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A host factor supports retrotransposition of the TRE5-A population in Dictyostelium cells by suppressing an Argonaute protein
Univ Jena, Inst Pharm, Dept Pharmaceut Biol, D-07743 Jena, Germany..
Univ Jena, Inst Pharm, Dept Pharmaceut Biol, D-07743 Jena, Germany..
Univ Jena, Inst Pharm, Dept Pharmaceut Biol, D-07743 Jena, Germany..
Swedish Univ Agr Sci, Biomed Ctr, Dept Mol Biol, Uppsala, Sweden..
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2015 (English)In: Mobile DNA, ISSN 1759-8753, E-ISSN 1759-8753, Vol. 6, 14Article in journal (Refereed) Published
Abstract [en]

Background: In the compact and haploid genome of Dictyostelium discoideum control of transposon activity is of particular importance to maintain viability. The non-long terminal repeat retrotransposon TRE5-A amplifies continuously in D. discoideum cells even though it produces considerable amounts of minus-strand (antisense) RNA in the presence of an active RNA interference machinery. Removal of the host-encoded C-module-binding factor (CbfA) from D. discoideum cells resulted in a more than 90 % reduction of both plus-and minus-strand RNA of TRE5-A and a strong decrease of the retrotransposition activity of the cellular TRE5-A population. Transcriptome analysis revealed an approximately 230-fold overexpression of the gene coding for the Argonaute-like protein AgnC in a CbfA-depleted mutant. Results: The D. discoideum genome contains orthologs of RNA-dependent RNA polymerases, Dicer-like proteins, and Argonaute proteins that are supposed to represent RNA interference pathways. We analyzed available mutants in these genes for altered expression of TRE5-A. We found that the retrotransposon was overexpressed in mutants lacking the Argonaute proteins AgnC and AgnE. Because the agnC gene is barely expressed in wild-type cells, probably due to repression by CbfA, we employed a new method of promoter-swapping to overexpress agnC in a CbfA-independent manner. In these strains we established an in vivo retrotransposition assay that determines the retrotransposition frequency of the cellular TRE5-A population. We observed that both the TRE5-A steady-state RNA level and retrotransposition rate dropped to less than 10 % of wild-type in the agnC overexpressor strains. Conclusions: The data suggest that TRE5-A amplification is controlled by a distinct pathway of the Dictyostelium RNA interference machinery that does not require RNA-dependent RNA polymerases but involves AgnC. This control is at least partially overcome by the activity of CbfA, a factor derived from the retrotransposon's host. This unusual regulation of mobile element activity most likely had a profound effect on genome evolution in D. discoideum.

Place, publisher, year, edition, pages
2015. Vol. 6, 14
Keyword [en]
Dictyostelium, Retrotransposition, siRNA, RNAi, Argonaute
National Category
URN: urn:nbn:se:uu:diva-262949DOI: 10.1186/s13100-015-0045-5ISI: 000360527400001PubMedID: 26339297OAI: oai:DiVA.org:uu-262949DiVA: diva2:858410
Swedish Research Council
Available from: 2015-10-02 Created: 2015-09-23 Last updated: 2015-10-02Bibliographically approved

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