Genomic architecture of phenotypic divergence between two hybridizing plant species along an elevational gradient
Hybrid zones that occur across environmental gradients provide excellent opportunities for studying the maintenance of divergent adaptations in the presence of gene flow. They also provide insight into the biodiversity implications of future species contact and hybridization in a changing world. We...
Saved in:
Published in | AoB plants Vol. 8 |
---|---|
Main Authors | , , |
Format | Journal Article |
Language | English |
Published |
England
Oxford University Press
01.01.2016
|
Series | Editor's choice |
Subjects | |
Online Access | Get full text |
Cover
Loading…
Abstract | Hybrid zones that occur across environmental gradients provide excellent opportunities for studying the maintenance of divergent adaptations in the presence of gene flow. They also provide insight into the biodiversity implications of future species contact and hybridization in a changing world. We studied divergent morphology between two Senecio (ragwort) species that form a natural hybrid zone with respect to elevation on Mount Etna, Italy, using a quantitative trait locus (QTL) mapping approach. We found signals of divergent selection with increased genetic differentiation close to QTLs. Extensive interactions between QTLs and traits suggested a QTL architecture that is resistant to hybridization.
Knowledge of the genetic basis of phenotypic divergence between species and how such divergence is caused and maintained is crucial to an understanding of speciation and the generation of biodiversity. The hybrid zone between Senecio aethnensis and S. chrysanthemifolius on Mount Etna, Sicily, provides a well-studied example of species divergence in response to conditions at different elevations, despite hybridization and gene flow. Here, we investigate the genetic architecture of divergence between these two species using a combination of quantitative trait locus (QTL) mapping and genetic differentiation measures based on genetic marker analysis. A QTL architecture characterized by physical QTL clustering, epistatic interactions between QTLs, and pleiotropy was identified, and is consistent with the presence of divergent QTL complexes resistant to gene flow. A role for divergent selection between species was indicated by significant negative associations between levels of interspecific genetic differentiation at mapped marker gene loci and map distance from QTLs and hybrid incompatibility loci. Within-species selection contributing to interspecific differentiation was evidenced by negative associations between interspecific genetic differentiation and genetic diversity within species. These results show that the two Senecio species, while subject to gene flow, maintain divergent genomic regions consistent with local selection within species and selection against hybrids between species which, in turn, contribute to the maintenance of their distinct phenotypic differences. |
---|---|
AbstractList | Knowledge of the genetic basis of phenotypic divergence between species and how such divergence is caused and maintained is crucial to an understanding of speciation and the generation of biodiversity. The hybrid zone between Senecio aethnensis and S. chrysanthemifolius on Mount Etna, Sicily, provides a well-studied example of species divergence in response to conditions at different elevations, despite hybridization and gene flow. Here, we investigate the genetic architecture of divergence between these two species using a combination of quantitative trait locus (QTL) mapping and genetic differentiation measures based on genetic marker analysis. A QTL architecture characterized by physical QTL clustering, epistatic interactions between QTLs, and pleiotropy was identified, and is consistent with the presence of divergent QTL complexes resistant to gene flow. A role for divergent selection between species was indicated by significant negative associations between levels of interspecific genetic differentiation at mapped marker gene loci and map distance from QTLs and hybrid incompatibility loci. Within-species selection contributing to interspecific differentiation was evidenced by negative associations between interspecific genetic differentiation and genetic diversity within species. These results show that the two Senecio species, while subject to gene flow, maintain divergent genomic regions consistent with local selection within species and selection against hybrids between species which, in turn, contribute to the maintenance of their distinct phenotypic differences.Knowledge of the genetic basis of phenotypic divergence between species and how such divergence is caused and maintained is crucial to an understanding of speciation and the generation of biodiversity. The hybrid zone between Senecio aethnensis and S. chrysanthemifolius on Mount Etna, Sicily, provides a well-studied example of species divergence in response to conditions at different elevations, despite hybridization and gene flow. Here, we investigate the genetic architecture of divergence between these two species using a combination of quantitative trait locus (QTL) mapping and genetic differentiation measures based on genetic marker analysis. A QTL architecture characterized by physical QTL clustering, epistatic interactions between QTLs, and pleiotropy was identified, and is consistent with the presence of divergent QTL complexes resistant to gene flow. A role for divergent selection between species was indicated by significant negative associations between levels of interspecific genetic differentiation at mapped marker gene loci and map distance from QTLs and hybrid incompatibility loci. Within-species selection contributing to interspecific differentiation was evidenced by negative associations between interspecific genetic differentiation and genetic diversity within species. These results show that the two Senecio species, while subject to gene flow, maintain divergent genomic regions consistent with local selection within species and selection against hybrids between species which, in turn, contribute to the maintenance of their distinct phenotypic differences. Hybrid zones that occur across environmental gradients provide excellent opportunities for studying the maintenance of divergent adaptations in the presence of gene flow. They also provide insight into the biodiversity implications of future species contact and hybridization in a changing world. We studied divergent morphology between two Senecio (ragwort) species that form a natural hybrid zone with respect to elevation on Mount Etna, Italy, using a quantitative trait locus (QTL) mapping approach. We found signals of divergent selection with increased genetic differentiation close to QTLs. Extensive interactions between QTLs and traits suggested a QTL architecture that is resistant to hybridization. Knowledge of the genetic basis of phenotypic divergence between species and how such divergence is caused and maintained is crucial to an understanding of speciation and the generation of biodiversity. The hybrid zone between Senecio aethnensis and S. chrysanthemifolius on Mount Etna, Sicily, provides a well-studied example of species divergence in response to conditions at different elevations, despite hybridization and gene flow. Here, we investigate the genetic architecture of divergence between these two species using a combination of quantitative trait locus (QTL) mapping and genetic differentiation measures based on genetic marker analysis. A QTL architecture characterized by physical QTL clustering, epistatic interactions between QTLs, and pleiotropy was identified, and is consistent with the presence of divergent QTL complexes resistant to gene flow. A role for divergent selection between species was indicated by significant negative associations between levels of interspecific genetic differentiation at mapped marker gene loci and map distance from QTLs and hybrid incompatibility loci. Within-species selection contributing to interspecific differentiation was evidenced by negative associations between interspecific genetic differentiation and genetic diversity within species. These results show that the two Senecio species, while subject to gene flow, maintain divergent genomic regions consistent with local selection within species and selection against hybrids between species which, in turn, contribute to the maintenance of their distinct phenotypic differences. Hybrid zones that occur across environmental gradients provide excellent opportunities for studying the maintenance of divergent adaptations in the presence of gene flow. They also provide insight into the biodiversity implications of future species contact and hybridization in a changing world. We studied divergent morphology between two Senecio (ragwort) species that form a natural hybrid zone with respect to elevation on Mount Etna, Italy, using a quantitative trait locus (QTL) mapping approach. We found signals of divergent selection with increased genetic differentiation close to QTLs. Extensive interactions between QTLs and traits suggested a QTL architecture that is resistant to hybridization. Knowledge of the genetic basis of phenotypic divergence between species and how such divergence is caused and maintained is crucial to an understanding of speciation and the generation of biodiversity. The hybrid zone between Senecio aethnensis and S. chrysanthemifolius on Mount Etna, Sicily, provides a well-studied example of species divergence in response to conditions at different elevations, despite hybridization and gene flow. Here, we investigate the genetic architecture of divergence between these two species using a combination of quantitative trait locus (QTL) mapping and genetic differentiation measures based on genetic marker analysis. A QTL architecture characterized by physical QTL clustering, epistatic interactions between QTLs, and pleiotropy was identified, and is consistent with the presence of divergent QTL complexes resistant to gene flow. A role for divergent selection between species was indicated by significant negative associations between levels of interspecific genetic differentiation at mapped marker gene loci and map distance from QTLs and hybrid incompatibility loci. Within-species selection contributing to interspecific differentiation was evidenced by negative associations between interspecific genetic differentiation and genetic diversity within species. These results show that the two Senecio species, while subject to gene flow, maintain divergent genomic regions consistent with local selection within species and selection against hybrids between species which, in turn, contribute to the maintenance of their distinct phenotypic differences. Knowledge of the genetic basis of phenotypic divergence between species and how such divergence is caused and maintained is crucial to an understanding of speciation and the generation of biodiversity. The hybrid zone between Senecio aethnensis and S. chrysanthemifolius on Mount Etna, Sicily, provides a well-studied example of species divergence in response to conditions at different elevations, despite hybridization and gene flow. Here, we investigate the genetic architecture of divergence between these two species using a combination of quantitative trait locus (QTL) mapping and genetic differentiation measures based on genetic marker analysis. A QTL architecture characterized by physical QTL clustering, epistatic interactions between QTLs, and pleiotropy was identified, and is consistent with the presence of divergent QTL complexes resistant to gene flow. A role for divergent selection between species was indicated by significant negative associations between levels of interspecific genetic differentiation at mapped marker gene loci and map distance from QTLs and hybrid incompatibility loci. Within-species selection contributing to interspecific differentiation was evidenced by negative associations between interspecific genetic differentiation and genetic diversity within species. These results show that the two Senecio species, while subject to gene flow, maintain divergent genomic regions consistent with local selection within species and selection against hybrids between species which, in turn, contribute to the maintenance of their distinct phenotypic differences. |
Author | Abbott, Richard J. Brennan, Adrian C. Hiscock, Simon J. |
Author_xml | – sequence: 1 givenname: Adrian C. surname: Brennan fullname: Brennan, Adrian C. email: a.c.brennan@durham.ac.uk organization: University of St Andrews – sequence: 2 givenname: Simon J. surname: Hiscock fullname: Hiscock, Simon J. organization: University of Bristol – sequence: 3 givenname: Richard J. surname: Abbott fullname: Abbott, Richard J. organization: University of St Andrews |
BackLink | https://www.ncbi.nlm.nih.gov/pubmed/27083198$$D View this record in MEDLINE/PubMed |
BookMark | eNqFUc9rHCEYlZLSpGmOvQaPuUzjj3F0LoEQ0rQQ6KU9i-N8u2txdaLOLpu_vra7DWkg1Ivie773_N57dBRiAIQ-UvKJkp5fmjhM3lxOfksYe4NOGGlpw5SgR8_Ox-gs55-kLs5U15J36JhJojjt1Ql6uIMQ185ik-zKFbBlToDjAk-rCpTdVKHRbSAtIVjAA5QtQMBlG_FqNyQ3ukcXlrimCAXnCayDjI2P9c4EDB42prgYjMfLZEYHoXxAbxfGZzg77Kfox-fb7zdfmvtvd19vru8b2zJSms4QwgglgonBjmPLpKCMEsXYSDsKjHadoobwgauWSCnVSFknuOFyEFJ2jJ-iq73uNA9rGG21TsbrKbm1STsdjdP_IsGt9DJudKuUlEJUgYuDQIoPM-Si1y5b8PWrEOesqex5T5lo-0o9f-71ZPJ3zpXQ7Ak2xZwTLJ4olOjfVep9lXpfZeXzF3zryp9J1qjOv_rqkDjO038MfgFncLRc |
CitedBy_id | crossref_primary_10_1007_s00035_018_0211_8 crossref_primary_10_1111_jse_12267 crossref_primary_10_1007_s00606_017_1420_0 crossref_primary_10_1038_s41437_022_00576_4 crossref_primary_10_1111_mec_15319 crossref_primary_10_1093_aobpla_ply007 crossref_primary_10_1111_mec_14481 crossref_primary_10_3389_fpls_2022_907363 crossref_primary_10_1101_cshperspect_a041440 crossref_primary_10_1080_17550874_2017_1400127 crossref_primary_10_1093_aobpla_ply078 |
Cites_doi | 10.1038/nature10944 10.1111/j.1471-8286.2004.00845.x 10.1534/genetics.105.047985 10.1111/j.1471-8286.2005.01155.x 10.1038/hdy.1986.135 10.1111/j.1420-9101.2012.02599.x 10.1046/j.1469-8137.2002.00420.x 10.1126/science.1086949 10.1111/j.0014-3820.2001.tb00628.x 10.1073/pnas.1219381110 10.1111/j.1365-294X.2008.03921.x 10.1093/genetics/152.3.1203 10.1093/genetics/140.3.1111 10.1111/j.1558-5646.2009.00622.x 10.1098/rstb.2011.0263 10.1093/genetics/138.3.963 10.1111/j.1558-5646.2007.00214.x 10.1111/j.1469-8137.2009.02944.x 10.1111/mec.12127 10.1111/evo.12663 10.1093/molbev/mst168 10.1371/journal.pbio.1000500 10.1038/hdy.2012.62 10.1016/S0169-5347(97)81027-0 10.1093/genetics/159.4.1701 10.1016/S0169-5347(01)02177-2 10.1016/j.tree.2011.04.005 10.1534/genetics.104.031195 10.1093/gbe/evt127 10.1111/j.1365-294X.2011.05350.x 10.1111/j.0014-3820.2005.tb00967.x 10.1111/j.1558-5646.2011.01269.x 10.1111/evo.12062 10.1111/j.1558-5646.2009.00943.x 10.1098/rstb.2011.0199 10.1111/mec.12796 10.1098/rstb.2011.0196 10.1534/genetics.108.089938 10.1111/jeb.12765 10.1098/rstb.2011.0197 10.1098/rstb.2013.0346 10.1093/molbev/msm066 10.1111/j.1365-294X.2011.05080.x 10.1093/czoolo/59.1.53 10.1046/j.1420-9101.2001.00335.x 10.1371/journal.pbio.0030285 10.1093/acprof:osobl/9780199587100.001.0001 10.1111/j.1365-294X.2008.03946.x 10.1371/journal.pgen.1000232 10.1111/mec.13618 10.1534/genetics.108.092221 10.1038/hdy.2014.14 10.1111/evo.12725 10.1111/j.1755-0998.2010.02847.x 10.1093/genetics/163.3.939 10.1038/sj.hdy.6800937 |
ContentType | Journal Article |
Copyright | Published by Oxford University Press on behalf of the Annals of Botany Company. 2016 Published by Oxford University Press on behalf of the Annals of Botany Company. |
Copyright_xml | – notice: Published by Oxford University Press on behalf of the Annals of Botany Company. 2016 – notice: Published by Oxford University Press on behalf of the Annals of Botany Company. |
DBID | TOX AAYXX CITATION NPM 7X8 5PM |
DOI | 10.1093/aobpla/plw022 |
DatabaseName | Oxford Journals Open Access Collection CrossRef PubMed MEDLINE - Academic PubMed Central (Full Participant titles) |
DatabaseTitle | CrossRef PubMed MEDLINE - Academic |
DatabaseTitleList | MEDLINE - Academic PubMed CrossRef |
Database_xml | – sequence: 1 dbid: NPM name: PubMed url: https://proxy.k.utb.cz/login?url=http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed sourceTypes: Index Database – sequence: 2 dbid: TOX name: Oxford Journals Open Access Collection url: https://academic.oup.com/journals/ sourceTypes: Publisher |
DeliveryMethod | fulltext_linktorsrc |
Discipline | Botany |
EISSN | 2041-2851 |
ExternalDocumentID | PMC4887755 27083198 10_1093_aobpla_plw022 10.1093/aobpla/plw022 |
Genre | Journal Article |
GrantInformation_xml | – fundername: Grant No. grantid: 264125; EcoGenes – fundername: Natural Environment Research Council (NERC) grantid: NE/D014166/1 – fundername: European Commission 7th Framework Programme Capacities Work Programme grantid: FP7-REGPOT 2010-1 |
GroupedDBID | .I3 0R~ 2XV 4.4 5VS 5WA 6J9 70E AAFWJ AAKDD AAMVS AAOGV AAPPN AAPXW AAVAP ABPTD ABQLI ABXVV ACGFO ACGFS ACPRK ADBBV ADHZD ADRAZ AENEX AENZO AFPKN AFULF ALMA_UNASSIGNED_HOLDINGS ALUQC AOIJS BAYMD BCNDV BTTYL C1A CIDKT CZ4 D~K E3Z ECGQY EJD GROUPED_DOAJ GX1 H13 HYE HZ~ IAO IFM ISR ITC KQ8 KSI M48 ML0 M~E O5R O5S OAWHX OJQWA OK1 PEELM RD5 RNS ROL ROX RPM RXO TOX WG7 X7H ~91 ~D7 ~S- 7X2 AAYXX ABEJV ABGNP AEUYN AFKRA AMNDL ATCPS BBNVY BENPR BHPHI CCPQU CITATION HCIFZ M0K M7P PATMY PHGZM PHGZT PIMPY PYCSY NPM 7X8 PQGLB 5PM |
ID | FETCH-LOGICAL-c420t-6a002010525bcdd42751210822d161e216681a03b38407778d12653a37b577623 |
IEDL.DBID | M48 |
ISSN | 2041-2851 |
IngestDate | Thu Aug 21 18:14:45 EDT 2025 Thu Jul 10 22:59:47 EDT 2025 Wed Feb 19 02:08:29 EST 2025 Tue Jul 01 05:16:58 EDT 2025 Thu Apr 24 23:03:14 EDT 2025 Wed Aug 28 03:21:16 EDT 2024 |
IsDoiOpenAccess | true |
IsOpenAccess | true |
IsPeerReviewed | true |
IsScholarly | true |
Keywords | QTL architecture selection QTL interactions phenotypic divergence Genetic differentiation hybridization speciation |
Language | English |
License | This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited. http://creativecommons.org/licenses/by/4.0 Published by Oxford University Press on behalf of the Annals of Botany Company. |
LinkModel | DirectLink |
MergedId | FETCHMERGED-LOGICAL-c420t-6a002010525bcdd42751210822d161e216681a03b38407778d12653a37b577623 |
Notes | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 Associate Editor: Diana Wolf |
OpenAccessLink | http://journals.scholarsportal.info/openUrl.xqy?doi=10.1093/aobpla/plw022 |
PMID | 27083198 |
PQID | 1793912549 |
PQPubID | 23479 |
ParticipantIDs | pubmedcentral_primary_oai_pubmedcentral_nih_gov_4887755 proquest_miscellaneous_1793912549 pubmed_primary_27083198 crossref_primary_10_1093_aobpla_plw022 crossref_citationtrail_10_1093_aobpla_plw022 oup_primary_10_1093_aobpla_plw022 |
ProviderPackageCode | CITATION AAYXX |
PublicationCentury | 2000 |
PublicationDate | 2016-01-01 |
PublicationDateYYYYMMDD | 2016-01-01 |
PublicationDate_xml | – month: 01 year: 2016 text: 2016-01-01 day: 01 |
PublicationDecade | 2010 |
PublicationPlace | England |
PublicationPlace_xml | – name: England |
PublicationSeriesTitle | Editor's choice |
PublicationTitle | AoB plants |
PublicationTitleAlternate | AoB Plants |
PublicationYear | 2016 |
Publisher | Oxford University Press |
Publisher_xml | – name: Oxford University Press |
References | Gompert (2025040414162685300_PLW022C23) 2012; 367 Foll (2025040414162685300_PLW022C21) 2008; 180 Wang (2025040414162685300_PLW022C59) 2011 Jiang (2025040414162685300_PLW022C26) 1995; 140 Servedio (2025040414162685300_PLW022C50) 2011; 26 Breitling (2025040414162685300_PLW022C7) 2008; 4 Lexer (2025040414162685300_PLW022C31) 2005; 169 Smadja (2025040414162685300_PLW022C51) 2011; 20 Nosil (2025040414162685300_PLW022C38) 2012; 367 Chapman (2025040414162685300_PLW022C11) 2016; 29 Cruikshank (2025040414162685300_PLW022C15) 2014; 23 Yeaman (2025040414162685300_PLW022C62) 2013; 110 Strasburg (2025040414162685300_PLW022C53) 2012; 367 R Development Core Team (2025040414162685300_PLW022C45) 2011 Whiteley (2025040414162685300_PLW022C60) 2008; 180 Coyne (2025040414162685300_PLW022C14) 2004 Twyford (2025040414162685300_PLW022C57) 2015; 69 Turelli (2025040414162685300_PLW022C55) 2001; 16 Rieseberg (2025040414162685300_PLW022C47) 2003; 301 Taylor (2025040414162685300_PLW022C54) 2012; 110 Kao (2025040414162685300_PLW022C29) 1999; 152 Lincoln (2025040414162685300_PLW022C32) 1993 Excoffier (2025040414162685300_PLW022C16) 2010; 10 Barton (2025040414162685300_PLW022C3) 1986; 57 Bouck (2025040414162685300_PLW022C6) 2007; 61 Lowry (2025040414162685300_PLW022C34) 2010; 8 Orr (2025040414162685300_PLW022C41) 2001; 55 Osborne (2025040414162685300_PLW022C42) 2013; 5 Lindtke (2025040414162685300_PLW022C33) 2015; 69 Nosil (2025040414162685300_PLW022C39) 2009; 18 Gagnaire (2025040414162685300_PLW022C22) 2013; 22 Brennan (2025040414162685300_PLW022C9) 2014; 113 Yeaman (2025040414162685300_PLW022C63) 2011; 65 Abbott (2025040414162685300_PLW022C1) 2013; 26 Filatov (2025040414162685300_PLW022C20) 2016 Rogers (2025040414162685300_PLW022C49) 2013; 59 Turner (2025040414162685300_PLW022C56) 2005; 3 Paterson (2025040414162685300_PLW022C43) 2002; 154 Chapman (2025040414162685300_PLW022C10) 2013; 30 Feder (2025040414162685300_PLW022C17) 2010; 64 Abbott (2025040414162685300_PLW022C2) 2014; 369 Feder (2025040414162685300_PLW022C18) 2003; 163 Kalinowsky (2025040414162685300_PLW022C28) 2005; 5 Wu (2025040414162685300_PLW022C61) 2001; 14 Fishman (2025040414162685300_PLW022C100) 2001; 159 James (2025040414162685300_PLW022C25) 2005; 59 Peakall (2025040414162685300_PLW022C44) 2006; 6 Rogers (2025040414162685300_PLW022C48) 2007; 24 Churchill (2025040414162685300_PLW022C12) 1994; 138 Brennan (2025040414162685300_PLW022C8) 2009; 183 Barton (2025040414162685300_PLW022C4) 2009; 63 Muir (2025040414162685300_PLW022C35) 2013; 67 Via (2025040414162685300_PLW022C58) 2008; 17 Stinchcombe (2025040414162685300_PLW022C52) 2008; 100 Zeng (2025040414162685300_PLW022C101) 1994; 136 Fenster (2025040414162685300_PLW022C19) 1997; 12 Kirkpatrick (2025040414162685300_PLW022C30) 2006; 173 Jones (2025040414162685300_PLW022C27) 2012; 484 Nosil (2025040414162685300_PLW022C37) 2012 Renaut (2025040414162685300_PLW022C46) 2012; 367 Bierne (2025040414162685300_PLW022C5) 2011; 20 |
References_xml | – volume: 484 start-page: 55 year: 2012 ident: 2025040414162685300_PLW022C27 article-title: The genomic basis of adaptive evolution in threespine sticklebacks publication-title: Nature doi: 10.1038/nature10944 – volume: 5 start-page: 187 year: 2005 ident: 2025040414162685300_PLW022C28 article-title: HP-RARE 1.0: a computer program for performing rarefaction on measures of allelic richness publication-title: Molecular Ecology Notes doi: 10.1111/j.1471-8286.2004.00845.x – volume: 173 start-page: 419 year: 2006 ident: 2025040414162685300_PLW022C30 article-title: Chromosome inversions, local adaptation and speciation publication-title: Genetics doi: 10.1534/genetics.105.047985 – volume: 6 start-page: 288 year: 2006 ident: 2025040414162685300_PLW022C44 article-title: GENALEX 6: genetic analysis in Excel. Population genetic software for teaching and research publication-title: Molecular Ecology Notes doi: 10.1111/j.1471-8286.2005.01155.x – volume: 57 start-page: 357 year: 1986 ident: 2025040414162685300_PLW022C3 article-title: The barrier to genetic exchange between hybridising populations publication-title: Heredity doi: 10.1038/hdy.1986.135 – volume: 26 start-page: 229 year: 2013 ident: 2025040414162685300_PLW022C1 article-title: Hybridization and speciation publication-title: Journal of Evolutionary Biology doi: 10.1111/j.1420-9101.2012.02599.x – volume: 154 start-page: 591 year: 2002 ident: 2025040414162685300_PLW022C43 article-title: What has QTL mapping taught us about plant domestication? publication-title: New Phytologist doi: 10.1046/j.1469-8137.2002.00420.x – volume: 301 start-page: 1211 year: 2003 ident: 2025040414162685300_PLW022C47 article-title: Major ecological transitions in wild sunflowers facilitated by hybridization publication-title: Science doi: 10.1126/science.1086949 – volume: 55 start-page: 1085 year: 2001 ident: 2025040414162685300_PLW022C41 article-title: The evolution of postzygotic isolation: accumulating Dobzhansky-Muller incompatibilities publication-title: Evolution doi: 10.1111/j.0014-3820.2001.tb00628.x – volume: 110 start-page: E1743 year: 2013 ident: 2025040414162685300_PLW022C62 article-title: Genomic rearrangements and the evolution of clusters of locally adaptive loci publication-title: Proceedings of the National Academy of Sciences of the USA doi: 10.1073/pnas.1219381110 – volume: 17 start-page: 4334 year: 2008 ident: 2025040414162685300_PLW022C58 article-title: The genetic mosaic suggests a new role for hitchhiking in ecological speciation publication-title: Molecular Ecology doi: 10.1111/j.1365-294X.2008.03921.x – volume: 152 start-page: 1203 year: 1999 ident: 2025040414162685300_PLW022C29 article-title: Multiple interval mapping for quantitative trait loci publication-title: Genetics doi: 10.1093/genetics/152.3.1203 – volume: 140 start-page: 1111 year: 1995 ident: 2025040414162685300_PLW022C26 article-title: Multiple trait analysis of genetic mapping for quantitative trait loci publication-title: Genetics doi: 10.1093/genetics/140.3.1111 – volume: 63 start-page: 1171 year: 2009 ident: 2025040414162685300_PLW022C4 article-title: The evolution of strong reproductive isolation publication-title: Evolution doi: 10.1111/j.1558-5646.2009.00622.x – volume: 367 start-page: 332 year: 2012 ident: 2025040414162685300_PLW022C38 article-title: Genomic divergence during speciation: causes and consequences publication-title: Philosophical Transactions of the Royal Society Series B doi: 10.1098/rstb.2011.0263 – volume: 138 start-page: 963 year: 1994 ident: 2025040414162685300_PLW022C12 article-title: Empirical threshold values for quantitative trait mapping publication-title: Genetics doi: 10.1093/genetics/138.3.963 – volume: 61 start-page: 2308 year: 2007 ident: 2025040414162685300_PLW022C6 article-title: QTL analysis of floral traits in Louisiana Iris hybrids publication-title: Evolution doi: 10.1111/j.1558-5646.2007.00214.x – volume: 183 start-page: 702 year: 2009 ident: 2025040414162685300_PLW022C8 article-title: Adaptation and selection in the Senecio (Asteraceae) hybrid zone on Mount Etna, Sicily publication-title: New Phytologist doi: 10.1111/j.1469-8137.2009.02944.x – year: 1993 ident: 2025040414162685300_PLW022C32 article-title: Constructing genetic linkage maps with MAPMAKER/EXP version 3.0: A tutorial and reference manual – volume-title: R: a language and environment for statistical computing year: 2011 ident: 2025040414162685300_PLW022C45 – volume: 22 start-page: 3036 year: 2013 ident: 2025040414162685300_PLW022C22 article-title: Mapping phenotypic, expression and transmission ratio distortion QTL using RAD markers in the Lake Whitefish ( Coregonus clupeaformis ) publication-title: Molecular Ecology doi: 10.1111/mec.12127 – volume: 69 start-page: 1476 year: 2015 ident: 2025040414162685300_PLW022C57 article-title: Adaptive divergence in the monkey flower Mimulus guttatus is maintained by a chromosomal inversion publication-title: Evolution doi: 10.1111/evo.12663 – volume: 30 start-page: 2553 year: 2013 ident: 2025040414162685300_PLW022C10 article-title: Genomic divergence during speciation driven by adaptation to altitude publication-title: Molecular Biology and Evolution doi: 10.1093/molbev/mst168 – volume: 8 start-page: e1000500 year: 2010 ident: 2025040414162685300_PLW022C34 article-title: A widespread chromosomal inversion polymorphism contributes to a major life-history transition, local adaptation, and reproductive isolation publication-title: PLoS Biology doi: 10.1371/journal.pbio.1000500 – volume: 110 start-page: 63 year: 2012 ident: 2025040414162685300_PLW022C54 article-title: Genomic collinearity and the genetic architecture of floral differences between the homoploid hybrid species Iris nelsonii and one of its progenitors, Iris hexagona publication-title: Heredity doi: 10.1038/hdy.2012.62 – volume: 12 start-page: 282 year: 1997 ident: 2025040414162685300_PLW022C19 article-title: Epistasis and its consequences for the evolution of natural populations publication-title: Trends in Ecology and Evolution doi: 10.1016/S0169-5347(97)81027-0 – volume: 159 start-page: 1701 year: 2001 ident: 2025040414162685300_PLW022C100 article-title: A genetic map in the Mimulus guttatus species complex reveals transmission ratio distortion due to heterospecific interactions publication-title: Genetics doi: 10.1093/genetics/159.4.1701 – volume-title: Windows QTL Cartographer 2.5. year: 2011 ident: 2025040414162685300_PLW022C59 – volume: 16 start-page: 330 year: 2001 ident: 2025040414162685300_PLW022C55 article-title: Theory and speciation publication-title: Trends in Ecology and Evolution doi: 10.1016/S0169-5347(01)02177-2 – volume: 26 start-page: 389 year: 2011 ident: 2025040414162685300_PLW022C50 article-title: Magic traits in speciation: ‘magic’ but not rare? publication-title: Trends in Ecology and Evolution doi: 10.1016/j.tree.2011.04.005 – volume: 169 start-page: 2225 year: 2005 ident: 2025040414162685300_PLW022C31 article-title: Genetics of species differences in the wild annual sunflowers, Helianthus annuus and H. petiolaris publication-title: Genetics doi: 10.1534/genetics.104.031195 – volume: 5 start-page: 1704 year: 2013 ident: 2025040414162685300_PLW022C42 article-title: Rapid speciation with gene flow following the formation of Mt. Etna publication-title: Genome Biology and Evolution doi: 10.1093/gbe/evt127 – volume: 20 start-page: 5123 year: 2011 ident: 2025040414162685300_PLW022C51 article-title: A framework for comparing processes of speciation in the presence of gene flow publication-title: Molecular Ecology doi: 10.1111/j.1365-294X.2011.05350.x – volume: 59 start-page: 2533 year: 2005 ident: 2025040414162685300_PLW022C25 article-title: Recent, allopatric, homoploid hybrid speciation: the origin of Senecio squalidus (Asteraceae) in the British Isles from a hybrid zone on Mount Etna, Sicily publication-title: Evolution doi: 10.1111/j.0014-3820.2005.tb00967.x – volume-title: Speciation year: 2004 ident: 2025040414162685300_PLW022C14 – volume: 65 start-page: 1897 year: 2011 ident: 2025040414162685300_PLW022C63 article-title: The genetic architecture of adaptation under migration–selection balance publication-title: Evolution doi: 10.1111/j.1558-5646.2011.01269.x – volume: 67 start-page: 3032 year: 2013 ident: 2025040414162685300_PLW022C35 article-title: Recent ecological selection on regulatory divergence is shaping clinal variation in Senecio on Mount Etna publication-title: Evolution doi: 10.1111/evo.12062 – volume: 64 start-page: 1729 year: 2010 ident: 2025040414162685300_PLW022C17 article-title: The efficacy of divergence hitchhiking in generating genomic islands during ecological speciation publication-title: Evolution doi: 10.1111/j.1558-5646.2009.00943.x – volume: 367 start-page: 364 year: 2012 ident: 2025040414162685300_PLW022C53 article-title: What can patterns of differentiation across plant genomes tell us about adaptation and speciation? publication-title: Philosophical Transactions of the Royal Society Series B doi: 10.1098/rstb.2011.0199 – volume: 23 start-page: 3133 year: 2014 ident: 2025040414162685300_PLW022C15 article-title: Reanalysis suggests that genomic islands of speciation are due to reduced diversity, not reduced gene flow publication-title: Molecular Ecology doi: 10.1111/mec.12796 – volume: 367 start-page: 439 year: 2012 ident: 2025040414162685300_PLW022C23 article-title: Genomics of isolation in hybrids publication-title: Philosophical Transactions of the Royal Society Series B doi: 10.1098/rstb.2011.0196 – volume: 180 start-page: 147 year: 2008 ident: 2025040414162685300_PLW022C60 article-title: The phenomics and expression quantitative trait locus mapping of brain transcriptomes regulating adaptive divergence in Lake Whitefish species pairs ( Coregonus sp.) publication-title: Genetics doi: 10.1534/genetics.108.089938 – volume: 29 start-page: 98 year: 2016 ident: 2025040414162685300_PLW022C11 article-title: The genomic bases of morphological divergence and reproductive isolation driven by ecological speciation in Senecio (Asteraceae) publication-title: Journal Evolutionary Biology doi: 10.1111/jeb.12765 – volume: 367 start-page: 354 year: 2012 ident: 2025040414162685300_PLW022C46 article-title: Genome-wide patterns of divergence during speciation: the lake whitefish case study. publication-title: Philosophical Transactions of the Royal Society Series B doi: 10.1098/rstb.2011.0197 – volume: 369 start-page: 20130346 year: 2014 ident: 2025040414162685300_PLW022C2 article-title: Altitudinal gradients, plant hybrid zones and evolutionary novelty publication-title: Philosophical Transactions of the Royal Society Series B doi: 10.1098/rstb.2013.0346 – volume: 24 start-page: 1423 year: 2007 ident: 2025040414162685300_PLW022C48 article-title: The genetic architecture of ecological speciation and the association with signatures of selection in natural lake whitefish ( Coregonus sp. Salmonidae) species pairs publication-title: Molecular Biology and Evolution doi: 10.1093/molbev/msm066 – volume: 20 start-page: 2044 year: 2011 ident: 2025040414162685300_PLW022C5 article-title: The coupling hypothesis: why genome scans may fail to map local adaptation genes publication-title: Molecular Ecology doi: 10.1111/j.1365-294X.2011.05080.x – volume: 136 start-page: 1457 year: 1994 ident: 2025040414162685300_PLW022C101 article-title: Precision mapping of quantitative trait loci publication-title: Genetics doi: 10.1111/j.1558-5646.2011.01269.x – volume: 59 start-page: 53 year: 2013 ident: 2025040414162685300_PLW022C49 article-title: The consequences of genomic architecture on ecological speciation in postglacial fishes publication-title: Current Zoology doi: 10.1093/czoolo/59.1.53 – volume: 14 start-page: 851 year: 2001 ident: 2025040414162685300_PLW022C61 article-title: The genic view of the process of speciation publication-title: Journal of Evolutionary Biology doi: 10.1046/j.1420-9101.2001.00335.x – volume: 3 start-page: e285 year: 2005 ident: 2025040414162685300_PLW022C56 article-title: Genomic islands of speciation in Anopheles gambiae publication-title: PLoS Biology doi: 10.1371/journal.pbio.0030285 – volume-title: Ecological speciation year: 2012 ident: 2025040414162685300_PLW022C37 doi: 10.1093/acprof:osobl/9780199587100.001.0001 – volume: 18 start-page: 375 year: 2009 ident: 2025040414162685300_PLW022C39 article-title: Divergent selection and heterogeneous genomic divergence publication-title: Molecular Ecology doi: 10.1111/j.1365-294X.2008.03946.x – volume: 4 start-page: e1000232 year: 2008 ident: 2025040414162685300_PLW022C7 article-title: Genetical genomics: spotlight on QTL hotspots publication-title: PLoS Genetics doi: 10.1371/journal.pgen.1000232 – year: 2016 ident: 2025040414162685300_PLW022C20 article-title: Demographic history of speciation in a Senecio altitudinal hybrid zone on Mt. Etna publication-title: Molecular Ecology doi: 10.1111/mec.13618 – volume: 180 start-page: 977 year: 2008 ident: 2025040414162685300_PLW022C21 article-title: A genome-scan method to identify selected loci appropriate for both dominant and codominant markers: a Bayesian perspective publication-title: Genetics doi: 10.1534/genetics.108.092221 – volume: 113 start-page: 195 year: 2014 ident: 2025040414162685300_PLW022C9 article-title: Interspecific crossing and genetic mapping reveal intrinsic genomic incompatibility between two Senecio species that form a hybrid zone on Mount Etna, Sicily publication-title: Heredity doi: 10.1038/hdy.2014.14 – volume: 69 start-page: 1987 year: 2015 ident: 2025040414162685300_PLW022C33 article-title: The genetic architecture of hybrid incompatibilities and their effect on barriers to introgression in secondary contact publication-title: Evolution doi: 10.1111/evo.12725 – volume: 10 start-page: 564 year: 2010 ident: 2025040414162685300_PLW022C16 article-title: Arlequin suite ver 3.5: a new series of programs to perform population genetics analyses under Linux and Windows publication-title: Molecular Ecology Resources doi: 10.1111/j.1755-0998.2010.02847.x – volume: 163 start-page: 939 year: 2003 ident: 2025040414162685300_PLW022C18 article-title: Evidence for inversion polymorphism related to sympatric host race formation in the apple maggot fly, Rhagoletis pomonella publication-title: Genetics doi: 10.1093/genetics/163.3.939 – volume: 100 start-page: 158 year: 2008 ident: 2025040414162685300_PLW022C52 article-title: Combining population genomics and quantitative genetics: finding the genes underlying ecologically important traits publication-title: Heredity doi: 10.1038/sj.hdy.6800937 |
SSID | ssj0000328640 |
Score | 2.0676887 |
Snippet | Hybrid zones that occur across environmental gradients provide excellent opportunities for studying the maintenance of divergent adaptations in the presence of... Knowledge of the genetic basis of phenotypic divergence between species and how such divergence is caused and maintained is crucial to an understanding of... |
SourceID | pubmedcentral proquest pubmed crossref oup |
SourceType | Open Access Repository Aggregation Database Index Database Enrichment Source Publisher |
Title | Genomic architecture of phenotypic divergence between two hybridizing plant species along an elevational gradient |
URI | https://www.ncbi.nlm.nih.gov/pubmed/27083198 https://www.proquest.com/docview/1793912549 https://pubmed.ncbi.nlm.nih.gov/PMC4887755 |
Volume | 8 |
hasFullText | 1 |
inHoldings | 1 |
isFullTextHit | |
isPrint | |
link | http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwjV1Lb9QwEB7RlgMXxJvlsTIS4kRoYsee7AEhirZUSC0IdaW9RU7sbStFyXabqiy_npnEXXZ5CC45JCMr8cQz39gz3wC81BhnpfVxpH2SRqkdYVQoY6JZqTJy0KWOY65GPjwyB5P001RPf1IKhQm8-GNox_2kJovqzbfz5Tta8G8DGdKubYp5ZXfn1RU5pC3YIaeEvEYPA9LvjLKSmenKI2WcJpEkoBEYN38bYcNDbVS9rYHPX3Mo15zS_h24HdCkeN-r_y7c8PU9uLnXEOJb3ofzj74rOhbrpwWimQnO62ra5ZweOc7L6Ag5RUjZEu1VI06XXMl19p0cm6B3rlvBJZkUVQtbNXTP1oIL08NOojhZdJlj7QOY7I-PPxxEocVCVKYybiNjGS8m3MyuKJ1LJWpmFCPU4AgKepkYkyU2VoWiQBARM5dIo5VVWGgkO6oewnbd1P4xCDQzJKzp3MyY1ClH0MI7ZyRaV6jCmAG8vp7WvAz849wGo8r7c3CV91rIey0M4NVKfN4Tb_xN8AXp6J8y1xrMafnwmYitfXN5kbN9GiUcJQ_gUa_R1VASuQ3bKBsAbuh6JcDU3JtP6rPTjqKbzCKi1k_-9yOewi1SQ9jbeQbb7eLSPye00xZD2MJ4PISdvfHRl6_Dbs9g2P3bdD3-PP0BHXsHFw |
linkProvider | Scholars Portal |
openUrl | ctx_ver=Z39.88-2004&ctx_enc=info%3Aofi%2Fenc%3AUTF-8&rfr_id=info%3Asid%2Fsummon.serialssolutions.com&rft_val_fmt=info%3Aofi%2Ffmt%3Akev%3Amtx%3Ajournal&rft.genre=article&rft.atitle=Genomic+architecture+of+phenotypic+divergence+between+two+hybridizing+plant+species+along+an+elevational+gradient&rft.jtitle=AoB+plants&rft.au=Brennan%2C+Adrian+C.&rft.au=Hiscock%2C+Simon+J.&rft.au=Abbott%2C+Richard+J.&rft.date=2016-01-01&rft.issn=2041-2851&rft.eissn=2041-2851&rft.volume=8&rft_id=info:doi/10.1093%2Faobpla%2Fplw022&rft.externalDBID=n%2Fa&rft.externalDocID=10_1093_aobpla_plw022 |
thumbnail_l | http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/lc.gif&issn=2041-2851&client=summon |
thumbnail_m | http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/mc.gif&issn=2041-2851&client=summon |
thumbnail_s | http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/sc.gif&issn=2041-2851&client=summon |