Brena Van-Lume1, Yennifer Mata-Sucre1, Mariana Báez1, Tiago Ribeiro1,2, Bruno Huettel3, Edeline Gagnon4, Ilia J Leitch5, Andrea Pedrosa-Harand1, Gwilym P Lewis5, Gustavo Souza6. 1. Laboratory of Plant Cytogenetics and Evolution, Department of Botany, Federal University of Pernambuco, Rua Nelson Chaves S/N, Cidade Universitária, Recife, PE, 50670-420, Brazil. 2. Department of Botany and Ecology, Institute of Biosciences, Federal University of Mato Grosso, Av. Fernando Correa da Costa, 2.367, Boa Esperança, Cuiabá, MT, 78060-900, Brazil. 3. Max Planck-Genome-center Cologne, Cologne, Germany. 4. Royal Botanic Garden Edinburgh, 20A Inverleith Row, Edinburgh, EH3 5NZ, UK. 5. Department of Comparative Plant and Fungal Biology, Royal Botanic Gardens, Kew, Richmond, Surrey, TW9 3AB, UK. 6. Laboratory of Plant Cytogenetics and Evolution, Department of Botany, Federal University of Pernambuco, Rua Nelson Chaves S/N, Cidade Universitária, Recife, PE, 50670-420, Brazil. luiz.rodriguessouza@ufpe.br.
Abstract
MAIN CONCLUSION: We demonstrated by cytogenomic analysis that the proximal heterochromatin of the Northeast Brazilian species of Caesalpinia group is enriched with phylogenetically conserved Ty3/Gypsy-Tekay RT, but diverge in the presence of Ty3/Gypsy-Athila RT and satDNA. The Caesalpinia Group includes 225 species and 27 monophyletic genera of which four occur in Northeastern Brazil: Erythrostemon (1 sp.), Cenostigma (7 spp.), Libidibia (1 sp.), and Paubrasilia (1 sp.). The last three genera are placed in different clades in the Caesalpinia Group phylogeny, and yet they are characterized by having a numerically stable karyotype 2n = 24 (16 M+8A) and GC-rich heterochromatic bands (chromomycin A3 positive/CMA+ bands) in the proximal chromosome regions. To characterize the composition of their heterochromatin and test for the homology of these chromosomal regions, genomic DNA was extracted from Cenostigma microphyllum, Libidibia ferrea, and Paubrasilia echinata, and sequenced at low coverage using the Illumina platform. The genomic repetitive fractions were characterized using a Galaxy/RepeatExplorer-Elixir platform. The most abundant elements of each genome were chromosomally located by fluorescent in situ hybridization (FISH) and compared to the CMA+ heterochromatin distribution. The repetitive fraction of the genomes of C. microphyllum, L. ferrea, and P. echinata were estimated to be 41.70%, 38.44%, and 72.51%, respectively. Ty3/Gypsy retrotransposons (RT), specifically the Tekay lineage, were the most abundant repeats in each of the three genomes. FISH mapping revealed species-specific patterns for the Tekay elements in the proximal regions of the chromosomes, co-localized with CMA+ bands. Other species-specific patterns were observed, e.g., for the Ty3/Gypsy RT Athila elements which were found in all the proximal heterochromatin of L. ferrea or restricted to the acrocentric chromosomes of C. microphyllum. This Athila labeling co-localized with satellite DNAs (satDNAs). Although the Caesalpinia Group diverged around 55 Mya, our results suggest an ancestral colonization of Tekay RT in the proximal heterochromatin. Thus, the present-day composition of the pericentromeric heterochromatin in these Northeast Brazilian species is a combination of the maintenance of an ancestral Tekay distribution with a species-specific accumulation of other repeats.
MAIN CONCLUSION: We demonstrated by cytogenomic analysis that the proximal heterochromatin of the Northeast Brazilian species of Caesalpinia group is enriched with phylogenetically conserved Ty3/Gypsy-Tekay RT, but diverge in the presence of Ty3/Gypsy-Athila RT and satDNA. The Caesalpinia Group includes 225 species and 27 monophyletic genera of which four occur in Northeastern Brazil: Erythrostemon (1 sp.), Cenostigma (7 spp.), Libidibia (1 sp.), and Paubrasilia (1 sp.). The last three genera are placed in different clades in the Caesalpinia Group phylogeny, and yet they are characterized by having a numerically stable karyotype 2n = 24 (16 M+8A) and GC-rich heterochromatic bands (chromomycin A3 positive/CMA+ bands) in the proximal chromosome regions. To characterize the composition of their heterochromatin and test for the homology of these chromosomal regions, genomic DNA was extracted from Cenostigma microphyllum, Libidibia ferrea, and Paubrasilia echinata, and sequenced at low coverage using the Illumina platform. The genomic repetitive fractions were characterized using a Galaxy/RepeatExplorer-Elixir platform. The most abundant elements of each genome were chromosomally located by fluorescent in situ hybridization (FISH) and compared to the CMA+ heterochromatin distribution. The repetitive fraction of the genomes of C. microphyllum, L. ferrea, and P. echinata were estimated to be 41.70%, 38.44%, and 72.51%, respectively. Ty3/Gypsy retrotransposons (RT), specifically the Tekay lineage, were the most abundant repeats in each of the three genomes. FISH mapping revealed species-specific patterns for the Tekay elements in the proximal regions of the chromosomes, co-localized with CMA+ bands. Other species-specific patterns were observed, e.g., for the Ty3/Gypsy RT Athila elements which were found in all the proximal heterochromatin of L. ferrea or restricted to the acrocentric chromosomes of C. microphyllum. This Athila labeling co-localized with satellite DNAs (satDNAs). Although the Caesalpinia Group diverged around 55 Mya, our results suggest an ancestral colonization of Tekay RT in the proximal heterochromatin. Thus, the present-day composition of the pericentromeric heterochromatin in these Northeast Brazilian species is a combination of the maintenance of an ancestral Tekay distribution with a species-specific accumulation of other repeats.
Authors: Pavel Neumann; Alice Navrátilová; Andrea Koblížková; Eduard Kejnovský; Eva Hřibová; Roman Hobza; Alex Widmer; Jaroslav Doležel; Jiří Macas Journal: Mob DNA Date: 2011-03-03
Authors: Chia-Hui Lin; Bing Li; Selene Swanson; Ying Zhang; Laurence Florens; Michael P Washburn; Susan M Abmayr; Jerry L Workman Journal: Mol Cell Date: 2008-12-05 Impact factor: 17.970
Authors: Renata de Castro Nunes; Simon Orozco-Arias; Dominique Crouzillat; Lukas A Mueller; Suzy R Strickler; Patrick Descombes; Coralie Fournier; Deborah Moine; Alexandre de Kochko; Priscila M Yuyama; André L L Vanzela; Romain Guyot Journal: Front Plant Sci Date: 2018-02-15 Impact factor: 5.753
Authors: Sergio S Samoluk; Laura M I Chalup; Carolina Chavarro; Germán Robledo; David J Bertioli; Scott A Jackson; Guillermo Seijo Journal: Planta Date: 2019-01-24 Impact factor: 4.116
Authors: Beatrice Weber; Tony Heitkam; Daniela Holtgräwe; Bernd Weisshaar; André E Minoche; Juliane C Dohm; Heinz Himmelbauer; Thomas Schmidt Journal: Mob DNA Date: 2013-03-01
Authors: Jiří Macas; Petr Novák; Jaume Pellicer; Jana Čížková; Andrea Koblížková; Pavel Neumann; Iva Fuková; Jaroslav Doležel; Laura J Kelly; Ilia J Leitch Journal: PLoS One Date: 2015-11-25 Impact factor: 3.240
Authors: Amalia Ibiapino; Mariana Báez; Miguel A García; Mihai Costea; Saša Stefanović; Andrea Pedrosa-Harand Journal: Chromosome Res Date: 2022-01-28 Impact factor: 5.239
Authors: Paulo Aecyo; André Marques; Bruno Huettel; Ana Silva; Tiago Esposito; Elâine Ribeiro; Inara R Leal; Edeline Gagnon; Gustavo Souza; Andrea Pedrosa-Harand Journal: Planta Date: 2021-07-08 Impact factor: 4.116