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DIRS retrotransposons amplify via linear, single-stranded cDNA intermediates

The Dictyostelium Intermediate Repeat Sequence 1 (DIRS-1) is the name-giving member of the DIRS order of tyrosine recombinase retrotransposons. In Dictyostelium discoideum, DIRS-1 is highly amplified and enriched in heterochromatic centromers of the D. discoideum genome. We show here that DIRS-1 it...

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Autores principales: Malicki, Marek, Spaller, Thomas, Winckler, Thomas, Hammann, Christian
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7192593/
https://www.ncbi.nlm.nih.gov/pubmed/32170321
http://dx.doi.org/10.1093/nar/gkaa160
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author Malicki, Marek
Spaller, Thomas
Winckler, Thomas
Hammann, Christian
author_facet Malicki, Marek
Spaller, Thomas
Winckler, Thomas
Hammann, Christian
author_sort Malicki, Marek
collection PubMed
description The Dictyostelium Intermediate Repeat Sequence 1 (DIRS-1) is the name-giving member of the DIRS order of tyrosine recombinase retrotransposons. In Dictyostelium discoideum, DIRS-1 is highly amplified and enriched in heterochromatic centromers of the D. discoideum genome. We show here that DIRS-1 it tightly controlled by the D. discoideum RNA interference machinery and is only mobilized in mutants lacking either the RNA dependent RNA polymerase RrpC or the Argonaute protein AgnA. DIRS retrotransposons contain an internal complementary region (ICR) that is thought to be required to reconstitute a full-length element from incomplete RNA transcripts. Using different versions of D. discoideum DIRS-1 equipped with retrotransposition marker genes, we show experimentally that the ICR is in fact essential to complete retrotransposition. We further show that DIRS-1 produces a mixture of single-stranded, mostly linear extrachromosomal cDNA intermediates. If this cDNA is isolated and transformed into D. discoideum cells, it can be used by DIRS-1 proteins to complete productive retrotransposition. This work provides the first experimental evidence to propose a general retrotransposition mechanism of the class of DIRS like tyrosine recombinase retrotransposons.
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spelling pubmed-71925932020-05-06 DIRS retrotransposons amplify via linear, single-stranded cDNA intermediates Malicki, Marek Spaller, Thomas Winckler, Thomas Hammann, Christian Nucleic Acids Res Gene regulation, Chromatin and Epigenetics The Dictyostelium Intermediate Repeat Sequence 1 (DIRS-1) is the name-giving member of the DIRS order of tyrosine recombinase retrotransposons. In Dictyostelium discoideum, DIRS-1 is highly amplified and enriched in heterochromatic centromers of the D. discoideum genome. We show here that DIRS-1 it tightly controlled by the D. discoideum RNA interference machinery and is only mobilized in mutants lacking either the RNA dependent RNA polymerase RrpC or the Argonaute protein AgnA. DIRS retrotransposons contain an internal complementary region (ICR) that is thought to be required to reconstitute a full-length element from incomplete RNA transcripts. Using different versions of D. discoideum DIRS-1 equipped with retrotransposition marker genes, we show experimentally that the ICR is in fact essential to complete retrotransposition. We further show that DIRS-1 produces a mixture of single-stranded, mostly linear extrachromosomal cDNA intermediates. If this cDNA is isolated and transformed into D. discoideum cells, it can be used by DIRS-1 proteins to complete productive retrotransposition. This work provides the first experimental evidence to propose a general retrotransposition mechanism of the class of DIRS like tyrosine recombinase retrotransposons. Oxford University Press 2020-05-07 2020-03-14 /pmc/articles/PMC7192593/ /pubmed/32170321 http://dx.doi.org/10.1093/nar/gkaa160 Text en © The Author(s) 2020. Published by Oxford University Press on behalf of Nucleic Acids Research. http://creativecommons.org/licenses/by-nc/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com
spellingShingle Gene regulation, Chromatin and Epigenetics
Malicki, Marek
Spaller, Thomas
Winckler, Thomas
Hammann, Christian
DIRS retrotransposons amplify via linear, single-stranded cDNA intermediates
title DIRS retrotransposons amplify via linear, single-stranded cDNA intermediates
title_full DIRS retrotransposons amplify via linear, single-stranded cDNA intermediates
title_fullStr DIRS retrotransposons amplify via linear, single-stranded cDNA intermediates
title_full_unstemmed DIRS retrotransposons amplify via linear, single-stranded cDNA intermediates
title_short DIRS retrotransposons amplify via linear, single-stranded cDNA intermediates
title_sort dirs retrotransposons amplify via linear, single-stranded cdna intermediates
topic Gene regulation, Chromatin and Epigenetics
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7192593/
https://www.ncbi.nlm.nih.gov/pubmed/32170321
http://dx.doi.org/10.1093/nar/gkaa160
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