Evidence map›Paper›PMID 38989862›Full record

ArticleeLife2024

Human DDX6 regulates translation and decay of inefficiently translated mRNAs.

Ramona Weber, Chung-Te Chang

Abstract read
In one paragraph

Article in eLife, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
–field-weighted citation impact
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

19 citing papers in PubMed.

  1. Live-attenuatedVirulence · 2026
    Article
  2. Article
  3. Article
  4. mCell death & disease · 2026
    Article
  5. Article
  6. Article
  7. Review
  8. Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. Article
  14. Review
  15. Article
  16. Article
  17. Article
  18. Article
  19. Review
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.

Ramona WeberDepartment of Biochemistry, Max Planck Institute for Developmental Biology, Tübingen, Germany.ORCID https://orcid.org/0000-0003-4176-1685
Chung-Te ChangDepartment of Biochemistry, Max Planck Institute for Developmental Biology, Tübingen, Germany.ORCID https://orcid.org/0000-0002-4792-1646

Funding

National Science and Technology Council NSTC111-2311-B-A49-005-Yen Tjing Ling Medical Foundation CI-112-13
6 · The paper itself

Abstract

Recent findings indicate that the translation elongation rate influences mRNA stability. One of the factors that has been implicated in this link between mRNA decay and translation speed is the yeast DEAD-box helicase Dhh1p. Here, we demonstrated that the human ortholog of Dhh1p, DDX6, triggers the deadenylation-dependent decay of inefficiently translated mRNAs in human cells. DDX6 interacts with the ribosome through the Phe-Asp-Phe (FDF) motif in its RecA2 domain. Furthermore, RecA2-mediated interactions and ATPase activity are both required for DDX6 to destabilize inefficiently translated mRNAs. Using ribosome profiling and RNA sequencing, we identified two classes of endogenous mRNAs that are regulated in a DDX6-dependent manner. The identified targets are either translationally regulated or regulated at the steady-state-level and either exhibit signatures of poor overall translation or of locally reduced ribosome translocation rates. Transferring the identified sequence stretches into a reporter mRNA caused translation- and DDX6-dependent degradation of the reporter mRNA. In summary, these results identify DDX6 as a crucial regulator of mRNA translation and decay triggered by slow ribosome movement and provide insights into the mechanism by which DDX6 destabilizes inefficiently translated mRNAs.

Indexed as

DEAD-box RNA HelicasesProtein BiosynthesisProto-Oncogene ProteinsRNA, MessengerRNA StabilityHEK293 CellsHumansRibosomesDDX6 protein, humanDEAD-box RNA HelicasesProto-Oncogene ProteinsRNA, MessengerbiochemistryCCR4-NOT complexchemical biologychromosomescodon optimizationDDX6gene expressionhumanmRNA decayribosome stalling

Identifiers

PMID38989862
PMCPMC11239181

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.