Evidence map›Paper›PMID 35029647›Full record

ArticleAnnals of botany2023

Down, then up: non-parallel genome size changes and a descending chromosome series in a recent radiation of the Australian allotetraploid plant species, Nicotiana section Suaveolentes (Solanaceae).

Mark W Chase, Rosabelle Samuel, Andrew R Leitch, Maïté S Guignard, John G Conran, Felipe Nollet, Paul Fletcher, Aljaž Jakob, Luiz A Cauz-Santos, Gabriel Vignolle and 4 more

Abstract read
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Article in Annals of botany, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

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0cells of the map it votes in
10citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

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2 · The registry

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3 · Its place in the literature

Who cites it

10 citing papers in PubMed.

  1. Article
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  9. The nature and organization of satellite DNAs inFrontiers in plant science · 2023
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4 · The record

Corrections and comments

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5 · Who and what money

Authors and funding

14 authors.

Mark W ChaseRoyal Botanic Gardens, Kew, Richmond TW9 3DS, UK.
Rosabelle SamuelDepartment of Botany and Biodiversity Research, University of Vienna, Rennweg 14, A-1030 Vienna, Austria.ORCID 0000-0003-0197-4854
Andrew R LeitchSchool of Biological and Chemical Sciences, Queen Mary University of London, Mile End Road, London E1 4NS, UK.
Maïté S GuignardRoyal Botanic Gardens, Kew, Richmond TW9 3DS, UK.
John G ConranACEBB & SGC, School of Biological Sciences, The University of Adelaide, SA 5005Australia.
Felipe NolletUniversidade Federal Rural de Pernambuco, Centro de Ciências Biológicas, Departamento de Botânica, Rua Manuel de Medeiros, S/N, Dois Irmãos, 52171-900 Recife, Pernambuco, Brazil.
Paul FletcherSchool of Biological and Chemical Sciences, Queen Mary University of London, Mile End Road, London E1 4NS, UK.
Aljaž JakobDepartment of Botany and Biodiversity Research, University of Vienna, Rennweg 14, A-1030 Vienna, Austria.
Luiz A Cauz-SantosDepartment of Botany and Biodiversity Research, University of Vienna, Rennweg 14, A-1030 Vienna, Austria.
Gabriel VignolleDepartment of Botany and Biodiversity Research, University of Vienna, Rennweg 14, A-1030 Vienna, Austria.
Steven DodsworthSchool of Biological Sciences, University of Portsmouth, Portsmouth PO1 2DY, UK.
Maarten J M ChristenhuszDepartment of Environment and Agriculture, Curtin University, Perth, Western Australia, Australia.
Maria Teresa BurilACEBB & SGC, School of Biological Sciences, The University of Adelaide, SA 5005Australia.
Ovidiu PaunDepartment of Botany and Biodiversity Research, University of Vienna, Rennweg 14, A-1030 Vienna, Austria.ORCID 0000-0002-8295-4937

Funding

Austrian Science Fund FWF P 33028
6 · The paper itself

Abstract

BACKGROUND AND

aimsThe extent to which genome size and chromosome numbers evolve in concert is little understood, particularly after polyploidy (whole-genome duplication), when a genome returns to a diploid-like condition (diploidization). We study this phenomenon in 46 species of allotetraploid Nicotiana section Suaveolentes (Solanaceae), which formed <6 million years ago and radiated in the arid centre of Australia.

methodsWe analysed newly assessed genome sizes and chromosome numbers within the context of a restriction site-associated nuclear DNA (RADseq) phylogenetic framework. KEY

resultsRADseq generated a well-supported phylogenetic tree, in which multiple accessions from each species formed unique genetic clusters. Chromosome numbers and genome sizes vary from n = 2x = 15 to 24 and 2.7 to 5.8 pg/1C nucleus, respectively. Decreases in both genome size and chromosome number occur, although neither consistently nor in parallel. Species with the lowest chromosome numbers (n = 15-18) do not possess the smallest genome sizes and, although N. heterantha has retained the ancestral chromosome complement, n = 2x = 24, it nonetheless has the smallest genome size, even smaller than that of the modern representatives of ancestral diploids.

conclusionsThe results indicate that decreases in genome size and chromosome number occur in parallel down to a chromosome number threshold, n = 20, below which genome size increases, a phenomenon potentially explained by decreasing rates of recombination over fewer chromosomes. We hypothesize that, more generally in plants, major decreases in genome size post-polyploidization take place while chromosome numbers are still high because in these stages elimination of retrotransposons and other repetitive elements is more efficient. Once such major genome size change has been accomplished, then dysploid chromosome reductions take place to reorganize these smaller genomes, producing species with small genomes and low chromosome numbers such as those observed in many annual angiosperms, including Arabidopsis.

Indexed as

NicotianaSolanaceaeAustraliaChromosomes, PlantEvolution, MolecularGenome, PlantGenome SizePhylogenyPolyploidyVegetablesAllotetraploid evolutionAustralian endemicsC-valuediploidizationdysploidyepigeneticsmodel organismNicotiana benthamianaNicotiana sect. SuaveolentespolyploidySolanaceaeWGD

Identifiers

PMID35029647
PMCPMC9904355

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.