Evidence map›Paper›PMID 20185544›Full record

ArticleRNA (New York, N.Y.)2010

Genome-wide analysis reveals distinct substrate specificities of Rrp6, Dis3, and core exosome subunits.

Daniel L Kiss, Erik D Andrulis

Open access · bronzeAbstract read
In one paragraph

Article in RNA (New York, N.Y.), 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 40 papers.

0numbers the graph read from it
0cells of the map it votes in
40citing papers in PubMed
2.7field-weighted citation impact, top 10% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

40 citing papers in PubMed, 57 citations in OpenAlex.

  1. Review
  2. Article
  3. Polyadenylated versions of small non-coding RNAs inMicrobial cell (Graz, Austria) · 2024
    Article
  4. Review
  5. Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. RNA Exosomes and Their Cofactors.Methods in molecular biology (Clifton, N.J.) · 2020
    Review
  13. The RNA Exosome and Human Disease.Methods in molecular biology (Clifton, N.J.) · 2020
    Review
  14. Review
  15. Long Noncoding RNAs in Plants.Advances in experimental medicine and biology · 2017
    Review
  16. Article
  17. Article
  18. Article
  19. The regulation and functions of the nuclear RNA exosome complex.Nature reviews. Molecular cell biology · 2016
    Review
  20. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

2 authors at 1 institution in 1 country.

Daniel L KissDepartment of Molecular Biology and Microbiology, School of Medicine, Case Western Reserve University, Cleveland, Ohio 44106-4960, USA.
Erik D Andrulis
Case Western Reserve University · US

Funding

Compartmentalized Exosome Structure and FunctionR01GM072820 · NIGMS · CASE WESTERN RESERVE UNIVERSITY · PI ANDRULIS, ERIK D · 2006 to 2010
$1.4M
NIGMS NIH HHS GM072820NIGMS NIH HHS R01 GM072820
6 · The paper itself

Abstract

The RNA processing exosome complex was originally defined as an evolutionarily conserved multisubunit complex of ribonucleases responsible for the processing and/or turnover of stable RNAs. The exosome complex is also involved in the surveillance of mRNAs in both the nucleus and the cytoplasm, including nonsense-mediated decay (NMD) targets. The detailed mechanisms for how individual exosome subunits participate in each of these RNA metabolic pathways remains unclear. Here, we use RNAi to deplete exosome subunits, the exonucleases Rrp6 and Dis3, and an exosome cofactor in Drosophila melanogaster S2 tissue culture cells and assay the effects on global mRNA levels using gene expression microarrays. Consistent with the RNA degradative activities ascribed to the exosome, most mRNAs are increased. Notably, these stabilized mRNAs possess 3' untranslated regions that are longer than the representative transcriptomic average. Moreover, our results reveal substantial differences in the pools of affected mRNAs for each depleted subunit. For example, approximately 25% of the affected transcripts in Rrp6 depleted cells represent NMD substrates. While the affected mRNAs were dissimilar, they encode proteins that function in similar cellular pathways. We conclude that individual exosome subunits are largely functionally independent at the transcript level, but are interdependent on a transcriptomic level.

Indexed as

AnimalsCells, CulturedDrosophila melanogasterDrosophila ProteinsExosome Multienzyme Ribonuclease ComplexGenome, InsectGenome-Wide Association StudyRibonucleasesRNA InterferenceRNA, MessengerRNA, Small InterferingSubstrate SpecificityDis3 protein, DrosophilaDrosophila ProteinsExosome Multienzyme Ribonuclease ComplexRibonucleasesRNA, MessengerRNA, Small InterferingRrp6 protein, Drosophila

Identifiers

PMID20185544
PMCPMC2844625
OpenAlexW2162167658

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.