Project acronym AGINGSEXDIFF
Project Aging Differently: Understanding Sex Differences in Reproductive, Demographic and Functional Senescence
Researcher (PI) Alexei Maklakov
Host Institution (HI) UPPSALA UNIVERSITET
Call Details Starting Grant (StG), LS8, ERC-2010-StG_20091118
Summary Sex differences in life span and aging are ubiquitous across the animal kingdom and represent a
long-standing challenge in evolutionary biology. In most species, including humans, sexes differ not
only in how long they live and when they start to senesce, but also in how they react to
environmental interventions aimed at prolonging their life span or decelerating the onset of aging.
Therefore, sex differences in life span and aging have important implications beyond the questions
posed by fundamental science. Both evolutionary reasons and medical implications of sex
differences in demographic, reproductive and physiological senescence are and will be crucial
targets of present and future research in the biology of aging. Here I propose a two-step approach
that can provide a significant breakthrough in our understanding of the biological basis of sex
differences in aging. First, I propose to resolve the age-old conundrum regarding the role of sexspecific
mortality rate in sex differences in aging by developing a series of targeted experimental
evolution studies in a novel model organism – the nematode, Caenorhabditis remanei. Second, I
address the role of intra-locus sexual conflict in the evolution of aging by combining novel
methodology from nutritional ecology – the Geometric Framework – with artificial selection
approach using the cricket Teleogryllus commodus and the fruitfly Drosophila melanogaster. I will
directly test the hypothesis that intra-locus sexual conflict mediates aging by restricting the
adaptive evolution of diet choice. By combining techniques from evolutionary biology and
nutritional ecology, this proposal will raise EU’s profile in integrative research, and contribute to
the training of young scientists in this rapidly developing field.
Summary
Sex differences in life span and aging are ubiquitous across the animal kingdom and represent a
long-standing challenge in evolutionary biology. In most species, including humans, sexes differ not
only in how long they live and when they start to senesce, but also in how they react to
environmental interventions aimed at prolonging their life span or decelerating the onset of aging.
Therefore, sex differences in life span and aging have important implications beyond the questions
posed by fundamental science. Both evolutionary reasons and medical implications of sex
differences in demographic, reproductive and physiological senescence are and will be crucial
targets of present and future research in the biology of aging. Here I propose a two-step approach
that can provide a significant breakthrough in our understanding of the biological basis of sex
differences in aging. First, I propose to resolve the age-old conundrum regarding the role of sexspecific
mortality rate in sex differences in aging by developing a series of targeted experimental
evolution studies in a novel model organism – the nematode, Caenorhabditis remanei. Second, I
address the role of intra-locus sexual conflict in the evolution of aging by combining novel
methodology from nutritional ecology – the Geometric Framework – with artificial selection
approach using the cricket Teleogryllus commodus and the fruitfly Drosophila melanogaster. I will
directly test the hypothesis that intra-locus sexual conflict mediates aging by restricting the
adaptive evolution of diet choice. By combining techniques from evolutionary biology and
nutritional ecology, this proposal will raise EU’s profile in integrative research, and contribute to
the training of young scientists in this rapidly developing field.
Max ERC Funding
1 391 904 €
Duration
Start date: 2010-12-01, End date: 2016-05-31
Project acronym AVIAN DIMORPHISM
Project The genomic and transcriptomic locus of sex-specific selection in birds
Researcher (PI) Judith Elizabeth Mank
Host Institution (HI) University College London
Call Details Starting Grant (StG), LS8, ERC-2010-StG_20091118
Summary It has long been understood that genes contribute to phenotypes that are then the basis of selection. However, the nature and process of this relationship remains largely theoretical, and the relative contribution of change in gene expression and coding sequence to phenotypic diversification is unclear. The aim of this proposal is to fuse information about sexually dimorphic phenotypes, the mating systems and sexually antagonistic selective agents that shape sexual dimorphism, and the sex-biased gene expression patterns that encode sexual dimorphisms, in order to create a cohesive integrated understanding of the relationship between evolution, the genome, and the animal form. The primary approach of this project is to harnesses emergent DNA sequencing technologies in order to measure evolutionary change in gene expression and coding sequence in response to different sex-specific selection regimes in a clade of birds with divergent mating systems. Sex-specific selection pressures arise in large part as a consequence of mating system, however males and females share nearly identical genomes, especially in the vertebrates where the sex chromosomes house very small proportions of the overall transcriptome. This single shared genome creates sex-specific phenotypes via different gene expression levels in females and males, and these sex-biased genes connect sexual dimorphisms, and the sexually antagonistic selection pressures that shape them, with the regions of the genome that encode them.
The Galloanserae (fowl and waterfowl) will be used to in the proposed project, as this clade combines the necessary requirements of both variation in mating systems and a well-conserved reference genome (chicken). The study species selected from within the Galloanserae for the proposal exhibit a range of sexual dimorphism and sperm competition, and this will be exploited with next generation (454 and Illumina) genomic and transcriptomic data to study the gene expression patterns that underlie sexual dimorphisms, and the evolutionary pressures acting on them. This work will be complemented by the development of mathematical models of sex-specific evolution that will be tested against the gene expression and gene sequence data in order to understand the mechanisms by which sex-specific selection regimes, arising largely from mating systems, shape the phenotype via the genome.
Summary
It has long been understood that genes contribute to phenotypes that are then the basis of selection. However, the nature and process of this relationship remains largely theoretical, and the relative contribution of change in gene expression and coding sequence to phenotypic diversification is unclear. The aim of this proposal is to fuse information about sexually dimorphic phenotypes, the mating systems and sexually antagonistic selective agents that shape sexual dimorphism, and the sex-biased gene expression patterns that encode sexual dimorphisms, in order to create a cohesive integrated understanding of the relationship between evolution, the genome, and the animal form. The primary approach of this project is to harnesses emergent DNA sequencing technologies in order to measure evolutionary change in gene expression and coding sequence in response to different sex-specific selection regimes in a clade of birds with divergent mating systems. Sex-specific selection pressures arise in large part as a consequence of mating system, however males and females share nearly identical genomes, especially in the vertebrates where the sex chromosomes house very small proportions of the overall transcriptome. This single shared genome creates sex-specific phenotypes via different gene expression levels in females and males, and these sex-biased genes connect sexual dimorphisms, and the sexually antagonistic selection pressures that shape them, with the regions of the genome that encode them.
The Galloanserae (fowl and waterfowl) will be used to in the proposed project, as this clade combines the necessary requirements of both variation in mating systems and a well-conserved reference genome (chicken). The study species selected from within the Galloanserae for the proposal exhibit a range of sexual dimorphism and sperm competition, and this will be exploited with next generation (454 and Illumina) genomic and transcriptomic data to study the gene expression patterns that underlie sexual dimorphisms, and the evolutionary pressures acting on them. This work will be complemented by the development of mathematical models of sex-specific evolution that will be tested against the gene expression and gene sequence data in order to understand the mechanisms by which sex-specific selection regimes, arising largely from mating systems, shape the phenotype via the genome.
Max ERC Funding
1 350 804 €
Duration
Start date: 2011-01-01, End date: 2016-07-31
Project acronym BIG_IDEA
Project Building an Integrated Genetic Infectious Disease Epidemiology Approach
Researcher (PI) Francois Balloux
Host Institution (HI) University College London
Call Details Starting Grant (StG), LS8, ERC-2010-StG_20091118
Summary Epidemiology and public health planning will increasingly rely on the analysis of genetic sequence data. The recent swine-derived influenza A/H1N1 pandemic may represent a tipping point in this trend, as it is arguably the first time when multiple strains of a human pathogen have been sequenced essentially in real time from the very beginning of its spread. However, the full potential of genetic information cannot be fully exploited to infer the spread of epidemics due to the lack of statistical methodologies capable of reconstructing transmission routes from genetic data structured both in time and space. To address this urgent need, we propose to develop a methodological framework for the reconstruction of the spatiotemporal dynamics of disease outbreaks and epidemics based on genetic sequence data. Rather than reconstructing most recent common ancestors as in phylogenetics, we will directly infer the most likely ancestries among the sampled isolates. This represents an entirely novel paradigm and allows for the development of statistically coherent and powerful inference software within a Bayesian framework. The methodological framework will be developed in parallel with the analysis of real genetic/genomic data from important human pathogens. We will in particular focus on the 2009 A/H1N1 pandemic influenza, methicilin-resistant Staphylococcus aureus clones (MRSAs), Batrachochytrium dendrobatidis, a fungus currently devastating amphibian populations worldwide. The tools we are proposing to develop are likely to impact radically on the field of infectious disease epidemiology and affect the way infectious emerging pathogens are monitored by biologists and public health professionals.
Summary
Epidemiology and public health planning will increasingly rely on the analysis of genetic sequence data. The recent swine-derived influenza A/H1N1 pandemic may represent a tipping point in this trend, as it is arguably the first time when multiple strains of a human pathogen have been sequenced essentially in real time from the very beginning of its spread. However, the full potential of genetic information cannot be fully exploited to infer the spread of epidemics due to the lack of statistical methodologies capable of reconstructing transmission routes from genetic data structured both in time and space. To address this urgent need, we propose to develop a methodological framework for the reconstruction of the spatiotemporal dynamics of disease outbreaks and epidemics based on genetic sequence data. Rather than reconstructing most recent common ancestors as in phylogenetics, we will directly infer the most likely ancestries among the sampled isolates. This represents an entirely novel paradigm and allows for the development of statistically coherent and powerful inference software within a Bayesian framework. The methodological framework will be developed in parallel with the analysis of real genetic/genomic data from important human pathogens. We will in particular focus on the 2009 A/H1N1 pandemic influenza, methicilin-resistant Staphylococcus aureus clones (MRSAs), Batrachochytrium dendrobatidis, a fungus currently devastating amphibian populations worldwide. The tools we are proposing to develop are likely to impact radically on the field of infectious disease epidemiology and affect the way infectious emerging pathogens are monitored by biologists and public health professionals.
Max ERC Funding
1 483 080 €
Duration
Start date: 2010-11-01, End date: 2015-10-31
Project acronym BLUELEAF
Project The adaptive advantages, evolution and development of iridescence in leaves
Researcher (PI) Heather Whitney
Host Institution (HI) UNIVERSITY OF BRISTOL
Call Details Starting Grant (StG), LS8, ERC-2010-StG_20091118
Summary Iridescence is a form of structural colour which changes hue according to the angle from which it is viewed. Blue iridescence caused by multilayers has been described on the leaves of taxonomically diverse species such as the lycophyte Selaginella uncinata and the angiosperm Begonia pavonina. While much is known about the role of leaf pigment colour, the adaptive role of leaf iridescence is unknown. Hypotheses have been put forward including 1) iridescence acts as disruptive camouflage against herbivores 2) it enhances light sensing and capture in low light conditions 3) it is a photoprotective mechanism to protect shade-adapted plants against high light levels. These hypotheses are not mutually exclusive: each function may be of varying importance in different environments. To understand any one function, we need a interdisciplinary approach considering all three potential functions and their interactions. The objective of my research would be to test these hypotheses, using animal behavioural and plant physiological methods, to determine the functions of leaf iridescence and how the plant has adapted to the reflection of developmentally vital wavelengths. Use of molecular and bioinformatics methods will elucidate the genes that control the production of this potentially multifunctional optical phenomenon. This research will provide a pioneering study into the generation, developmental impact and adaptive significance of iridescence in leaves. It would also answer questions at the frontiers of several fields including those of plant evolution, insect vision, methods of camouflage, the generation and role of animal iridescence, and could also potentially inspire synthetic biomimetic applications.
Summary
Iridescence is a form of structural colour which changes hue according to the angle from which it is viewed. Blue iridescence caused by multilayers has been described on the leaves of taxonomically diverse species such as the lycophyte Selaginella uncinata and the angiosperm Begonia pavonina. While much is known about the role of leaf pigment colour, the adaptive role of leaf iridescence is unknown. Hypotheses have been put forward including 1) iridescence acts as disruptive camouflage against herbivores 2) it enhances light sensing and capture in low light conditions 3) it is a photoprotective mechanism to protect shade-adapted plants against high light levels. These hypotheses are not mutually exclusive: each function may be of varying importance in different environments. To understand any one function, we need a interdisciplinary approach considering all three potential functions and their interactions. The objective of my research would be to test these hypotheses, using animal behavioural and plant physiological methods, to determine the functions of leaf iridescence and how the plant has adapted to the reflection of developmentally vital wavelengths. Use of molecular and bioinformatics methods will elucidate the genes that control the production of this potentially multifunctional optical phenomenon. This research will provide a pioneering study into the generation, developmental impact and adaptive significance of iridescence in leaves. It would also answer questions at the frontiers of several fields including those of plant evolution, insect vision, methods of camouflage, the generation and role of animal iridescence, and could also potentially inspire synthetic biomimetic applications.
Max ERC Funding
1 118 378 €
Duration
Start date: 2011-01-01, End date: 2016-07-31
Project acronym DIVERSITY
Project Evolution of Pathogen and Host Diversity
Researcher (PI) Sunetra Gupta
Host Institution (HI) THE CHANCELLOR, MASTERS AND SCHOLARS OF THE UNIVERSITY OF OXFORD
Call Details Advanced Grant (AdG), LS8, ERC-2010-AdG_20100317
Summary The study of host-pathogen systems is of central importance to the control of infectious disease, but also provides unique opportunities to observe evolution in action. Many pathogen species have diversified under selection pressures from the host; conversely, genes that are important in host defence also exhibit high degrees of polymorphism. This proposal divides into two parts: (1) the evolution of pathogen diversity under host immune selection, and (2) the evolution of host diversity under pathogen selection. I have developed a body of theoretical work showing that discrete population structures can arise through immune selection rather than limitations on genetic exchange. The predictions of this framework concerning the structure and dynamics of antigenic, metabolic and virulence genes will be empirically tested using three different systems: the bacterial pathogen, Neisseira meningitidis, the influenza virus, and the malaria parasite, Plasmodium falciparum. The current theory will also be expanded and modified to address a number of outstanding questions such whether it can explain the occurrence of influenza pandemics. With regard to host diversity, we will be attempting to validate and extend a novel framework incoporating epistatic interactions between malaria-protective genetic disorders of haemoglobin to understand their intriguing geographical distribution and their mode of action against the malarial disease. We will also be exploring the potential of mechanisms that can organise pathogens into discrete strains to generate patterns among host genes responsible for pathogen recognition, such as the Major Histocompatibility Complex. The co-evolution of hosts and pathogens under immune selection thus forms the ultimate theme of this proposal.
Summary
The study of host-pathogen systems is of central importance to the control of infectious disease, but also provides unique opportunities to observe evolution in action. Many pathogen species have diversified under selection pressures from the host; conversely, genes that are important in host defence also exhibit high degrees of polymorphism. This proposal divides into two parts: (1) the evolution of pathogen diversity under host immune selection, and (2) the evolution of host diversity under pathogen selection. I have developed a body of theoretical work showing that discrete population structures can arise through immune selection rather than limitations on genetic exchange. The predictions of this framework concerning the structure and dynamics of antigenic, metabolic and virulence genes will be empirically tested using three different systems: the bacterial pathogen, Neisseira meningitidis, the influenza virus, and the malaria parasite, Plasmodium falciparum. The current theory will also be expanded and modified to address a number of outstanding questions such whether it can explain the occurrence of influenza pandemics. With regard to host diversity, we will be attempting to validate and extend a novel framework incoporating epistatic interactions between malaria-protective genetic disorders of haemoglobin to understand their intriguing geographical distribution and their mode of action against the malarial disease. We will also be exploring the potential of mechanisms that can organise pathogens into discrete strains to generate patterns among host genes responsible for pathogen recognition, such as the Major Histocompatibility Complex. The co-evolution of hosts and pathogens under immune selection thus forms the ultimate theme of this proposal.
Max ERC Funding
1 670 632 €
Duration
Start date: 2011-06-01, End date: 2017-05-31
Project acronym EARLYWARNING
Project Generic Early Warning Signals for Critical Transitions
Researcher (PI) Marten Scheffer
Host Institution (HI) WAGENINGEN UNIVERSITY
Call Details Advanced Grant (AdG), LS8, ERC-2010-AdG_20100317
Summary Abrupt shifts occasionally reshape complex systems in nature ranging in scale from lakes and reefs to regional climate systems. Such shifts sometimes represent critical transitions in the sense that they happen at tipping points where runaway change propels the system towards an alterative contrasting state. Although the mechanism of critical transitions can often be reconstructed in the hindsight, we are virtually unable to predict when they will happen in advance. Simulation models for complex environmental systems are simply not good enough to predict tipping points, and there is little hope that this will change over the coming decades. The proposed project is aimed at developing an alternative way to predict critical transitions. We aim at finding early warning signals for such transitions that are generic in the sense that they work irrespective of the (often poorly known) mechanisms responsible for the tipping points. Mathematical theory indicates that this might be possible. However, although excitement about these ideas is emerging, we are far from having a cohesive theory, let alone practical approaches for predicting critical transitions in large complex systems like lakes, coral reefs or the climate. I will work towards this goal with my team along three lines: 1) Develop a comprehensive theory of early warning signals using analytical mathematical techniques as well as models ranging in character from simple and transparent to elaborate and realistic; 2) Test the theory on experimental plankton systems kept in controlled microcosms; and 3) Analyze data from real systems that go through catastrophic transitions. The anticipated results would imply a major breakthrough in a field of research that is exiting as well as highly relevant to society. If we are successful, it would allow us to anticipate critical transitions even in large complex systems where we have little hope of predicting tipping points on the basis of mechanistic models.
Summary
Abrupt shifts occasionally reshape complex systems in nature ranging in scale from lakes and reefs to regional climate systems. Such shifts sometimes represent critical transitions in the sense that they happen at tipping points where runaway change propels the system towards an alterative contrasting state. Although the mechanism of critical transitions can often be reconstructed in the hindsight, we are virtually unable to predict when they will happen in advance. Simulation models for complex environmental systems are simply not good enough to predict tipping points, and there is little hope that this will change over the coming decades. The proposed project is aimed at developing an alternative way to predict critical transitions. We aim at finding early warning signals for such transitions that are generic in the sense that they work irrespective of the (often poorly known) mechanisms responsible for the tipping points. Mathematical theory indicates that this might be possible. However, although excitement about these ideas is emerging, we are far from having a cohesive theory, let alone practical approaches for predicting critical transitions in large complex systems like lakes, coral reefs or the climate. I will work towards this goal with my team along three lines: 1) Develop a comprehensive theory of early warning signals using analytical mathematical techniques as well as models ranging in character from simple and transparent to elaborate and realistic; 2) Test the theory on experimental plankton systems kept in controlled microcosms; and 3) Analyze data from real systems that go through catastrophic transitions. The anticipated results would imply a major breakthrough in a field of research that is exiting as well as highly relevant to society. If we are successful, it would allow us to anticipate critical transitions even in large complex systems where we have little hope of predicting tipping points on the basis of mechanistic models.
Max ERC Funding
2 299 171 €
Duration
Start date: 2011-06-01, End date: 2016-05-31
Project acronym ECOADAPT
Project Microbial adaptation within ecosystems
Researcher (PI) Isabel Antunes Mendes Gordo
Host Institution (HI) FUNDACAO CALOUSTE GULBENKIAN
Call Details Starting Grant (StG), LS8, ERC-2010-StG_20091118
Summary All natural populations are constantly subject to new mutations, and frequently face new environments, to which they adapt. Knowledge of the genetics of adaptation should provide the centerpiece of a unified theory of evolution. Despite its extreme importance, the process of adaptation is far from being understood. How does the shape of distribution of fitness effects of mutations depend on the environment? What is the importance of epistasis in adaptive evolution? are still open questions. While empirical observations on advantageous mutations are extremely difficult, recent technical advances allow us to start tackling these questions with an unprecedented accuracy. Here we will combine different methods in a novel powerful marker system to track adaptive mutations as they become incorporated into bacterial populations adapting to different environments and as they fix. Interestingly theory suggest that some generalities may underlie the process of adaptation and that ecology may be important in the dynamics and statistical laws of adaptation. Experimental evolution with bacteria presents us with the opportunity to directly measure key parameters and to test theoretical predictions about the genetic basis of adaptive evolution in increasingly complex ecosystems. As Dobzansky pointed out The greater the diversity of inhabitants in a territory, the more adaptive opportunities exist in it. The main goal of this research project is to measure rates and effects of adaptive mutations, as well as patterns of epistasis amongst beneficial mutations in environments with different strengths of abiotic versus biotic interactions.
Summary
All natural populations are constantly subject to new mutations, and frequently face new environments, to which they adapt. Knowledge of the genetics of adaptation should provide the centerpiece of a unified theory of evolution. Despite its extreme importance, the process of adaptation is far from being understood. How does the shape of distribution of fitness effects of mutations depend on the environment? What is the importance of epistasis in adaptive evolution? are still open questions. While empirical observations on advantageous mutations are extremely difficult, recent technical advances allow us to start tackling these questions with an unprecedented accuracy. Here we will combine different methods in a novel powerful marker system to track adaptive mutations as they become incorporated into bacterial populations adapting to different environments and as they fix. Interestingly theory suggest that some generalities may underlie the process of adaptation and that ecology may be important in the dynamics and statistical laws of adaptation. Experimental evolution with bacteria presents us with the opportunity to directly measure key parameters and to test theoretical predictions about the genetic basis of adaptive evolution in increasingly complex ecosystems. As Dobzansky pointed out The greater the diversity of inhabitants in a territory, the more adaptive opportunities exist in it. The main goal of this research project is to measure rates and effects of adaptive mutations, as well as patterns of epistasis amongst beneficial mutations in environments with different strengths of abiotic versus biotic interactions.
Max ERC Funding
1 167 600 €
Duration
Start date: 2010-12-01, End date: 2015-11-30
Project acronym ECOLIGHT
Project Ecological effects of light pollution
Researcher (PI) Kevin John Gaston
Host Institution (HI) THE UNIVERSITY OF EXETER
Call Details Advanced Grant (AdG), LS8, ERC-2010-AdG_20100317
Summary The last 100 years have seen the dramatic spread of an evolutionarily unprecedented environmental change. Across huge areas, the spatial patterns and temporal cycles of light and dark that have previously remained approximately constant have been disrupted by the introduction of artificial night-time lights. This raises major concerns, given that light and dark provide critical resources and environmental conditions for organisms and play key roles in their physiology, growth, behaviour and reproduction, including the entrainment of internal biological clocks to local time. Indeed, it has long been recognised that light pollution of the night is likely to have profound consequences for the structure and functioning of populations and communities. Nonetheless, empirical studies of these effects remain wanting. This project will bring about a step change in understanding of the ecological consequences of night-time light pollution, addressing the principal question: How does the experimental manipulation of artificial night-time light influence population abundance, species composition and community structure? This will be answered using linked experimental studies. The results will have wide ramifications for understanding of the influences of rapid environmental change on population and community structure and of measures by which these can best be ameliorated.
Summary
The last 100 years have seen the dramatic spread of an evolutionarily unprecedented environmental change. Across huge areas, the spatial patterns and temporal cycles of light and dark that have previously remained approximately constant have been disrupted by the introduction of artificial night-time lights. This raises major concerns, given that light and dark provide critical resources and environmental conditions for organisms and play key roles in their physiology, growth, behaviour and reproduction, including the entrainment of internal biological clocks to local time. Indeed, it has long been recognised that light pollution of the night is likely to have profound consequences for the structure and functioning of populations and communities. Nonetheless, empirical studies of these effects remain wanting. This project will bring about a step change in understanding of the ecological consequences of night-time light pollution, addressing the principal question: How does the experimental manipulation of artificial night-time light influence population abundance, species composition and community structure? This will be answered using linked experimental studies. The results will have wide ramifications for understanding of the influences of rapid environmental change on population and community structure and of measures by which these can best be ameliorated.
Max ERC Funding
1 600 000 €
Duration
Start date: 2011-05-01, End date: 2017-04-30
Project acronym ECOTELO
Project The ecological significance of telomere dynamics: environments, individuals and inheritance
Researcher (PI) Patricia Monaghan
Host Institution (HI) UNIVERSITY OF GLASGOW
Call Details Advanced Grant (AdG), LS8, ERC-2010-AdG_20100317
Summary The current pace of change is such that many organisms face ever more rapid and severe fluctuations in their physical and biotic environments. A major challenge for ecologists and evolutionary biologists is in understanding how this will influence individuals, populations and ecosystems, and over what time scale such effects will occur. There is now great interest in so called 'maternal effects', which can generate rapid phenotypic responses, with both positive and negative fitness consequences in an ecological timeframe. In this project, I propose to examine a hitherto unconsidered route whereby the state of the mother alters the DNA that her offspring inherit, with profound effects on offspring reproductive performance and potential lifespan. This route is the effect of maternal state on telomeres, the DNA sequences that cap chromosomes ends; changes in the length and loss rate of telomeres could affect the longevity and reproductive output of individuals, their offspring and even grand-offspring. We still know very little about what telomere loss measurable at the cellular level actually means for organismal level performance, how it is influenced by environmental factors and intergenerational maternal effects, and how telomere dynamics relate to Darwinian fitness parameters. We lack experimental studies that track telomere loss within individuals subjected to varying environmental circumstances and relate this to organismal level outcomes for parents and offspring. I plan to address this gap in our understanding in a novel and innovative experimental programme that tests the idea that the effects of environmental stressors on senescence rates and lifespan are linked to accelerated telomere loss and that, through this route, can affect more than one generation.
Summary
The current pace of change is such that many organisms face ever more rapid and severe fluctuations in their physical and biotic environments. A major challenge for ecologists and evolutionary biologists is in understanding how this will influence individuals, populations and ecosystems, and over what time scale such effects will occur. There is now great interest in so called 'maternal effects', which can generate rapid phenotypic responses, with both positive and negative fitness consequences in an ecological timeframe. In this project, I propose to examine a hitherto unconsidered route whereby the state of the mother alters the DNA that her offspring inherit, with profound effects on offspring reproductive performance and potential lifespan. This route is the effect of maternal state on telomeres, the DNA sequences that cap chromosomes ends; changes in the length and loss rate of telomeres could affect the longevity and reproductive output of individuals, their offspring and even grand-offspring. We still know very little about what telomere loss measurable at the cellular level actually means for organismal level performance, how it is influenced by environmental factors and intergenerational maternal effects, and how telomere dynamics relate to Darwinian fitness parameters. We lack experimental studies that track telomere loss within individuals subjected to varying environmental circumstances and relate this to organismal level outcomes for parents and offspring. I plan to address this gap in our understanding in a novel and innovative experimental programme that tests the idea that the effects of environmental stressors on senescence rates and lifespan are linked to accelerated telomere loss and that, through this route, can affect more than one generation.
Max ERC Funding
2 113 818 €
Duration
Start date: 2011-04-01, End date: 2016-07-31
Project acronym ENDOSEXDET
Project The impact of endosymbionts on the evolution of host sex determination mechanisms
Researcher (PI) Richard Cordaux
Host Institution (HI) CENTRE NATIONAL DE LA RECHERCHE SCIENTIFIQUE CNRS
Call Details Starting Grant (StG), LS8, ERC-2010-StG_20091118
Summary Appreciation of endosymbiosis, a type of symbiosis in which a microbial partner lives within its host cells, as an important source of evolutionary novelty has developed relatively recently. In this proposal, we investigate a fundamental evolutionary process influenced by bacterial endosymbionts: the mechanisms of sex determination of their eukaryotic hosts.
In animals, the most common system of sex determination is genetic. It can also be affected by inherited bacterial endosymbionts. However, very few systems have been analyzed and there is no extensive empirical evidence of how endosymbionts can shape host sex-determining systems. In the isopod crustacean Armadillidium vulgare, genetic sex determination follows female heterogamety. However, many A. vulgare populations harbour Wolbachia bacterial endosymbionts which can invert genetic males into phenotypic functional females.
Other sex-determining factors have been identified in A. vulgare: a feminizing f element which may be a Wolbachia genome fragment carrying feminization information inserted into the host nuclear genome, and a masculinizing gene which can restore the male sex in the presence of the f element, as a result of a genetic conflict. Thus, sex determination mechanisms in A. vulgare seem to be largely driven by Wolbachia endosymbionts. However, the molecular genetic basis and evolutionary history of all these sex-determining factors is unknown.
The A. vulgare/Wolbachia model provides a unique opportunity for directly investigating the impact of endosymbionts on the evolution of host sex determination mechanisms at the molecular genetic level. We will address this issue using the latest developments of molecular genetics technologies, such as next-generation DNA sequencing and high throughput genotyping.
Summary
Appreciation of endosymbiosis, a type of symbiosis in which a microbial partner lives within its host cells, as an important source of evolutionary novelty has developed relatively recently. In this proposal, we investigate a fundamental evolutionary process influenced by bacterial endosymbionts: the mechanisms of sex determination of their eukaryotic hosts.
In animals, the most common system of sex determination is genetic. It can also be affected by inherited bacterial endosymbionts. However, very few systems have been analyzed and there is no extensive empirical evidence of how endosymbionts can shape host sex-determining systems. In the isopod crustacean Armadillidium vulgare, genetic sex determination follows female heterogamety. However, many A. vulgare populations harbour Wolbachia bacterial endosymbionts which can invert genetic males into phenotypic functional females.
Other sex-determining factors have been identified in A. vulgare: a feminizing f element which may be a Wolbachia genome fragment carrying feminization information inserted into the host nuclear genome, and a masculinizing gene which can restore the male sex in the presence of the f element, as a result of a genetic conflict. Thus, sex determination mechanisms in A. vulgare seem to be largely driven by Wolbachia endosymbionts. However, the molecular genetic basis and evolutionary history of all these sex-determining factors is unknown.
The A. vulgare/Wolbachia model provides a unique opportunity for directly investigating the impact of endosymbionts on the evolution of host sex determination mechanisms at the molecular genetic level. We will address this issue using the latest developments of molecular genetics technologies, such as next-generation DNA sequencing and high throughput genotyping.
Max ERC Funding
1 403 285 €
Duration
Start date: 2011-01-01, End date: 2015-12-31