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Telomere‐centric genome repatterning determines recurring chromosome number reductions during the evolution of eukaryotes

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What this work says

Outgoing claims: the papers this work cites, builds on, or argues with.

inferredcites →https://doi.org/10.1007/s001220050026openalex-snapshot
Comparative mapping reveals a complex relationship between the pearl millet genome and those of foxtail millet and rice
inferredcites →https://doi.org/10.1007/s10577-011-9240-5openalex-snapshot
Inactivation of a centromere during the formation of a translocation in maize
inferredcites →https://doi.org/10.1016/j.jgg.2012.01.006openalex-snapshot
Dicentric Chromosome Formation and Epigenetics of Centromere Formation in Plants
inferredcites →https://doi.org/10.1016/j.pbi.2005.01.005openalex-snapshot
Updating the ‘Crop Circle’
inferredcites →https://doi.org/10.1016/j.pbi.2010.01.004openalex-snapshot
Accessing genetic diversity for crop improvement
inferredcites →https://doi.org/10.1016/j.tig.2010.12.003openalex-snapshot
Population genetics of genomics-based crop improvement methods
inferredcites →https://doi.org/10.1016/j.tig.2011.03.004openalex-snapshot
Interpretation of karyotype evolution should consider chromosome structural constraints
inferredcites →https://doi.org/10.1016/s1097-2765(03)00531-8openalex-snapshot
Indecent Exposure
inferredcites →https://doi.org/10.1016/s1534-5807(04)00059-0openalex-snapshot
Dynamics of Homologous Chromosome Pairing during Meiotic Prophase in Fission Yeast
inferredcites →https://doi.org/10.1038/35003085openalex-snapshot
A tale of ends
inferredcites →https://doi.org/10.1038/35085086openalex-snapshot
A bouquet makes ends meet
inferredcites →https://doi.org/10.1038/hdy.2010.56openalex-snapshot
Statistical properties of QTL linkage mapping in biparental genetic populations
inferredcites →https://doi.org/10.1038/nature03895openalex-snapshot
The map-based sequence of the rice genome
inferredcites →https://doi.org/10.1038/nature06148openalex-snapshot
The grapevine genome sequence suggests ancestral hexaploidization in major angiosperm phyla
inferredcites →https://doi.org/10.1038/nature07723openalex-snapshot
The Sorghum bicolor genome and the diversification of grasses
inferredcites →https://doi.org/10.1038/nature08747openalex-snapshot
Genome sequencing and analysis of the model grass Brachypodium distachyon
inferredcites →https://doi.org/10.1038/nature11241openalex-snapshot
The banana (Musa acuminata) genome and the evolution of monocotyledonous plants
inferredcites →https://doi.org/10.1038/nrg2224openalex-snapshot
Finding a match: how do homologous sequences get together for recombination?
inferredcites →https://doi.org/10.1073/pnas.0307901101openalex-snapshot
Ancient polyploidization predating divergence of the cereals, and its consequences for comparative genomics
inferredcites →https://doi.org/10.1073/pnas.0504235102openalex-snapshot
Stable barley chromosomes without centromeric repeats
inferredcites →https://doi.org/10.1073/pnas.0509650103openalex-snapshot
High frequency of centromere inactivation resulting in stable dicentric chromosomes of maize
inferredcites →https://doi.org/10.1073/pnas.0510791103openalex-snapshot
Mechanisms of chromosome number reduction in Arabidopsis thaliana and related Brassicaceae species
inferredcites →https://doi.org/10.1073/pnas.0902350106openalex-snapshot
Reconstruction of monocotelydoneous proto-chromosomes reveals faster evolution in plants than in animals
inferredcites →https://doi.org/10.1073/pnas.0908195106openalex-snapshot
Genome comparisons reveal a dominant mechanism of chromosome number reduction in grasses and accelerated genome evolution in Triticeae
inferredcites →https://doi.org/10.1073/pnas.25.8.405openalex-snapshot
The Behavior in Successive Nuclear Divisions of a Chromosome Broken at Meiosis
inferredcites →https://doi.org/10.1093/bfgp/elq006openalex-snapshot
Realizing the potential of genomics for crop improvement
inferredcites →https://doi.org/10.1093/emboj/19.14.3831openalex-snapshot
Telomere‐led bouquet formation facilitates homologous chromosome pairing and restricts ectopic interaction in fission yeast meiosis
inferredcites →https://doi.org/10.1093/genetics/160.4.1651openalex-snapshot
Gene Loss, Silencing and Activation in a Newly Synthesized Wheat Allotetraploid
inferredcites →https://doi.org/10.1093/nar/19.17.4780openalex-snapshot
Improved telomere detection using a telomere repeat probe (TTAGGG) n generated by PCR
inferredcites →https://doi.org/10.1097/hp.0b013e3182307758openalex-snapshot
Validation of QuickScan Dicentric Chromosome Analysis for High Throughput Radiation Biological Dosimetry
inferredcites →https://doi.org/10.1098/rstb.2009.0320openalex-snapshot
Mutation and the evolution of recombination
inferredcites →https://doi.org/10.1101/gad.1869110openalex-snapshot
De novo telomere formation is suppressed by the Mec1-dependent inhibition of Cdc13 accumulation at DNA breaks
inferredcites →https://doi.org/10.1101/gr.109744.110openalex-snapshot
Ancestral grass karyotype reconstruction unravels new mechanisms of genome shuffling as a source of plant evolution
inferredcites →https://doi.org/10.1101/gr.2332504openalex-snapshot
Close Split of Sorghum and Maize Genome Progenitors
inferredcites →https://doi.org/10.1101/gr.3436305openalex-snapshot
Comparative genome analyses of Arabidopsis spp.: Inferring chromosomal rearrangement events in the evolutionary history of A. thaliana
inferredcites →https://doi.org/10.1105/tpc.107.056309openalex-snapshot
Identification and Characterization of Shared Duplications between Rice and Wheat Provide New Insight into Grass Genome Evolution
inferredcites →https://doi.org/10.1105/tpc.110.080622openalex-snapshot
Seventy Million Years of Concerted Evolution of a Homoeologous Chromosome Pair, in Parallel, in Major Poaceae Lineages
inferredcites →https://doi.org/10.1105/tpc.111.230611openalex-snapshot
De Novo Telomere Formation in Arabidopsis Tetraploids
inferredcites →https://doi.org/10.1111/j.1469-8137.2004.01293.xopenalex-snapshot
Duplication and DNA segmental loss in the rice genome: implications for diploidization
inferredcites →https://doi.org/10.1126/science.1153917openalex-snapshot
Synteny and Collinearity in Plant Genomes
inferredcites →https://doi.org/10.1126/science.1178534openalex-snapshot
The B73 Maize Genome: Complexity, Diversity, and Dynamics
inferredcites →https://doi.org/10.1126/science.288.5474.2141openalex-snapshot
Telomeres Keep On Rappin'
inferredcites →https://doi.org/10.1136/jmg.2006.045476openalex-snapshot
Molecular characterisation of a mosaicism with a complex chromosome rearrangement: evidence for coincident chromosome healing by telomere capture and neo-telomere formation
inferredcites →https://doi.org/10.1159/000121080openalex-snapshot
The cytogenetics of homologous chromosome pairing in meiosis in plants
inferredcites →https://doi.org/10.1242/jcs.01363openalex-snapshot
A bouquet of chromosomes
inferredcites →https://doi.org/10.1371/journal.pbio.1000409openalex-snapshot
Following Tetraploidy in Maize, a Short Deletion Mechanism Removed Genes Preferentially from One of the Two Homeologs
inferredcites →https://doi.org/10.1371/journal.pgen.1000463openalex-snapshot
Large-Scale Selective Sweep among Segregation Distorter Chromosomes in African Populations of Drosophila melanogaster
inferredcites →https://doi.org/10.1371/journal.pgen.1002190openalex-snapshot
Mechanisms of Chromosome Number Evolution in Yeast
inferredcites →https://doi.org/10.1534/genetics.103.022343openalex-snapshot
Comparing the Linkage Maps of the Close Relatives Arabidopsis lyrata and A. thaliana
inferredcites →https://doi.org/10.1534/genetics.106.057554openalex-snapshot
Numerous and Rapid Nonstochastic Modifications of Gene Products in Newly SynthesizedBrassica napusAllotetraploids
inferredcites →https://doi.org/10.3732/ajb.92.4.761openalex-snapshot
Genome evolution among cruciferous plants: a lecture from the comparison of the genetic maps of three diploid species— Capsella rubella , Arabidopsis lyrata subsp. petraea , and A. thaliana
inferredcites →https://doi.org/10.4238/vol9-1gmr707openalex-snapshot
Ring chromosome instability evaluation in six patients with autosomal rings

What points at this work

Incoming claims: where this work appears in other papers’ reference lists and arguments.

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inferred← citeshttps://doi.org/10.1093/hr/uhab030openalex-snapshot
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inferred← citeshttps://doi.org/10.1111/nph.17361openalex-snapshot
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inferred← citeshttps://doi.org/10.1360/ssv-2020-0042openalex-snapshot
Evolutionary genomics model of chromosome number reduction and B chromosome production
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Illegitimate Recombination between Duplicated Genes Generated from Recursive Polyploidizations Accelerated the Divergence of the Genus Arachis
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The Concept of Neuromuscular Repatterning in Dancers: A Systematic Review
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inferred← citeshttps://doi.org/10.3390/plants10112541openalex-snapshot
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“End-to-End Chromosome Fusion” as the Main Driver of Descending Dysploidy in Vigna lasiocarpa (Mart. ex Benth.) Verdc. (Leguminosae Juss.)
inferred← citeshttps://doi.org/10.3732/ajb.1600134openalex-snapshot
Chromosome number reduction in the sister clade of Carica papaya with concomitant genome size doubling
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Ancestral chromosome karyotype construction and large-scale analysis of CAM biosynthesis genes in ice plant and representative plants
inferred← citeshttps://doi.org/10.4995/thesis/10251/125697openalex-snapshot
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Additional file 1 of An updated explanation of ancestral karyotype changes and reconstruction of evolutionary trajectories to form Camelina sativa chromosomes
inferred← citeshttps://doi.org/10.6084/m9.figshare.13083344openalex-snapshot
Additional file 2 of An updated explanation of ancestral karyotype changes and reconstruction of evolutionary trajectories to form Camelina sativa chromosomes
inferred← citeshttps://doi.org/10.6084/m9.figshare.16935696openalex-snapshot
Additional file 10 of High-quality reference genome sequences of two coconut cultivars provide insights into evolution of monocot chromosomes and differentiation of fiber content and plant height
inferred← citeshttps://doi.org/10.6084/m9.figshare.16935702openalex-snapshot
Additional file 11 of High-quality reference genome sequences of two coconut cultivars provide insights into evolution of monocot chromosomes and differentiation of fiber content and plant height
inferred← citeshttps://doi.org/10.6084/m9.figshare.16935705openalex-snapshot
Additional file 12 of High-quality reference genome sequences of two coconut cultivars provide insights into evolution of monocot chromosomes and differentiation of fiber content and plant height
inferred← citeshttps://doi.org/10.6084/m9.figshare.16935708openalex-snapshot
Additional file 13 of High-quality reference genome sequences of two coconut cultivars provide insights into evolution of monocot chromosomes and differentiation of fiber content and plant height
inferred← citeshttps://doi.org/10.6084/m9.figshare.16935714openalex-snapshot
Additional file 14 of High-quality reference genome sequences of two coconut cultivars provide insights into evolution of monocot chromosomes and differentiation of fiber content and plant height
inferred← citeshttps://doi.org/10.6084/m9.figshare.16935717openalex-snapshot
Additional file 15 of High-quality reference genome sequences of two coconut cultivars provide insights into evolution of monocot chromosomes and differentiation of fiber content and plant height
inferred← citeshttps://doi.org/10.6084/m9.figshare.16935723openalex-snapshot
Additional file 16 of High-quality reference genome sequences of two coconut cultivars provide insights into evolution of monocot chromosomes and differentiation of fiber content and plant height
inferred← citeshttps://doi.org/10.6084/m9.figshare.16935726openalex-snapshot
Additional file 17 of High-quality reference genome sequences of two coconut cultivars provide insights into evolution of monocot chromosomes and differentiation of fiber content and plant height
inferred← citeshttps://doi.org/10.6084/m9.figshare.16935729openalex-snapshot
Additional file 18 of High-quality reference genome sequences of two coconut cultivars provide insights into evolution of monocot chromosomes and differentiation of fiber content and plant height
inferred← citeshttps://doi.org/10.6084/m9.figshare.16935732openalex-snapshot
Additional file 19 of High-quality reference genome sequences of two coconut cultivars provide insights into evolution of monocot chromosomes and differentiation of fiber content and plant height
inferred← citeshttps://doi.org/10.6084/m9.figshare.16935735openalex-snapshot
Additional file 1 of High-quality reference genome sequences of two coconut cultivars provide insights into evolution of monocot chromosomes and differentiation of fiber content and plant height
inferred← citeshttps://doi.org/10.6084/m9.figshare.16935738openalex-snapshot
Additional file 20 of High-quality reference genome sequences of two coconut cultivars provide insights into evolution of monocot chromosomes and differentiation of fiber content and plant height
inferred← citeshttps://doi.org/10.6084/m9.figshare.16935741openalex-snapshot
Additional file 21 of High-quality reference genome sequences of two coconut cultivars provide insights into evolution of monocot chromosomes and differentiation of fiber content and plant height
inferred← citeshttps://doi.org/10.6084/m9.figshare.16935744openalex-snapshot
Additional file 22 of High-quality reference genome sequences of two coconut cultivars provide insights into evolution of monocot chromosomes and differentiation of fiber content and plant height
inferred← citeshttps://doi.org/10.6084/m9.figshare.16935747openalex-snapshot
Additional file 23 of High-quality reference genome sequences of two coconut cultivars provide insights into evolution of monocot chromosomes and differentiation of fiber content and plant height
inferred← citeshttps://doi.org/10.6084/m9.figshare.16935753openalex-snapshot
Additional file 24 of High-quality reference genome sequences of two coconut cultivars provide insights into evolution of monocot chromosomes and differentiation of fiber content and plant height
inferred← citeshttps://doi.org/10.6084/m9.figshare.16935756openalex-snapshot
Additional file 2 of High-quality reference genome sequences of two coconut cultivars provide insights into evolution of monocot chromosomes and differentiation of fiber content and plant height
inferred← citeshttps://doi.org/10.6084/m9.figshare.16935759openalex-snapshot
Additional file 3 of High-quality reference genome sequences of two coconut cultivars provide insights into evolution of monocot chromosomes and differentiation of fiber content and plant height
inferred← citeshttps://doi.org/10.6084/m9.figshare.16935765openalex-snapshot
Additional file 4 of High-quality reference genome sequences of two coconut cultivars provide insights into evolution of monocot chromosomes and differentiation of fiber content and plant height
inferred← citeshttps://doi.org/10.6084/m9.figshare.16935768openalex-snapshot
Additional file 5 of High-quality reference genome sequences of two coconut cultivars provide insights into evolution of monocot chromosomes and differentiation of fiber content and plant height
inferred← citeshttps://doi.org/10.6084/m9.figshare.16935771openalex-snapshot
Additional file 6 of High-quality reference genome sequences of two coconut cultivars provide insights into evolution of monocot chromosomes and differentiation of fiber content and plant height
inferred← citeshttps://doi.org/10.6084/m9.figshare.16935774openalex-snapshot
Additional file 7 of High-quality reference genome sequences of two coconut cultivars provide insights into evolution of monocot chromosomes and differentiation of fiber content and plant height
inferred← citeshttps://doi.org/10.6084/m9.figshare.16935777openalex-snapshot
Additional file 8 of High-quality reference genome sequences of two coconut cultivars provide insights into evolution of monocot chromosomes and differentiation of fiber content and plant height
inferred← citeshttps://doi.org/10.6084/m9.figshare.16935780openalex-snapshot
Additional file 9 of High-quality reference genome sequences of two coconut cultivars provide insights into evolution of monocot chromosomes and differentiation of fiber content and plant height
inferred← citeshttps://doi.org/10.6084/m9.figshare.20088218openalex-snapshot
Additional file 1 of Conversion between duplicated genes generated by polyploidization contributes to the divergence of poplar and willow
inferred← citeshttps://doi.org/10.6084/m9.figshare.20088221openalex-snapshot
Additional file 2 of Conversion between duplicated genes generated by polyploidization contributes to the divergence of poplar and willow
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