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Evolution of age-specific decline in stress phenotypes is driven by both antagonistic pleiotropy and mutation accumulation

https://doi.org/10.1101/115931
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What this work says

Outgoing claims: the papers this work cites, builds on, or argues with.

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Why organisms age: Evolution of senescence under positive pleiotropy?
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Patterns of Age-specific Means and Genetic Variances of Mortality Rates Predicted by the Mutation-Accumulation Theory of Ageing
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ggplot2: Elegant Graphics for Data Analysis
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Expression of genetic and environmental variation during ageing
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Expression of genetic and environmental variation during ageing
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Characterisation and limitations of the rapid cold-hardening response in the housefly Musca domestica (Diptera: Muscidae)
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The moulding of senescence by natural selection
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Selection on stress resistance increases longevity in Drosophila melanogaster
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Rapid cold hardening increases cold and chilling tolerances more than acclimation in the adults of the sycamore lace bug, Corythucha ciliata (Say) (Hemiptera: Tingidae)
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Acclimation, shock and hardening in the cold
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Misexpression screen delineates novel genes controlling Drosophila lifespan
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Oxidative stress and aging reduce COX I RNA and cytochrome oxidase activity in Drosophila
inferredcites →https://doi.org/10.1016/s0960-9822(02)00808-4openalex-snapshot
Genome-Wide Transcript Profiles in Aging and Calorically Restricted Drosophila melanogaster
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Evolution in Age-Structured Populations
inferredcites →https://doi.org/10.1038/362305a0openalex-snapshot
Optimally, mutation and the evolution of ageing
inferredcites →https://doi.org/10.1038/nature10811openalex-snapshot
The Drosophila melanogaster Genetic Reference Panel
inferredcites →https://doi.org/10.1038/ncomms5338openalex-snapshot
Genome-wide analysis in Drosophila reveals age-specific effects of SNPs on fitness traits
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Quantitative genetic tests of recent senescence theory: age-specific mortality and male fertility in Drosophila melanogaster
inferredcites →https://doi.org/10.1038/sj.hdy.6800786openalex-snapshot
Quantitative trait loci for thermotolerance phenotypes in Drosophila melanogaster
inferredcites →https://doi.org/10.1038/srep28999openalex-snapshot
Cold acclimation wholly reorganizes the Drosophila melanogaster transcriptome and metabolome
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Stress temperatures and quantitative variation in Drosophila melanogaster
inferredcites →https://doi.org/10.1073/pnas.1306656110openalex-snapshot
The age-specific force of natural selection and biodemographic walls of death
inferredcites →https://doi.org/10.1073/pnas.1400841111openalex-snapshot
Evolutionary shaping of demographic schedules
inferredcites →https://doi.org/10.1073/pnas.1503456112openalex-snapshot
Constraints, independence, and evolution of thermal plasticity: Probing genetic architecture of long- and short-term thermal acclimation
inferredcites →https://doi.org/10.1073/pnas.192360899openalex-snapshot
Directional selection is the primary cause of phenotypic diversification
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A test of evolutionary theories of aging
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Age-specific inbreeding depression and components of genetic variance in relation to the evolution of senescence.
inferredcites →https://doi.org/10.1093/genetics/138.3.773openalex-snapshot
The effects of spontaneous mutation on quantitative traits. I. Variances and covariances of life history traits.
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Age-Specific Patterns of Genetic Variance in Drosophila melanogaster. II. Fecundity and Its Genetic Covariance With Age-Specific Mortality
inferredcites →https://doi.org/10.1093/genetics/148.1.287openalex-snapshot
Age-Specific Properties of Spontaneous Mutations Affecting Mortality in Drosophila melanogaster
inferredcites →https://doi.org/10.1093/genetics/149.4.2099openalex-snapshot
Testing Natural Selection vs. Genetic Drift in Phenotypic Evolution Using Quantitative Trait Locus Data
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Orr's Quantitative Trait Loci Sign Test Under Conditions of Trait Ascertainment
inferredcites →https://doi.org/10.1093/gerona/glv047openalex-snapshot
Longevity GWAS Using theDrosophilaGenetic Reference Panel
inferredcites →https://doi.org/10.1093/gerona/glv193openalex-snapshot
Age-related Decline of Abiotic Stress Tolerance in YoungDrosophila melanogasterAdults
inferredcites →https://doi.org/10.1098/rspb.2009.0183openalex-snapshot
What can genetic variation tell us about the evolution of senescence?
inferredcites →https://doi.org/10.1098/rstb.2012.0005openalex-snapshot
Predicting organismal vulnerability to climate warming: roles of behaviour, physiology and adaptation
inferredcites →https://doi.org/10.1101/gr.171546.113openalex-snapshot
Natural variation in genome architecture among 205 Drosophila melanogaster Genetic Reference Panel lines
inferredcites →https://doi.org/10.1111/evo.12946openalex-snapshot
Retired flies, hidden plateaus, and the evolution of senescence in Drosophila melanogaster
inferredcites →https://doi.org/10.1111/j.1365-2435.2009.01615.xopenalex-snapshot
Field tests reveal genetic variation for performance at low temperatures in Drosophila melanogaster
inferredcites →https://doi.org/10.1111/j.1365-3032.2009.00677.xopenalex-snapshot
Hardening trumps acclimation in improving cold tolerance of Drosophila melanogaster larvae
inferredcites →https://doi.org/10.1111/j.1420-9101.2004.00871.xopenalex-snapshot
Evidence for a robust sex‐specific trade‐off between cold resistance and starvation resistance in Drosophila melanogaster
inferredcites →https://doi.org/10.1111/j.1420-9101.2011.02428.xopenalex-snapshot
Evolution of starvation resistance in Drosophila melanogaster : measurement of direct and correlated responses to artificial selection
inferredcites →https://doi.org/10.1111/j.1469-185x.2008.00046.xopenalex-snapshot
Insect thermal tolerance: what is the role of ontogeny, ageing and senescence?
inferredcites →https://doi.org/10.1111/j.1558-5646.1957.tb02911.xopenalex-snapshot
PLEIOTROPY, NATURAL SELECTION, AND THE EVOLUTION OF SENESCENCE
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LABORATORY EVOLUTION OF POSTPONED SENESCENCE INDROSOPHILA MELANOGASTER
inferredcites →https://doi.org/10.1111/j.1558-5646.1988.tb04134.xopenalex-snapshot
ANTAGONISTIC PLEIOTROPY: AN INTERSPECIFICDROSOPHILACOMPARISON
inferredcites →https://doi.org/10.1111/jeb.12183openalex-snapshot
Transcriptomic analysis of inbreeding depression in cold‐sensitive Drosophila melanogaster shows upregulation of the immune response
inferredcites →https://doi.org/10.1111/jeb.12321openalex-snapshot
Developmental thermal plasticity among D rosophila melanogaster populations
inferredcites →https://doi.org/10.1111/jeb.12690openalex-snapshot
Seasonal variation in life history traits in two Drosophila species
inferredcites →https://doi.org/10.1126/science.238.4832.1415openalex-snapshot
A Rapid Cold-Hardening Process in Insects
inferredcites →https://doi.org/10.1146/annurev-ecolsys-102710-145055openalex-snapshot
Physiological Correlates of Geographic Range in Animals
inferredcites →https://doi.org/10.1186/gb-2007-8-7-r129openalex-snapshot
FlyMine: an integrated database for Drosophila and Anopheles genomics
inferredcites →https://doi.org/10.1242/jeb.01685openalex-snapshot
Low temperature acclimated populations of the grain aphidSitobion avenaeretain ability to rapidly cold harden with enhanced fitness
inferredcites →https://doi.org/10.1242/jeb.058032openalex-snapshot
Predicting the physiological performance of ectotherms in fluctuating thermal environments
inferredcites →https://doi.org/10.1242/jeb.148.1.245openalex-snapshot
A rapid cold-hardening response protecting against cold shock injury in Drosophila melanogaster
inferredcites →https://doi.org/10.1242/jeb.204.9.1659openalex-snapshot
Rapid Cold-Hardening of Drosophila Melanogaster (Diptera: Drosophilidae) During Ecologically Based Thermoperiodic Cycles
inferredcites →https://doi.org/10.1371/journal.pgen.1004775openalex-snapshot
Genomic Evidence of Rapid and Stable Adaptive Oscillations over Seasonal Time Scales in Drosophila
inferredcites →https://doi.org/10.1534/g3.112.003228openalex-snapshot
Resampling QTL Effects in the QTL Sign Test Leads to Incongruous Sensitivity to Variance in Effect Size
inferredcites →https://doi.org/10.1534/genetics.105.048520openalex-snapshot
Quantitative Trait Loci With Age-Specific Effects on Fecundity in Drosophila melanogaster
inferredcites →https://doi.org/10.1534/genetics.106.070078openalex-snapshot
Age Specificity of Inbreeding Load inDrosophila melanogasterand Implications For the Evolution of Late-Life Mortality Plateaus
inferredcites →https://doi.org/10.1534/genetics.114.169276openalex-snapshot
Quantitative Genetic Analysis Indicates Natural Selection on Leaf Phenotypes Across Wild Tomato Species (Solanumsect.Lycopersicon; Solanaceae)
inferredcites →https://doi.org/10.2307/2406060openalex-snapshot
Pleiotropy, Natural Selection, and the Evolution of Senescence
inferredcites →https://doi.org/10.2307/2409234openalex-snapshot
Antagonistic Pleiotropy: An Interspecific Drosophila Comparison
inferredcites →https://doi.org/10.32614/r.manualsopenalex-snapshot
R: A Language and Environment for Statistical Computing
inferredcites →https://doi.org/10.5694/j.1326-5377.1953.tb84985.xopenalex-snapshot
AN UNSOLVED PROBLEM OF BIOLOGY
inferredcites →https://doi.org/10.5860/choice.28-5664openalex-snapshot
Evolutionary biology of aging
inferredcites →https://doi.org/10.5962/bhl.title.27468openalex-snapshot
The genetical theory of natural selection

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inferred← citeshttps://doi.org/10.1093/g3journal/jkae015openalex-snapshot
Gene expression variation underlying tissue-specific responses to copper stress in Drosophila melanogaster
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