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11th ICRS Abstract book - Nova Southeastern University

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Poster Mini-Symposium 6: Ecological and Evolutionary Genomics of Coral Reef Organisms<br />

6.160<br />

Intracolonial Genotypic Variations And Heterozygosity Excess Of A Scleractinian<br />

Coral Pocillopora Damicornis<br />

Shang-Ru YEOH 1 , Chang-Feng DAI* 1<br />

1 Institute of Oceanography, National Taiwan <strong>University</strong>, Taipei, Taiwan<br />

The naturally occurring intraorganismal genetic heterogeneity (IGH) and heterozygosity<br />

excess of Pocillopora damicornis populations were studied in southern Taiwan. Two<br />

populations of P. damicornis were sampled exhaustively in a fine-scale and an additional<br />

population was sampled randomly for index comparisons (n = 107). Identities of colonies<br />

were characterized genotypically with seven microsatellite markers. Both genuine<br />

clonemates (colonies with identical multilocus genotypes) and genotypic varieties that<br />

differed only slightly from them were found. In order to discern whether these genotypic<br />

varieties were the coincidental products of sexual reproductions, we redefined the clones<br />

into clonal lineages (genuine clonemates and their closely-related clonal varieties) with a<br />

threshold value determined from the frequency histogram of pairwise genotypic distances<br />

between all multilocus genotype (MLG)-pairs under the infinite allele model (IAM). Ten<br />

distinct clonal lineages (C1 to C10) were defined and intracolonial genetic variations<br />

were observed in all but one clonal lineage, suggesting that autonomous genetic changes<br />

such as somatic mutations and mitotic gene conversions might occur frequently in the<br />

clonal population of P. damicornis. Moreover, allele-sharings among several clonal<br />

lineages were also observed, implying that allogeneic fusions might occur between<br />

individuals of newly settled larvae and young colonies, either intraclonally or<br />

interclonally. In addition, heterozygosity excess, a phenomenon that was rarely observed<br />

in the sessile marine invertebrates, was found to prevail in all three populations. This<br />

observation was probably a result derived from an interplay between negative assortative<br />

mating, selection for heterozygotes, and asexual reproductions.<br />

6.161<br />

Comparative Coral Mitogenomics And Its Application To Phylogenetic, Population<br />

Genetic And Biodiversity Studies<br />

Jean-François FLOT* 1 , Simon TILLIER 1<br />

1 Département Systématique et Evolution, Muséum National d'Histoire Naturelle, Paris,<br />

France<br />

The mitochondrial genomes of scleractinian corals used to be considered uniform in<br />

terms of gene content and order (Medina et al. 2006) as all corals sequenced had been<br />

found to conform to the Acropora tenuis model (van Oppen et al. 2002). Moreover, the<br />

apparently slow rate of evolution of coral mitochondrial DNA (Shearer et al. 2002) was<br />

generally thought to preclude its use in population genetic studies (Hellberg 2006).<br />

New data, however, have started to emerge that challenge this view: the mitochondrial<br />

genome of Pocillopora contains two hypervariable regions, located respectively in an<br />

intergenic region and in a novel open reading frame (ORF) (Flot and Tillier 2007). This<br />

ORF is also present in Madracis, Seriatopora and Stylophora, and we have observed<br />

other original gene arrangements involving for instance the duplication of a tRNA gene.<br />

In Pocillopora, hypervariable regions appear variable enough for population genetic<br />

studies: this shows that, in some groups of corals at least, mitochondrial sequence<br />

markers can be much more useful than previously thought.<br />

Flot J-F, Tillier S (2007) The mitochondrial genome of Pocillopora (Cnidaria:<br />

Scleractinia) contains two variable regions: The putative D-loop and a novel ORF of<br />

unknown function. Gene 401:80-87<br />

Hellberg M (2006) No variation and low synonymous substitution rates in coral mtDNA<br />

despite high nuclear variation. BMC Evol Biol 6:24<br />

Medina M, Collins AG, Takaoka TL, Kuehl JV, Boore JL (2006) Naked corals: skeleton<br />

loss in Scleractinia. Proc Natl Acad Sci U S A 103:9096-9100<br />

Shearer TL, van Oppen MJH, Romano SL, Wörheide G (2002) Slow mitochondrial DNA<br />

sequence evolution in the Anthozoa (Cnidaria). Mol Ecol 11:2475-2487<br />

van Oppen MJ, Catmull J, McDonald BJ, Hislop NR, Hagerman PJ, Miller DJ (2002)<br />

The mitochondrial genome of Acropora tenuis (Cnidaria; Scleractinia) contains a large<br />

group I intron and a candidate control region. J Mol Evol 55:1-13<br />

303

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