Evidence map›Paper›PMID 40243440›Full record

ReviewInternational journal of molecular sciences2025

The Central FacilitaTOR: Coordinating Transcription and Translation in Eukaryotes.

Summer E Adams-Brown, Ke Zhang Reid

Abstract readReview
In one paragraph

Review in International journal of molecular sciences, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. 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.

Summer E Adams-BrownDepartment of Biology, Wake Forest University, Winston-Salem, NC 27109, USA.
Ke Zhang ReidDepartment of Biology, Wake Forest University, Winston-Salem, NC 27109, USA.ORCID 0000-0003-1973-0874

Funding

Functional diversity of large ribosomal protein 27 and small ribosomal protein 19 paralogsR15GM157708 · NIGMS · WAKE FOREST UNIVERSITY · PI REID, KE ZHANG · 2024 to 2024
$429k
National Institutes of Health of United States R15GM157708-01NIGMS NIH HHS R15 GM157708
6 · The paper itself

Abstract

One of the biggest challenges to eukaryotic gene expression is coordinating transcription in the nucleus and protein synthesis in the cytoplasm. However, little is known about how these major steps in gene expression are connected. The Target of Rapamycin (TOR) signaling pathway is crucial in connecting these critical phases of gene expression. Highly conserved among eukaryotic cells, TOR regulates growth, metabolism, and cellular equilibrium in response to changes in nutrients, energy levels, and stress conditions. This review examines the extensive role of TOR in gene expression regulation. We highlight how TOR is involved in phosphorylation, remodeling chromatin structure, and managing the factors that facilitate transcription and translation. Furthermore, the critical functions of TOR extend to processing RNA, assembling RNA-protein complexes, and managing their export from the nucleus, demonstrating its wide-reaching impact throughout the cell. Our discussion emphasizes the integral roles of TOR in bridging the processes of transcription and translation and explores how it orchestrates these complex cellular processes.

Indexed as

EukaryotaEukaryotic CellsProtein BiosynthesisTOR Serine-Threonine KinasesTranscription, GeneticAnimalsGene Expression RegulationHumansPhosphorylationSignal TransductionTOR Serine-Threonine KinasesmRNA turnoverribosome biogenesisRNA exportRNA processingstress responseTORtranscriptiontranslation

Identifiers

PMID40243440
PMCPMC11989106

What OpenQuestion holds

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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.