Complex Polyploids: Origins, Genomic Composition, and Role of Introgressed Alleles
Jazyk angličtina Země Anglie, Velká Británie Médium print
Typ dokumentu časopisecké články
Grantová podpora
2016-00780
Swedish Research Council for Sustainable Development
676876
European Union's Horizon 2020 Research and Innovation Programme
PubMed
38613229
PubMed Central
PMC11282369
DOI
10.1093/sysbio/syae012
PII: 7645150
Knihovny.cz E-zdroje
- Klíčová slova
- Allopolyploidy, Betula, autopolyploidy, gene flow, genomic polarization, homoeologs, interploidal, introgressive hybridization, polyploid phylogenetics, polyploidization simulation, reticulate evolution,
- MeSH
- alely * MeSH
- bříza * genetika klasifikace MeSH
- fylogeneze * MeSH
- genom rostlinný * MeSH
- genová introgrese MeSH
- hybridizace genetická MeSH
- polyploidie * MeSH
- Publikační typ
- časopisecké články MeSH
Introgression allows polyploid species to acquire new genomic content from diploid progenitors or from other unrelated diploid or polyploid lineages, contributing to genetic diversity and facilitating adaptive allele discovery. In some cases, high levels of introgression elicit the replacement of large numbers of alleles inherited from the polyploid's ancestral species, profoundly reshaping the polyploid's genomic composition. In such complex polyploids, it is often difficult to determine which taxa were the progenitor species and which taxa provided additional introgressive blocks through subsequent hybridization. Here, we use population-level genomic data to reconstruct the phylogenetic history of Betula pubescens (downy birch), a tetraploid species often assumed to be of allopolyploid origin and which is known to hybridize with at least four other birch species. This was achieved by modeling polyploidization and introgression events under the multispecies coalescent and then using an approximate Bayesian computation rejection algorithm to evaluate and compare competing polyploidization models. We provide evidence that B. pubescens is the outcome of an autoploid genome doubling event in the common ancestor of B. pendula and its extant sister species, B. platyphylla, that took place approximately 178,000-188,000 generations ago. Extensive hybridization with B. pendula, B. nana, and B. humilis followed in the aftermath of autopolyploidization, with the relative contribution of each of these species to the B. pubescens genome varying markedly across the species' range. Functional analysis of B. pubescens loci containing alleles introgressed from B. nana identified multiple genes involved in climate adaptation, while loci containing alleles derived from B. humilis revealed several genes involved in the regulation of meiotic stability and pollen viability in plant species.
Department of Forest Sciences University of Helsinki 00014 Helsinki Finland
Science for Life Laboratory Uppsala University 75237 Uppsala Sweden
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Albertin W., Marullo P. 2012. Polyploidy in fungi: evolution after whole-genome duplication. Proc. R Soc. B. Biol. Sci. 279:2497–2509. PubMed PMC
Amborella Genome Project. 2013. The Amborella genome and the evolution of flowering plants. Science 342:1241089. PubMed
Anamthawat-Jónsson K., Tomasson T. 1990. Cytogenetics of hybrid introgression in Icelandic birch. Hereditas 112:65–70.
Anamthawat-Jónsson K., Thór Thórsson A. 2003. Natural hybridisation in birch: triploid hybrids between Betula nana and B. pubescens. Plant Cell Tissue Organ. Cult. 75:99–107.
Arnold B., Kim S.-T., Bomblies K. 2015. Single geographic origin of a widespread autotetraploid Arabidopsis arenosa lineage followed by interploidy admixture. Mol. Biol. Evol. 32:1382–1395. PubMed
Arnold B.J., Lahner B., DaCosta J.M., Weisman C.M., Hollister J.D., Salt D.E., Bomblies K., Yant L. 2016. Borrowed alleles and convergence in serpentine adaptation. Proc. Natl. Acad. Sci. U.S.A. 113:8320–8325. PubMed PMC
Ashburner K., McAllister H.A. 2013. The genus Betula: a taxonomic revision of birches:26-28. London: Kew Publishing.
Atkinson M.D. 1992. Betula pendula Roth (B. Verrucosa Ehrh.) and B. pubescens Ehrh. J. Ecol. 80:837–870.
Aury J.-M., Jaillon O., Duret L., Noel B., Jubin C., Porcel B.M., Ségurens B., Daubin V., Anthouard V., Aiach N., Arnaiz O., Billaut A., Beisson J., Blanc I., Bouhouche K., Câmara F., Duharcourt S., Guigo R., Gogendeau D., Katinka M., Keller A.-M., Kissmehl R., Klotz C., Koll F., Le Mouël A., Lepère G., Malinsky S., Nowacki M., Nowak J.K., Plattner H., Poulain J., Ruiz F., Serrano V., Zagulski M., Dessen P., Bétermier M., Weissenbach J., Scarpelli C., Schächter V., Sperling L., Meyer E., Cohen J., Wincker P. 2006. Global trends of whole-genome duplications revealed by the ciliate Paramecium tetraurelia. Nature 444:171–178. PubMed
Baack E., Melo M.C., Rieseberg L.H., Ortiz-Barrientos D. 2015. The origins of reproductive isolation in plants. New Phytol. 207:968–984. PubMed
Baduel P., Bray S., Vallejo-Marin M., Kolář F., Yant L. 2018. The “Polyploid Hop”: shifting challenges and opportunities over the evolutionary lifespan of genome duplications. Front. Ecol. Evol. 6:1–19.
Bagherieh-Najjar M.B., de Vries O.M.H., Hille J., Dijkwel P.P. 2005. Arabidopsis RecQl4A suppresses homologous recombination and modulates DNA damage responses. Plant J. 43:789–798. PubMed
Bao S., Tibbetts R.S., Brumbaugh K.M., Fang Y., Richardson D.A., Ali A., Chen S.M., Abraham R.T., Wang X.-F. 2001. ATR/ATM-mediated phosphorylation of human Rad17 is required for genotoxic stress responses. Nature 411:969–974. PubMed
Barker M.S., Arrigo N., Baniaga A.E., Li Z., Levin D.A. 2016. On the relative abundance of autopolyploids and allopolyploids. New Phytol. 210:391–398. PubMed
Barton N.H., Hewitt G.M. 1989. Adaptation, speciation and hybrid zones. Nature 341:497–503. PubMed
Beaumont M.A., Zhang W., Balding D.J. 2002. Approximate Bayesian computation in population genetics. Genetics. 162:2025–2035. PubMed PMC
Beaumont M.A. 2019. Approximate Bayesian computation. Annu. Rev. Stat. Appl. 6:379–403.
Berthelot C., Brunet F., Chalopin D., Juanchich A., Bernard M., Noël B., Bento P., Da Silva C., Labadie K., Alberti A., Aury J.-M., Louis A., Dehais P., Bardou P., Montfort J., Klopp C., Cabau C., Gaspin C., Thorgaard G.H., Boussaha M., Quillet E., Guyomard R., Galiana D., Bobe J., Volff J.-N., Genêt C., Wincker P., Jaillon O., Crollius H.R., Guiguen Y. 2014. The rainbow trout genome provides novel insights into evolution after whole-genome duplication in vertebrates. Nat. Commun. 5:3657. PubMed PMC
Bertrand Y.J.K., Scheen A.-C., Marcussen T., Pfeil B.E., de Sousa F., Oxelman B. 2015. Assignment of homoeologs to parental genomes in allopolyploids for species tree inference, with an example from Fumaria (Papaveraceae). Syst. Biol. 64:448–471. PubMed
Bleeker W., Hurka H. 2001. Introgressive hybridization in Rorippa (Brassicaceae): gene flow and its consequences in natural and anthropogenic habitats. Mol. Ecol. 10:2013–2022. PubMed
Bleeker W. 2003. Hybridization and Rorippa austriaca (Brassicaceae) invasion in Germany. Mol. Ecol. 12:1831–1841. PubMed
Blischak P.D., Mabry M.E., Conant G.C., Pires J.C. 2018. Integrating networks, phylogenomics, and population genomics for the study of polyploidy. Annu. Rev. Ecol. Evol. Syst. 49:253–278.
Bomblies K., Higgins J.D., Yant L. 2015. Meiosis evolves: adaptation to external and internal environments. New Phytol. 208:306–323. PubMed
Bomblies K. 2023. Learning to tango with four (or more): the molecular basis of adaptation to polyploid meiosis. Plant Reprod. 36:107–124. PubMed PMC
Bowers J.E., Chapman B.A., Rong J., Paterson A.H. 2003. Unravelling angiosperm genome evolution by phylogenetic analysis of chromosomal duplication events. Nature 422:433–438. PubMed
Braasch I., Postlethwait J.H. 2012. Polyploidy in fish and the teleost genome duplication. In: Soltis P.S., Soltis D.E., editors. Polyploidy and genome evolution. Berlin, Heidelberg: Springer. p. 341–383.
Brown I.R., Al-Dawoody D. 1979. Observations on meiosis in three cytotypes of Betula alba L. New Phytol. 83:801–811.
Bryant D., Moulton V. 2004. Neighbor-Net: an agglomerative method for the construction of phylogenetic networks. Mol. Biol. Evol. 21:255–265. PubMed
Burns R., Mandáková T., Gunis J., Soto-Jiménez L.M., Liu C., Lysak M.A., Novikova P.Y., Nordborg M. 2021. Gradual evolution of allopolyploidy in Arabidopsis suecica. Nat. Ecol. Evol. 5:1367–1381. PubMed PMC
Caldwell K.S., Michelmore R.W. 2009. Arabidopsis thaliana genes encoding defense signaling and recognition proteins exhibit contrasting evolutionary dynamics. Genetics 181:671–684. PubMed PMC
Cao H., Bowling S.A., Gordon A.S., Dong X. 1994. Characterization of an arabidopsis mutant that is nonresponsive to inducers of systemic acquired resistance. Plant Cell. 6:1583–1592. PubMed PMC
Cerca J., Armstrong E.E., Vizueta J., Fernández R., Dimitrov D., Petersen B., Prost S., Rozas J., Petrov D., Gillespie R.G. 2021. The Tetragnatha kauaiensis genome sheds light on the origins of genomic novelty in spiders. Genome Biol. Evol. 13:evab262. PubMed PMC
Chalhoub B., Denoeud F., Liu S., Parkin I.A.P., Tang H., Wang X., Chiquet J., Belcram H., Tong C., Samans B., Corréa M., Da Silva C., Just J., Falentin C., Koh C.S., Le Clainche I., Bernard M., Bento P., Noel B., Labadie K., Alberti A., Charles M., Arnaud D., Guo H., Daviaud C., Alamery S., Jabbari K., Zhao M., Edger P.P., Chelaifa H., Tack D., Lassalle G., Mestiri I., Schnel N., Le Paslier M.-C., Fan G., Renault V., Bayer P.E., Golicz A.A., Manoli S., Lee T.-H., Thi V.H.D., Chalabi S., Hu Q., Fan C., Tollenaere R., Lu Y., Battail C., Shen J., Sidebottom C.H.D., Wang X., Canaguier A., Chauveau A., Bérard A., Deniot G., Guan M., Liu Z., Sun F., Lim Y.P., Lyons E., Town C.D., Bancroft I., Wang X., Meng J., Ma J., Pires J.C., King G.J., Brunel D., Delourme R., Renard M., Aury J.-M., Adams K.L., Batley J., Snowdon R.J., Tost J., Edwards D., Zhou Y., Hua W., Sharpe A.G., Paterson A.H., Guan C., Wincker P. 2014. Early allopolyploid evolution in the post-Neolithic Brassica napus oilseed genome. Science 345:950–953. PubMed
Chen X., Lu L., Mayer K.S., Scalf M., Qian S., Lomax A., Smith L.M., Zhong X. 2016. POWERDRESS interacts with HISTONE DEACETYLASE 9 to promote aging in Arabidopsis. eLife 5:e17214. PubMed PMC
Chen S., Wang Y., Yu L., Zheng T., Wang S., Yue Z., Jiang J., Kumari S., Zheng C., Tang H., Li J., Li Y., Chen J., Zhang W., Kuang H., Robertson J.S., Zhao P.X., Li H., Shu S., Yordanov Y.S., Huang H., Goodstein D.M., Gai Y., Qi Q., Min J., Xu C., Wang S., Qu G.-Z., Paterson A.H., Sankoff D., Wei H., Liu G., Yang C. 2021. Genome sequence and evolution of Betula platyphylla. Hortic. Res. 8:37. PubMed PMC
Cheng H., Liu J., Wen J., Nie X., Xu L., Chen N., Li Z., Wang Q., Zheng Z., Li M., Cui L., Liu Z., Bian J., Wang Z., Xu S., Yang Q., Appels R., Han D., Song W., Sun Q., Jiang Y. 2019. Frequent intra- and inter-species introgression shapes the landscape of genetic variation in bread wheat. Genome Biol. 20:136. PubMed PMC
Chenuil A., Galtier N., Berrebi P. 1999. A test of the hypothesis of an autopolyploid vs. allopolyploid origin for a tetraploid lineage: application to the genus Barbus (Cyprinidae). Heredity 82 Pt 4:373–380. PubMed
Chester M., Gallagher J.P., Symonds V.V., Cruz da Silva A.V., Mavrodiev E.V., Leitch A.R., Soltis P.S., Soltis D.E. 2012. Extensive chromosomal variation in a recently formed natural allopolyploid species, Tragopogon miscellus (Asteraceae). Proc. Natl. Acad. Sci. U.S.A. 109:1176–1181. PubMed PMC
Cifuentes M., Grandont L., Moore G., Chèvre A.M., Jenczewski E. 2010. Genetic regulation of meiosis in polyploid species: new insights into an old question. New Phytol. 186:29–36. PubMed
Cingolani P., Platts A., Wang L.L., Coon M., Nguyen T., Wang L., Land S.J., Lu X., Ruden D.M. 2012. A program for annotating and predicting the effects of single nucleotide polymorphisms, SnpEff. Fly 6:80–92. PubMed PMC
Clark L.V., Stewart J.R., Nishiwaki A., Toma Y., Kjeldsen J.B., Jørgensen U., Zhao H., Peng J., Yoo J.H., Heo K., Yu C.Y., Yamada T., Sacks E.J. 2015. Genetic structure of Miscanthus sinensis and Miscanthus sacchariflorus in Japan indicates a gradient of bidirectional but asymmetric introgression. J. Exp. Bot. 66:4213–4225. PubMed PMC
Comai L. 2005. The advantages and disadvantages of being polyploid. Nat. Rev. Genet. 6:836–846. PubMed
Cornish-Bowden A. 1985. Nomenclature for incompletely specified bases in nucleic acid sequences: recommendations 1984. Nucleic Acids Res. 13:3021–3030. PubMed PMC
Danecek P., Bonfield J.K., Liddle J., Marshall J., Ohan V., Pollard M.O., Whitwham A., Keane T., McCarthy S.A., Davies R.M., Li H. 2021. Twelve years of SAMtools and BCFtools. GigaScience. 10:1–4. PubMed PMC
Dasmahapatra K.K., Walters J.R., Briscoe A.D., Davey J.W., Whibley A., Nadeau N.J., Zimin A.V., Hughes D.S.T., Ferguson L.C., Martin S.H., Salazar C., Lewis J.J., Adler S., Ahn S.-J., Baker D.A., Baxter S.W., Chamberlain N.L., Chauhan R., Counterman B.A., Dalmay T., Gilbert L.E., Gordon K., Heckel D.G., Hines H.M., Hoff K.J., Holland P.W.H., Jacquin-Joly E., Jiggins F.M., Jones R.T., Kapan D.D., Kersey P., Lamas G., Lawson D., Mapleson D., Maroja L.S., Martin A., Moxon S., Palmér W.J., Papa R., Papanicolaou A., Pauchet Y., Ray D.A., Rosser N., Salzberg S.L., Supple M.A., Surridge A., Tenger-Trolander A., Vogel H., Wilkinson P.A., Wilson D., Yorke J.A., Yuan F., Balmuth A.L., Eland C., Gharbi K., Thomson M., Gibbs R.A., Han Y., Jayaseelan J.C., Kovar C., Mathew T., Muzny D.M., Ongeri F., Pu L.-L., Qu J., Thornton R.L., Worley K.C., Wu Y.-Q., Linares M., Blaxter M.L., ffrench-Constant R.H., Joron M., Kronforst M.R., Mullen S.P., Reed R.D., Scherer S.E., Richards S., Mallet J., Owen McMillan W., Jiggins C.D., The Heliconius Genome Consortium. 2012. Butterfly genome reveals promiscuous exchange of mimicry adaptations among species. Nature. 487:94–98. PubMed PMC
De Bodt S., Maere S., Van de Peer Y. 2005. Genome duplication and the origin of angiosperms. Trends Ecol. Evol. 20:591–597. PubMed
de Groot W.J., Thomas P.A., Wein R.W. 1997. Betula nana L. and Betula glandulosa Michx. J. Ecol. 85:241–264.
Dehal P., Boore J.L. 2005. Two rounds of whole genome duplication in the ancestral vertebrate. PLoS Biol. 3:e314. PubMed PMC
Ding J., Zhang B., Li Y., André D., Nilsson O. 2021. Phytochrome B and PHYTOCHROME INTERACTING FACTOR8 modulate seasonal growth in trees. New Phytol. 232:2339–2352. PubMed
Dong M.A., Farré E.M., Thomashow M.F. 2011. CIRCADIAN CLOCK-ASSOCIATED 1 and LATE ELONGATED HYPOCOTYL regulate expression of the C-REPEAT BINDING FACTOR (CBF) pathway in Arabidopsis. Proc. Natl. Acad. Sci. U.S.A. 108:7241–7246. PubMed PMC
Dowling T.E., Secor C.L. 1997. The role of hybridization and introgression in the diversification of animals. Annu. Rev. Ecol. Syst. 28:593–619.
Eidesen P.B., Alsos I.G., Brochmann C. 2015. Comparative analyses of plastid and AFLP data suggest different colonization history and asymmetric hybridization between Betula pubescens and B. nana. Mol. Ecol. 24:3993–4009. PubMed
Ellstrand N.C. 2014. Is gene flow the most important evolutionary force in plants? Am. J. Bot. 101:737–753. PubMed
Enns L.C., Kanaoka M.M., Torii K.U., Comai L., Okada K., Cleland R.E. 2005. Two callose synthases, GSL1 and GSL5, play an essential and redundant role in plant and pollen development and in fertility. Plant Mol. Biol. 58:333–349. PubMed
Excoffier L., Foll M., Petit R.J. 2009. Genetic consequences of range expansions. Annu. Rev. Ecol. Evol. Syst. 40:481–501.
Excoffier L., Dupanloup I., Huerta-Sánchez E., Sousa V.C., Foll M. 2013. Robust demographic inference from genomic and SNP data. PLoS Genet. 9:e1003905. PubMed PMC
Felber F. 1991. Establishment of a tetraploid cytotype in a diploid population: effect of relative fitness of the cytotypes. J. Evol. Biol. 4:195–207.
Filiault D.L., Wessinger C.A., Dinneny J.R., Lutes J., Borevitz J.O., Weigel D., Chory J., Maloof J.N. 2008. Amino acid polymorphisms in Arabidopsis phytochrome B cause differential responses to light. Proc. Natl. Acad. Sci. U.S.A. 105:3157–3162. PubMed PMC
Fletcher W., Yang Z. 2009. INDELible: a flexible simulator of biological sequence evolution. Mol. Biol. Evol. 26:1879–1888. PubMed PMC
Fontaine M.C., Pease J.B., Steele A., Waterhouse R.M., Neafsey D.E., Sharakhov I.V., Jiang X., Hall A.B., Catteruccia F., Kakani E., Mitchell S.N., Wu Y.-C., Smith H.A., Love R.R., Lawniczak M.K., Slotman M.A., Emrich S.J., Hahn M.W., Besansky N.J. 2015. Extensive introgression in a malaria vector species complex revealed by phylogenomics. Science 347:1258524. PubMed PMC
Fraïsse C., Popovic I., Mazoyer C., Spataro B., Delmotte S., Romiguier J., Loire E., Simon A., Galtier N., Duret L., Bierne N., Vekemans X., Roux C. 2021. DILS: demographic inferences with linked selection by using ABC. Mol. Ecol. Resour. 21:2629–2644. PubMed
Freyman W.A., Johnson M.G., Rothfels C.J. 2023. homologizer: phylogenetic phasing of gene copies into polyploid subgenomes. Methods Ecol. Evol. 14:1230–1244. PubMed
Fujiwara S., Oda A., Yoshida R., Niinuma K., Miyata K., Tomozoe Y., Tajima T., Nakagawa M., Hayashi K., Coupland G., Mizoguchi T. 2008. Circadian clock proteins LHY and CCA1 regulate SVP protein accumulation to control flowering in Arabidopsis. Plant Cell 20:2960–2971. PubMed PMC
Gaeta R.T., Chris Pires J. 2010. Homoeologous recombination in allopolyploids: the polyploid ratchet. New Phytol. 186:18–28. PubMed
Grant P.R., Grant B.R. 1992. Hybridization of bird species. Science 256:193–197. PubMed
Grant P.R., Grant B.R. 2020. Triad hybridization via a conduit species. Proc. Natl. Acad. Sci. U.S.A. 117:7888–7896. PubMed PMC
Gutenkunst R.N., Hernandez R.D., Williamson S.H., Bustamante C.D. 2009. Inferring the joint demographic history of multiple populations from multidimensional SNP frequency data. PLoS Genet. 5:e1000695. PubMed PMC
Hajdu A., Ádám E., Sheerin D.J., Dobos O., Bernula P., Hiltbrunner A., Kozma-Bognár L., Nagy F. 2015. High-level expression and phosphorylation of phytochrome B modulates flowering time in Arabidopsis. Plant J. 83:794–805. PubMed
Hardigan M.A., Laimbeer F.P.E., Newton L., Crisovan E., Hamilton J.P., Vaillancourt B., Wiegert-Rininger K., Wood J.C., Douches D.S., Farré E.M., Veilleux R.E., Buell C.R. 2017. Genome diversity of tuber-bearing Solanum uncovers complex evolutionary history and targets of domestication in the cultivated potato. Proc. Natl. Acad. Sci. USA 114:E9999–E10008. PubMed PMC
Hartung F., Suer S., Knoll A., Wurz-Wildersinn R., Puchta H. 2008. Topoisomerase 3α and RMI1 suppress somatic crossovers and are essential for resolution of meiotic recombination intermediates in Arabidopsis thaliana. PLoS Genet. 4:e1000285. PubMed PMC
Heitzeberg F., Chen I.-P., Hartung F., Orel N., Angelis K.J., Puchta H. 2004. The Rad17 homologue of Arabidopsis is involved in the regulation of DNA damage repair and homologous recombination. Plant J. 38:954–968. PubMed
Heled J., Drummond A.J. 2010. Bayesian inference of species trees from multilocus data. Mol. Biol. Evol. 27:570–580. PubMed PMC
Higgins J.D., Ferdous M., Osman K., Franklin F.C.H. 2011. The RecQ helicase AtRECQ4A is required to remove inter-chromosomal telomeric connections that arise during meiotic recombination in Arabidopsis. Plant J. 65:492–502. PubMed
Hohmann N., Schmickl R., Chiang T.-Y., Lučanová M., Kolář F., Marhold K., Koch M.A. 2014. Taming the wild: resolving the gene pools of non-model Arabidopsis lineages. BMC Evol. Biol. 14:224. PubMed PMC
Hohmann N., Koch M.A. 2017. An Arabidopsis introgression zone studied at high spatio-temporal resolution: interglacial and multiple genetic contact exemplified using whole nuclear and plastid genomes. BMC Genom. 18:1–18. PubMed PMC
Howland D.E., Oliver R.P., Davy A.J. 1995. Morphological and molecular variation in natural populations of Betula. New Phytol. 130:117–124.
Hu Q., Zhang C., Xue Z., Ma L., Liu W., Shen Y., Ma B., Cheng Z. 2018. OsRAD17 is required for meiotic double-strand break repair and plays a redundant role with OsZIP4 in synaptonemal complex assembly. Front. Plant Sci. 9:1236. PubMed PMC
Husband B.C. 2004. The role of triploid hybrids in the evolutionary dynamics of mixed-ploidy populations. Biol. J. Linn. Soc. 82:537–546.
Huson D.H., Bryant D. 2006. Application of phylogenetic networks in evolutionary studies. Mol. Biol. Evol. 23:254–267. PubMed
Ingvarsson P.K., Garcia M.V., Luquez V., Hall D., Jansson S. 2008. Nucleotide polymorphism and phenotypic associations within and around the phytochrome B2 Locus in European Aspen (Populus tremula, Salicaceae). Genetics 178:2217–2226. PubMed PMC
Jadwiszczak K.A., Banaszek A., Jabłońska E., Sozinov O.V. 2012. Chloroplast DNA variation of Betula humilis Schrk. in Poland and Belarus. Tree Genet. Genomes 8:1017–1030.
Järvinen P., Palmé A., Morales L.O., Lännenpää M., Keinänen M., Sopanen T., Lascoux M. 2004. Phylogenetic relationships of Betula species (Betulaceae) based on nuclear ADH and chloroplast matK sequences. Am. J. Bot. 91:1834–1845. PubMed
Jeffers, R. M. 1971. Research at the Institute of Forest Genetics, Rhinelander, Wisconsin. USDA Forest Service, Research Paper NC-67, p. 17.
Jiang X., Song Q., Ye W., Chen Z.J. 2021. Concerted genomic and epigenomic changes accompany stabilization of Arabidopsis allopolyploids. Nat. Ecol. Evol. 5:1382–1393. PubMed PMC
Johnsson H. 1944. Triploidy in Betula alba L. Bot. Kotiser. 97:85.
Jombart T., Devillard S., Balloux F. 2010. Discriminant analysis of principal components: a new method for the analysis of genetically structured populations. BMC Genet. 11:94–15. PubMed PMC
Jones G., Sagitov S., Oxelman B. 2013. Statistical inference of allopolyploid species networks in the presence of incomplete lineage sorting. Syst. Biol. 62:467–478. PubMed
Jørgensen M.H., Ehrich D., Schmickl R., Koch M.A., Brysting A.K. 2011. Interspecific and interploidal gene flow in Central European Arabidopsis (Brassicaceae). BMC Evol. Biol. 11:346. PubMed PMC
Joubès J., Raffaele S., Bourdenx B., Garcia C., Laroche-Traineau J., Moreau P., Domergue F., Lessire R. 2008. The VLCFA elongase gene family in Arabidopsis thaliana: phylogenetic analysis, 3D modelling and expression profiling. Plant Mol. Biol. 67:547–566. PubMed
Jung J.-H., Domijan M., Klose C., Biswas S., Ezer D., Gao M., Khattak A.K., Box M.S., Charoensawan V., Cortijo S., Kumar M., Grant A., Locke J.C.W., Schäfer E., Jaeger K.E., Wigge P.A. 2016. Phytochromes function as thermosensors in Arabidopsis. Science 354:886–889. PubMed
Kaczorowski K.A., Quail P.H. 2003. Arabidopsis PSEUDO-RESPONSE REGULATOR7 is a signaling intermediate in phytochrome-regulated seedling deetiolation and phasing of the circadian clock. Plant Cell 15:2654–2665. PubMed PMC
Kamm J., Terhorst J., Durbin R., Song Y.S. 2020. Efficiently inferring the demographic history of many populations with allele count data. J. Am. Stat. Assoc. 115:1472–1487. PubMed PMC
Keightley P.D., Jackson B.C. 2018. Inferring the probability of the derived vs. the ancestral allelic state at a polymorphic site. Genetics 209:897–906. PubMed PMC
Keller I., Wagner C.E., Greuter L., Mwaiko S., Selz O.M., Sivasundar A., Wittwer S., Seehausen O. 2013. Population genomic signatures of divergent adaptation, gene flow and hybrid speciation in the rapid radiation of Lake Victoria cichlid fishes. Mol. Ecol. 22:2848–2863. PubMed
Kellis M., Birren B.W., Lander E.S. 2004. Proof and evolutionary analysis of ancient genome duplication in the yeast Saccharomyces cerevisiae. Nature 428:617–624. PubMed
Kim H.-J., Kim Y.-K., Park J.-Y., Kim J. 2002. Light signalling mediated by phytochrome plays an important role in cold-induced gene expression through the C-repeat/dehydration responsive element (C/DRE) in Arabidopsis thaliana. Plant J. 29:693–704. PubMed
Kim M., Cui M.-L., Cubas P., Gillies A., Lee K., Chapman M.A., Abbott R.J., Coen E. 2008. Regulatory genes control a key morphological and ecological trait transferred between species. Science 322:1116–1119. PubMed
Kim Y., Park S., Gilmour S.J., Thomashow M.F. 2013. Roles of CAMTA transcription factors and salicylic acid in configuring the low-temperature transcriptome and freezing tolerance of Arabidopsis. Plant J. 75:364–376. PubMed
Kim Y.J., Wang R., Gao L., Li D., Xu C., Mang H., Jeon J., Chen X., Zhong X., Kwak J.M., Mo B., Xiao L., Chen X. 2016. POWERDRESS and HDA9 interact and promote histone H3 deacetylation at specific genomic sites in Arabidopsis. Proc. Natl. Acad. Sci. U.S.A. 113:14858–14863. PubMed PMC
Koch M.A., Matschinger M. 2007. Evolution and genetic differentiation among relatives of Arabidopsis thaliana. Proc. Natl. Acad. Sci. U.S.A. 104:6272–6277. PubMed PMC
Koch M.A. 2019. The plant model system Arabidopsis set in an evolutionary, systematic, and spatio-temporal context. J. Exp. Bot. 70:55–67. PubMed
Koropachinskii I.Y. 2013. Natural hybridization and taxonomy of birches in North Asia. Contemp. Probl. Ecol. 6:350–369.
Krehenwinkel H., Tautz D. 2013. Northern range expansion of European populations of the wasp spider Argiope bruennichi is associated with global warming–correlated genetic admixture and population-specific temperature adaptations. Mol. Ecol. 22:2232–2248. PubMed
Lafon-Placette C., Johannessen I.M., Hornslien K.S., Ali M.F., Bjerkan K.N., Bramsiepe J., Glöckle B.M., Rebernig C.A., Brysting A.K., Grini P.E., Köhler C. 2017. Endosperm-based hybridization barriers explain the pattern of gene flow between Arabidopsis lyrata and Arabidopsis arenosa in Central Europe. Proc. Natl. Acad. Sci. USA 114:E1027–E1035. PubMed PMC
Lamichhaney S., Berglund J., Almén M.S., Maqbool K., Grabherr M., Martinez-Barrio A., Promerová M., Rubin C.-J., Wang C., Zamani N., Grant B.R., Grant P.R., Webster M.T., Andersson L. 2015. Evolution of Darwin’s finches and their beaks revealed by genome sequencing. Nature 518:371–375. PubMed
Lashermes P., Hueber Y., Combes M.-C., Severac D., Dereeper A. 2016. Inter-genomic DNA exchanges and homeologous gene silencing shaped the nascent allopolyploid coffee genome (Coffea arabica L.). G3 (Bethesda, Md.) 6:2937–2948. PubMed PMC
Lautenschlager U., Wagner F., Oberprieler C. 2020. AllCoPol: inferring allele co-ancestry in polyploids. BMC Bioinf. 21:441. PubMed PMC
Leal J.L., Milesi P., Salojärvi J., Lascoux M. 2023. Phylogenetic analysis of allotetraploid species using polarized genomic sequences. Syst. Biol. 72:372–390. PubMed PMC
Legris M., Klose C., Burgie E.S., Rojas C.C.R., Neme M., Hiltbrunner A., Wigge P.A., Schäfer E., Vierstra R.D., Casal J.J. 2016. Phytochrome B integrates light and temperature signals in Arabidopsis. Science 354:897–900. PubMed
Li J., Shoup S., Chen Z. 2005. Phylogenetics of Betula (Betulaceae) inferred from sequences of nuclear ribosomal DNA. Rhodora 107:69–86.
Li J., Shoup S., Chen Z. 2007. Phylogenetic relationships of diploid species of Betula (Betulaceae) inferred from DNA sequences of nuclear nitrate reductase. Syst. Bot. 32:357–365.
Li H., Durbin R. 2009. Fast and accurate short read alignment with Burrows–Wheeler transform. Bioinformatics 25:1754–1760. PubMed PMC
Li F., Fan G., Lu C., Xiao G., Zou C., Kohel R.J., Ma Z., Shang H., Ma X., Wu J., Liang X., Huang G., Percy R.G., Liu K., Yang W., Chen W., Du X., Shi C., Yuan Y., Ye W., Liu X., Zhang X., Liu W., Wei H., Wei S., Huang G., Zhang X., Zhu S., Zhang H., Sun F., Wang X., Liang J., Wang J., He Q., Huang L., Wang J., Cui J., Song G., Wang K., Xu X., Yu J.Z., Zhu Y., Yu S. 2015. Genome sequence of cultivated Upland cotton (Gossypium hirsutum TM-1) provides insights into genome evolution. Nat. Biotechnol. 33:524–530. PubMed
Li Z., Tiley G.P., Galuska S.R., Reardon C.R., Kidder T.I., Rundell R.J., Barker M.S. 2018a. Multiple large-scale gene and genome duplications during the evolution of hexapods. Proc. Natl. Acad. Sci. U.S.A. 115:4713–4718. PubMed PMC
Li X., Yu H., Jiao Y., Shahid M.Q., Wu J., Liu X. 2018b. Genome-wide analysis of DNA polymorphisms, the methylome and transcriptome revealed that multiple factors are associated with low pollen fertility in autotetraploid rice. PLoS One 13:e0201854. PubMed PMC
Li L., Milesi P., Tiret M., Chen J., Sendrowski J., Baison J., Chen Z., Zhou L., Karlsson B., Berlin M., Westin J., Garcia-Gil M.R., Wu H.X., Lascoux M. 2022. Teasing apart the joint effect of demography and natural selection in the birth of a contact zone. New Phytol. 236:1976–1987. PubMed PMC
Lihová J., Kučera J., Perný M., Marhold K. 2007. Hybridization between two polyploid Cardamine (Brassicaceae) species in North-western Spain: discordance between morphological and genetic variation patterns. Ann. Bot. 99:1083–1096. PubMed PMC
Lim C.J., Park J., Shen M., Park H.J., Cheong M.S., Park K.S., Baek D., Bae M.J., Ali A., Jan M., Lee S.Y., Lee B., Kim W.-Y., Pardo J.M., Yun D.-J. 2020. The histone-modifying complex PWR/HOS15/HD2C epigenetically regulates cold tolerance. Plant Physiol. 184:1097–1111. PubMed PMC
Liu Z., Hall J.D., Mount D.W. 2001. Arabidopsis UVH3 gene is a homolog of the Saccharomyces cerevisiae RAD2 and human XPG DNA repair genes. Plant J. 26:329–338. PubMed
Lloyd A., Bomblies K. 2016. Meiosis in autopolyploid and allopolyploid Arabidopsis. Curr. Opin. Plant Biol. 30:116–122. PubMed
Lloyd A., Blary A., Charif D., Charpentier C., Tran J., Balzergue S., Delannoy E., Rigaill G., Jenczewski E. 2018. Homoeologous exchanges cause extensive dosage-dependent gene expression changes in an allopolyploid crop. New Phytol. 217:367–377. PubMed
Ma L.-J., Ibrahim A.S., Skory C., Grabherr M.G., Burger G., Butler M., Elias M., Idnurm A., Lang B.F., Sone T., Abe A., Calvo S.E., Corrochano L.M., Engels R., Fu J., Hansberg W., Kim J.-M., Kodira C.D., Koehrsen M.J., Liu B., Miranda-Saavedra D., O’Leary S., Ortiz-Castellanos L., Poulter R., Rodriguez-Romero J., Ruiz-Herrera J., Shen Y.-Q., Zeng Q., Galagan J., Birren B.W., Cuomo C.A., Wickes B.L. 2009. Genomic analysis of the basal lineage fungus Rhizopus oryzae reveals a whole-genome duplication. PLoS Genet. 5:e1000549. PubMed PMC
Macqueen D.J., Johnston I.A. 2014. A well-constrained estimate for the timing of the salmonid whole genome duplication reveals major decoupling from species diversification. Proc. Biol. Sci. 281:20132881. PubMed PMC
Maddison W.P., Knowles L.L. 2006. Inferring phylogeny despite incomplete lineage sorting. Syst. Biol. 55:21–30. PubMed
Mallet J. 2005. Hybridization as an invasion of the genome. Trends Ecol. Evol. 20:229–237. PubMed
Mallet J. 2007. Hybrid speciation. Nature 446:279–283. PubMed
Mallet J., Besansky N., Hahn M.W. 2016. How reticulated are species? Bioessays 38:140–149. PubMed PMC
Mallo D., De Oliveira Martins L., Posada D. 2016. SimPhy: phylogenomic simulation of gene, locus, and species trees. Syst. Biol. 65:334–344. PubMed PMC
Mandel J.R., Barker M.S., Bayer R.J., Dikow R.B., Gao T.-G., Jones K.E., Keeley S., Kilian N., Ma H., Siniscalchi C.M., Susanna A., Thapa R., Watson L., Funk V.A. 2017. The Compositae Tree of Life in the age of phylogenomics. J. Syst. Evol. 55:405–410.
Marburger S., Monnahan P., Seear P.J., Martin S.H., Koch J., Paajanen P., Bohutínská M., Higgins J.D., Schmickl R., Yant L. 2019. Interspecific introgression mediates adaptation to whole genome duplication. Nat. Commun. 10:5218. PubMed PMC
Marhold K., Lihová J. 2006. Polyploidy, hybridization and reticulate evolution: lessons from the Brassicaceae. Plant Syst. Evol. 259:143–174.
Maruyama K., Takeda M., Kidokoro S., Yamada K., Sakuma Y., Urano K., Fujita M., Yoshiwara K., Matsukura S., Morishita Y., Sasaki R., Suzuki H., Saito K., Shibata D., Shinozaki K., Yamaguchi-Shinozaki K. 2009. Metabolic pathways involved in cold acclimation identified by integrated analysis of metabolites and transcripts regulated by DREB1A and DREB2A. Plant Physiol. 150:1972–1980. PubMed PMC
McCormack J.E., Huang H., Knowles L.L. 2009. Maximum likelihood estimates of species trees: how accuracy of phylogenetic inference depends upon the divergence history and sampling design. Syst. Biol. 58:501–508. PubMed
McDonald D.B., Parchman T.L., Bower M.R., Hubert W.A., Rahel F.J. 2008. An introduced and a native vertebrate hybridize to form a genetic bridge to a second native species. Proc. Natl. Acad. Sci. U.S.A. 105:10837–10842. PubMed PMC
McKenna A., Hanna M., Banks E., Sivachenko A., Cibulskis K., Kernytsky A., Garimella K., Altshuler D., Gabriel S., Daly M., DePristo M.A. 2010. The Genome Analysis Toolkit: a MapReduce framework for analyzing next-generation DNA sequencing data. Genome Res. 20:1297–1303. PubMed PMC
Meier J.I., Marques D.A., Mwaiko S., Wagner C.E., Excoffier L., Seehausen O. 2017. Ancient hybridization fuels rapid cichlid fish adaptive radiations. Nat. Commun. 8:14363. PubMed PMC
Merret R., Descombin J., Juan Y., Favory J.-J., Carpentier M.-C., Chaparro C., Charng Y., Deragon J.-M., Bousquet-Antonelli C. 2013. XRN4 and LARP1 are required for a heat-triggered mRNA decay pathway involved in plant acclimation and survival during thermal stress. Cell Rep. 5:1279–1293. PubMed
Minh B.Q., Schmidt H.A., Chernomor O., Schrempf D., Woodhams M.D., von Haeseler A., Lanfear R. 2020. IQ-TREE 2: new models and efficient methods for phylogenetic inference in the genomic era. Mol. Biol. Evol. 37:1530–1534. PubMed PMC
Mirarab S., Bayzid M.S., Warnow T. 2016. Evaluating summary methods for multilocus species tree estimation in the presence of incomplete lineage sorting. Syst. Biol. 65:366–380. PubMed
Monnahan P., Kolář F., Baduel P., Sailer C., Koch J., Horvath R., Laenen B., Schmickl R., Paajanen P., Šrámková G., Bohutínská M., Arnold B., Weisman C.M., Marhold K., Slotte T., Bomblies K., Yant L. 2019. Pervasive population genomic consequences of genome duplication in Arabidopsis arenosa. Nat. Ecol. Evol. 3:457–468. PubMed
Morgan C., White M.A., Franklin F.C.H., Zickler D., Kleckner N., Bomblies K. 2021. Evolution of crossover interference enables stable autopolyploidy by ensuring pairwise partner connections in Arabidopsis arenosa. Curr. Biol. 31:4713–4726.e4. PubMed PMC
Muñoz-Rodríguez P., Carruthers T., Wood J.R.I., Williams B.R.M., Weitemier K., Kronmiller B., Ellis D., Anglin N.L., Longway L., Harris S.A., Rausher M.D., Kelly S., Liston A., Scotland R.W. 2018. Reconciling conflicting phylogenies in the origin of sweet potato and dispersal to polynesia. Curr. Biol. 28:1246–1256.e12. PubMed
Nibau C., Gonzalo A., Evans A., Sweet-Jones W., Phillips D., Lloyd A. 2022. Meiosis in allopolyploid Arabidopsis suecica. Plant J. 111:1110–1122. PubMed PMC
Nieto Feliner G., Casacuberta J., Wendel J.F. 2020. Genomics of evolutionary novelty in hybrids and polyploids. Front. Genet. 11:1–21. PubMed PMC
Nossa C.W., Havlak P., Yue J.-X., Lv J., Vincent K.Y., Brockmann H.J., Putnam N.H. 2014. Joint assembly and genetic mapping of the Atlantic horseshoe crab genome reveals ancient whole genome duplication. GigaScience 3:2047–217X-3–9. PubMed PMC
Novikova P.Y., Tsuchimatsu T., Simon S., Nizhynska V., Voronin V., Burns R., Fedorenko O.M., Holm S., Säll T., Prat E., Marande W., Castric V., Nordborg M. 2017. Genome sequencing reveals the origin of the Allotetraploid Arabidopsis suecica. Mol. Biol. Evol. 34:957–968. PubMed PMC
Novikova P.Y., Brennan I.G., Booker W., Mahony M., Doughty P., Lemmon A.R., Lemmon E.M., Roberts J.D., Yant L., de Peer Y.V., Keogh J.S., Donnellan S.C. 2020. Polyploidy breaks speciation barriers in Australian burrowing frogs Neobatrachus. PLoS Genet. 16:e1008769. PubMed PMC
Oberprieler C., Wagner F., Tomasello S., Konowalik K. 2017. A permutation approach for inferring species networks from gene trees in polyploid complexes by minimising deep coalescences. Methods Ecol. Evol. 8:835–849.
Opgenoorth L., Dauphin B., Benavides R., Heer K., Alizoti P., Martínez-Sancho E., Alía R., Ambrosio O., Audrey A., Auñón F., Avanzi C., Avramidou E., Bagnoli F., Barbas E., Bastias C.C., Bastien C., Ballesteros E., Beffa G., Bernier F., Bignalet H., Bodineau G., Bouic D., Brodbeck S., Brunetto W., Buchovska J., Buy M., Cabanillas-Saldaña A.M., Carvalho B., Cheval N., Climent J.M., Correard M., Cremer E., Danusevičius D., Del Caño F., Denou J.-L., di Gerardi N., Dokhelar B., Ducousso A., Eskild Nilsen A., Farsakoglou A.-M., Fonti P., Ganopoulos I., García del Barrio J.M., Gilg O., González-Martínez S.C., Graf R., Gray A., Grivet D., Gugerli F., Hartleitner C., Hollenbach E., Hurel A., Issehut B., Jean F., Jorge V., Jouineau A., Kappner J.-P., Kärkkäinen K., Kesälahti R., Knutzen F., Kujala S.T., Kumpula T.A., Labriola M., Lalanne C., Lambertz J., Lascoux M., Lejeune V., Le-Provost G., Levillain J., Liesebach M., López-Quiroga D., Meier B., Malliarou E., Marchon J., Mariotte N., Mas A., Matesanz S., Meischner H., Michotey C., Milesi P., Morganti S., Nievergelt D., Notivol E., Ostreng G., Pakull B., Perry A., Piotti A., Plomion C., Poinot N., Pringarbe M., Puzos L., Pyhäjärvi T., Raffin A., Ramírez-Valiente J.A., Rellstab C., Remi D., Richter S., Robledo-Arnuncio J.J., San Segundo S., Savolainen O., Schueler S., Schneck V., Scotti I., Semerikov V., Slámová L., Sønstebø J.H., Spanu I., Thevenet J., Tollefsrud M.M., Turion N., Vendramin G.G., Villar M., von Arx G., Westin J., Fady B., Myking T., Valladares F., Aravanopoulos F.A., Cavers S. 2021. The GenTree Platform: growth traits and tree-level environmental data in 12 European forest tree species. GigaScience 10:giab010. PubMed PMC
Oxelman B., Brysting A.K., Jones G.R., Marcussen T., Oberprieler C., Pfeil B.E. 2017. Phylogenetics of allopolyploids. Annu. Rev. Ecol. Evol. Syst. 48:543–557.
Palmé A.E., Su Q., Palsson S., Lascoux M. 2004. Extensive sharing of chloroplast haplotypes among European birches indicates hybridization among Betula pendula, B. pubescens and B. nana. Mol. Ecol. 13:167–178. PubMed
Pardo-Diaz C., Salazar C., Baxter S.W., Merot C., Figueiredo-Ready W., Joron M., McMillan W.O., Jiggins C.D. 2012. Adaptive introgression across species boundaries in Heliconius butterflies. PLoS Genet. 8:e1002752. PubMed PMC
Pickrell J.K., Pritchard J.K. 2012. Inference of population splits and mixtures from genome-wide allele frequency data. PLoS Genet. 8:e1002967. PubMed PMC
Pritchard J.K., Stephens M., Donnelly P. 2000. Inference of population structure using Multilocus genotype data. Genetics 155:945–959. PubMed PMC
Rabiee M., Sayyari E., Mirarab S. 2019. Multi-allele species reconstruction using ASTRAL. Mol. Phylogenet. Evol. 130:286–296. PubMed
Ramsey J., Schemske D.W. 1998. Pathways, mechanisms, and rates of polyploid formation in flowering plants. Annu. Rev. Ecol. Syst. 29:467–501.
Ramsey J., Schemske D.W. 2002. Neopolyploidy in flowering plants. Annu. Rev. Ecol. Syst. 33:589–639.
Renard J., Niñoles R., Martínez-Almonacid I., Gayubas B., Mateos-Fernández R., Bissoli G., Bueso E., Serrano R., Gadea J. 2020. Identification of novel seed longevity genes related to oxidative stress and seed coat by genome-wide association studies and reverse genetics. Plant Cell Environ. 43:2523–2539. PubMed
Rieseberg L.H., Archer M.A., Wayne R.K. 1999. Transgressive segregation, adaptation and speciation. Heredity 83 ( Pt 4):363–372. PubMed
Rieseberg L.H., Willis J.H. 2007. Plant speciation. Science 317:910–914. PubMed PMC
Rius M., Darling J.A. 2014. How important is intraspecific genetic admixture to the success of colonising populations? Trends Ecol. Evol. 29:233–242. PubMed
Robertson F.M., Gundappa M.K., Grammes F., Hvidsten T.R., Redmond A.K., Lien S., Martin S.A.M., Holland P.W.H., Sandve S.R., Macqueen D.J. 2017. Lineage-specific rediploidization is a mechanism to explain time-lags between genome duplication and evolutionary diversification. Genome Biol. 18:111. PubMed PMC
Rothfels C.J. 2021. Polyploid phylogenetics. New Phytol. 230:66–72. PubMed
Roux C., Pannell J.R. 2015. Inferring the mode of origin of polyploid species from next-generation sequence data. Mol. Ecol. 24:1047–1059. PubMed
Salojärvi J., Smolander O.-P., Nieminen K., Rajaraman S., Safronov O., Safdari P., Lamminmäki A., Immanen J., Lan T., Tanskanen J., Rastas P., Amiryousefi A., Jayaprakash B., Kammonen J.I., Hagqvist R., Eswaran G., Ahonen V.H., Serra J.A., Asiegbu F.O., de Dios Barajas-Lopez J., Blande D., Blokhina O., Blomster T., Broholm S., Brosché M., Cui F., Dardick C., Ehonen S.E., Elomaa P., Escamez S., Fagerstedt K.V., Fujii H., Gauthier A., Gollan P.J., Halimaa P., Heino P.I., Himanen K., Hollender C., Kangasjärvi S., Kauppinen L., Kelleher C.T., Kontunen-Soppela S., Koskinen J.P., Kovalchuk A., Kärenlampi S.O., Kärkönen A.K., Lim K.-J., Leppälä J., Macpherson L., Mikola J., Mouhu K., Mähönen A.P., Niinemets U., Oksanen E., Overmyer K., Palva E.T., Pazouki L., Pennanen V., Puhakainen T., Poczai P., Possen B.J.H.M., Punkkinen M., Rahikainen M.M., Rousi M., Ruonala R., van der Schoot C., Shapiguzov A., Sierla M., Sipilä T.P., Sutela S., Teeri T.H., Tervahauta A.I., Vaattovaara A., Vahala J., Vetchinnikova L., Welling A., Wrzaczek M., Xu E., Paulin L.G., Schulman A.H., Lascoux M., Albert V.A., Auvinen P., Helariutta Y., Kangasjärvi J. 2017. Genome sequencing and population genomic analyses provide insights into the adaptive landscape of silver birch. Nat. Genet. 49:904–912. PubMed
Salojärvi J., Rambani A., Yu Z., Guyot R., Strickler S., Lepelley M., Wang C., Rajaraman S., Rastas P., Zheng C., Muñoz D.S., Meidanis J., Paschoal A.R., Bawin Y., Krabbenhoft T., Wang Z.Q., Fleck S., Aussel R., Bellanger L., Charpagne A., Fournier C., Kassam M., Lefebvre G., Métairon S., Moine D., Rigoreau M., Stolte J., Hamon P., Couturon E., Tranchant-Dubreuil C., Mukherjee M., Lan T., Engelhardt J., Stadler P., Lemos S.M.C.D., Suzuki S.I., Sumirat U., Man W.C., Dauchot N., Orozco-Arias S., Garavito A., Kiwuka C., Musoli P., Nalukenge A., Guichoux E., Reinout H., Smit M., Carretero-Paulet L., Filho O.G., Braghini M.T., Padilha L., Sera G.H., Ruttink T., Henry R., Marraccini P., de Peer Y.V., Andrade A., Domingues D., Giuliano G., Mueller L., Pereira L.F., Plaisance S., Poncet V., Rombauts S., Sankoff D., Albert V.A., Crouzillat D., de Kochko A., Descombes P. 2023. The genome and population genomics of allopolyploid Coffea arabica reveal the diversification history of modern coffee cultivars. bioRxiv::2023.09.06.556570. PubMed PMC
Schenk M.F., Thienpont C.-N., Koopman W.J.M., Gilissen L.J.W.J., Smulders M.J.M. 2008. Phylogenetic relationships in Betula (Betulaceae) based on AFLP markers. Tree Genet. Genomes 4:911–924.
Schmickl R., Marburger S., Bray S., Yant L. 2017. Hybrids and horizontal transfer: introgression allows adaptive allele discovery. J. Exp. Bot. 68:5453–5470. PubMed
Schmickl R., Yant L. 2021. Adaptive introgression: how polyploidy reshapes gene flow landscapes. New Phytol. 230:457–461. PubMed
Schwager E.E., Sharma P.P., Clarke T., Leite D.J., Wierschin T., Pechmann M., Akiyama-Oda Y., Esposito L., Bechsgaard J., Bilde T., Buffry A.D., Chao H., Dinh H., Doddapaneni H., Dugan S., Eibner C., Extavour C.G., Funch P., Garb J., Gonzalez L.B., Gonzalez V.L., Griffiths-Jones S., Han Y., Hayashi C., Hilbrant M., Hughes D.S.T., Janssen R., Lee S.L., Maeso I., Murali S.C., Muzny D.M., Nunes da Fonseca R., Paese C.L.B., Qu J., Ronshaugen M., Schomburg C., Schönauer A., Stollewerk A., Torres-Oliva M., Turetzek N., Vanthournout B., Werren J.H., Wolff C., Worley K.C., Bucher G., Gibbs R.A., Coddington J., Oda H., Stanke M., Ayoub N.A., Prpic N.-M., Flot J.-F., Posnien N., Richards S., McGregor A.P. 2017. The house spider genome reveals an ancient whole-genome duplication during arachnid evolution. BMC Biol. 15:62. PubMed PMC
Seear P.J., France M.G., Gregory C.L., Heavens D., Schmickl R., Yant L., Higgins J.D. 2020. A novel allele of ASY3 is associated with greater meiotic stability in autotetraploid Arabidopsis lyrata. PLoS Genet. 16:e1008900. PubMed PMC
Seehausen O. 2006. African cichlid fish: a model system in adaptive radiation research. Proc. Biol. Sci. 273:1987–1998. PubMed PMC
Séguéla-Arnaud M., Crismani W., Larchevêque C., Mazel J., Froger N., Choinard S., Lemhemdi A., Macaisne N., Van Leene J., Gevaert K., De Jaeger G., Chelysheva L., Mercier R. 2015. Multiple mechanisms limit meiotic crossovers: TOP3α and two BLM homologs antagonize crossovers in parallel to FANCM. Proc. Natl. Acad. Sci. U.S.A. 112:4713–4718. PubMed PMC
Seo M., Hanada A., Kuwahara A., Endo A., Okamoto M., Yamauchi Y., North H., Marion-Poll A., Sun T., Koshiba T., Kamiya Y., Yamaguchi S., Nambara E. 2006. Regulation of hormone metabolism in Arabidopsis seeds: phytochrome regulation of abscisic acid metabolism and abscisic acid regulation of gibberellin metabolism. Plant J. 48:354–366. PubMed
Serra H., Lambing C., Griffin C.H., Topp S.D., Nageswaran D.C., Underwood C.J., Ziolkowski P.A., Séguéla-Arnaud M., Fernandes J.B., Mercier R., Henderson I.R. 2018. Massive crossover elevation via combination of HEI10 and recq4a recq4b during Arabidopsis meiosis. Proc. Natl. Acad. Sci. U.S.A. 115:2437–2442. PubMed PMC
Shen H., Luong P., Huq E. 2007. The F-box protein MAX2 functions as a positive regulator of photomorphogenesis in arabidopsis. Plant Physiol. 145:1471–1483. PubMed PMC
Shi X., Sun X., Zhang Z., Feng D., Zhang Q., Han L., Wu J., Lu T. 2015. GLUCAN SYNTHASE-LIKE 5 (GSL5) plays an essential role in male fertility by regulating callose metabolism during microsporogenesis in rice. Plant Cell Physiol. 56:497–509. PubMed
Sicard A., Kappel C., Josephs E.B., Lee Y.W., Marona C., Stinchcombe J.R., Wright S.I., Lenhard M. 2015. Divergent sorting of a balanced ancestral polymorphism underlies the establishment of gene-flow barriers in Capsella. Nat. Commun. 6:7960. PubMed PMC
Slotte T., Huang H., Lascoux M., Ceplitis A. 2008. Polyploid speciation did not confer instant reproductive isolation in capsella (Brassicaceae). Mol. Biol. Evol. 25:1472–1481. PubMed
Solís-Lemus C., Bastide P., Ané C. 2017. PhyloNetworks: a package for phylogenetic networks. Mol. Biol. Evol. 34:3292–3298. PubMed
Soltis P.S., Soltis D.E. 2009. The role of hybridization in plant speciation. Annu. Rev. Plant Biol. 60:561–588. PubMed
Somers D.E., Devlin P.F., Kay S.A. 1998. Phytochromes and cryptochromes in the entrainment of the Arabidopsis circadian clock. Science. 282:1488–1490. PubMed
Spoelhof J.P., Soltis P.S., Soltis D.E. 2017. Pure polyploidy: closing the gaps in autopolyploid research. J. Syst. Evol.. 55:340–352.
Stebbins G.L. 1956. Cytogenetics and evolution of the grass family. Am. J. Bot. 43:890–905.
Stebbins G. 1971. Chromosomal evolution in higher plants. London: Edward Arnold Ltd.
Stern K. 1965. Tetrasome spaltung bei Betula pubescens. Silvae Genet. 14:56–57.
Suarez-Gonzalez A., Hefer C.A., Lexer C., Douglas C.J., Cronk Q.C.B. 2018. Introgression from Populus balsamifera underlies adaptively significant variation and range boundaries in P. trichocarpa. New Phytol. 217:416–427. PubMed
Sun F., Fan G., Hu Q., Zhou Y., Guan M., Tong C., Li J., Du D., Qi C., Jiang L., Liu W., Huang S., Chen W., Yu J., Mei D., Meng J., Zeng P., Shi J., Liu K., Wang X., Wang X., Long Y., Liang X., Hu Z., Huang G., Dong C., Zhang H., Li J., Zhang Y., Li L., Shi C., Wang J., Lee S.M.-Y., Guan C., Xu X., Liu S., Liu X., Chalhoub B., Hua W., Wang H. 2017. The high-quality genome of Brassica napus cultivar “ZS11” reveals the introgression history in semi-winter morphotype. Plant J. 92:452–468. PubMed
Tavaré S., Balding D.J., Griffiths R.C., Donnelly P. 1997. Inferring coalescence times from DNA sequence data. Genetics 145:505–518. PubMed PMC
Than C., Ruths D., Nakhleh L. 2008. PhyloNet: a software package for analyzing and reconstructing reticulate evolutionary relationships. BMC Bioinf. 9:322. PubMed PMC
Thórsson ÆH.T., Salmela E., Anamthawat-Jónsson K. 2001. Morphological, cytogenetic, and molecular evidence for introgressive hybridization in birch. J. Hered. 92:404–408. PubMed
Truong C., Palmé A.E., Felber F. 2007. Recent invasion of the mountain birch Betula pubescens ssp. tortuosa above the treeline due to climate change: genetic and ecological study in northern Sweden. J. Evol. Biol. 20:369–380. PubMed
Tsuda Y., Semerikov V., Sebastiani F., Vendramin G.G., Lascoux M. 2017. Multispecies genetic structure and hybridization in the Betula genus across Eurasia. Mol. Ecol. 26:589–605. PubMed
Van de Peer Y., Mizrachi E., Marchal K. 2017. The evolutionary significance of polyploidy. Nat. Rev. Genet. 18:411–424. PubMed
Wagner N.D., He L., Hörandl E. 2020. Phylogenomic relationships and evolution of polyploid salix species revealed by RAD sequencing data. Front. Plant Sci. 11:1077. PubMed PMC
Walters S.M. 1968. Betula L. in Britain. Pro. Bot. Soc. Br. Isl. 7:179–180.
Wang N., Borrell J.S., Bodles W.J.A., Kuttapitiya A., Nichols R.A., Buggs R.J.A. 2014. Molecular footprints of the Holocene retreat of dwarf birch in Britain. Mol. Ecol. 23:2771–2782. PubMed PMC
Wang N., McAllister H.A., Bartlett P.R., Buggs R.J.A. 2016. Molecular phylogeny and genome size evolution of the genus Betula (Betulaceae). Ann. Bot. 117:1023–1035. PubMed PMC
Wang Z., Miao H., Liu J., Xu B., Yao X., Xu C., Zhao S., Fang X., Jia C., Wang J., Zhang J., Li J., Xu Y., Wang J., Ma W., Wu Z., Yu L., Yang Y., Liu C., Guo Y., Sun S., Baurens F.-C., Martin G., Salmon F., Garsmeur O., Yahiaoui N., Hervouet C., Rouard M., Laboureau N., Habas R., Ricci S., Peng M., Guo A., Xie J., Li Y., Ding Z., Yan Y., Tie W., D’Hont A., Hu W., Jin Z. 2019. Musa balbisiana genome reveals subgenome evolution and functional divergence. Nat. Plants 5:810–821. PubMed PMC
Wang N., Kelly L.J., McAllister H.A., Zohren J., Buggs R.J.A. 2021. Resolving phylogeny and polyploid parentage using genus-wide genome-wide sequence data from birch trees. Mol. Phylogenet. Evol. 160:107126. PubMed
Wen D., Yu Y., Zhu J., Nakhleh L. 2018. Inferring phylogenetic networks using PhyloNet. Syst. Biol. 67:735–740. PubMed PMC
Whitney K.D., Randell R.A., Rieseberg L.H. 2006. Adaptive introgression of herbivore resistance traits in the weedy sunflower Helianthus annuus. Am. Nat. 167:794–807. PubMed
Winkler M., Escobar García P., Gattringer A., Sonnleitner M., Hülber K., Schönswetter P., Schneeweiss G.M. 2017. A novel method to infer the origin of polyploids from Amplified Fragment Length Polymorphism data reveals that the alpine polyploid complex of Senecio carniolicus (Asteraceae) evolved mainly via autopolyploidy. Mol. Ecol. Resour. 17:877–892. PubMed
Wolfe K.H., Shields D.C. 1997. Molecular evidence for an ancient duplication of the entire yeast genome. Nature 387:708–713. PubMed
Wood T.E., Takebayashi N., Barker M.S., Mayrose I., Greenspoon P.B., Rieseberg L.H. 2009. The frequency of polyploid speciation in vascular plants. Proc. Natl. Acad. Sci. U.S.A. 106:13875–13879. PubMed PMC
Wu Y., Lin F., Zhou Y., Wang J., Sun S., Wang B., Zhang Z., Li G., Lin X., Wang X., Sun Y., Dong Q., Xu C., Gong L., Wendel J.F., Zhang Z., Liu B. 2021. Genomic mosaicism due to homoeologous exchange generates extensive phenotypic diversity in nascent allopolyploids. Natl. Sci. Rev. 8:nwaa277. PubMed PMC
Xiong Z., Gaeta R.T., Edger P.P., Cao Y., Zhao K., Zhang S., Pires J.C. 2021. Chromosome inheritance and meiotic stability in allopolyploid Brassica napus. G3 (Bethesda, Md.). 11:jkaa011. PubMed PMC
Yan Z., Cao Z., Liu Y., Ogilvie H.A., Nakhleh L. 2022. Maximum parsimony inference of phylogenetic networks in the presence of polyploid complexes. Syst. Biol. 71:706–720. PubMed PMC
Yano R., Nakamura M., Yoneyama T., Nishida I. 2005. Starch-related α-glucan/water dikinase is involved in the cold-induced development of freezing tolerance in arabidopsis. Plant Physiol. 138:837–846. PubMed PMC
Yant L., Hollister J.D., Wright K.M., Arnold B.J., Higgins J.D., Franklin F.C.H., Bomblies K. 2013. Meiotic adaptation to genome duplication in Arabidopsis arenosa. Curr. Biol. 23:2151–2156. PubMed PMC
Yoshida K., Schuenemann V.J., Cano L.M., Pais M., Mishra B., Sharma R., Lanz C., Martin F.N., Kamoun S., Krause J., Thines M., Weigel D., Burbano H.A. 2013. The rise and fall of the Phytophthora infestans lineage that triggered the Irish potato famine. eLife 2:e00731. PubMed PMC
Zhang C., Ogilvie H.A., Drummond A.J., Stadler T. 2018a. Bayesian inference of species networks from multilocus sequence data. Mol. Biol. Evol. 35:504–517. PubMed PMC
Zhang C., Rabiee M., Sayyari E., Mirarab S. 2018b. ASTRAL-III: polynomial time species tree reconstruction from partially resolved gene trees. BMC Bioinf. 19:153. PubMed PMC
Zhang T., Jing J.-L., Liu L., He Y. 2021. ZmRAD17 is required for accurate double-strand break repair during maize male meiosis. Front. Plant Sci. 12:1–9. PubMed PMC
Zhou B.-B.S., Elledge S.J. 2000. The DNA damage response: putting checkpoints in perspective. Nature. 408:433–439. PubMed
Zohren J., Wang N., Kardailsky I., Borrell J.S., Joecker A., Nichols R.A., Buggs R.J.A. 2016. Unidirectional diploid–tetraploid introgression among British birch trees with shifting ranges shown by restriction site-associated markers. Mol. Ecol. 25:2413–2426. PubMed PMC