby, 1846)<br />
Andreas Altenburger and Andreas Wanninger<br />
University <strong>of</strong> Copenhagen, Institute <strong>of</strong> Biology, Research Group for<br />
Comparative Zoology, Universitetsparken 15, Building 3, 2100<br />
Copenhagen, Denmark<br />
We investigated development and muscle formation in larvae <strong>of</strong> the<br />
articulate brachiopods Argyrotheca cordata, A. cistellula and<br />
Terebratalia transversa using immunocytochemistry combined with<br />
confocal laser scanning microscopy. Full grown larvae are threelobed<br />
and express two pairs <strong>of</strong> bristles. Muscle development in the<br />
three species investigated shows a number <strong>of</strong> similarities. As such,<br />
the first anlagen <strong>of</strong> the musculature develop in the bristle pouches<br />
and the pedicle lobe. Late-stage larvae show a network <strong>of</strong><br />
longitudinal muscles running from the apical to the pedicle lobe as<br />
well as transversal muscles situated in the apical lobe. Strong<br />
muscles attach to both the bristles pouches and the pedicle lobe. We<br />
found only few similarities between the larval myoanatomy <strong>of</strong><br />
brachiopods and the hitherto investigated representatives <strong>of</strong> the two<br />
other lophophorate phyla, Phoronida and Ectoprocta. This may be<br />
due to an early evolutionary split <strong>of</strong> the ontogenetic pathways <strong>of</strong><br />
Brachiopoda, Phoronida and Ectoprocta.<br />
The evolutionary origin <strong>of</strong> the bilaterian CNS<br />
Detlev Arendt<br />
EMBL Heidelberg, Germany<br />
Animal nervous systems are composed <strong>of</strong> neuron types specialized<br />
for functions as diverse as light perception or hormone secretion.<br />
While some animals such as cnidarians have few neuron types,<br />
human neuron types count in hundreds. Understanding the evolution<br />
<strong>of</strong> neuron types is key to understanding the evolution <strong>of</strong> animal<br />
nervous systems<br />
The recent advent <strong>of</strong> molecular fingerprints for defining cell types<br />
sets the stage the study <strong>of</strong> neuron type evolution. Each neuron type<br />
displays a unique pr<strong>of</strong>ile <strong>of</strong> expressed genes, which encode<br />
transcription factors, microRNAs and differentiation gene batteries.<br />
Since many <strong>of</strong> these genes are deeply conserved in animal evolution,<br />
this allows the identification <strong>of</strong> homologous cell types over large<br />
evolutionary distances. Molecular fingerprint comparisons also allow<br />
identifying, within a given species, sister cell types that are related by<br />
evolutionary diversification.<br />
In my lab, we are currently generating an expression pr<strong>of</strong>iling atlas<br />
for all cell types <strong>of</strong> the developing Platynereis nervous system by a<br />
novel technique, Wholemount In Silico Expression Pr<strong>of</strong>iling. This<br />
technique provides a close-to-complete inventory <strong>of</strong> neuron type<br />
molecular fingerprints in the Platynereis brain. We use this to identify<br />
homologous cell types between annelids and other bilaterians such<br />
as insects and vertebrates. This approach will be exemplified for the<br />
mushroom bodies, the associative centre <strong>of</strong> the annelid brain, and<br />
for the various types <strong>of</strong> photoreceptor cells that harbour the<br />
Platynereis brain. I will discuss the implications <strong>of</strong> these data for our<br />
understaning <strong>of</strong> the origin <strong>of</strong> the bilaterian brain.<br />
Evolution and development <strong>of</strong> the ascidian neural gland<br />
complex<br />
Hélène Auger, Shungo Kano, Laurent Legendre and Jean-Stéphane<br />
Joly<br />
INRA MSNC Group, DEPSN, Institut A. Fessard, CNRS, 1 Avenue<br />
de la Terrasse, 91198 Gif-sur-Yvette, France.<br />
The cerebral ganglion <strong>of</strong> adult ascidians is apposed to the neural<br />
gland complex. This later has three parts: a ciliated funnel, a ciliated<br />
duct and one neural gland. I will first report our progress on the study<br />
<strong>of</strong> the ciliated funnel epithelium.<br />
S11 - Evolution and Development<br />
- 38 -<br />
We have looked for genes expressed in this cell type, proposed to be<br />
related to some <strong>of</strong> the vertebrate pituitary endocrine cells. These<br />
experiments are based on in situ hybridization experiments, and on<br />
micro-array experiments on fluorescent epithelia micro-dissected<br />
from GFP expressing transgenic lines. The neural gland is another<br />
organ whose homology with vertebrate organs is still debated. It is a<br />
spongious sac with a folded epithelium. It has been suggested that it<br />
is involved in osmoregulation, with the ciliated duct generating an<br />
unidirectional influx <strong>of</strong> seawater into the neural gland. In Deyts et al.<br />
(2006), we reported that the ascidian neuropeptide G-proteincoupled<br />
receptors, the vertebrate homologues <strong>of</strong> which are involved<br />
in homeostasis, are expressed in the neural gland complex. More<br />
recently, ISH on thick sections revealed that vertebrate markers<br />
specifically found in the choroid plexus, such as Transthyretin or<br />
Gelsolin, are also expressed in the ascidian neural gland. These<br />
results highlighted similarities between the ascidian neural gland and<br />
the vertebrate circumventricular organs. Circumventricular organs<br />
are located along the midlines <strong>of</strong> vertebrate brain ventricles. They<br />
appear to be associated with multiple functions, at first as<br />
transducers <strong>of</strong> information between the blood, neurons and the<br />
cerebrospinal fluid. Among them, the vertebrate choroid plexus, a<br />
neural circumventricular organ, produces large quantities <strong>of</strong><br />
cerebrospinal fluid.<br />
These findings, together with electrophysiological experiments and<br />
cell lineage analysis through metamorphosis should allow us to<br />
determine more precisely the ontological origin and morphogenesis<br />
<strong>of</strong> the neural gland and its function in ascidians. This leads us to<br />
raise hypotheses on the origin in chordates <strong>of</strong> neuroendocrine and<br />
endocrine cell types associated with nervous system.<br />
The segmented ancestor <strong>of</strong> protostomes and the origin <strong>of</strong><br />
parasegmental patterning<br />
Guillaume Balavoine<br />
Centre de Génétique Moléculaire du CNRS, avenue de la Terrasse,<br />
91198, Gif-sur-Yvette, France<br />
The comparison <strong>of</strong> the genetic processes <strong>of</strong> segment formation in<br />
three distant groups <strong>of</strong> bilaterian metazoans (arthropods, insects and<br />
annelids) has opened a heated debate that considerably impacts on<br />
our conceptions <strong>of</strong> metazoan evolution: was the last common<br />
ancestor <strong>of</strong> protostome and deuterostome animals a metameric<br />
organism? Processes <strong>of</strong> segment formation can be divided in three<br />
steps: the proliferation <strong>of</strong> axial tissues, the production <strong>of</strong> a periodic<br />
segmentation signal along this axis and the patterning <strong>of</strong> the subparts<br />
<strong>of</strong> individual segments. While the ?cascade? <strong>of</strong> metamere<br />
patterning genes <strong>of</strong> the fruitfly and the known mechanisms <strong>of</strong> somite<br />
formation in vertebrates have little in common, intriguing similarities<br />
have been uncovered in other model animals. Gene expression and<br />
interference data suggest that the Notch pathway may be involved in<br />
synchronising a periodic segmental signal in some arthropods<br />
(spiders, centipedes) in a similar way as in vertebrates. Also, a<br />
number <strong>of</strong> genes have been shown to present similar ?segment<br />
polarity? patterns in the marine annelid Platynereis dumerilii and<br />
arthropods. Pharmacological treatments suggest that the hedgehog<br />
pathway is involved in regulating the individual segmental patterns in<br />
Platynereis in the same way as in arthropods. The spatial<br />
relationships between these annelid ?segment polarity? patterns are<br />
remarkably similar to their arthropod homologues and leave few<br />
doubts on the segmented architecture <strong>of</strong> the protostome ancestor<br />
body. Additionally, they suggest that annelid segments are<br />
homologous with arthropod parasegments. A scenario for the origin<br />
<strong>of</strong> arthropod parasegmental patterning is proposed.