Evidence map›Paper›PMID 36449697›Full record

ReviewFEMS microbiology reviews2023

Mitochondrial genome maintenance-the kinetoplast story.

Simona Amodeo, Irina Bregy, Torsten Ochsenreiter

Open access · hybridAbstract readReview
In one paragraph

Review in FEMS microbiology reviews, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
4.5field-weighted citation impact, top 4% 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

18 citing papers in PubMed, 34 citations in OpenAlex.

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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

3 authors at 1 institution in 1 country.

Simona AmodeoInstitute of Cell Biology, University of Bern, Baltzerstrasse 4, 3012 Bern, Switzerland.
Irina BregyInstitute of Cell Biology, University of Bern, Baltzerstrasse 4, 3012 Bern, Switzerland.
Torsten OchsenreiterInstitute of Cell Biology, University of Bern, Baltzerstrasse 4, 3012 Bern, Switzerland.ORCID 0000-0002-8846-8526
University of Bern · CH

Funding

Swiss National Science Foundation 177096
6 · The paper itself

Abstract

Mitochondrial DNA replication is an essential process in most eukaryotes. Similar to the diversity in mitochondrial genome size and organization in the different eukaryotic supergroups, there is considerable diversity in the replication process of the mitochondrial DNA. In this review, we summarize the current knowledge of mitochondrial DNA replication and the associated factors in trypanosomes with a focus on Trypanosoma brucei, and provide a new model of minicircle replication for this protozoan parasite. The model assumes the mitochondrial DNA (kinetoplast DNA, kDNA) of T. brucei to be loosely diploid in nature and the replication of the genome to occur at two replication centers at the opposing ends of the kDNA disc (also known as antipodal sites, APS). The new model is consistent with the localization of most replication factors and in contrast to the current model, it does not require the assumption of an unknown sorting and transport complex moving freshly replicated DNA to the APS. In combination with the previously proposed sexual stages of the parasite in the insect vector, the new model provides a mechanism for maintenance of the mitochondrial genetic diversity.

Indexed as

DNA, KinetoplastGenome, MitochondrialDNA, MitochondrialDNA ReplicationMitochondriaProtozoan ProteinsDNA, KinetoplastDNA, MitochondrialProtozoan ProteinskDNAkinetoplastmitochondrial DNAmitochondrial DNA replicationtrypanosomes

Identifiers

PMID36449697
PMCPMC10719067
OpenAlexW4310571525

What Socratic holds

Textmetadata
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 Socratic graph.