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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.

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