Network Models of TEM β-Lactamase Mutations Coevolving under Antibiotic Selection Show Modular Structure and Anticipate Evolutionary Trajectories 英文参考文献.docVIP
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Network Models of TEM β-Lactamase Mutations Coevolving under Antibiotic Selection Show Modular Structure and Anticipate Evolutionary Trajectories 英文参考文献
NetworkModelsofTEMb-LactamaseMutations
CoevolvingunderAntibioticSelectionShowModular
StructureandAnticipateEvolutionaryTrajectories
VioletaBelevaGuthrie1,JenniferAllen2,ManelCamps2,RachelKarchin1*
1Department of Biomedical Engineering and Institute for Computational Medicine, Johns Hopkins University, Baltimore, Maryland, United States of America,
2DepartmentofEnvironmentalToxicology,UniversityofCaliforniaSantaCruz,SantaCruz,California,UnitedStatesofAmerica
Abstract
Understandinghownovelfunctionsevolve(geneticadaptation)isacriticalgoalofevolutionarybiology.Amongasexual
organisms,geneticadaptationinvolvesmultiplemutationsthatfrequentlyinteractinanon-linearfashion(epistasis).Non-
linearinteractionsposeaformidablechallengeforthecomputationalpredictionofmutationeffects.Hereweusetherecent
evolutionofb-lactamaseunderantibioticselectionasamodelforgeneticadaptation.Webuildanetworkofcoevolving
residues(possiblefunctionalinteractions),inwhichnodesaremutantresiduepositionsandlinksrepresenttwopositions
found mutated together in the same sequence. Most often these pairs occur in the setting of more complex mutants.
Focusingonextended-spectrumresistantsequences,weusenetwork-theoreticaltoolstoidentifytriplemutanttrajectories
oflikelyspecialsignificanceforadaptation.Weextrapolateevolutionarypaths(n=3)thatincreaseresistanceandthatare
longerthantheunitsusedtobuildthenetwork(n=2).Thesepathsconsistofalimitednumberofresiduepositionsandare
enrichedforknowntriplemutantcombinationsthatincreasecefotaximeresistance.Wefindthatthepairsofresiduesused
tobuildthenetworkfrequentlydecreaseresistance comparedtotheircorrespondingsinglets.Thisisasurprisingresult,
giventhattheircoevolutionsuggestsaselectiveadvantage.Thus,b-lactamaseadaptationishighlyepistatic.Ourmethod
canidentifytripletsthatincreaseresistancedespitetheunderlyingruggedfitnesslandscapeandhastheuniqueabilityto
makepredictionsbyplacingeachmutantresiduepositioninitsfunctionalcontext.Ourapproachrequiresonlysequence
information,sufficie
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