A stochastic model for the development of Bateson-Dobzhansky-Muller incompatibilities that incorporates protein interaction networks

scientific article published on 29 March 2012

A stochastic model for the development of Bateson-Dobzhansky-Muller incompatibilities that incorporates protein interaction networks is …
instance of (P31):
scholarly articleQ13442814

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P356DOI10.1016/J.MBS.2012.03.006
P932PMC publication ID5797834
P698PubMed publication ID22465838
P5875ResearchGate publication ID223978781
P894zbMATH Open document ID1352.92063

P2093author name stringPeter Olofsson
Karen Macpherson
Kevin Livingstone
Andrius Dagilis
Garner Cochran
Kerry A Seitz
P2860cites workDominance, epistasis and the genetics of postzygotic isolationQ34609169
Complex epistasis and the genetic basis of hybrid sterility in the Drosophila pseudoobscura Bogota-USA hybridization.Q34612806
The molecular evolutionary basis of species formationQ37669190
Dynamics of hybrid incompatibility in gene networks in a constant environmentQ41677928
Determinants of divergent adaptation and Dobzhansky-Muller interaction in experimental yeast populationsQ42147858
Divergent evolution of duplicate genes leads to genetic incompatibilities within A. thalianaQ44749998
A Test of the Snowball Theory for the Rate of Evolution of Hybrid IncompatibilitiesQ51619902
Genetic architecture and postzygotic reproductive isolation: evolution of Bateson-Dobzhansky-Muller incompatibilities in a polygenic model.Q51647767
Hybrid dysfunction: population genetic and quantitative genetic perspectives.Q51691418
Accumulation of Dobzhansky-Muller incompatibilities within a spatially structured populationQ73142403
The yeast protein interaction network evolves rapidly and contains few redundant duplicate genesQ74071558
The evolution of postzygotic isolation: accumulating Dobzhansky-Muller incompatibilitiesQ74273365
Hybrid Incompatibility “Snowballs” Between Solanum SpeciesQ85041068
PERSPECTIVE: MODELS OF SPECIATION: WHAT HAVE WE LEARNED IN 40 YEARS?Q22065124
BioGRID: a general repository for interaction datasetsQ24538650
Rates of speciation in the fossil recordQ28765243
Lethality and centrality in protein networksQ29547267
Accumulating Dobzhansky-Muller incompatibilities: reconciling theory and dataQ30946080
A genome-wide analysis reveals no nuclear dobzhansky-muller pairs of determinants of speciation between S. cerevisiae and S. paradoxus, but suggests more complex incompatibilitiesQ33649856
Genetics of reproductive isolation in the Drosophila simulans clade: complex epistasis underlying hybrid male sterilityQ33962864
The population genetics of speciation: the evolution of hybrid incompatibilitiesQ33964957
Speciation genes in plantsQ34076779
Modular organization of cellular networksQ34329388
Rice pollen hybrid incompatibility caused by reciprocal gene loss of duplicated genesQ34377486
P433issue1
P6104maintained by WikiProjectWikiProject MathematicsQ8487137
P1104number of pages5
P304page(s)49-53
P577publication date2012-03-29
P1433published inMathematical BiosciencesQ2199138
P1476titleA stochastic model for the development of Bateson-Dobzhansky-Muller incompatibilities that incorporates protein interaction networks
P478volume238

Reverse relations

cites work (P2860)
Q92139986Admixture mapping in interspecific Populus hybrids identifies classes of genomic architectures for phytochemical, morphological and growth traits
Q35230104Models of speciation: where are we now?
Q57134585Speciation genes are more likely to have discordant gene trees
Q39070449Spiraling Complexity: A Test of the Snowball Effect in a Computational Model of RNA Folding
Q52315036Systematic analysis of complex genetic interactions.
Q36050102The Pace of Hybrid Incompatibility Evolution in House Mice.
Q64065896The evolution of hybrid fitness during speciation
Q37241461The evolution of hybrid incompatibilities along a phylogeny.
Q46700797The genetic architecture of hybrid incompatibilities and their effect on barriers to introgression in secondary contact
Q49209238The probability of speciation on an interaction network with unequal substitution rates