Evidence map›Paper›PMID 27436287›Full record

ArticleNucleic acids research2016

Length heterogeneity at conserved sequence block 2 in human mitochondrial DNA acts as a rheostat for RNA polymerase POLRMT activity.

Benedict G Tan, Frederick C Wellesley, Nigel J Savery, Mark D Szczelkun

Abstract read
In one paragraph

Article in Nucleic acids research, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing 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

20 citing papers in PubMed.

  1. Mechanisms and regulation of human mitochondrial transcription.Nature reviews. Molecular cell biology · 2024
    Review
  2. Article
  3. Article
  4. Article
  5. Nuclear genetic control of mtDNA copy number and heteroplasmy in humans.medRxiv : the preprint server for health sciences · 2023
    Article
  6. Mitochondrial DNAFrontiers in ophthalmology · 2023
    Article
  7. Article
  8. Spectroscopic Characterization of Mitochondrial G-Quadruplexes.International journal of molecular sciences · 2022
    Article
  9. To Be a Champion of the 24-h Ultramarathon Race. If Not the Heart ... Mosaic Theory?International journal of environmental research and public health · 2021
    Article
  10. High expression of theJournal of gastrointestinal oncology · 2020
    Article
  11. Article
  12. Mitochondrial Genetic Drift after Nuclear Transfer in Oocytes.International journal of molecular sciences · 2020
    Review
  13. Article
  14. Article
  15. Article
  16. Article
  17. Structural basis of mitochondrial transcription.Nature structural & molecular biology · 2018
    Review
  18. Article
  19. Mitochondrial DNA replication: a PrimPol perspective.Biochemical Society transactions · 2017
    Review
  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

4 authors.

Benedict G TanDNA-Protein Interactions Unit, School of Biochemistry, University of Bristol, Bristol BS8 1TD, UK.
Frederick C WellesleyDNA-Protein Interactions Unit, School of Biochemistry, University of Bristol, Bristol BS8 1TD, UK.
Nigel J SaveryDNA-Protein Interactions Unit, School of Biochemistry, University of Bristol, Bristol BS8 1TD, UK n.j.savery@bristol.ac.uk.
Mark D SzczelkunDNA-Protein Interactions Unit, School of Biochemistry, University of Bristol, Bristol BS8 1TD, UK mark.szczelkun@bristol.ac.uk.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The guanine (G)-tract of conserved sequence block 2 (CSB 2) in human mitochondrial DNA can result in transcription termination due to formation of a hybrid G-quadruplex between the nascent RNA and the nontemplate DNA strand. This structure can then influence genome replication, stability and localization. Here we surveyed the frequency of variation in sequence identity and length at CSB 2 amongst human mitochondrial genomes and used in vitro transcription to assess the effects of this length heterogeneity on the activity of the mitochondrial RNA polymerase, POLRMT. In general, increased G-tract length correlated with increased termination levels. However, variation in the population favoured CSB 2 sequences which produced efficient termination while particularly weak or strong signals were avoided. For all variants examined, the 3' end of the transcripts mapped to the same downstream sequences and were prevented from terminating by addition of the transcription factor TEFM. We propose that CSB 2 length heterogeneity allows variation in the efficiency of transcription termination without affecting the position of the products or the capacity for regulation by TEFM.

Indexed as

AdenineBase SequenceConserved SequenceDNA-Directed RNA PolymerasesDNA, MitochondrialGenome, MitochondrialG-QuadruplexesHumansMitochondrial ProteinsOpen Reading FramesPromoter Regions, GeneticTranscription FactorsTranscription Termination, GeneticAdenineDNA-Directed RNA PolymerasesDNA, MitochondrialMitochondrial ProteinsPOLRMT protein, humanTEFM protein, humanTranscription Factors

Identifiers

PMID27436287
PMCPMC5027508

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.