LINE-1 amplification accompanies explosive genome repatterning in rodents.

Chromosome Res

Laboratoire Origine, Structure et Evolution de la Biodiversité, Muséum National d'Histoire Naturelle, 55, rue Buffon, F75005, Paris, France.

Published: May 2005

AI Article Synopsis

  • - Transposable elements (TEs), particularly LINE-1 retrotransposons, can cause significant karyotypic changes in rodents from the genus Taterillus, which recently experienced major genome rearrangements.
  • - Through FISH and Southern blot analyses, the study found that LINE-1 elements were significantly amplified and irregularly distributed in the most rearranged chromosomes, indicating a possible link between LINE-1 activity and chromosomal evolution.
  • - The findings suggest that the genome repatterning may trigger temporary stress phases that relax certain epigenetic controls, like DNA methylation, enabling the amplification of transposable elements in the Taterillus species.

Article Abstract

Transposable elements (TEs) sometimes induce karyotypic changes following recombination, breakage and rearrangement. We used FISH and Southern blot analyses to investigate the amount and distribution of LINE-1 retrotransposons in rodents (genus Taterillus, Muridae, Gerbillinae) that have recently undergone an important genome repatterning. Our results were interpreted in a known phylogenetic framework and clearly showed that LINE-1 elements were greatly amplified and non-randomly distributed in the most rearranged karyotypes. A comparison between FISH and conventional banding patterns provided evidence that LINE-1 insertion sites and chromosome breakpoints were not strongly correlated, thus suggesting that LINE-1 amplification subsequently accompanied Taterillus chromosome evolution. Similar patterns are observed in some cases of genomic stresses (hybrid genomes, cancer and DNA-damaged cells) and usually associated with DNA hypomethylation. We propose that intensively repatterned genomes face transient stress phases during which some epigenetic features, such as DNA methylation, are relaxed, thus allowing TE amplification.

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Source
http://dx.doi.org/10.1007/s10577-005-5265-yDOI Listing

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