Literature DB >> 30172008

Hybridization and polyploidization within the Chenopodium album aggregate analysed by means of cytological and molecular markers.

Bohumil Mandák1, Karol Krak2, Petr Vít2, Maria N Lomonosova3, Alexander Belyayev4, Farzaneh Habibi5, Lei Wang6, Jan Douda7, Helena Štorchová8.   

Abstract

Hybridization and polyploidization represent an important speciation mechanism in the diploid-polyploid complex of the Chenopodium album aggregate. In the present study we successfully reconstructed the evolutionary histories of the majority of Eurasian representatives of the C. album aggregate, resulting in the most comprehensive phylogenetic analysis of this taxonomically intricate group of species to date. We applied a combination of classical karyology for precise chromosome number determination, genomic in-situ hybridization for the determination of genomic composition, flow cytometry for the estimation of genome size and sequencing of plastid (cpDNA) and nuclear (ribosomal internal transcribed spacer - ITS and the introns of the FLOWERING LOCUS T LIKE genes - FTL) markers for a phylogenetic reconstruction and the identification of parental genomes in polyploid taxa. The FTL markers identified eight well supported evolutionary lineages. Five of them include at least one diploid species, and the remaining three comprise solely the subgenomes of polyploids that probably represent extinct or unknown diploid taxa. The existence of eight basic diploid lineages explains the origin of seven Eurasian polyploid groups and brings evidence of a nearly unlimited number of subgenomic combinations. The supposed promiscuity generated new species wherever different diploid lineages met each other and gave rise to tetraploid species or whenever they met other tetraploid species to produce hexaploid species throughout their evolutionary history. Finally, we unravelled a surprisingly simple scheme of polyploid species formation within the C. album aggregate. We determined seven groups of polyploid species differing in their origin in either Eurasia or Africa and convincingly demonstrated that (1) all Chenopodium polyploid species under study are of allopolyploid origin, (2) there are eight major monophyletic evolutionary lineages represented by extant or extinct/unknown diploid taxa, (3) those monophyletic lineages represent individual subgenomes, (4) hybridization among the lineages created seven subgenomic combinations of polyploid taxa, (5) taxa represented by particular subgenome combinations were further subjected to diversification, and (6) the majority of species are relatively young, not exceeding the age of the Quaternary period.
Copyright © 2018 Elsevier Inc. All rights reserved.

Entities:  

Keywords:  Allopolyploidy; Chenopodium; FTL genes; Hybridization; cpDNA; nrDNA ITS

Mesh:

Substances:

Year:  2018        PMID: 30172008     DOI: 10.1016/j.ympev.2018.08.016

Source DB:  PubMed          Journal:  Mol Phylogenet Evol        ISSN: 1055-7903            Impact factor:   4.286


  8 in total

1.  Multiple Drivers of High Species Diversity and Endemism Among Alyssum Annuals in the Mediterranean: The Evolutionary Significance of the Aegean Hotspot.

Authors:  Veronika Cetlová; Judita Zozomová-Lihová; Andrea Melichárková; Lenka Mártonfiová; Stanislav Španiel
Journal:  Front Plant Sci       Date:  2021-04-27       Impact factor: 5.753

2.  Transposons and satellite DNA: on the origin of the major satellite DNA family in the Chenopodium genome.

Authors:  Alexander Belyayev; Jiřina Josefiová; Michaela Jandová; Václav Mahelka; Karol Krak; Bohumil Mandák
Journal:  Mob DNA       Date:  2020-06-26

3.  Natural History of a Satellite DNA Family: From the Ancestral Genome Component to Species-Specific Sequences, Concerted and Non-Concerted Evolution.

Authors:  Alexander Belyayev; Jiřina Josefiová; Michaela Jandová; Ruslan Kalendar; Karol Krak; Bohumil Mandák
Journal:  Int J Mol Sci       Date:  2019-03-09       Impact factor: 5.923

4.  The structural diversity of CACTA transposons in genomes of Chenopodium (Amaranthaceae, Caryophyllales) species: specific traits and comparison with the similar elements of angiosperms.

Authors:  Alexander Belyayev; Jiřina Josefiová; Michaela Jandová; Ruslan Kalendar; Václav Mahelka; Bohumil Mandák; Karol Krak
Journal:  Mob DNA       Date:  2022-04-04

5.  Chromosome-Scale Genome Assembly of the Hexaploid Taiwanese Goosefoot "Djulis" (Chenopodium formosanum).

Authors:  David E Jarvis; John S Sproul; Beatriz Navarro-Domínguez; Karol Krak; Kate Jaggi; Yung-Fen Huang; Tzu-Yun Huang; Tzu Che Lin; Eric N Jellen; Peter J Maughan
Journal:  Genome Biol Evol       Date:  2022-08-03       Impact factor: 4.065

6.  Chenopodium ficifolium flowers under long days without upregulation of FLOWERING LOCUS T (FT) homologs.

Authors:  Helena Štorchová; Helena Hubáčková; Oushadee A J Abeyawardana; Jana Walterová; Zuzana Vondráková; Kateřina Eliášová; Bohumil Mandák
Journal:  Planta       Date:  2019-10-04       Impact factor: 4.116

Review 7.  A Review of Chenopodium quinoa (Willd.) Diseases-An Updated Perspective.

Authors:  Carla Colque-Little; Daniel Buchvaldt Amby; Christian Andreasen
Journal:  Plants (Basel)       Date:  2021-06-16

8.  The major satellite DNA families of the diploid Chenopodium album aggregate species: Arguments for and against the "library hypothesis".

Authors:  Alexander Belyayev; Michaela Jandová; Jiřina Josefiová; Ruslan Kalendar; Václav Mahelka; Bohumil Mandák; Karol Krak
Journal:  PLoS One       Date:  2020-10-27       Impact factor: 3.240

  8 in total

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