Cargando…

Transposon Invasion of the Paramecium Germline Genome Countered by a Domesticated PiggyBac Transposase and the NHEJ Pathway

Sequences related to transposons constitute a large fraction of extant genomes, but insertions within coding sequences have generally not been tolerated during evolution. Thanks to their unique nuclear dimorphism and to their original mechanism of programmed DNA elimination from their somatic nucleu...

Descripción completa

Detalles Bibliográficos
Autores principales: Dubois, Emeline, Bischerour, Julien, Marmignon, Antoine, Mathy, Nathalie, Régnier, Vinciane, Bétermier, Mireille
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3408717/
https://www.ncbi.nlm.nih.gov/pubmed/22888464
http://dx.doi.org/10.1155/2012/436196
_version_ 1782239497522511872
author Dubois, Emeline
Bischerour, Julien
Marmignon, Antoine
Mathy, Nathalie
Régnier, Vinciane
Bétermier, Mireille
author_facet Dubois, Emeline
Bischerour, Julien
Marmignon, Antoine
Mathy, Nathalie
Régnier, Vinciane
Bétermier, Mireille
author_sort Dubois, Emeline
collection PubMed
description Sequences related to transposons constitute a large fraction of extant genomes, but insertions within coding sequences have generally not been tolerated during evolution. Thanks to their unique nuclear dimorphism and to their original mechanism of programmed DNA elimination from their somatic nucleus (macronucleus), ciliates are emerging model organisms for the study of the impact of transposable elements on genomes. The germline genome of the ciliate Paramecium, located in its micronucleus, contains thousands of short intervening sequences, the IESs, which interrupt 47% of genes. Recent data provided support to the hypothesis that an evolutionary link exists between Paramecium IESs and Tc1/mariner transposons. During development of the macronucleus, IESs are excised precisely thanks to the coordinated action of PiggyMac, a domesticated piggyBac transposase, and of the NHEJ double-strand break repair pathway. A PiggyMac homolog is also required for developmentally programmed DNA elimination in another ciliate, Tetrahymena. Here, we present an overview of the life cycle of these unicellular eukaryotes and of the developmentally programmed genome rearrangements that take place at each sexual cycle. We discuss how ancient domestication of a piggyBac transposase might have allowed Tc1/mariner elements to spread throughout the germline genome of Paramecium, without strong counterselection against insertion within genes.
format Online
Article
Text
id pubmed-3408717
institution National Center for Biotechnology Information
language English
publishDate 2012
publisher Hindawi Publishing Corporation
record_format MEDLINE/PubMed
spelling pubmed-34087172012-08-10 Transposon Invasion of the Paramecium Germline Genome Countered by a Domesticated PiggyBac Transposase and the NHEJ Pathway Dubois, Emeline Bischerour, Julien Marmignon, Antoine Mathy, Nathalie Régnier, Vinciane Bétermier, Mireille Int J Evol Biol Review Article Sequences related to transposons constitute a large fraction of extant genomes, but insertions within coding sequences have generally not been tolerated during evolution. Thanks to their unique nuclear dimorphism and to their original mechanism of programmed DNA elimination from their somatic nucleus (macronucleus), ciliates are emerging model organisms for the study of the impact of transposable elements on genomes. The germline genome of the ciliate Paramecium, located in its micronucleus, contains thousands of short intervening sequences, the IESs, which interrupt 47% of genes. Recent data provided support to the hypothesis that an evolutionary link exists between Paramecium IESs and Tc1/mariner transposons. During development of the macronucleus, IESs are excised precisely thanks to the coordinated action of PiggyMac, a domesticated piggyBac transposase, and of the NHEJ double-strand break repair pathway. A PiggyMac homolog is also required for developmentally programmed DNA elimination in another ciliate, Tetrahymena. Here, we present an overview of the life cycle of these unicellular eukaryotes and of the developmentally programmed genome rearrangements that take place at each sexual cycle. We discuss how ancient domestication of a piggyBac transposase might have allowed Tc1/mariner elements to spread throughout the germline genome of Paramecium, without strong counterselection against insertion within genes. Hindawi Publishing Corporation 2012 2012-07-22 /pmc/articles/PMC3408717/ /pubmed/22888464 http://dx.doi.org/10.1155/2012/436196 Text en Copyright © 2012 Emeline Dubois et al. https://creativecommons.org/licenses/by/3.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Review Article
Dubois, Emeline
Bischerour, Julien
Marmignon, Antoine
Mathy, Nathalie
Régnier, Vinciane
Bétermier, Mireille
Transposon Invasion of the Paramecium Germline Genome Countered by a Domesticated PiggyBac Transposase and the NHEJ Pathway
title Transposon Invasion of the Paramecium Germline Genome Countered by a Domesticated PiggyBac Transposase and the NHEJ Pathway
title_full Transposon Invasion of the Paramecium Germline Genome Countered by a Domesticated PiggyBac Transposase and the NHEJ Pathway
title_fullStr Transposon Invasion of the Paramecium Germline Genome Countered by a Domesticated PiggyBac Transposase and the NHEJ Pathway
title_full_unstemmed Transposon Invasion of the Paramecium Germline Genome Countered by a Domesticated PiggyBac Transposase and the NHEJ Pathway
title_short Transposon Invasion of the Paramecium Germline Genome Countered by a Domesticated PiggyBac Transposase and the NHEJ Pathway
title_sort transposon invasion of the paramecium germline genome countered by a domesticated piggybac transposase and the nhej pathway
topic Review Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3408717/
https://www.ncbi.nlm.nih.gov/pubmed/22888464
http://dx.doi.org/10.1155/2012/436196
work_keys_str_mv AT duboisemeline transposoninvasionoftheparameciumgermlinegenomecounteredbyadomesticatedpiggybactransposaseandthenhejpathway
AT bischerourjulien transposoninvasionoftheparameciumgermlinegenomecounteredbyadomesticatedpiggybactransposaseandthenhejpathway
AT marmignonantoine transposoninvasionoftheparameciumgermlinegenomecounteredbyadomesticatedpiggybactransposaseandthenhejpathway
AT mathynathalie transposoninvasionoftheparameciumgermlinegenomecounteredbyadomesticatedpiggybactransposaseandthenhejpathway
AT regniervinciane transposoninvasionoftheparameciumgermlinegenomecounteredbyadomesticatedpiggybactransposaseandthenhejpathway
AT betermiermireille transposoninvasionoftheparameciumgermlinegenomecounteredbyadomesticatedpiggybactransposaseandthenhejpathway