Widespread genome duplications throughout the history of flowering plants.

By Liying Cui, P. K. Wall, J. Leebens-Mack, Bruce G. Lindsay, D. Soltis, J. Doyle, Pamela S. Soltis, J. Carlson, K. Arumuganathan, Abdelali Barakat and 3 more. Genome Research, 2006

714 citations recorded by the source corpus.

Subfields: Genetics, Plant Science

View Paper: https://www.semanticscholar.org/paper/1e0b9b10d9371ac1edd773df00b468b6f735c014

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Citations in the corpus

Mating Consequences of Polyploid Evolution in Flowering Plants: Current Trends and Insights from Synthetic Polyploids (2008, background): “Based on chromosome number, between 57% and 70% of angiosperm species have been estimated to be polyploid (Grant 1963; Masterson 1994); this value may be closer to 100% if one considers the incidence of paleopolyploids detected through comparative genomics (Wolfe 2001; Cui et al. 2006).”
The Amborella Genome and the Evolution of Flowering Plants (2013, background): “The prevalence of WGDs in monocots and other basal angiosperms ( 34 – 37 ) limits the possibility of identifying such genomes.”
Draft genome of the living fossil Ginkgo biloba (2016, result): “The latter of these time periods is consistent with that previously reported for seed plants [46–48], while the former time period is far later than when Gingko and conifers diverged, indicating a potential independent WGD event postdating the origin of Ginkgo by at least 170 mya [49].”
Polyploidy and angiosperm diversification. (2009, methodology): “" Despite its relatively high chromosome number of 2 n = 26, very few duplicate gene pairs were detected in Amborella based on the initial 8629 ESTs analyzed by Cui et al. (2006) , and no K s signal for ancient genome duplication was observed.”
Plants with double genomes might have had a better chance to survive the Cretaceous–Tertiary extinction event (2009, background): “Peaks in age distributions at similar KS values have been found for other plant species as well (14, 15, 18, 19).”
Unraveling ancient hexaploidy through multiply-aligned angiosperm gene maps. (2008, result): “One phylogenetic model placed Vitis within the eurosid I clade (Jaillon et al. 2007), in contrast with the prevailing view of the Vitaceae as sister to both eurosid I and eurosid II (Davies et al. 2004; Soltis et al. 2005).”
Complexity of the Alternative Splicing Landscape in Plants[C][W][OPEN] (2013, background): “The lack of an in vitro splicing assay in plants has been amajor limitation in studying the mechanisms involved in intron recognition and spliceosome assembly in plants (Barta et al., 2012).”
The evolutionary significance of ancient genome duplications (2009, background): “Evidence from cytogenetic analyses, morphological studies of fossil and extant species and, more recently, whole-genome and EST analyses suggests that most (60–70%) flowering plants have a polyploid ancestr”
The role of hybridization in plant speciation. (2009, background): “In the absence of complete genome sequences, ESTs (expressed sequence tags) are an important source of genomic data that can be used to infer occurrences of ancient genome duplication (22, 39, 168).”
Hybridization, polyploidy and invasion: lessons from Spartina (Poaceae) (2009, background): “Hedge et al. 2004; Cottet et al. 2007 ), and Spartina anglica is now listed among the 100 ‘‘World’s worst’’ invaders (IUCN 2000).”
Genomic Changes in Resynthesized Brassica napus and Their Effect on Gene Expression and Phenotype[W][OA] (2007, background): “Genomic Changes in Resynthesized Brassica napus and Their”