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Deleterious Mutation Accumulation and the Long-Term Fate of Chromosomal Inversions

https://doi.org/10.1101/606012
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What this work says

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

inferredcites →https://doi.org/10.1007/bf00122932openalex-snapshot
The role of genic selection in the establishment of inversion polymorphism in Drosophila subobscura
inferredcites →https://doi.org/10.1007/bf00293412openalex-snapshot
Heteromorphism for chromosome 1, a requirement for normal development in crested newts
inferredcites →https://doi.org/10.1007/bf00426369openalex-snapshot
Chromosome distribution and catenation in Rhoeo spathacea var. concolor
inferredcites →https://doi.org/10.1016/0027-5107(64)90047-8openalex-snapshot
The relation of recombination to mutational advance
inferredcites →https://doi.org/10.1016/j.cub.2009.02.039openalex-snapshot
Reduced Effectiveness of Selection Caused by a Lack of Recombination
inferredcites →https://doi.org/10.1016/j.cub.2015.11.069openalex-snapshot
Divergence and Functional Degradation of a Sex Chromosome-like Supergene
inferredcites →https://doi.org/10.1016/j.cub.2018.07.004openalex-snapshot
Local Inversion Heterozygosity Alters Recombination throughout the Genome
inferredcites →https://doi.org/10.1016/j.tree.2018.04.002openalex-snapshot
Eco-Evolutionary Genomics of Chromosomal Inversions
inferredcites →https://doi.org/10.1016/j.tree.2018.12.005openalex-snapshot
Evolving Inversions
inferredcites →https://doi.org/10.1016/s0168-9525(03)00116-1openalex-snapshot
Biased gene conversion: implications for genome and sex evolution
inferredcites →https://doi.org/10.1017/s0016672300012684openalex-snapshot
Associative overdominance caused by linked detrimental mutations
inferredcites →https://doi.org/10.1017/s0016672300030111openalex-snapshot
Accumulation of P elements in minority inversions in natural populations ofDrosophila melanogaster
inferredcites →https://doi.org/10.1017/s0016672300031086openalex-snapshot
Mutation accumulation in finite outbreeding and inbreeding populations
inferredcites →https://doi.org/10.1017/s0016672300034029openalex-snapshot
Background selection and patterns of genetic diversity inDrosophila melanogaster
inferredcites →https://doi.org/10.1017/s0016672397002899openalex-snapshot
Rapid fixation of deleterious alleles can be caused by Muller's ratchet
inferredcites →https://doi.org/10.1038/hdy.1965.48openalex-snapshot
Complex hybridity in Isotoma petræa
inferredcites →https://doi.org/10.1038/hdy.1979.85openalex-snapshot
A model for the evolution of translocation heterozygosity
inferredcites →https://doi.org/10.1038/hdy.1985.36openalex-snapshot
Genie and karyotypic selection on an inversion polymorphism in the seaweed fly, Coelopa frigida
inferredcites →https://doi.org/10.1038/hdy.1994.103openalex-snapshot
Inversion polymorphism and accumulation of lethals in selected lines of Drosophila melanogaster
inferredcites →https://doi.org/10.1038/nature05388openalex-snapshot
Direct estimation of per nucleotide and genomic deleterious mutation rates in Drosophila
inferredcites →https://doi.org/10.1038/s41559-017-0235-2openalex-snapshot
A sex-linked supergene controls sperm morphology and swimming speed in a songbird
inferredcites →https://doi.org/10.1073/pnas.212277199openalex-snapshot
Linkage limits the power of natural selection in Drosophila
inferredcites →https://doi.org/10.1073/pnas.41.5.289openalex-snapshot
AN EXTREME CASE OF HETEROSIS IN A CENTRAL AMERICAN POPULATION OF DROSOPHILA TROPICALIS
inferredcites →https://doi.org/10.1073/pnas.93.7.2873openalex-snapshot
Accelerated evolution and Muller's rachet in endosymbiotic bacteria.
inferredcites →https://doi.org/10.1093/gbe/evr081openalex-snapshot
Effects of Inversions on Within- and Between-Species Recombination and Divergence
inferredcites →https://doi.org/10.1093/genetics/137.3.815openalex-snapshot
Transposable element numbers in cosmopolitan inversions from a natural population of Drosophila melanogaster.
inferredcites →https://doi.org/10.1093/genetics/146.2.695openalex-snapshot
Recombination and Gene Flux Caused by Gene Conversion and Crossing Over in Inversion Heterokaryotypes
inferredcites →https://doi.org/10.1093/genetics/155.2.685openalex-snapshot
Effect of Inversion Polymorphism on the Neutral Nucleotide Variability of Linked Chromosomal Regions in Drosophila
inferredcites →https://doi.org/10.1093/genetics/48.3.361openalex-snapshot
GENETICS OF NATURAL POPULATIONS. XXXII. INBREEDING AND THE MUTATIONAL AND BALANCED GENETIC LOADS IN NATURAL POPULATIONS OF DROSOPHILA PSEUDOOBSCURA
inferredcites →https://doi.org/10.1093/genetics/50.4.711openalex-snapshot
THE GENETIC STRUCTURE OF NATURAL POPULATIONS OF DROSOPHILA MELANOGASTER. II. OVERDOMINANCE OF SPONTANEOUS MUTANT POLYGENES CONTROLLING VIABILITY IN HOMOZYGOUS GENETIC BACKGROUND
inferredcites →https://doi.org/10.1093/genetics/57.4.741openalex-snapshot
FREQUENCY CHANGES OF NEW INVERSIONS IN POPULATIONS UNDER MUTATION-SELECTION EQUILIBRIA
inferredcites →https://doi.org/10.1093/genetics/58.1.125openalex-snapshot
RECOMBINATION-INDUCED CHROMOSOMAL HETEROSIS
inferredcites →https://doi.org/10.1093/genetics/61.4.859openalex-snapshot
CHROMOSOMAL POLYMORPHISM AND GENETIC LOAD IN DROSOPHILA PSEUDOOBSCURA
inferredcites →https://doi.org/10.1093/genetics/72.4.691openalex-snapshot
FACTORS INFLUENCING FITNESS IN CHROMOSOMAL STRAINS IN DROSOPHILA SUBOBSCURA
inferredcites →https://doi.org/10.1093/genetics/78.2.737openalex-snapshot
THE EVOLUTIONARY ADVANTAGE OF RECOMBINATION
inferredcites →https://doi.org/10.1093/molbev/msu056openalex-snapshot
The Relation between Recombination Rate and Patterns of Molecular Evolution and Variation in Drosophila melanogaster
inferredcites →https://doi.org/10.1093/molbev/msw211openalex-snapshot
SLiM 2: Flexible, Interactive Forward Genetic Simulations
inferredcites →https://doi.org/10.1093/oxfordjournals.molbev.a040074openalex-snapshot
Reduced natural selection associated with low recombination in Drosophila melanogaster.
inferredcites →https://doi.org/10.1098/rstb.2011.0199openalex-snapshot
What can patterns of differentiation across plant genomes tell us about adaptation and speciation?
inferredcites →https://doi.org/10.1098/rstb.2011.0246openalex-snapshot
Coalescent patterns for chromosomal inversions in divergent populations
inferredcites →https://doi.org/10.1101/736504openalex-snapshot
Mutation accumulation in chromosomal inversions maintains wing pattern polymorphism in a butterfly
inferredcites →https://doi.org/10.1101/748004openalex-snapshot
Transition from background selection to associative overdominance promotes diversity in regions of low recombination
inferredcites →https://doi.org/10.1111/brv.12213openalex-snapshot
Chromosomal polymorphism in mammals: an evolutionary perspective
inferredcites →https://doi.org/10.1111/evo.12663openalex-snapshot
Adaptive divergence in the monkey flowerMimulus guttatusis maintained by a chromosomal inversion
inferredcites →https://doi.org/10.1111/j.1365-2583.2007.00764.xopenalex-snapshot
Genetic exchange in 2La inversion heterokaryotypes of Anopheles gambiae
inferredcites →https://doi.org/10.1111/j.1365-294x.2008.03946.xopenalex-snapshot
Divergent selection and heterogeneous genomic divergence
inferredcites →https://doi.org/10.1111/j.1558-5646.1969.tb03528.xopenalex-snapshot
CHROMOSOME TRANSLOCATIONS INGAYOPHYTUM(ONAGRACEAE)
inferredcites →https://doi.org/10.1111/j.1558-5646.1995.tb04434.xopenalex-snapshot
MUTATIONAL MELTDOWNS IN SEXUAL POPULATIONS
inferredcites →https://doi.org/10.1111/j.1558-5646.2008.00504.xopenalex-snapshot
SELECTION IN HETEROGENEOUS ENVIRONMENTS MAINTAINS THE GENE ARRANGEMENT POLYMORPHISM OF DROSOPHILA PSEUDOOBSCURA
inferredcites →https://doi.org/10.1111/j.1558-5646.2011.01269.xopenalex-snapshot
THE GENETIC ARCHITECTURE OF ADAPTATION UNDER MIGRATION-SELECTION BALANCE
inferredcites →https://doi.org/10.1111/j.1558-5646.2012.01836.xopenalex-snapshot
REPRODUCTIVE ISOLATION AND LOCAL ADAPTATION QUANTIFIED FOR A CHROMOSOME INVERSION IN A MALARIA MOSQUITO
inferredcites →https://doi.org/10.1111/jeb.12856openalex-snapshot
Tracking changes in chromosomal arrangements and their genetic content during adaptation
inferredcites →https://doi.org/10.1111/mec.14280openalex-snapshot
Long‐term balancing selection on chromosomal variants associated with crypsis in a stick insect
inferredcites →https://doi.org/10.1111/mec.14921openalex-snapshot
Pervasive gene conversion in chromosomal inversion heterozygotes
inferredcites →https://doi.org/10.1111/mec.14923openalex-snapshot
How chromosomal rearrangements shape adaptation and speciation: Case studies in Drosophila pseudoobscura and its sibling species Drosophila persimilis
inferredcites →https://doi.org/10.1111/mec.15066openalex-snapshot
Going beyond SNPs: The role of structural genomic variants in adaptive evolution and species diversification
inferredcites →https://doi.org/10.1111/mec.15936openalex-snapshot
Unboxing mutations: Connecting mutation types with evolutionary consequences
inferredcites →https://doi.org/10.1371/journal.pbio.1000500openalex-snapshot
A Widespread Chromosomal Inversion Polymorphism Contributes to a Major Life-History Transition, Local Adaptation, and Reproductive Isolation
inferredcites →https://doi.org/10.1371/journal.pbio.1000501openalex-snapshot
How and Why Chromosome Inversions Evolve
inferredcites →https://doi.org/10.1371/journal.pgen.0010056openalex-snapshot
Discovery of Human Inversion Polymorphisms by Comparative Analysis of Human and Chimpanzee DNA Sequence Assemblies
inferredcites →https://doi.org/10.1534/g3.111.001396openalex-snapshot
A Whole-Chromosome Analysis of Meiotic Recombination inDrosophila melanogaster
inferredcites →https://doi.org/10.1534/genetics.105.047985openalex-snapshot
Chromosome Inversions, Local Adaptation and Speciation
inferredcites →https://doi.org/10.1534/genetics.107.082743openalex-snapshot
The Effects of Recombination Rate on the Distribution and Abundance of Transposable Elements
inferredcites →https://doi.org/10.1534/genetics.113.156935openalex-snapshot
Robust Forward Simulations of Recurrent Hitchhiking

What points at this work

Incoming claims: where this work appears in other papers’ reference lists and arguments.

inferred← citeshttps://doi.org/10.1016/j.cub.2019.11.063openalex-snapshot
Transition from Background Selection to Associative Overdominance Promotes Diversity in Regions of Low Recombination
inferred← citeshttps://doi.org/10.1016/j.cub.2020.05.011openalex-snapshot
Balanced lethal systems
inferred← citeshttps://doi.org/10.1016/j.tree.2020.03.002openalex-snapshot
A Roadmap for Understanding the Evolutionary Significance of Structural Genomic Variation
inferred← citeshttps://doi.org/10.1016/j.tree.2020.04.007openalex-snapshot
The Persistence of Polymorphisms across Species Radiations
inferred← citeshttps://doi.org/10.1016/j.tree.2025.08.004openalex-snapshot
Beyond supergenes: the diverse roles of inversions in trait evolution
inferred← citeshttps://doi.org/10.1038/s41467-020-14479-7openalex-snapshot
Balancing selection via life-history trade-offs maintains an inversion polymorphism in a seaweed fly
inferred← citeshttps://doi.org/10.1038/s41588-020-00771-1openalex-snapshot
Mutation load at a mimicry supergene sheds new light on the evolution of inversion polymorphisms
inferred← citeshttps://doi.org/10.1101/2020.11.19.389577openalex-snapshot
Admixture can readily lead to the formation of supergenes
inferred← citeshttps://doi.org/10.1101/2024.10.25.620277openalex-snapshot
Conserved gene content and unique phylogenetic history characterize the ‘bloopergene’ underlying Triturus’ balanced lethal system
inferred← citeshttps://doi.org/10.1101/748004openalex-snapshot
Transition from background selection to associative overdominance promotes diversity in regions of low recombination
inferred← citeshttps://doi.org/10.1111/1755-0998.13602openalex-snapshot
Extensive sequence divergence between the reference genomes of two zebrafish strains, Tuebingen and AB
inferred← citeshttps://doi.org/10.1111/evo.14129openalex-snapshot
Evolution and genetic architecture of disassortative mating at a locus under heterozygote advantage
inferred← citeshttps://doi.org/10.1111/mec.15565openalex-snapshot
Copy number variants outperform SNPs to reveal genotype–temperature association in a marine species
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