Evidence map›Paper›PMID 31656086›Full record

ReviewCritical reviews in biochemistry and molecular biology2019

Feedback to the central dogma: cytoplasmic mRNA decay and transcription are interdependent processes.

Ella Hartenian, Britt A Glaunsinger

Open access · greenAbstract readReview
In one paragraph

Review in Critical reviews in biochemistry and molecular biology, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 32 papers.

0numbers the graph read from it
0cells of the map it votes in
32citing papers in PubMed
2.8field-weighted citation impact, top 8% 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

32 citing papers in PubMed, 75 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Review
  9. Article
  10. Article
  11. Article
  12. Article
  13. Article
  14. SARS-CoV-2 Nsp1 traps RNA in the nucleus to escape immune detection.Proceedings of the National Academy of Sciences of the United States of America · 2024
    Article
  15. Review
  16. Review
  17. Article
  18. Article
  19. Enhanced gene regulation by cooperation between mRNA decay and gene transcription.Biochimica et biophysica acta. Gene regulatory mechanisms · 2023
    Article
  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 2 institutions in 1 country.

Ella HartenianDepartment of Molecular & Cell Biology, University of California, Berkeley, CA, USA.ORCID 0000-0001-9277-2152
Britt A GlaunsingerDepartment of Molecular & Cell Biology, University of California, Berkeley, CA, USA.ORCID 0000-0003-0479-9377
Howard Hughes Medical Institute · USUniversity of California, Berkeley · US

Funding

Disruption of Cellular RNA Processing by Kaposi's Sarcoma-Associated HerpesvirusR01CA136367 · NCI · UNIVERSITY OF CALIFORNIA BERKELEY · PI Britt A Glaunsinger · 2010 to 2026
$5.8M
Regulation of Gammaherpesviral Late Gene ExpressionR01AI122528 · NIAID · UNIVERSITY OF CALIFORNIA BERKELEY · PI Britt A Glaunsinger · 2016 to 2026
$4.2M
Howard Hughes Medical InstituteNCI NIH HHS R01 CA136367NIAID NIH HHS R01 AI122528
6 · The paper itself

Abstract

Transcription and RNA decay are key determinants of gene expression; these processes are typically considered as the uncoupled beginning and end of the messenger RNA (mRNA) lifecycle. Here we describe the growing number of studies demonstrating interplay between these spatially disparate processes in eukaryotes. Specifically, cells can maintain mRNA levels by buffering against changes in mRNA stability or transcription, and can also respond to virally induced accelerated decay by reducing RNA polymerase II gene expression. In addition to these global responses, there is also evidence that mRNAs containing a premature stop codon can cause transcriptional upregulation of homologous genes in a targeted fashion. In each of these systems, RNA binding proteins (RBPs), particularly those involved in mRNA degradation, are critical for cytoplasmic to nuclear communication. Although their specific mechanistic contributions are yet to be fully elucidated, differential trafficking of RBPs between subcellular compartments are likely to play a central role in regulating this gene expression feedback pathway.

Indexed as

Transcription, GeneticAnimalsCell NucleusCodon, TerminatorCytoplasmExoribonucleasesGene ExpressionHomeostasisHumansInfectionsMicrotubule-Associated ProteinsRNA-Binding ProteinsRNA, MessengerRNA Polymerase IIRNA StabilityCodon, TerminatorExoribonucleasesMicrotubule-Associated ProteinsRNA-Binding ProteinsRNA, MessengerRNA Polymerase IIXRN1 protein, humangenetic bufferinghost shutoffmRNA decayNITCtranscriptionXrn1

Identifiers

PMID31656086
PMCPMC6871655
OpenAlexW2982113925

What OpenQuestion holds

Textmetadata
LicenceTDM
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.