Mail Address: Comparative
Genomics Centre,
Molecular Sciences Bldg
21, James Cook University,
Townsville, 4811, Queensland,
Australia
Telephone: 61-7-4781 6265
Fax: 61-7-4781 6078

| Our understanding of metazoan genome evolution is based on a small number of complete genome sequences and large EST (Express Sequence Tags) datasets that represent only a few complex animals. Of necessity, therefore, deductions about the evolutionary origins and structures of human genes are largely based on comparisons with the genomes of the insects Drosophila melanogaster and Anopheles gambiae, the nematode Caenorhabditis elegans and the yeasts Saccharomyces cerevisiae and Schizosaccharomyces pombe. The study of the evolution of developmental genes has identified some spectacular examples of conservation of developmental programs, particularly between D. melanogaster and vertebrates. However, a significant number of D. melanogaster and C. elegans genes are highly modified, and the extent of gene loss in these organisms is unknown. Substantial differences between the D. melanogaster and C. elegans genomes, together with the fact that the nematodes and arthropods are now regarded as more closely related than was previously the case, imply that comparisons based only on these organisms may give a misleading view of the ancestral metazoan. |
In terms of understanding the evolution of metazoan genetic and
developmental complexity, the Cnidaria are likely to be critically important,
as this phylum is regarded as the sister group to the Bilateria. For these
reasons, we are using a local cnidarian, the reef-building coral Acropora,
as a model system in order to investigate several issues central to the
evolution of developmental mechanisms. Over the last few years, we
have established most of the standard molecular methods (in situ hybridisation
technology etc.) and tools (genetic libraries etc.) for Acropora, and this
has lead to increasing recognition of its value as a comparator by the
international community. At present we are using Acropora to address several
questions that are central to nervous system development and the evolution
of developmental mechanisms.
Anthozoan cnidarians such as Acropora possess the most 'primitive'
present-day nervous systems, a morphologically homogeneous nerve net. However,
an ongoing EST project that we are carrying out has identified a large
number of genes involved in specifying and patterning the advanced nervous
systems of flies and mammals. We have shown that several of these genes
are expressed in the coral in patterns that resemble those seen in vertebrates.
In addition, the cnidarian nervous system appears to be entirely dispensable,
as it is possible to indefinitely culture hydra after destroying all nerve
cells and the interstitial cells that give rise to them. Therefore despite
its apparent simplicity, plasticity and regenerative capabilities, the
cnidarian nervous system is patterned by genes related to those of vertebrates.
Cnidarians are therefore potentially highly informative for many aspects
of nervous system specification and regeneration.
| We use Acropora as a model for understanding the evolutionary
processes affecting sessile marine invertebrates in general, as these appear
to evolve in very different ways to the terrestrial animals upon which
much of our understanding of evolutionary processes is based. One of the
major differences between these systems is that many sessile marine invertebrates
release their gametes into the water column where fertilization takes place.
This creates unparalleled opportunities for interspecific hybridization
and introgression between species, as has been documented for many species
of reef corals. Molecular data and experimental breeding trials have confirmed
that interspecific hybridisation occurs and is likely to have contributed
to the evolution of modern Indo-Pacific coral species including the genus
Acropora
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Coral spawning is an intense period of activity for us as, over a period of a few days each year, we try to collect and preserve sufficient embryonic and larval coral material to sustain lab activities for the rest of the year. We also carry out many experiments on the reproductive and developmental biology of Acropora at that time. Fieldwork during coral spawning is generally carried out from Magnetic sland, and takes place following the full moon in mid-late October. The fact that the main reefs generally spawn one lunar month after inshore reefs (such as those around Magnetic Island enables us also to collect material from the Universityís research station on Orpheus Island if we need to. We have also carried out fieldwork on the West Australian reefs, which spawn during autumn rather than spring |
| All reef-building corals form obligate symbioses with unicellular algae belonging to the dinoflagellate genus Symbiodinium (nominally a single genus but actually a highly diverse group of organisms) the ability of corals to calcify at rates required to build reefs requires high levels of photosynthesis in their algal symbionts. We are interested in both basic and evolutionary genetics of dinoflagellate. Dinoflagellates are unique eukaryotes in many ways for example, components of their light-harvesting complexes are unrelated to any known proteins, and they do not contain true histone proteins. Little is known about the molecular basis of the interaction of the algae with their coral hosts, nor about the specificity of the interaction. |
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Graduate Students
Comparative Genomics Centre, Center, James Cook University, Key words: Coral, Genetics, gene, genome, DNA, linkage, Autoimmune diabetes, Type 1 diabetes mellitus, childhood diabetes, lupus, systemic lupus erythematosus, haemolytic anaemia, hemolytic anemia, Coombs' test, antinuclear antibodies, renal failure, glomerulonephritis, gastritis, type A gastritis, pernicious anemia.