sh.sePublications
Change search
CiteExportLink to record
Permanent link

Direct link
Cite
Citation style
  • apa
  • ieee
  • modern-language-association-8th-edition
  • vancouver
  • harvard-anglia-ruskin-university
  • apa-old-doi-prefix.csl
  • sodertorns-hogskola-harvard.csl
  • sodertorns-hogskola-oxford.csl
  • Other style
More styles
Language
  • de-DE
  • en-GB
  • en-US
  • fi-FI
  • nn-NO
  • nn-NB
  • sv-SE
  • Other locale
More languages
Output format
  • html
  • text
  • asciidoc
  • rtf
ABCE1 Is a Highly Conserved RNA Silencing Suppressor
Tallinn University of Technology, Tallinn, Estonia / Competence Centre for Cancer Research, Tallinn, Estonia .
Tallinn University of Technology, Tallinn, Estonia / Competence Centre for Cancer Research, Tallinn, Estonia .
Tallinn University of Technology, Tallinn, Estonia.
Tallinn University of Technology, Tallinn, Estonia.
Show others and affiliations
2015 (English)In: PLOS ONE, E-ISSN 1932-6203, Vol. 10, no 2, article id e0116702Article in journal (Refereed) Published
Abstract [en]

ATP-binding cassette sub-family E member 1 (ABCE1) is a highly conserved protein among eukaryotes and archaea. Recent studies have identified ABCE1 as a ribosome-recycling factor important for translation termination in mammalian cells, yeast and also archaea. Here we report another conserved function of ABCE1. We have previously described AtRLI2, the homolog of ABCE1 in the plant Arabidopsis thaliana, as an endogenous suppressor of RNA silencing. In this study we show that this function is conserved: human ABCE1 is able to suppress RNA silencing in Nicotiana benthamiana plants, in mammalian HEK293 cells and in the worm Caenorhabditis elegans. Using co-immunoprecipitation and mass spectrometry, we found a number of potential ABCE1-interacting proteins that might support its function as an endogenous suppressor of RNA interference. The interactor candidates are associated with epigenetic regulation, transcription, RNA processing and mRNA surveillance. In addition, one of the identified proteins is translin, which together with its binding partner TRAX supports RNA interference.

Place, publisher, year, edition, pages
2015. Vol. 10, no 2, article id e0116702
National Category
Biological Sciences
Identifiers
URN: urn:nbn:se:sh:diva-26400DOI: 10.1371/journal.pone.0116702ISI: 000349444900060PubMedID: 25659154Scopus ID: 2-s2.0-84922720162OAI: oai:DiVA.org:sh-26400DiVA, id: diva2:787992
Funder
The Foundation for Baltic and East European Studies, 300501Available from: 2015-02-12 Created: 2015-02-12 Last updated: 2021-06-14Bibliographically approved

Open Access in DiVA

No full text in DiVA

Other links

Publisher's full textPubMedScopusPMC Full text

Authority records

Smialowska, AgataKylsten, PerEkwall, KarlSwoboda, Peter

Search in DiVA

By author/editor
Smialowska, AgataKylsten, PerEkwall, KarlSwoboda, Peter
By organisation
School of Natural Sciences, Technology and Environmental Studies
In the same journal
PLOS ONE
Biological Sciences

Search outside of DiVA

GoogleGoogle Scholar

doi
pubmed
urn-nbn

Altmetric score

doi
pubmed
urn-nbn
Total: 233 hits
CiteExportLink to record
Permanent link

Direct link
Cite
Citation style
  • apa
  • ieee
  • modern-language-association-8th-edition
  • vancouver
  • harvard-anglia-ruskin-university
  • apa-old-doi-prefix.csl
  • sodertorns-hogskola-harvard.csl
  • sodertorns-hogskola-oxford.csl
  • Other style
More styles
Language
  • de-DE
  • en-GB
  • en-US
  • fi-FI
  • nn-NO
  • nn-NB
  • sv-SE
  • Other locale
More languages
Output format
  • html
  • text
  • asciidoc
  • rtf