Fast diploidization in close mesopolyploid relatives of Arabidopsis

. 2010 Jul ; 22 (7) : 2277-90. [epub] 20100716

Jazyk angličtina Země Anglie, Velká Británie Médium print-electronic

Typ dokumentu časopisecké články, práce podpořená grantem

Perzistentní odkaz   https://www.medvik.cz/link/pmid20639445

Mesopolyploid whole-genome duplication (WGD) was revealed in the ancestry of Australian Brassicaceae species with diploid-like chromosome numbers (n = 4 to 6). Multicolor comparative chromosome painting was used to reconstruct complete cytogenetic maps of the cryptic ancient polyploids. Cytogenetic analysis showed that the karyotype of the Australian Camelineae species descended from the eight ancestral chromosomes (n = 8) through allopolyploid WGD followed by the extensive reduction of chromosome number. Nuclear and maternal gene phylogenies corroborated the hybrid origin of the mesotetraploid ancestor and suggest that the hybridization event occurred approximately 6 to 9 million years ago. The four, five, and six fusion chromosome pairs of the analyzed close relatives of Arabidopsis thaliana represent complex mosaics of duplicated ancestral genomic blocks reshuffled by numerous chromosome rearrangements. Unequal reciprocal translocations with or without preceeding pericentric inversions and purported end-to-end chromosome fusions accompanied by inactivation and/or loss of centromeres are hypothesized to be the main pathways for the observed chromosome number reduction. Our results underline the significance of multiple rounds of WGD in the angiosperm genome evolution and demonstrate that chromosome number per se is not a reliable indicator of ploidy level.

Zobrazit více v PubMed

Al-Shehbaz I.A., Beilstein M.A., Kellogg E.A. (2006). Systematics and phylogeny of the Brassicaceae (Cruciferae): An overview. Plant Syst. Evol. 259: 89–120

Arabidopsis Genome Initiative (2000). Analysis of the genome sequence of the flowering plant Arabidopsis thaliana. Nature 408: 796–815 PubMed

Barker M.S., Kane N.C., Matvienko M., Kozik A., Michelmore R.W., Knap S.J., Rieseberg L.H. (2008). Multiple paleopolyploidizations during the evolution of the Compositae reveal parallel patterns of duplicate gene retention after millions of years. Mol. Biol. Evol. 25: 2445–2455 PubMed PMC

Barker M.S., Vogel H., Schranz M.E. (2009). Paleopolyploidy in the Brassicales: Analyses of the Cleome transcriptome elucidate the history of genome duplications in Arabidopsis and other Brassicales. Genome Biol. Evol. 1: 1–9 PubMed PMC

Birchler J.A., Veitia R.A. (2007). The gene balance hypothesis: from classical genetics to modern genomics. Plant Cell 19: 395–402 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

Caputo P., Cozzolino S., Gaudio L., Moretti A., Stevenson D.W. (1996). Karyology and phylogeny of some Mesoamerican species of Zamia (Zamiaceae). Am. J. Bot. 83: 1513–1520

Carlsen T., Bleeker W., Hurka H., Elven R., Brochmann C. (2009). Biogeography and phylogeny of Cardamine (Brassicaceae). PLoS ONE 96: 215–236

Cronquist A. (1981). An Integrated System of Classification of Flowering Plants. (New York: Columbia University Press; ).

Cui L., et al. (2006). Widespread genome duplications throughout the history of flowering plants. Genome Res. 16: 738–739 PubMed PMC

De Bodt S., Maere S., Van der Peer Y. (2005). Genome duplication and the origin of angiosperms. Trends Ecol. Evol. 20: 591–597 PubMed

Dierschke T., Mandáková T., Lysak M.A., Mummenhoff K. (2009). A bicontinental origin of polyploid Australian/New Zealand Lepidium species (Brassicaceae)? Evidence from genomic in situ hybridization. Ann. Bot. (Lond.) 104: 681–688 PubMed PMC

Drummond A.J., Rambaut A. (2007). BEAST: Bayesian evolutionary analysis by sampling trees. BMC Evol. Biol. 7: 214. PubMed PMC

Edgar R.C. (2004). MUSCLE: Multiple sequence alignment with high accuracy and high throughput. Nucleic Acids Res. 32: 1792–1797 PubMed PMC

Edger P.P., Pires J.C. (2009). Gene and genome duplications: The impact of dosage-sensitivity of the fate of nuclear genes. Chromosome Res. 17: 699–717 PubMed

Favarger C. (1961). Sur l’emploi des nombres chromo-somiques en géographie botanique historique. Ber. Geobot. Inst. Rübel 32: 119–146

Fawcett J.A., Maere S., Van de Peer Y. (2009). Plants with double genomes might have had a better chance to survive the Cretaceous-Tertiary extinction event. Proc. Natl. Acad. Sci. USA 106: 5737–5742 PubMed PMC

Ferreri G.C., Liscinsky D.M., Mack J.A., Eldridge M.D.B., O’Neill R.J. (2005). Retention of latent centromeres in the mammalian genome. J. Hered. 96: 217–224 PubMed

Franzke A., German D., Al-Shehbaz I.A., Mummenhoff K. (2009). Arabidopsis family ties: Molecular phylogeny and age estimates in the Brassicaceae. Taxon 58: 425–437

Freeling M. (2008). The evolutionary position of subfunctionalization, downgraded. Genome Dyn. 4: 25–40 PubMed

Gaeta R.T., Pires J.C., Iniguez-Luy F., Leon E., Osborn T.C. (2007). Genomic changes in resynthesized Brassica napus and their effect on gene expression and phenotype. Plant Cell 19: 3403–3417 PubMed PMC

Gandolfo M.A., Nixon K.C., Crepet W.L. (1998). A new fossil flower from the Turonian of New Jersey: Dressiantha bicarpellata gen. et sp. nov. (Capparales). Am. J. Bot. 85: 964–974 PubMed

Goldman N., Yang Z. (1994). A codon-based model of nucleotide substitution for protein-coding DNA sequences. Mol. Biol. Evol. 11: 725–736 PubMed

Grant V. (1981). Plant Speciation. (New York: Columbia University Press; ).

Guerra M. (2008). Chromosome numbers in plant cytotaxonomy: Concepts and implications. Cytogenet. Genome Res. 120: 339–350 PubMed

Han F., Gao Z., Birchler J.A. (2009). Reactivation of an inactive centromere reveals epigenetic and structural components for centromere specification in maize. Plant Cell 21: 1929–1939 PubMed PMC

Han F., Lamb J.C., Birchler J.A. (2006). High frequency of centromere inactivation resulting in stable dicentric chromosomes of maize. Proc. Natl. Acad. Sci. USA 103: 3238–3243 PubMed PMC

Han Y., Zhang Z., Liu C., Liu J., Huang S., Jiang J., Lin W. (2009). Centromere repositioning in cucurbit species: Implication of the genomic impact from centromere activation and inactivation. Proc. Natl. Acad. Sci. USA 106: 14937–14941 PubMed PMC

Hegarty M.J., Hiscock S.J. (2008). Genomic clues to the evolutionary success of polyploid plants. Curr. Biol. 18: 435–444 PubMed

Ijdo J.W., Wells R.A., Baldini A., Reeders S.T. (1991a). Improved telomere detection using a telomere repeat probe (TTAGGG)n generated by PCR. Nucleic Acids Res. 19: 4780. PubMed PMC

Ijdo J.W., Wells R.A.W., Baldini A., Reeders S.T. (1991b). The origin of human chromosome 2: An ancestral telomere-telomere fusion. Proc. Natl. Acad. Sci. USA 88: 9051–9055 PubMed PMC

Imai H.T., Taylor R.W. (1989). Chromosomal polymorphisms ivolving telomere fusion, centromeric inactivation and centromere shift in the ant Myrmecia (pilosula) n = 1. Chromosoma 98: 456–460

Jaillon O., Aury J.M., Wincker P. (2009). “Changing by doubling”, the impact of whole genome duplications in the evolution of eukaryotes. C. R. Biol. 332: 241–253 PubMed

Joly S., Heenan P.B., Lockhart P.J. (2009). A Pleistocene inter-tribal allopolyploidization event precedes the species radiation of Pachycladon (Brassicaceae) in New Zealand. Mol. Phylogenet. Evol. 51: 365–372 PubMed

Kim S., Sultan S.E., Donoghue M.J. (2008). Allopolyploid speciation in Persicaria (Polygonaceae): Insights from a low-copy nuclear region. Proc. Natl. Acad. Sci. USA 105: 12370–12375 PubMed PMC

Kaczmarek M., Koczyk G., Ziolkowski P.A., Babula-Skowronska D., Sadowski J. (2009). Comparative analysis of the Brassica oleracea genetic map and the Arabidopsis thaliana genome. Genome 52: 620–633 PubMed

Koch M.A., Haubold B., Mitchell-Olds T. (2000). Comparative evolutionary analysis of chalcone synthase and alcohol dehydrogenase loci in Arabidopsis, Arabis, and related genera (Brassicaceae). Mol. Biol. Evol. 17: 1483–1498 PubMed

Kocsis E., Trus B.L., Steer C.J., Bisher M.E., Steven A.C. (1991). Image averaging of flexible fibrous macromolecules: The clathrin triskelion has an elastic proximal segment. J. Struct. Biol. 107: 6–14 PubMed

Kopecký D., Lukaszewski A.J., Doležel J. (2008). Cytogenetics of Festulolium (Festuca × Lolium hybrids). Cytogenet. Genome Res. 120: 370–383 PubMed

Krzywinski M., Schein J., Birol I., Connors J., Gascoyne R., Horsman D., Jones S.J., Marra M.A. (2009). Circos: An information aesthetic for comparative genomics. Genome Res. 19: 1639–1645 PubMed PMC

Lagercrantz U., Lydiate D. (1996). Comparative genome mapping in Brassica. Genetics 144: 1903–1910 PubMed PMC

Leitch I.J., Kahandawala I., Suda J., Hanson L., Ingrouille M.J., Chase M.W., Fay M.F. (2009). Genome size diversity in orchids: Consequences and evolution. Ann. Bot. (Lond.) 104: 469–481 PubMed PMC

Lim K.Y., Soltis D.E., Soltis P.S., Tate J., Matyasek R., Srubarova H., Kovarik A., Pires J.C., Xiong Z., Leitch A.R. (2008). Rapid chromosome evolution in recently formed polyploids in Tragopogon (Asteraceae). PLoS ONE 3: e3353. PubMed PMC

Luo M.C., et al. (2009). Genome comparisons reveal a dominant mechanism of chromosome number reduction in grasses and accelerated genome evolution in Triticeae. Proc. Natl. Acad. Sci. USA 106: 15780–15785 PubMed PMC

Lysak M.A., Berr A., Pecinka A., Schmidt R., McBreen K., Schubert I. (2006). Mechanisms of chromosome number reduction in Arabidopsis thaliana and related Brassicaceae species. Proc. Natl. Acad. Sci. USA 103: 5224–5229 PubMed PMC

Lysak M.A., Cheung K., Kitschke M., Bureš P. (2007). Ancestral chromosomal blocks are triplicated in Brassiceae species with varying chromosome number and genome size. Plant Physiol. 145: 402–410 PubMed PMC

Lysak M.A., Koch M.A., Pecinka A., Schubert I. (2005). Chromosome triplication found across the tribe Brassiceae. Genome Res. 15: 516–525 PubMed PMC

Mai D.H. (1995). Tertiäre vegetationsgeschichte Europas. (Jena, Stuttgart, New York: Gustav Fisher; ).

Mandáková T., Lysak M.A. (2008). Chromosomal phylogeny and karyotype evolution in x=7 crucifer species (Brassicaceae). Plant Cell 20: 2559–2570 PubMed PMC

Ming R., et al. (2008). The draft genome of the transgenic tropical fruit tree papaya (Carica papaya Linnaeus). Nature 452: 991–996 PubMed PMC

Mummenhoff K., Franzke A. (2007). Gone with the bird: Late Tertiary and Quaternary intercontinental long-distance dispersal and allopolyploidization in plants. Syst. Biodivers. 5: 255–260

Panjabi P., Jagannath A., Bisht N.C., Padmaja K.L., Sharma S., Gupta V., Pradhan A.K., Pental D. (2008). Comparative mapping of Brassica juncea and Arabidopsis thaliana using Intron Polymorphism (IP) markers: Homoeologous relationships, diversification and evolution of the A, B and C Brassica genomes. BMC Genomics 9: 113. PubMed PMC

Parkin I.A.P., Gulden S.M., Sharpe A.G., Lukens L., Trick M., Osborn T.C., Lydiate D.J. (2005). Segmental structure of the Brassica napus genome based on comparative analysis with Arabidopsis thaliana. Genetics 171: 765–781 PubMed PMC

Posada D., Crandall K.A. (1998). Modeltest: Testing the model of DNA substitution. Bioinformatics 14: 817–818 PubMed

Roosens N.H.C.J., Willems G., Gode C., Courseaux A., Saumitou-Laprade P. (2008). The use of comparative genome analysis and syntenic relationships allows extrapolating the position of Zn tolerance QTL regions from Arabidopsis halleri into Arabidopsis thaliana. Plant Soil 306: 105–116

Salse J., Bolot S., Throude M., Jouffe V., Piegu B., Quraishi U.M., Calcagno T., Cooke R., Delseny M., Feuillet C. (2008). Identification and characterization of shared duplications between rice and wheat provide new insight into grass genome evolution. Plant Cell 20: 11–24 PubMed PMC

Schlueter J.A., Dixon P., Granger C., Grant D., Clark L., Doyle J.J., Schoemaker R.C. (2004). Mining EST databases to resolve evolutionary events in major crop species. Genome 47: 868–876 PubMed

Schranz M.E., Lysak M.A., Mitchell-Olds T. (2006). The ABC’s of comparative genomics in the Brassicaceae: Building blocks of crucifer genomes. Trends Plant Sci. 11: 535–542 PubMed

Schranz M.E., Mitchell-Olds T. (2006). Independent ancient polyploidy events in the sister families Brassicaceae and Cleomaceae. Plant Cell 18: 1152–1165 PubMed PMC

Schranz M.E., Windsor A.J., Song B.-H., Lawton-Rauh A., Mitchell-Olds T. (2007). Comparative genetic mapping in Boechera stricta, a close relative of Arabidopsis. Plant Physiol. 144: 286–298 PubMed PMC

Schubert I. (2007). Chromosome evolution. Curr. Opin. Plant Biol. 10: 109–115 PubMed

Schwarzbach A.E., Rieseberg L.H. (2002). Likely multiple origins of a diploid hybrid sunflower species. Mol. Ecol. 11: 1703–1715 PubMed

Sears E.R., Camara A. (1952). A transmissible dicentric chromosome. Genetics 37: 125–135 PubMed PMC

Sémon M., Wolfe K.H. (2007). Rearrangement rate following the whole-genome duplication in teleosts. Mol. Biol. Evol. 24: 860–867 PubMed

Shimizu-Inatsugi R., Lihova J., Iwanaga H., Kudoh H., Marhold K., Savolainen O., Watanabe K., Yakubov V.V., Shimizu K.K. (2009). The allopolyploid Arabidopsis kamchatica originated from multiple individuals of Arabidopsis lyrata and Arabidopsis halleri. Mol. Ecol. 18: 4024–4048 PubMed

Soltis D.E., Albert V.A., Leebens-Mack J., Bell C.D., Paterson A.H., Zheng C., Sankoff D., dePamphilis C.W., Wall P.K., Soltis P.S. (2009). Polyploidy and angiosperm diversification. Am. J. Bot. 96: 336–348 PubMed

Soltis D.E., Soltis P.S., Schemske D.W., Hancock J.F., Thompson J.N., Husband B.C., Judd W.S. (2007). Autopolyploidy in angiosperms: Have we grossly underestimated the number of species? Taxon 56: 13–30

Tang H., Bowers J.E., Wang X., Ming X., Alam M., Paterson A.H. (2008). Synteny and collinearity in plant genomes. Science 320: 486–488 PubMed

Thomas B.C., Pedersen B., Freeling M. (2006). Following tetraploidy in an Arabidopsis ancestor, genes were removed preferentially from one homeolog leaving clusters enriched in dose-sensitive genes. Genome Res. 16: 934–946 PubMed PMC

Town C.D., et al. (2006). Comparative genomics of Brassica oleracea and Arabidopsis thaliana reveal gene loss, fragmentation, and dispersal after polyploidy. Plant Cell 18: 1348–1359 PubMed PMC

Veitia R.A., Bottani S., Birchler J.A. (2008). Cellular reactions to gene dosage imbalance: Genomic, transcriptomic and proteomic effects. Trends Genet. 24: 390–397 PubMed

Ventura M., Antonacci F., Cardone M.F., Stanyon R., D’Addabbo P., Cellamare A., Sprague L.J., Eichler E.E., Archidiacono N., Rocchi M. (2007). Evolutionary formation of new centromeres in macaque. Science 316: 243–246 PubMed

Ventura M., et al. (2004). Recurrent sites for new centromere seeding. Genome Res. 14: 1696–1703 PubMed PMC

Wood T.E., Takebayashi N., Barker M.S., Mayrose I., Greenspoond P.B., Rieseberg L.H. (2009). The frequency of polyploid speciation in vascular plants. Proc. Natl. Acad. Sci. USA 106: 13875–13879 PubMed PMC

Yang T.J., et al. (2006). Sequence-level analysis of the diploidization process in the triplicated FLOWERING LOCUS C region of Brassica rapa. Plant Cell 18: 1339–1347 PubMed PMC

Yang Z. (1997). PAML: A program package for phylogenetic analysis by maximum likelihood. Comput. Appl. Biosci. 13: 555–556 PubMed

Ziolkowski P.A., Kaczmarek M., Babula D., Sadowski J. (2006). Genome evolution in Arabidopsis/Brassica: Conservation and divergence of ancient rearranged segments and their breakpoints. Plant J. 47: 63–74 PubMed

Nejnovějších 20 citací...

Zobrazit více v
Medvik | PubMed

Interploidy gene flow via a 'pentaploid bridge' and ploidy reduction in Cystopteris fragilis fern complex (Cystopteridaceae: Polypodiales)

. 2023 Dec ; 36 (4) : 321-331. [epub] 20230802

The evolution of the hypotetraploid Catolobus pendulus genome - the poorly known sister species of Capsella

. 2023 ; 14 () : 1165140. [epub] 20230508

Genome diploidization associates with cladogenesis, trait disparity, and plastid gene evolution

. 2022 Aug 29 ; 190 (1) : 403-420.

Celebrating Mendel, McClintock, and Darlington: On end-to-end chromosome fusions and nested chromosome fusions

. 2022 Jul 04 ; 34 (7) : 2475-2491.

A hypomorphic allele of telomerase uncovers the minimal functional length of telomeres in Arabidopsis

. 2021 Oct 02 ; 219 (2) : .

Revisiting the Karyotypes of Alligators and Caimans (Crocodylia, Alligatoridae) after a Half-Century Delay: Bridging the Gap in the Chromosomal Evolution of Reptiles

. 2021 Jun 05 ; 10 (6) : . [epub] 20210605

Linked by Ancestral Bonds: Multiple Whole-Genome Duplications and Reticulate Evolution in a Brassicaceae Tribe

. 2021 May 04 ; 38 (5) : 1695-1714.

Nested whole-genome duplications coincide with diversification and high morphological disparity in Brassicaceae

. 2020 Jul 30 ; 11 (1) : 3795. [epub] 20200730

Comparative analyses of DNA repeats and identification of a novel Fesreba centromeric element in fescues and ryegrasses

. 2020 Jun 17 ; 20 (1) : 280. [epub] 20200617

The story of promiscuous crucifers: origin and genome evolution of an invasive species, Cardamine occulta (Brassicaceae), and its relatives

. 2019 Sep 24 ; 124 (2) : 209-220.

Polyploid evolution: The ultimate way to grasp the nettle

. 2019 ; 14 (7) : e0218389. [epub] 20190701

Chromosome identification for the carnivorous plant Genlisea margaretae

. 2017 Jun ; 126 (3) : 389-397. [epub] 20160507

chromDraw: an R package for visualization of linear and circular karyotypes

. 2016 May ; 24 (2) : 217-23. [epub] 20160120

Repeated Whole-Genome Duplication, Karyotype Reshuffling, and Biased Retention of Stress-Responding Genes in Buckler Mustard

. 2016 Jan ; 28 (1) : 17-27. [epub] 20151214

A Time-Calibrated Road Map of Brassicaceae Species Radiation and Evolutionary History

. 2015 Oct ; 27 (10) : 2770-84. [epub] 20150926

Chromatin organization and cytological features of carnivorous Genlisea species with large genome size differences

. 2015 ; 6 () : 613. [epub] 20150820

Chromatin features of plant telomeric sequences at terminal vs. internal positions

. 2014 ; 5 () : 593. [epub] 20141104

The more the merrier: recent hybridization and polyploidy in cardamine

. 2013 Sep ; 25 (9) : 3280-95. [epub] 20130930

Island species radiation and karyotypic stasis in Pachycladon allopolyploids

. 2010 Nov 29 ; 10 () : 367. [epub] 20101129

Zobrazit více v PubMed

GENBANK
GQ926501, GQ926502, GQ926503, GQ926504, GQ926505, GQ926506, GQ926507, GQ926508, GQ926509, GQ926510, GQ926511, GQ926512, GQ926513, GQ926514, GQ926515, GQ926516, GQ926517, GQ926518, GQ926519, GQ926520, GQ926521, GQ926522, GQ926523, GQ926524, GQ926525, GQ926526, GQ926527, GQ926528, GQ926529, GQ926530, GQ926531, GQ926532, GQ926533, GQ926534, GQ926535, GQ926536, GQ926537, GQ926538, GQ926539, GQ926540, GQ926541, GQ926542, GQ926543, GQ926544, GQ926545, GQ926546, GQ926547, GQ926548, GQ926549, GQ926550, GQ926551, GQ926552, GQ926553, GQ926554, GQ926555, GQ926556, GQ926557, GQ926558, GQ926559, GQ926560, GQ926561, GQ926562, GQ926563, GQ926564, GQ926565, GQ926566, GQ926567, GQ926568

Najít záznam

Citační ukazatele

Nahrávání dat ...

Možnosti archivace

Nahrávání dat ...