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organisation - the Instituto Gulbenkian de Ciência

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EVOLUTIONARY<br />

GENETICS<br />

Henrique Teotónio Principal Investigator<br />

PhD in Evolutionary Genetics, Universida<strong>de</strong> <strong>de</strong> Lisboa, Portugal, 2000<br />

Postdoc, Princeton University<br />

Postdoc, University of Oregon Eugene<br />

Principal Investigator at <strong>the</strong> IGC since 2003<br />

The study of natural selection and its consequences are central to any un<strong>de</strong>rstanding<br />

of biology because <strong>the</strong>y provi<strong>de</strong> a framework for <strong>the</strong> origin, divergence<br />

and maintenance of diversity. We are specifically investigating how <strong>the</strong><br />

interactions between mating between individuals and meiotic recombination<br />

<strong>de</strong>termine <strong>the</strong> evolution of polygenic phenotypes. For this we use populations<br />

of C. elegans with standing diversity and alternative mating systems in <strong>de</strong>mographic<br />

conditions <strong>de</strong>fined by discrete non-overlapping generations at constant<br />

high population sizes. We <strong>the</strong>n manipulate <strong>the</strong> frequency of environmental<br />

change and follow <strong>the</strong> evolution of phenotypes and genotypes in real time.<br />

Analysis of data involves computer simulations of experimental evolution un<strong>de</strong>r<br />

several selection scenarios.<br />

THE INFLUENCE OF MATING, RECOMBINATION AND NATURAL SELECTION<br />

IN C. elegans EXPERIMENTAL EVOLUTION<br />

Un<strong>de</strong>rstanding adaptation following an environmental shift is necessary to<br />

explain <strong>the</strong> evolution of biological diversity. The mechanisms thought to limit<br />

diversity mating among related individuals because <strong>the</strong>y cause inbreeding, meiotic<br />

recombination because <strong>the</strong>y <strong>de</strong>termine extent of gametic linkage among<br />

loci, and <strong>the</strong> <strong>de</strong>gree of dominance or epistatic gene interactions because <strong>the</strong>y<br />

<strong>de</strong>fine natural selection. We aim to resolve <strong>the</strong> influence of <strong>the</strong>se mechanisms<br />

on <strong>the</strong> adaptation of large populations by employing an experimental evolution<br />

approach in <strong>the</strong> androdioecious nemato<strong>de</strong> Caenorhabditis elegans un<strong>de</strong>r<br />

varying levels of outcrossing rates, initial standing genetic variation and frequency<br />

of environmental change. During experimental evolution several levels<br />

of structural organization, from fitness-proxy and life history phenotypes to<br />

genome wi<strong>de</strong> RNA expression are characterized in <strong>the</strong>ir genetic and environmental<br />

components.<br />

GROUP MEMBERS<br />

Ivo Chelo (Post-doc)<br />

Yoannis Theologidis (Post-doc)<br />

Peter Sandner (Post-doc, started in June)<br />

Sara Carvalho (PhD stu<strong>de</strong>nt)<br />

Bruno Afonso (PhD stu<strong>de</strong>nt)<br />

Christine Goy (Lab Manager)<br />

Judit Nedli (Technician, started in September)<br />

COLLABORATORS<br />

Matt Rockman (New York University, USA)<br />

Boris Shraiman (University of California, Santa Barbara, USA)<br />

FUNDING<br />

European Research Council (ERC), European Commission<br />

Human Frontiers Science Programme (HFSP)<br />

PUBLIC ENGAGEMENT IN SCIENCE<br />

Radio Interview, February<br />

The project also inclu<strong>de</strong>s hitchhiking mapping of relevant loci, by whole<br />

genome linkage disequilibrium (LD) association mapping and computer simulations<br />

of directional and balancing selection during experimental evolution.<br />

We have completed <strong>the</strong> characterization of >350 SNPs in experimentally evolved<br />

populations and <strong>the</strong> characterization of reproduction and viability un<strong>de</strong>r several<br />

osmotic and anoxic environmental stress conditions.<br />

ROLE OF GENETIC INTERACTIONS AND RECOMBINATION IN EXPERIMENTAL<br />

EVOLUTION OF C. elegans<br />

Adaptation from standing genetic variation is central to <strong>the</strong> evolution of phenotypes,<br />

yet its <strong>de</strong>pen<strong>de</strong>nce on <strong>the</strong> molecular <strong>de</strong>tails that connect genotype,<br />

phenotype, and fitness is a major unsolved problem in genetics. The effect of<br />

recombination, in particular, is expected to <strong>de</strong>pend on <strong>the</strong> extent of genetic<br />

interaction among alleles. We propose a multidisciplinary investigation of <strong>the</strong><br />

roles of recombination and genetic interactions. We will study laboratory adaptation<br />

of C. elegans populations that start with high genetic variability and are<br />

engineered to have different rates of inbreeding and outcrossing. The project<br />

integrates experimentally <strong>de</strong>termined genome-wi<strong>de</strong> genotype distributions,<br />

multidimensional phenotype (gene expression) measurements, and fitness data<br />

across 100 generations of laboratory populations that differ in <strong>the</strong>ir rates of<br />

outcrossing. This integration forms <strong>the</strong> empirical test bed for <strong>the</strong>oretical mo<strong>de</strong>ls<br />

of <strong>the</strong> role of genomic architecture in adaptation.<br />

We will test <strong>the</strong> predicted positive correlation among non-additive genetic<br />

effects and levels of linkage disequilibrium across <strong>the</strong> genome. The <strong>de</strong>rivation<br />

of three ancestral populations for experimental evolution with exclusive selfing,<br />

mixed selfing and outcrossing and obligatory outcrossing has been achieved,<br />

as well as <strong>de</strong>rivation of recombinant inbred lines from population at genetic<br />

equilibrium.<br />

IGC ANNUAL REPORT ‘11<br />

RESEARCH GROUPS<br />

65

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