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repetitive component of the A genome of peanut (Arachis hypogaea) and its role in remodelling intergenic sequence space since its evolutionary divergence from the B genome

Background and AimsPeanut (Arachis hypogaea) is an allotetraploid (AABB-type genome) of recent origin, with a genome of about 2·8 Gb and a high repetitive content. This study reports an analysis of the repetitive component of the peanut A genome using bacterial artificial chromosome (BAC) clones fro...

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Bibliographic Details
Published in:Annals of botany 2013-08, Vol.112 (3), p.545-559
Main Authors: Bertioli, David J, Vidigal, Bruna, Nielen, Stephan, Ratnaparkhe, Milind B, Lee, Tae-Ho, Leal-Bertioli, Soraya C. M, Kim, Changsoo, Guimarães, Patricia M, Seijo, Guillermo, Schwarzacher, Trude, Paterson, Andrew H, Heslop-Harrison, Pat, Araujo, Ana C. G
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Language:English
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Summary:Background and AimsPeanut (Arachis hypogaea) is an allotetraploid (AABB-type genome) of recent origin, with a genome of about 2·8 Gb and a high repetitive content. This study reports an analysis of the repetitive component of the peanut A genome using bacterial artificial chromosome (BAC) clones from A. duranensis, the most probable A genome donor, and the probable consequences of the activity of these elements since the divergence of the peanut A and B genomes.MethodsThe repetitive content of the A genome was analysed by using A. duranensis BAC clones as probes for fluorescence in situ hybridization (BAC-FISH), and by sequencing and characterization of 12 genomic regions. For the analysis of the evolutionary dynamics, two A genome regions are compared with their B genome homeologues.Key ResultsBAC-FISH using 27 A. duranensis BAC clones as probes gave dispersed and repetitive DNA characteristic signals, predominantly in interstitial regions of the peanut A chromosomes. The sequences of 14 BAC clones showed complete and truncated copies of ten abundant long terminal repeat (LTR) retrotransposons, characterized here. Almost all dateable transposition events occurred
ISSN:0305-7364
1095-8290
DOI:10.1093/aob/mct128