Evidence map›Paper›PMID 25870104›Full record

ArticleMolecular and cellular biology2015

Competition between Decapping Complex Formation and Ubiquitin-Mediated Proteasomal Degradation Controls Human Dcp2 Decapping Activity.

Stacy L Erickson, Elizabeth O Corpuz, Jeffrey P Maloy, Christy Fillman, Kristofer Webb, Eric J Bennett, Jens Lykke-Andersen

Open access · bronzeAbstract read
In one paragraph

Article in Molecular and cellular biology, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
1.8field-weighted citation impact, top 15% 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

17 citing papers in PubMed, 26 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Eukaryotic mRNA Decapping Activation.Frontiers in genetics · 2022
    Review
  5. Article
  6. Review
  7. Article
  8. Review
  9. Article
  10. Article
  11. New insights into decapping enzymes and selective mRNA decay.Wiley interdisciplinary reviews. RNA · 2017
    Review
  12. Article
  13. Article
  14. Review
  15. Article
  16. Cytoplasmic mRNA turnover and ageing.Mechanisms of ageing and development · 2015
    Review
  17. 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

7 authors at 2 institutions in 1 country.

Stacy L EricksonDivision of Biological Sciences, University of California San Diego, La Jolla, California, USA Department of Molecular, Cellular and Developmental Biology, University of Colorado, Boulder, Colorado, USA.
Elizabeth O CorpuzDivision of Biological Sciences, University of California San Diego, La Jolla, California, USA.
Jeffrey P MaloyDivision of Biological Sciences, University of California San Diego, La Jolla, California, USA.
Christy FillmanDepartment of Molecular, Cellular and Developmental Biology, University of Colorado, Boulder, Colorado, USA.
Kristofer WebbDivision of Biological Sciences, University of California San Diego, La Jolla, California, USA.
Eric J BennettDivision of Biological Sciences, University of California San Diego, La Jolla, California, USA.
Jens Lykke-AndersenDivision of Biological Sciences, University of California San Diego, La Jolla, California, USA Department of Molecular, Cellular and Developmental Biology, University of Colorado, Boulder, Colorado, USA jlykkeandersen@ucsd.edu.
University of California, San Diego · USUniversity of Colorado Boulder · US

Funding

TRAINING IN SIGNAL TRANSDUCTION &CELL CYCLE REGULATIONT32GM008759 · NIGMS · UNIVERSITY OF COLORADO AT BOULDER · PI AHN, NATALIE G. · 2000 to 2020
$5.9M
Predoctoral Training Program in Signaling and Cellular Regulation INCLUDE Down Syndrome SupplementT32GM142607 · NIGMS · UNIVERSITY OF COLORADO · PI Sabrina Leigh Spencer, Tin Tin Su · 2021 to 2026
$3.6M
The Function of Processing Bodies in Human mRNA TurnoverR01GM077243 · NIGMS · UNIVERSITY OF COLORADO · PI LYKKE-ANDERSEN, JENS · 2007 to 2015
$1.7M
NIGMS NIH HHS R01 GM077243NIGMS NIH HHS T32 GM008759NIGMS NIH HHS T32 GM08759NIGMS NIH HHS T32 GM142607
6 · The paper itself

Abstract

mRNA decapping is a central step in eukaryotic mRNA decay that simultaneously shuts down translation initiation and activates mRNA degradation. A major complex responsible for decapping consists of the decapping enzyme Dcp2 in association with decapping enhancers. An important question is how the activity and accumulation of Dcp2 are regulated at the cellular level to ensure the specificity and fidelity of the Dcp2 decapping complex. Here, we show that human Dcp2 levels and activity are controlled by a competition between decapping complex assembly and Dcp2 degradation. This is mediated by a regulatory domain in the Dcp2 C terminus, which, on the one hand, promotes Dcp2 activation via decapping complex formation mediated by the decapping enhancer Hedls and, on the other hand, targets Dcp2 for ubiquitin-mediated proteasomal degradation in the absence of Hedls association. This competition between Dcp2 activation and degradation restricts the accumulation and activity of uncomplexed Dcp2, which may be important for preventing uncontrolled decapping or for regulating Dcp2 levels and activity according to cellular needs.

Indexed as

EndoribonucleasesHEK293 CellsHumansProteasome Endopeptidase ComplexProteinsProtein StabilityProtein Structure, TertiaryProteolysisUbiquitinDCP2 protein, humanEDC4 protein, humanEndoribonucleasesProteasome Endopeptidase ComplexProteinsUbiquitin

Identifiers

PMID25870104
PMCPMC4438239
OpenAlexW2015807059

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.