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Arcyptera fusca and Arcyptera tornosi repetitive DNA families: whole‐comparative genomic hybridization (W‐CGH) as a novel approach to the study of satellite DNA libraries
Author(s) -
PITA M.,
ZABALAGUIRRE M.,
ARROYO F.,
GOSÁLVEZ J.,
LÓPEZFERNÁNDEZ C.,
DE LA TORRE J.
Publication year - 2008
Publication title -
journal of evolutionary biology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.289
H-Index - 128
eISSN - 1420-9101
pISSN - 1010-061X
DOI - 10.1111/j.1420-9101.2007.01436.x
Subject(s) - biology , satellite dna , comparative genomic hybridization , repeated sequence , genetics , evolutionary biology , dna , genome , gene
Whole‐comparative genomic hybridization (W‐CGH) has been used to exemplify a simple methodology which allows identifying and mapping whole genome differences for highly repetitive DNA sequences between two related species of unknown genomic background. The use of this technique to the species binomy Arcyptera fusca / Arcyptera tornosi has allowed the identification of different DNA families mainly concentrated within the para‐/peri‐centromeric and distal heterochromatic regions of different chromosomes, which are differentially expanded in both genomes. Additionally, W‐CGH allowed chromosome mapping of particular euchromatic regions immersed in the chromosome arms which have been affected by processes of DNA amplification and losses. A molecular approach was also conducted to analyse satellite DNA families in these species. We have found three different families showing an unequal representation in both species. Two of these families showed a centromeric location (EcoRV‐390CEN and Sau3A‐419CEN), whereas the last one was located at distal heterochromatic regions (Sau3A‐197TEL). As A. fusca is a widely distributed species represented in most European high mountains, whereas A. tornosi is an endemic species represented in the Iberian Peninsula, the differences and resemblances reported here offer a good basis to support a close evolutionary relationship between both of the actually isolated species. Finally, W‐CGH allowed identification of an asynchronic pattern of heterochromatin condensation through early prophase (characteristic in both species) which is uncommon or probably has been poorly analysed within classical early condensing chromosome domains through meiosis. The congruence of the obtained cytological and molecular results is analysed in light of the ancestral genome relationship between both species.