Evidence map›Paper›PMID 25183523›Full record

ArticleNucleic acids research2014

Yeast mitochondrial RNAP conformational changes are regulated by interactions with the mitochondrial transcription factor.

Srdja Drakulic, Liping Wang, Jorge Cuéllar, Qing Guo, Gilberto Velázquez, Jaime Martín-Benito, Rui Sousa, José M Valpuesta

Open access · goldAbstract read
In one paragraph

Article in Nucleic acids research, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
0.3field-weighted citation impact, top 40% 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

4 citing papers in PubMed, 8 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. 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

8 authors at 2 institutions in 2 countries.

Srdja DrakulicDepartment for Macromolecular Structures, Centro Nacional de Biotecnología (CNB-CSIC), Madrid 28049, Spain.
Liping WangDepartment of Biochemistry, University of Texas Health Science Center, San Antonio, Texas, TX 78229-3900, USA.
Jorge CuéllarDepartment for Macromolecular Structures, Centro Nacional de Biotecnología (CNB-CSIC), Madrid 28049, Spain.
Qing GuoDepartment of Biochemistry, University of Texas Health Science Center, San Antonio, Texas, TX 78229-3900, USA.
Gilberto VelázquezDepartment of Biochemistry, University of Texas Health Science Center, San Antonio, Texas, TX 78229-3900, USA.
Jaime Martín-BenitoDepartment for Macromolecular Structures, Centro Nacional de Biotecnología (CNB-CSIC), Madrid 28049, Spain.
Rui SousaDepartment of Biochemistry, University of Texas Health Science Center, San Antonio, Texas, TX 78229-3900, USA sousa@biochem.uthscsa.edu.
José M ValpuestaDepartment for Macromolecular Structures, Centro Nacional de Biotecnología (CNB-CSIC), Madrid 28049, Spain jmv@cnb.csic.es.
Centro Nacional de Biotecnología · ESThe University of Texas Health Science Center at San Antonio · US

Funding

STRUCTURE/FUNCTION STUDIES OF T7 RNA POLYMERASER01GM052522 · NIGMS · UNIVERSITY OF TEXAS HLTH SCIENCE CENTER · PI SOUSA, RUI J. · 1995 to 2012
$3.6M
NIGMS NIH HHS GM0502552NIGMS NIH HHS R01 GM052522
6 · The paper itself

Abstract

Mitochondrial RNA polymerases (MtRNAPs) are members of the single-subunit RNAP family, the most well-characterized member being the RNAP from T7 bacteriophage. MtRNAPs are, however, functionally distinct in that they depend on one or more transcription factors to recognize and open the promoter and initiate transcription, while the phage RNAPs are capable of performing these tasks alone. Since the transcriptional mechanisms that are conserved in phage and mitochondrial RNAPs have been so effectively characterized in the phage enzymes, outstanding structure-mechanism questions concern those aspects that are distinct in the MtRNAPs, particularly the role of the mitochondrial transcription factor(s). To address these questions we have used both negative staining and cryo-EM to generate three-dimensional reconstructions of yeast MtRNAP initiation complexes with and without the mitochondrial transcription factor (MTF1), and of the elongation complex. Together with biochemical experiments, these data indicate that MTF1 uses multiple mechanisms to drive promoter opening, and that its interactions with the MtRNAP regulate the conformational changes undergone by the latter enzyme as it traverses the template strand.

Indexed as

Transcription Initiation, GeneticDNADNA-Binding ProteinsDNA-Directed RNA PolymerasesFungal ProteinsMitochondriaMitochondrial ProteinsModels, MolecularPromoter Regions, GeneticProtein ConformationTranscription Elongation, GeneticTranscription FactorsYeastsDNADNA-Binding ProteinsDNA-Directed RNA PolymerasesFungal ProteinsMitochondrial Proteinsmitochondrial transcription factor ATranscription Factors

Identifiers

PMID25183523
PMCPMC4176174
OpenAlexW2088934006

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.