Evidence map›Paper›PMID 29248739›Full record

ReviewBiochimica et biophysica acta. Gene regulatory mechanisms2018

Maf1 phenotypes and cell physiology.

Ian M Willis

Abstract readReview
In one paragraph

Review in Biochimica et biophysica acta. Gene regulatory mechanisms, 2018. 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
1.1field-weighted citation impact, top 22% 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, 28 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Article
  5. Article
  6. Article
  7. RNA Polymerases I and III in development and disease.Seminars in cell & developmental biology · 2023
    Review
  8. Article
  9. Review
  10. Article
  11. Article
  12. Article
  13. Activation and repression at the heart of human RNA polymerase III.Nature structural & molecular biology · 2021
    Article
  14. Article
  15. Article
  16. Article
  17. Metabolic programming a lean phenotype by deregulation of RNA polymerase III.Proceedings of the National Academy of Sciences of the United States of America · 2018
    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

1 author at 1 institution in 1 country.

Ian M WillisDepartments of Biochemistry and Systems and Computational Biology, Albert Einstein College of Medicine, Bronx, NY, USA. Electronic address: ian.willis@einstein.yu.edu.
Albert Einstein College of Medicine · US

Funding

Translational Research CoreP30DK020541 · NIDDK · ALBERT EINSTEIN COLLEGE OF MEDICINE, INC · PI STREAMSON C CHUA · 2015 to 2026
$27.7M
Special Animal CoreP30DK041296 · NIDDK · YESHIVA UNIVERSITY · PI GUPTA, SANJEEV · 1989 to 2018
$22.9M
MAF1 Function and Metabolic InefficiencyR01GM120358 · NIGMS · ALBERT EINSTEIN COLLEGE OF MEDICINE, INC · PI WILLIS, IAN M · 2016 to 2019
$2.2M
NIDDK NIH HHS P30 DK020541NIDDK NIH HHS P30 DK041296NIGMS NIH HHS R01 GM120358
6 · The paper itself

Abstract

As a master regulator of transcription by RNA polymerase (Pol) III, Maf1 represses the synthesis of highly abundant non-coding RNAs as anabolic signals dissipate, as the quality or quantity of nutrients decreases, and under a wide range of cellular and environmental stress conditions. Thus, Maf1 responds to changes in cell physiology to conserve metabolic energy and to help maintain appropriate levels of tRNAs and other essential non-coding RNAs. Studies in different model organisms and cell-based systems show that perturbations of Maf1 can also impact cell physiology and metabolism. These effects are mediated by changes in Pol III transcription and/or by effects of Maf1 on the expression of select Pol II-transcribed genes. Maf1 phenotypes can vary between different systems and are sometimes conflicting as in comparisons between Maf1 KO mice and cultured mammalian cells. These studies are reviewed in an effort to better appreciate the relationship between Maf1 function and cell physiology. This article is part of a Special Issue entitled: SI: Regulation of tRNA synthesis and modification in physiological conditions and disease edited by Dr. Boguta Magdalena.

Indexed as

Transcription, GeneticAnimalsCaenorhabditis elegans ProteinsEnergy MetabolismGene Expression RegulationGene Expression Regulation, FungalGluconeogenesisMafB Transcription FactorMammalsMiceMice, KnockoutMitochondriaModels, MolecularPhenotypeProtein ConformationRepressor ProteinsCaenorhabditis elegans ProteinsMaf1 protein, mouseMAF1 protein, S cerevisiaeMafB Transcription FactorRepressor ProteinsRNA Polymerase IIISaccharomyces cerevisiae ProteinsTranscription Factorscancerfutile cycleMaf1metabolismRNA polymerase IIItumor suppressor

Identifiers

PMID29248739
PMCPMC5882558
OpenAlexW2771271057

What OpenQuestion holds

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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.