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...

Full description

Saved in:
Bibliographic Details
Published inAoB plants Vol. 8
Main Authors Brennan, Adrian C., Hiscock, Simon J., Abbott, Richard J.
Format Journal Article
LanguageEnglish
Published England Oxford University Press 01.01.2016
SeriesEditor's choice
Subjects
Online AccessGet 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