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Incipient speciation in Drosophila melanogaster involves chemical signals. PDF

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Preview Incipient speciation in Drosophila melanogaster involves chemical signals.

Incipient speciation in Drosophila melanogaster involves chemical signals SUBJECTAREAS: MichelineGrillet1,2,ClaudeEveraerts1,BenjaminHouot1,3,MichaelG.Ritchie4,MatthewCobb2 ANIMALBEHAVIOUR &Jean-FrançoisFerveur1 SPECIATION EVOLUTIONARYBIOLOGY 1CentredesSciencesduGouˆtetdel’Alimentation,UMR6265CNRS,UMR1324INRA,Universite´deBourgogne,AgrosupDijon,6, MOLECULAREVOLUTION BdGabriel,21000Dijon,France,2FacultyofLifeSciences,UniversityofManchester,OxfordRoad,ManchesterM139PT,UK, 3Presentaddress:DepartmentofBiology,WVU,LifeScienceBuilding,53CampusDrive,Morgantown,WV26506,USA,4School ofBiology,UniversityofStAndrews,NorthHaugh,StAndrews,Fife,KY169TF,UK. Received 4July2011 ThesensoryandgeneticbasesofincipientspeciationbetweenstrainsofDrosophilamelanogasterfrom Accepted Zimbabweandthosefromelsewhereareunknown.Westudiedmatingbehaviourbetweeneightstrains–six 15December2011 fromZimbabwe,togetherwithtwocosmopolitanstrains.TheZimbabwestrainsshowedsignificantsexual isolationwhenpairedwithcosmopolitanmales,duetoZimbabwefemalesdiscriminatingagainstthese Published males.Ourresultsshowthatflies’cuticularhydrocarbons(CHs)wereinvolvedinthissexualisolation,but 19January2012 thatvisualandacousticsignalswerenot.ThematingfrequencyofZimbabwefemaleswashighly significantlynegativelycorrelatedwiththemale’srelativeamountof7-tricosene(%7-T),whilethematingof cosmopolitanfemaleswaspositivelycorrelatedwith%7-T.Variationintranscriptionlevelsoftwo Correspondenceand hydrocarbon-determininggenes,desat1anddesat2,didnotcorrelatewiththeobservedmatingpatterns. Ourstudyrepresentsastepforwardinourunderstandingofthesensoryprocessesinvolvedinthisclassic requestsformaterials caseofincipientspeciation. shouldbeaddressedto J.F.F.(jean-francois. ferveur@u-bourgogne. Sensorysignalsareusedbyanimalstoassessthesex,speciesandreproductivestatusoftheirpotentialmate1. fr) Theintraspecificdivergenceofsuchsignalsbetweenpopulationscanincreasetheirsexualisolationand ultimately lead to distinct species2. Although Drosophila melanogaster has a global distribution, several strains found in some geographic areas show non-random mating indicating partial sexual isolation3–5. The strongest documented case of intraspecific sexual isolation in this species is found between strains from Zimbabweandthosefromothergeographicareas(Cosmopolitanstrains).Inparticular,Zimbabwefemalesrarely mate with Cosmopolitan males whereas Cosmopolitan females show a high mating frequency with both ZimbabweandCosmopolitanmales6,7. Several D. melanogaster natural strains vary in their cuticular hydrocarbons (CHs), some of which play a pheromonalrole8.Mostfemalesproducehighlevelsof7,11-dienes(CHswithtwodoublebondsoncarbons7and 11),whereasthefemalesfromseveralWesternAfricanstrains(suchastheTaistrainfromIvoryCoast9,10)and fromtheCaribbean11producehighamountsof5,9-dienesandlowamountsof7,11-dienes.However,malesof Tai-likestrainsstillproducehighlevelsof7-monoenes(withasingledesaturationonC7)andnoorverylowlevels of5-monoenes9,12.Thesecompounds can actaspheromones: male-predominant 7-tricosene (7-T)stimulates femalematingbutinhibitsmalecourtship,while7,11-dienesenhancemalepreference13–16.Othercompounds mayalsobeinvolved:ithasbeensuggestedthat5-tricosene(5-T)inhibitsmalecourtshipinitiation,whiletherole of5,9-dienesisunclear–thesecompoundswereinitiallythoughttodecreasefemaleattractivityasshownby matinglevels,butthiswasnotconfirmed10,17. InD.melanogaster,theproductionofCHswithafirstdesaturationeitheronC7oronC5dependsonthe activity of desat1 and desat2, respectively. These are two closely linked genes that code for carbon-specific desaturaseenzymes17–19.Thedesat2geneisnotexpressedinCosmopolitanstrains,thusexplainingtheabsence of5,9-dienesinCosmopolitanfemales20.Themolecularstructureofthedesat2geneisapparentlyrelatedtothe degreeofsexualisolationinZimbabwefemales21,butnothingisknownofthesensorysignal(s)involvedinthis case of incipient speciation22,23. The desat1 gene has a pleiotropic effect on both the production of cuticular pheromonesandtheirdiscrimination24,25.Thesefindingsraisethetantalizingpossibilitythatdesat1anddesat2 arealsoinvolvedintheperceptionofC7-andC5-desaturatedhydrocarbonpheromones. Aftereliminatingvisualandauditorysignalsassourcesofsensorydiscriminationbetweenstrains,weexplored the relationship between the sexual isolation of Zimbabwe and Cosmopolitan strains and (i) their cuticular SCIENTIFICREPORTS |2:224|DOI:10.1038/srep00224 1 www.nature.com/scientificreports pheromonesand(ii)thetranscriptlevelsofdesat1anddesat2.After USAandDijon(Dij)fromFrance)inall64possiblecombinations investigating the mating patterns between six Zimbabwe and two andwemeasuredtheirmatingfrequenciesforonehour.Thisrevealed CosmopolitanstrainsandtheirCHprofiles,wechoseoneCosmo- significantassortativematingpatterns(Figure1):ALandDijfemales politan and one Zimbabwean strain to represent each group and tendedtoshowhigherlevelsofmatingwithALandDijmalesthan exploredtheroleofCHsindepth.Weshowedthepartialinvolve- with Z2–Z6 males, while Z2-6 females mated more frequently with ment of CHs in this case of sexual isolation by perfuming experi- Z2-6malesthanwithALandDijmales(Figure1A).Toquantifythe mentsandexploredthegeneticbasisofthecuticularhydrocarbons degree of sexual isolation, we calculated the joint isolation index variationbetweenthesetwostrainsbycomparingthelevelofdesat1 (I )foreachofthe64crossesbetweentheeighttypesoffly26.Over- psi anddesat2transcripts. all,theindexwashighlysignificant(TotalI 50.17,G 5561.5, psi 49df p,0.0001;TableS1). Results Surprisingly, Z1 flies behaved like AL and Dij flies (I 50.04; psi Zimbabwefemalestendnottocopulatewithcosmopolitanmales. t 50.64, p50.52; Figure 1B). These flies come from the 2755df WepairedmalesandfemalesfromsixstrainsfromZimbabwe(Z1-6) Zimbabwecapital(Harare)andshowacuticularhydrocarbonprofile and two cosmopolitan strains(Arkansas-Louisiana, (AL) from the closetothatofALandDijflies(seebelow).Cosmopolitan-typeflies Figure1|(A)MatingfrequencyofsinglepairsofmaleandfemalefliesfromAL,DijandZ1–Z6strains,shownasapercentage. Coupleswereobserved for60minutes.Eachboxrepresentsacrossbetweenthegenotypeofthefemale(rows)andofthemale(columns).Therelativesurfaceofthesquarefilledis proportionaltothematingfrequency.n534–156.(B)Dendrogramofahierarchicalclusteranalysis(unweightedpair-groupaveragelinkagemethod) oftheeightcosmopolitan-typeandZimbabweanstrains,comparingtheirmatingfrequencies.BranchlengthisproportionaltothepairwiseI (see psi MaterialsandMethods).Theeightstrainsaredividedinthreesignificantclusters(p50.05):thefirstone(‘‘Cosmopolitan-type’’)includetheAL,Dijand Z1flies,thesecond(Zimbabwean)includetheZ3toZ6flies,whereastheZ2fliesdifferfromthesetwogroups. SCIENTIFICREPORTS |2:224|DOI:10.1038/srep00224 2 www.nature.com/scientificreports havepreviouslybeendescribedinAfricanurbancentres,presumably intenseovipositorextrusion(generallyconsideredasarejectionres- duetohumantransport27,soonthebasisoftheCHdataweclassified ponse28)inresponsetoALmalesthantoZ6males(X 57.615,p5 2 Z1aspartoftheCosmopolitangroup.Asexpectedinstrainsshowing 0.022).Thecumulativematingcurvesforallfourcrossesinvolving incipientspeciation,thedistributionofmatingincrossesinvolving these two strains revealed significant differences: over the first 10 ZimbabwestrainsZ2–Z6andthosegroupedas‘Cosmopolitan’(AL, minutes,ALxALpairsshowedasignificantlyhighermatinglevel DijandZ1)revealedastrongasymmetricsexualisolation(I 50.35; (23%)thanZ6xZ6orALxZ6pairs(10%),whereasZ6xALpairs psi t 54.16, p50.0001, Figure 1B. All IA values for crosses be- alreadyshowedasignificantlylowermatinglevel(Figure2B).This 2755df psi tween‘Cosmopolitan’andZimbabwefliesweresignificant(p50.05; indicatesthatthefactor(s)thatleadZ6femalesnottomatewithAL TableS1),duetotherelativeabsenceofmatingbetweenZimbabwe malesaredetectedfromtheveryearliestmomentsoftheencounter femalesandCosmopolitanmales. betweenmaleandfemale. Weinvestigatedthesensoryeffectsresponsible fortheobserved matingpatternsbystudyingthecourtshipbehaviouroftheZ6and The nature of the stimulus provided by the male. We first AL strains (crosses are always given as female x male). We chose investigated whether the Z6 females were discriminating against a thesestrainsbecause they showedthemostextreme differences in visualsignalprovidedbytheALmales,bypaintingthefemales’eyes. matingpatternandincuticularhydrocarbonprofile(seebelow),and Thisunusualprocedurewasrequiredinordertomakethefemales canbetakenasexemplarsofthiscaseofincipientspeciation.First,we blindwhileenablingthemalestobehavenormally.Ithadnoeffecton exploredwhetherthetendencytopositiveassortativematinginZ6 the courtship intensity of sighted males compared to crosses with femaleswasduetoalteredmalebehaviour.Z6femalesinducedsig- sighted females, indicating that the males were not discriminating nificantlyhigherlevelsofcourtshipinALmalesthandidALfemales againstthefemalesbecauseofthepaintontheireyes,andtheZ6xAL (Figure2A),indicatingthatZ6femaleswerehighlyattractivetoAL crossstillinducedthehighestcourtshipindex(FigureS1).However, males.Thisinturnsuggests thatthetendency towardsisolation is sight-deprivedZ6femalesstillshowedvirtuallynomatingwithAL due to female discrimination by Z6 females of a sensory stimulus males,whereasmatingfrequenciesintheotherthreecrosseswereall providedbytheALmales,notduetoalteredmalebehaviours.This .40%(FigureS1).Asimilarmatingpatternwasobtainedunderred wasconfirmedbythefactthatZ6femalesmorefrequentlyshowed lightwhere bothpartners arevirtuallyblind: 48%ALand30%Z6 Figure2|(A)Mean(6SE)courtshipindicesinallfourcrossesbetweenALandZ6flies. Courtshipwasdefinedasthetimespentbyamaleshowing wingsvibration,femalegenitalialicking,circlingandcopulationattempt51.Pairsofflieswereobservedfor10minutes.n548–54.Lettersindicate significantdifferences.(B)CumulativematingcurvesinallfourcrossesbetweenALandZ6flies.Thetotalobservationperiodlastedfor60min. n596–156.Lettersindicatesignificantdifferences. SCIENTIFICREPORTS |2:224|DOI:10.1038/srep00224 3 www.nature.com/scientificreports malesmatedwithALfemales,comparedto2%and41%,respectively AL or Z6 males were used as donors, to produce desat1*AL* and with Z6 females. We conclude that male visual signals are not desat1*Z6*malesrespectively.Theperfumingprocedurealteredthe responsibleforthediscriminationshownbyZ6females. CHprofileofdesat1malestoaprofilebetweenthoseofdesat1males WenextstudiedwhethertheZ6femaleswereusingmalecourt- andthedonor(Figure6B).Perfumingdesat1maleswitheitherZ6or shipsongtodiscriminateagainsttheALmales.Recordingsofcourt- ALmalessignificantlyincreasedtheirsuccesswithALfemales,with shipsongfromALandZ6malesrevealedslightdifferencesbetween no difference between the treatments (Figure 6A). Strikingly, AL the two strains (Figure 3A). However, ablation of male wings and females showed higher mating frequencies than Z6 females in playbackofsyntheticsongmimickingthesedifferencesshowedthat all three crosses. We conclude that AL females are relatively thisdifferenceinsongplayednoroleinmatediscriminationbyZ6 indifferenttotheprecisecuticularcocktailcarriedbyamalefly,as females.Songwasimportanttomatingsuccess,becauseablationof long as it contains some ofthe relevant compounds. However, Z6 malewingsabolishedmatinginallbuttheALxALcross(mating5 females showed a significant increase in mating only when paired 20%),butmatingwasrestoredwhenwinglessmaleflieswereaccom- withdesat1*Z6*males,butnotwithdesat1*AL*males.Thisshows panied by playback of song typical of either their own strain or a that Z6 females are positively stimulated by the CH profile of Z6 heterotypicmale’ssong(Figure3B).Strikingly,.65%ofALmales males,andsuggeststhatCHmaleprofileandfemalepreferencesare mated with AL females when accompanied by playback, with no involved in this case of incipient speciation. However, the levels significantdifferencebetweenthetwoplaybacktypes,suggestingthat of mating shown in the Z6 x desat1*Z6* cross (Figure 6A) were AL females are highly stimulated by any type of D. melanogaster substantially lower than those in the unmanipulated homotypic courtship song. The persistence of very low mating of both kinds cross (Z6 x Z6 – Figure 3C), indicating that the pheromonal of female with Z6 wingless males accompanied by song playback profileoftheperfumedmaleswasstillnotoptimalforZ6females. indicatesthatthewingsofthesemalesareimportanteitherforthe Itispossiblethatthecombinationofthetwoprofiles(desat1males stimulationordetectionoffemales,orboth.Thesensorymodalities are rich in linear saturated alkanes, and Z6 males are rich in 5-T) involvedareunknownbutwepresumethemtobeprimarilychem- induced simultaneous antagonistic effects — repulsion and attrac- ical.Lastly,noZ6femalesmatedwithALmales,irrespectiveofthe tion — on the behaviour of Z6 females. The partial effect of per- typeofplayback,suggestingZ6femaleswerenotusingmalesongto fumingonmatingfrequency(20%insteadof45%)mayalsobedue discriminate against AL males. To test this hypothesis, we ablated totheabsenceoralterationofotherunknownpheromonalornon- female aristae, thereby deafening the females29–31. This procedure pheromonal signals in manipulated males. Z6 females were also significantly reduced mating by AL and Z6 females, but only in crossed with AL and Z6 males perfumed with either donor male homotypiccrosses(Figure3C).ThisindicatesthatALfemaleswere (Figure S2A). Z6 males showed higher mating frequency than AL equallystimulatedbytheacousticand/orthechemicalsignalspro- males,andtheperfumeofALmalesinducedaslightlyhighermating ducedbymalewingswhereasZ6femalesreliedmoreonthechemical responsethanthatseenwithZ6maleperfume.Thealteredfemale than on acoustic signals when paired with homotypic males. We responsemaybecausedby(i)thecomplexcombinationofthetwo concludethatanothersensorysignal,probablychemical,isrespons- CHprofiles (Figure S2B), (ii) the altered distribution of CHtopo- ibleforthetendencytoisolationintheZ6xALcross. graphy on the male cuticle35, and/or (iii) altered male behaviour Variation in cuticular hydrocarbons (CHs) has previously been producedbytheperfumingprocedure14,46. implicated in this assortative mating5–7, but no decisive evidence To identify which part of the male cuticular profile might be has been found. We found significant and complex CH variation involvedinthiscaseofincipientspeciation,wecalculatedcorrelation between these strains, which generally paralleled the differences coefficientsbetweenthemeancuticularcompositionofeachstrain, betweenthetwogroupsofstrainssuggestedbythematingpatterns anditsmatingperformance.ThematingfrequenciesofZ2-6females (Z2-6 vs Z1, AL and Dij) (Table S2). The most extreme CH dif- werehighlysignificantlynegativelycorrelatedwiththeproportionof ferences were observed between Z6 and AL flies (Figure 4). Z6 7-Tonthecuticleofthemalestheywerepairedwith(r520.458, females produced more C5-desaturated CHs (5-tricosene (5-T), d.f.538,p50.003).Forthethreecosmopolitan-typefemalesthe 5-pentacosene (5-P) and 5-heptacosene, 5, 9-hepta- and nona- situationwasthecompleteopposite:therewasasignificantpositive cosadienes), whereas AL females produced more of the equivalent correlationbetweenmatingfrequencyandtheproportionof7-Ton C7-desaturated CHs (7-tricosene (7-T), 7-pentacosene and 7- themale(r50.429,d.f.522,p50.036).Nosignificantcorrelations heptacosene,7,11-hepta-andnona-cosadienes).Similarly,Z6males werefoundbetweenmatingfrequencyandmale%5-T,5-T:7-Tratio produced significantly more 5-T than 7-T, while the opposite was or C5:C7 ratio for either group of females (data not shown). This trueinALmales.Multivariateanalysis(Figure5)showedvariability suggests that Zimbabwe females discriminate against males witha within Zimbabwe males – Z2, Z3 and Z4 showed an intermediate hydrocarbon bouquet containing a high proportion of 7-T, while positionbetweenZ5andZ6maleswithhighlevelsof5-T15-P1 cosmopolitan-type females are stimulated by 7-T-rich males. We n-heptacosaneandZ1,ALandDijmales(withhighlevelsof7-T1 concludethatthedifferencesincuticularhydrocarbonsplayarole n-tricosane). Even though Z2–Z6 males showed inter-strain vari- intheeffect.However,thisisnotthefullstory:other,asyetunknown, ationforthepercentageof5-T,theyallshowedasignificantlyhigher signalsmayalsocontributetothesensoryprofilethatstimulatesZ percentage of 5-T than Z1, AL and Dij males. Virtually all these femalesmost. compounds have previously been suggested to play a pheromonal Asaninitialexplorationofthegeneticbasesofthisvariation,we roleinD.melanogastercourtship10,13–15. usedRT-PCRtomeasurethelevelsofthedesat2transcriptandoffive This combined profile of male and female CHs in Zimbabwe desat1transcripts17–19,24,25inALandZ1flies,andinZ6andTai(Ivory strainsisunliketheprofilesofeithercosmopolitanorotherAfrican Coast)flies(Figure7;dataarepresentedasexpressionrelativetoAL strains;althoughtheC5:C7ratiofoundinZ2–Z6femalesissimilar flies).Taiflieswereincludedbecause–theypossessawell-studied tothatfoundinCentralAfricanstrains,thehighlevelsof5-Tshown CHprofilethatisintermediatebetweenthoseofZ6andALflies.The by Z2–Z6 males are unique4,9,10,20. This unique combination may cuticle ofTai males is mainly covered with7-monoenes (as in AL be a local adaptation to environmental parameters such as latitude males)whileTaifemalesmainlycarry5,9-dienes(asinZ6females). and/ortemperature22,32,33. desat1 and desat2 genes are both involved in the desaturation of fatty acids, a key step in the cuticular hydrocarbon biosynthesis Theroleofmalehydrocarbonsinisolation.Toinvestigatewhether pathway36,37. Inconclusive findings have linked desat2 to this case male CHs are used by females in selecting a mate, we perfumed of incipient speciation21, while desat1 is involved in the detection desat1 mutantmales, which lackany of theCHs described here34.. of cuticular hydrocarbons as well as their production24,25. desat2 SCIENTIFICREPORTS |2:224|DOI:10.1038/srep00224 4 www.nature.com/scientificreports Figure3|(A)CompositionofthecourtshipsongofALandZ6males.n510.(B)Isolationisnotduetoauditorysignalsfrommales.Matingfrequency inallfourcrossesbetweenALandZ6flieswasobservedfor60minutes.Maleshadtheirwingsclippedoffandwereeitherallowedtomateintheabsenceof anysong(Ø)orwereaccompaniedbyasyntheticsongcorrespondingtoALorZ6males.n55–56.(C)Isolationisnotduetosignalsdetectedbythe femalearistae.MatingfrequencyinallfourcrossesbetweenALandZ6flieswasobservedfor60minutes.Femaleswereeitherintact(‘Control’),orhad theiraristaeremoved(‘Aristae-’).n528–49.Lettersindicatesignificantdifferences. SCIENTIFICREPORTS |2:224|DOI:10.1038/srep00224 5 www.nature.com/scientificreports Figure4|Zimbabweandcosmopolitanflieshavequalitativelydifferentcuticularhydrocarbonprofiles. Typicalgaschromatographytracesareshown. Peakswereidentifiedbymassspectrometry.Keyforcompounds:A57,11-TD,B523MeBr19-T,C57-T,D55-T,E5n-C23,F59,13-PD,G57,11-PD, H55,9-PD,I59-P,J57-P,K55-P,L5n-C25,M59,13-HD,N57,11-HD,O527MeBr,P55,9-HD,Q57-H,R55-H,S5n-C27,T59,13-ND, U57,11-ND,V529MeBr,W55,9-ND,X5n-C29.CompoundshighlightedincyanandmagentaaredesaturatedonC5andC7,respectively.Detailed hydrocarboncompositionisshownonFig.S2. transcriptlevelsweresignificantlyhigherinthebodiesofZ6andTai fliesreactinginoppositewaystotheproportionof7-T,themaincu- fliesthaninZ1andALflies,withnodifferencebetweenthesexes ticularcomponentofmaleD.melanogasterfliesfromallstrainsexcept (Figure 7). Of the five desat1 transcripts, RC, RE and RB showed Zimbabwe. Zimbabwe females discriminate against cosmopolitan- significantinter-strainvariationbetweenmalestrains(Figure7),but likemalesonthebasisoftheproportionof7-TintheirCHbouquet, noneofthetranscriptswassignificantlydifferentsolelyinZ6males. whilefemalesfromotherstrainsarestimulatedbyhigherproportions Our data suggest that the desat2 gene is involved in the C5:C7 of this substance. Although we cannot exclude the possibility that ratiothatcharacterisesfemalesofbothZ6andTaiAfricanstrains. correlatedsignals,forexamplevolatilecompounds,arealsoinvolved However,thesex-specificdifferencebetweenthetwoAfricanstrains infemalediscrimination,thefactthattransferringALCHstodesat1 —lowlevelsof7-Tandhighlevelsof5-TinZ6malesbutnotinTai males did not significantly increase their mating levels with Z6 males—maybefurtherinfluencedbyeither(i)amoresubtletissue- females, while transfer of the Z6 profile did significantly increase specificvariationofdesat2expressioninmalesand/or(ii)adiffer- mating (Figure 6), indicates that the % of 7-T as a component of entialvariationofRAandREtranscriptsbetweenfemales.SinceRA thetotalCHbouquetmaypartiallyaccountfortheobservedpattern and RE are implicated in hydrocarbon production25, their interac- of isolation in these strains. In male D. melanogaster, 7-T plays an tionwithdesat2transcriptmayaffectmaleandfemaleCHprofiles inhibitoryroleinmale-malecourtshipandhasbeenshowntoactivate differently. bittergustatorysensoryneurons38.WehypothesisethatinZimbabwe femalesthereisasimilareffect,leadingthesefemalestoreject7-Trich Discussion males. Wehaveprovidedevidencethatcuticularhydrocarbonsareinvolved Although we found no evidence of quantitative differences in in this example of incipient speciation between D. melanogaster transcription levels of desat1 between two cosmopolitan lines and strains from Zimbabwe and from elsewhere in the world. Fur- two lines from Zimbabwe, it is possible that there is a qualitative thermore,wehaveshownthatthiseffectispartiallyduetofemale differenceintheformsofthisgeneinthesetwokindsofstrain.desat1 SCIENTIFICREPORTS |2:224|DOI:10.1038/srep00224 6 www.nature.com/scientificreports Figure5|Discriminantanalysisoffemale(A)andmale(B)fliesofalleightstrains,projectedontothefirsttwoprincipalcomponents. Probability ellipsescorrespondto95%probability.Thevariouscomponentsinthecuticularcocktail(A-X)werealsoprojectedontothesecomponents(arrows)to giveasenseofthedimensionality.Foreachsex,weconductedaforwardstepwisediscriminantanalysis(withanentrythresholdvalueofp50.05anda removalthresholdvalueofp50.10)usingtheadditive/logratiotransformedproportionoftheCHs)usingtheabsoluteamountoftheuncorrelatedCHs asquantitativevariablesandthestrainasaqualitativevariable.MagentaarrowsindicateC7compounds,cyanarrowsindicateC5compounds,black arrowsindicateotherscompounds.Forlegends,seefigure4. SCIENTIFICREPORTS |2:224|DOI:10.1038/srep00224 7 www.nature.com/scientificreports Figure6|(A)Chemicalsignalsarepartiallyresponsibleforisolation. CumulativematingcurvesforALandZ6femaleswithdesat1malesthatwere eitherunmanipulated(desat1)orreceivedhydrocarbonsfromALmales(desat1*AL*)orfromZ6males(desat1*Z6*).n548–80.Lettersindicate significantdifferences.(B)DiscriminantanalysisofmalefliesfromAL,Z6anddesat1strains,andfrommalesthathadpheromonetransfers (desat1*AL*anddesat1*Z6*),projectedontothefirsttwoprincipalcomponents.Equiprobableellipsescorrespondto95%probability.Thevarious componentsinthecuticularcocktailwerealsoprojectedontothesecomponents(arrows)togiveasenseofdimensionality.Weconductedaforward stepwisediscriminantanalysis(withanentrythresholdvalueofp50.05andaremovalthresholdvalueofp50.10)usingtheadditive/logratio transformedproportionoftheCHs)usingtheabsoluteamountoftheuncorrelatedCHsasquantitativevariablesandthestrainasaqualitativevariable. MagentaarrowsindicateC7compounds,cyanarrowsindicateC5compounds,blackarrowsindicateotherscompounds. simultaneously controls both the production and the detection of genesintermsoftheircombinedeffectsontheintraspecificvariation someDrosophilasexpheromones24,25.Thisoccursthroughdifferent forproductionandperceptionofpheromones. promoterregions25thatdriveitsexpressioninoenocytes(abdominal Ourdatahelpansweraconundrumthathasexistedforover15 tissues that control pheromone production)24,39; and in brain neu- years6,23 but they do not fully resolve this case of incipient spe- ronsinvolvedinpheromoneperception24,25.Zimbabwefemalesmay ciation. The factthat AL females apparently respondsignificantly carryaspecificformofthisgeneorofitspromoter(s)thatresultin tomanipulationofthemale’scourtshipsong,whereasZ6females alteredresponses.Wealsoneedtoexplore,bothatthegeneticand did not, suggests that there may be further differences between tissuelevels,thefunctionalrelationshipbetweendesat1anddesat2 thesestrains,whichmayaddtothepheromonally-drivenisolation SCIENTIFICREPORTS |2:224|DOI:10.1038/srep00224 8 www.nature.com/scientificreports Figure7|Transcriptionlevelsofdesat1anddesat2donotdirectlycorrelatewithmatingpatterns.RT-PCRwascarriedoutonthetranscriptionlevelsof desat1anddesat2formaleandfemalefliesfromTai(IvoryCoast),andZ6andZ1;differencesincomparisontoALfliesareshownasstarsabove/below bars(*:P,0.05;**:P,0.01).SignificantdifferencesintranscriptlevelsratiobetweenZ1,Z6andTaistrains(shownasdifferentlettersabove/belowbars) weredetectedwiththeRelativeExpressionSoftwareTool(REST,REST-MCSbetasoftwareversion247)wheretheiterationnumberwasfixedat2000. we have demonstrated here. Our findings indicate the potential until4to6daysold.Allexperimentswereperformedinat2460.5uCand6565% importance of sensory processes in speciation, and lay the basis humidity.Testswerecompletedoverseveraldaysandtookplace1–4hafterlightson. Onemalewasaspirated(withoutanaesthesia)underawatchglassusedasan forafullunderstandingofthisclassiccaseofincipientspeciation. observationchamber(1.6cm3).After10minutes,avirginfemalewasintroduced. Eachtestwasperformedfor60minutesinwhitelightandtheoverallfrequencyof Methods copulatingpairswasmeasuredforeachtreatment. Courtshipbehaviour.Flieswerepreparedasforthematingbehaviourtests.Asingle Strainsandflyhusbandry.AllD.melanogasterstrainswereraisedonyeast/cornmeal/ malewasaspirated(withoutanaesthesia)underawatchglassandthevirginfemale agarmediumandkeptat2460.5uCwith6565%humidityona12512light/dark wasintroduced10minuteslater.Eachtestwasperformedfor10minutesinwhite cycle.TheZimbabweandtheALlineswereprovidedbyProfessorJerryCoyne lightandthetimethatmalespentcourtingwasmeasured.Wethencalculatedthe (UniversityofChicago,Illinois).TheZimbabwelineswerecollectedin1990eitherin courtshipindex–thepercentageoftimethemalespentcourtingthefemale.Tomake theWildlifeReserveofSengwaforZ3,Z5andZ6lines,orinHarare,theZimbabwe thefemaleblind,wepaintedbothhereyeswithblacknailvarnish(‘MissHelen’ capital,forZ1,Z2andZ4lines.Forthesakeofsimplicity,wemodifiedthenamesofthe Zimbabwestrainsusedhere.TheoriginalnameswereZ15H23,Z25H18,Z35S6, nu112),usingasmallbrush.Thisprocedurewasperformedonehourbeforethetestto Z45H42,Z55Z53andZ65S30.ThecosmopolitanlineArkansas-Louisiana(AL) allowthevarnishtodry.Testsperformedinredlightproducedsimilarmating comesfromtheUnitedStates.TheDijon2000(Dij)linewascollectedbyDr.J-F patterns(seeResults&Discussion).Wethereforeconcludethatpaintingtheeyesdid FerveurinDijon(France)in2000.Althoughsomeofthesestrainshavebeenkeptin makethefliesblindanddidnotintroduceanyotherconfoundingsensoryvariable. thelaboratoryfor20years,ouraimwastostudyincipientspeciationratherthan whetherthesestrainsrepresentcurrentwild-typevariation.Moreimportantly,the Songrecordingandplayback.4–5dayoldmaleflieswereisolatedateclosionand performanceofthesestrainswasvirtuallyconstantcomparedtoresultsreportedinthe thenintroducedintotherecordingchambertogetherwithafemalethathaditswings 1990s6,7.Itshouldbenotedthatafterfiveyearsofacclimationinthelaboratory,wild- cutoff,topreventfemalewing-producedsoundsfrombeingrecorded.Malesongwas typefliesshownoimportantchangesinCH,courtshipormating40.Thedesat1linehas recordedusinganInsectavoxrecorder,linkedtoacomputer.Songwasfilteredbefore amutationinthedesat1geneanddesat1malesandfemalesshowdrasticallyreduced beingvisualisedonscreenusingtheAudacityprogrammeandanalysedwithSpike2 levelsof7-tricosene(7-T)and7,11-heptacosadiene(7,11-HD),respectively. software.ALandZ6malesproducedslightlydifferentsongs(Figure3A).Basedon thesedataandamoreextensivesurveyinColegraveetal.41artificialsongswere Behaviour.Matingbehaviour.AllflieswereisolatedunderlightCO anaesthesia0– synthesisedusingSignal(ElectronicDesign).Eachsongconsistedofanidentical 2 4haftereclosion.Maleflieswereheldindividuallyinfreshglassfoodvialsfor4or5 pulsesongaround300HzwithanIPIofeither35.5ms(representingthesongof daysbeforetesting.Femaleswerekeptfor4or5daysingroupsoffivetoten.Maleand Cosmopolitanflies)or30.3ms(representingthesongofZimbabweanflies). femalefliesusedasdonorsforhydrocarbontransferwerekeptinvialsingroupsof20 VariationinIPIfollowedarhythmiccycle42.Fulldetailsofsongsynthesisare SCIENTIFICREPORTS |2:224|DOI:10.1038/srep00224 9 www.nature.com/scientificreports describedinRitchieetal.43.Thedaybeforethetest,maleswereanaesthetisedbyCO2 4. Haerty,W.,Jallon,J.M.,Rouault,J.,Bazin,C.&Capy,P.Reproductiveisolationin andhadbothwingscompletelyremoved.Thematingcell,1.6cmdiameterx1cm naturalpopulationsofDrosophilamelanogasterfromBrazzaville(Congo). high,hadameshsurfaceandwasplacedonaloudspeaker(LCS2415)whichplayed Genetica116,215–224(2002). backthesyntheticsongat80dB.Thewholeapparatuswasplacedinasound- 5. Yukilevich,R.&True,J.R.Incipientsexualisolationamongcosmopolitan insulatedchamberat25uC.Thesongwascontinuallybroadcastthroughoutthe Drosophilamelanogasterpopulations.Evolution62,2112–2121(2008). durationoftheexperiment(30minutes). 6. Wu,C.I.etal.SexualisolationinDrosophilamelanogaster:apossiblecaseof incipientspeciation.ProcNatlAcadSciUSA92,2519–2523(1995). Cuticularhydrocarbons.Extractionandanalysis.Cuticularhydrocarbons(CHs) 7. Hollocher,H.,Ting,C.T.,Wu,M.L.&Wu,C.I.Incipientspeciationbysexual from4day-oldmaleandfemalefliesofthedifferentstrainswereanalyzedbygas isolationinDrosophilamelanogaster:extensivegeneticdivergencewithout chromatography(GC)followinghexaneextractionandtheadditionofsyntheticC26 reinforcement.Genetics147,1191–1201(1997). andC31hydrocarboninternalmarkers,accordingtostandardprocedures44.Analyses 8. Ferveur,J.F.Cuticularhydrocarbons:theirevolutionandrolesinDrosophila wereperformedwithaVarianCP3380chromatograph,fittedwithaflame-ionization pheromonalcommunication.BehavGenet35,279–295(2005). detector,withaCP-sil/5CBcapillarycolumn(Varian,25m30.32mmID)anda 9. Jallon,J.M.&Pechine,J.M.AnovelchemicalraceofDrosophilamelanogasterin split-splitlessinjectionsystem(operatingwithasplitflowof60ml/minandaseptum Africa.ComptesRendusDeLAcademieDesSciencesSerieIi309,1551–1556 purgeof3ml/min,openingofthesplitport30secafterinjection).Hydrogenwas (1989). usedascarriergas(50cm/secvelocityatroomtemperature).Theinjectorand 10.Ferveur,J.F.,Cobb,M.,Boukella,H.&Jallon,J.M.World-widevariationin detectortemperatureswere260and280uC,respectively.Thecolumnwasheld Drosophilamelanogastersexpheromone:behaviouraleffects,geneticbasesand isothermallyat140uCfor2min,thenprogrammedtoincreaseatarateof5uC/minto potentialevolutionaryconsequences.Genetica97,73–80(1996). 280uC.ThedatawereautomaticallycomputedandrecordedusingPCsoftware(Star 11.Yukilevich,R.&Yukilevich,R.&True,J.R.Africanmorphology,behaviorand 5.2,Varian). phermonesunderlieincipientsexualisolationbetweenusandCaribbean Hydrocarbontransfer.WeusedthemethodofCoyneetal.45.15receivermales Drosophilamelanogaster.Evolution62,2807–2828(2008). (desat1males)wereenclosedwith150killeddonormales(ALorZ6males)inafood 12.Jallon,J.M.AfewchemicalwordsexchangedbyDrosophiladuringcourtshipand vialovernightbeforeexperiment.Usingdeaddonorsavoidstheproblemofpotential mating.BehavGenet14,441–478(1984). socialinteractionsthatcanoccurwithlivedonors46.Toincreasethecontactbetween 13.Ferveur,J.F.&Sureau,G.Simultaneousinfluenceonmalecourtshipof donorsandreceivers,theplugofthevialwaspusheddown,leavinga0.5cmhigh stimulatoryandinhibitorypheromonesproducedbylivesex-mosaicDrosophila spacebetweenthefoodandtheplug.Transferefficiencywastestedusinggas melanogaster.ProcBiolSci263,967–973(1996). chromatography. 14.Grillet,M.,Dartevelle,L.&Ferveur,J.F.ADrosophilamalepheromoneaffects Fliestobeanalyzedfortheirbehavioralandchemicalcharacteristicswerecollected femalesexualreceptivity.ProcBiolSci273,315–323(2006). inparallel.Weusedahighlysensitivedetectionmethod(SolidPhaseMicro 15.Marcillac,F.&Ferveur,J.F.Asetoffemalepheromonesaffectsreproduction Extraction47)tocomparetheHCprofilesinthesetwosamples,andfoundnovariation before,duringandaftermatinginDrosophila.JExpBiol207,3927–3933(2007). otherthanthecompoundspassivelytransferedbetweenpartnersduringphysical 16.Billeter,J.C.,Atallah,J.,Krupp,J.J.,Millar,J.G.&Levine,J.D.Specializedcellstag interaction.Thesecompoundsarenotrelevantinthepresentstudy,whichfocusedon sexualandspeciesidentityinDrosophilamelanogaster.Nature461,987–991 precopulatorybehavior. (2009). 17.Coyne,J.A.,Wicker-Thomas,C.&Jallon,J.M.Ageneresponsibleforacuticular hydrocarbonpolymorphisminDrosophilamelanogaster.GenetRes73,189–203 Real-TimePCR.Wemeasuredtherelativeamountofthefivedesat1transcripts(RA, (1999). RC,RE,RBandRD)andofthedesat2transcriptin35to45headlessbodiesof5-day- 18.Wicker-Thomas,C.,Henriet,C.&DalleracR.Partialcharacterizationofafatty oldmales.RNAswereextractedbytheTrizolmethod(GIBCOBRL)andtreatedwith aciddesaturasegeneinDrosophilamelanogaster.InsectBiochemMolBiol27, RNase-freeDNasetoavoidcontaminationbygenomicDNA.TotalRNA(2mg)was 963–972(1997). reversetranscribedwiththeiScriptcDNASynthesisKit(Biorad).QuantativePCR 19.Dallerac,R.etal.ADelta9desaturasegenewithadifferentsubstratespecificityis reactionswereperformedwiththeIQSYBRGreensupermix(Biorad)inathermal responsibleforthecuticulardienehydrocarbonpolymorphisminDrosophila cycler(MyIQ,Biorad)accordingtotheprocedurerecommendedbythe melanogaster.ProcNatAcadSciUSA97,9449–9454(2000). manufacturer.TheqPCRreactionwasdoneinavolumeof20ml,by40cycles(95uC 20.Takahashi,A.,Tsaur,S.C.,Coyne,J.A.&Wu,C.I.Thenucleotidechanges for30sec,TMuCfor30secand72uCfor30sec),precededby3mindenaturation governingcuticularhydrocarbonvariationandtheirevolutioninDrosophila stepat98uCandfollowedbya1minelongationstepat72uC.TMofthehybridization melanogaster.ProcNatlAcadSciUSA98,3920–3925(2001). stepdependsontheprimerpairused(seeHouotetal.25).Eachreactionwas 21.Fang,S.,Takahashi,A.&Wu,C.I.Amutationinthepromoterofdesaturase2is performedintriplicateandthemeanofthethreeindependentbiologicalreplicates correlatedwithsexualisolationbetweenDrosophilabehavioralraces.Genetics wascalculated.AllresultswerenormalizedtotheActine5CmRNAlevel. 162,781–784(2002). 22.Greenberg,A.J.,Moran,J.R.,Coyne,J.A.&Wu,C.I.Ecologicaladaptation Statisticalanalysis.Matingfrequency.Formatingfrequencycomparisons,weused duringincipientspeciationrevealedbyprecisegenereplacement.Science302, JMATINGSoftware26tocomputethetotalIpsiandthepairwiseIpsiandIApsi. 1754–1757(2003). ThepairwiseIpsiwereusedasadissimilarityindextoachieveanagglomerative 23.Coyne,J.A.&Elwyn,S.Doesthedesaturase-2locusinDrosophilamelanogaster hierarchicalclustering(unweightedpair-groupaveragelinkagemethod).Toanalyse causeadaptationandsexualisolation?Evolution60,279–291(2006). cumulativematingfrequency,matinglevelswererecordedevery10minover60min 24.Marcillac,F.,Grosjean,Y.&Ferveur,J.F.Asinglemutationaltersproductionand andcomparedusingachi-squaretestwithacomputationofsignificancebycell. discriminationofDrosophilasexpheromones.ProcBiolSci272,303–309(2005). CourtshipIndiceswerecomparedwiththeKruskal-Wallistest,completedby 25.Houot,B.,Bousquet,F.&Ferveur,J.F.Theconsequencesofregulationofdesat1 Conover-Iman’smultiplepairwisecomparison(two-tailedwithBonferroni expressionforpheromoneemissionanddetectioninDrosophilamelanogaster. correction). Genetics185,1297–1309(2010). Cuticularprofiles.Formaleandfemalefliesofeachstrain,therelativeamountsof 26.Carvajal-Rodriguez,A.&Rolan-Alvarez,E.J.MATING:asoftwareforthe CHsweretransformedbyadditivelog-ratiotransformation(alr)48usingCoDaPack analysisofsexualselectionandsexualisolationeffectsfrommatingfrequency (v2.01.1)49;thezerovaluesweresubstitutedby1026valuesandthedenominatorwas data.BMCEvol.Biol.6,40–44(2006). takentobetheproportionofn-C29.Foreachsex,wecarriedoutastepwisedis- 27.Haerty,W.,Lesbats,M.&Capy,P.Pre-reproductiveisolationasaconsequenceof criminantanalysis(DA)(forward,entrythresholdvalue:p50.05andremoval allopatricdifferentiationbetweenpopulationsofDrosophilamelanogaster. thresholdvalue:p50.10)usingthealr-transformedCHproportionsasquantitative MolecularEcology14,3801–3807(2005). variablesandthestrain(orperfume)asthequalitativevariable. 28.Lasbleiz,C.,Everaerts,C.&Ferveur,J.F.CourtshipbehaviourofDrosophila ExceptforIpsi,statisticalanalyseswereconductedwithXLSTAT2007(Addinsoft, melanogasterrevisited.AnimalBehaviour72,1001–1012(2006). 2007). 29.Mayr,E.TheroleoftheantennaeinthematingbehavioroffemaleDrosophila. Transcriptlevels.StatisticalanalyseswereperformedusingXLSTATsoftware. Evolution4,149–154(1950). Significantdifferencesintranscriptlevelsratiobetweengenotypesweredetectedwith 30.Ewing,A.W.AntennaofDrosophilaasaLoveSongReceptor.Physiological theRelativeExpressionSoftwareTool(REST,REST-MCSbetasoftwareversion250) Entomology3,33–36(1978). andtheiterationnumberwasfixedat2000.Thistestisbasedontheprobabilityofan 31.Gopfert,M.C.&Robert,D.ThemechanicalbasisofDrosophilaaudition.J.Exp effectaslargeasthatobservedunderthenullhypothesis(noeffectofthetreatment), Biol205,1199–1208(2002). usingarandomizationtest(PairWiseFixedReallocationRandomisationTestE). 32.Rouault,J.,Capy,P.&Jallon,J.M.Variationsofmalecuticularhydrocarbonswith geoclimaticvariables:anadaptativemechanisminDrosophilamelanogaster? Genetica110,117–130(2000). 1. Alcock,J.AnimalBehavior:AnEvolutionaryApproach.6thEdition(Sunderland: 33.Rouault,J.D.,Marican,C.,Wicker-Thomas,C.&Jallon,J.M.Relationsbetween SinauerAssociates,Massachusetts,1998). cuticularhydrocarbon(HC)polymorphism,resistanceagainstdesiccationand 2. Coyne,J.A.&Orr,H.A.Speciation.(Sunderland:SinauerAssociates, breedingtemperature;amodelforHCevolutioninD.melanogasterand Massachusett,2004) D.simulans.Genetica120,195–212(2004). 3. Korol,A.etal.NonrandommatinginDrosophilamelanogasterlaboratory 34.Marcillac,F.,Bousquet,F.,Alabouvette,J.,Savarit,F.&Ferveur,J.F.Amutation populationsderivedfromcloselyadjacentecologicallycontrastingslopesat withmajoreffectsonDrosophilamelanogastersexpheromones.Genetics171, ‘‘EvolutionCanyon’’ProcNatlAcadSciUSA97,12637–12642(2007). 1617–1628(2005). SCIENTIFICREPORTS |2:224|DOI:10.1038/srep00224 10

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