Evidence map›Paper›PMID 32589966›Full record

ArticleMolecular cell2020

Selective 40S Footprinting Reveals Cap-Tethered Ribosome Scanning in Human Cells.

Jonathan Bohlen, Kai Fenzl, Günter Kramer, Bernd Bukau, Aurelio A Teleman

Abstract read
PubMed Publisher
In one paragraph

Article in Molecular cell, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 95 papers.

0numbers the graph read from it
0cells of the map it votes in
95citing papers in PubMed
8.0field-weighted citation impact, top 2% 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

95 citing papers in PubMed, 160 citations in OpenAlex.

  1. Review
  2. Review
  3. Article
  4. Article
  5. Review
  6. Review
  7. Article
  8. Review
  9. Review
  10. Article
  11. Review
  12. Article
  13. Structural insights into the role of eIF3 in translation mediated by the HCV IRES.Proceedings of the National Academy of Sciences of the United States of America · 2025
    Article
  14. Article
  15. Review
  16. Article
  17. Review
  18. Review
  19. Article
  20. Article

35 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

5 authors at 1 institution in 1 country.

Jonathan BohlenGerman Cancer Research Center (DKFZ), 69120 Heidelberg, Germany; CellNetworks - Cluster of Excellence, 69120 Heidelberg University, Germany; Heidelberg University, 69120 Heidelberg, Germany; Heidelberg Biosciences International Graduate School (HBIGS), 69120 Heidelberg, Germany; National Center for Tumor Diseases (NCT) partner site, 69120 Heidelberg, Germany.
Kai FenzlCenter for Molecular Biology of Heidelberg University (ZMBH) and German Cancer Research Center (DKFZ), DKFZ-ZMBH Alliance, Im Neuenheimer Feld 282, 69120 Heidelberg, Germany.
Günter KramerNational Center for Tumor Diseases (NCT) partner site, 69120 Heidelberg, Germany; Center for Molecular Biology of Heidelberg University (ZMBH) and German Cancer Research Center (DKFZ), DKFZ-ZMBH Alliance, Im Neuenheimer Feld 282, 69120 Heidelberg, Germany.
Bernd BukauNational Center for Tumor Diseases (NCT) partner site, 69120 Heidelberg, Germany; Center for Molecular Biology of Heidelberg University (ZMBH) and German Cancer Research Center (DKFZ), DKFZ-ZMBH Alliance, Im Neuenheimer Feld 282, 69120 Heidelberg, Germany.
Aurelio A TelemanGerman Cancer Research Center (DKFZ), 69120 Heidelberg, Germany; CellNetworks - Cluster of Excellence, 69120 Heidelberg University, Germany; Heidelberg University, 69120 Heidelberg, Germany; Heidelberg Biosciences International Graduate School (HBIGS), 69120 Heidelberg, Germany; National Center for Tumor Diseases (NCT) partner site, 69120 Heidelberg, Germany. Electronic address: a.teleman@dkfz.de.
German Cancer Research Center · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Translation regulation occurs largely during the initiation phase. Here, we develop selective 40S footprinting to visualize initiating 40S ribosomes on endogenous mRNAs in vivo. This reveals the positions on mRNAs where initiation factors join the ribosome to act and where they leave. We discover that in most human cells, most scanning ribosomes remain attached to the 5' cap. Consequently, only one ribosome scans a 5' UTR at a time, and 5' UTR length affects translation efficiency. We discover that eukaryotic initiation factor 3B (eIF3B,) eIF4G1, and eIF4E remain bound to 80S ribosomes as they begin translating, with a decay half-length of ∼12 codons. Hence, ribosomes retain these initiation factors while translating short upstream open reading frames (uORFs), providing an explanation for how ribosomes can reinitiate translation after uORFs in humans. This method will be of use for studying translation initiation mechanisms in vivo.

Indexed as

5' Untranslated RegionsPeptide Chain Initiation, TranslationalAnimalsCodon, InitiatorDNA FootprintingEukaryotic Initiation Factor-3Eukaryotic Initiation Factor-4EEukaryotic Initiation Factor-4GHeLa CellsHumansMiceNIH 3T3 CellsOpen Reading FramesRibosome SubunitsRibosome Subunits, Small, EukaryoticRNA, Messenger5' Untranslated RegionsCodon, InitiatorEIF3B protein, humanEIF4E protein, humanEIF4G1 protein, humanEukaryotic Initiation Factor-3Eukaryotic Initiation Factor-4EEukaryotic Initiation Factor-4GRNA, MessengerRNA, Transfer, Metcap-tetheringeukaryotic initiation factormRNA capreinitiationribosome footprintingscanningtranslational regulationtranslation initiation

Identifiers

PMID32589966
OpenAlexW3037971445

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.