Evidence map›Paper›PMID 34001130›Full record

ArticleBMC biology2021

Single-cell genomics unveils a canonical origin of the diverse mitochondrial genomes of euglenozoans.

Kristína Záhonová, Gordon Lax, Savar D Sinha, Guy Leonard, Thomas A Richards, Julius Lukeš, Jeremy G Wideman

Open access · goldAbstract read
In one paragraph

Article in BMC biology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
1.2field-weighted citation impact, top 21% 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

12 citing papers in PubMed, 21 citations in OpenAlex.

  1. Article
  2. Assembly and Annotation of Kinetoplastid and Diplonemid Mitochondrial Genomes.Methods in molecular biology (Clifton, N.J.) · 2026
    Article
  3. Euglenid Extrachromosomal DNA: Assembly and Annotation.Methods in molecular biology (Clifton, N.J.) · 2026
    Article
  4. Article
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  11. Mitochondrial RNA editing inComputational and structural biotechnology journal · 2022
    Article
  12. 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

7 authors at 5 institutions in 5 countries.

Kristína ZáhonováInstitute of Parasitology, Biology Centre, Czech Academy of Sciences, České Budějovice (Budweis), Czech Republic.
Gordon LaxDepartment of Botany, University of British Columbia, Vancouver, Canada.
Savar D SinhaCenter for Mechanisms of Evolution, Biodesign Institute, School of Life Sciences, Arizona State University, Tempe, USA.
Guy LeonardDepartment of Zoology, University of Oxford, Oxford, UK.
Thomas A RichardsDepartment of Zoology, University of Oxford, Oxford, UK.
Julius LukešInstitute of Parasitology, Biology Centre, Czech Academy of Sciences, České Budějovice (Budweis), Czech Republic. jula@paru.cas.cz.
Jeremy G WidemanCenter for Mechanisms of Evolution, Biodesign Institute, School of Life Sciences, Arizona State University, Tempe, USA. jeremy.wideman@asu.edu.ORCID 0000-0002-4426-9533
Arizona State University · USUniversity of Oxford · GBCharles University · CZSewanee: The University of the South · USUniversity of British Columbia · CA

Funding

Czech Ministry of Education 16_019/0000759Grantová Agentura České Republiky 20-07186SMinisterstvo Školství, Mládeže a Tělovýchovy ERC CZ LL1601Royal Society URF\R\191005
6 · The paper itself

Abstract

backgroundThe supergroup Euglenozoa unites heterotrophic flagellates from three major clades, kinetoplastids, diplonemids, and euglenids, each of which exhibits extremely divergent mitochondrial characteristics. Mitochondrial genomes (mtDNAs) of euglenids comprise multiple linear chromosomes carrying single genes, whereas mitochondrial chromosomes are circular non-catenated in diplonemids, but circular and catenated in kinetoplastids. In diplonemids and kinetoplastids, mitochondrial mRNAs require extensive and diverse editing and/or trans-splicing to produce mature transcripts. All known euglenozoan mtDNAs exhibit extremely short mitochondrial small (rns) and large (rnl) subunit rRNA genes, and absence of tRNA genes. How these features evolved from an ancestral bacteria-like circular mitochondrial genome remains unanswered.

resultsWe sequenced and assembled 20 euglenozoan single-cell amplified genomes (SAGs). In our phylogenetic and phylogenomic analyses, three SAGs were placed within kinetoplastids, 14 within diplonemids, one (EU2) within euglenids, and two SAGs with nearly identical small subunit rRNA gene (18S) sequences (EU17/18) branched as either a basal lineage of euglenids, or as a sister to all euglenozoans. Near-complete mitochondrial genomes were identified in EU2 and EU17/18. Surprisingly, both EU2 and EU17/18 mitochondrial contigs contained multiple genes and one tRNA gene. Furthermore, EU17/18 mtDNA possessed several features unique among euglenozoans including full-length rns and rnl genes, six mitoribosomal genes, and nad11, all likely on a single chromosome.

conclusionsOur data strongly suggest that EU17/18 is an early-branching euglenozoan with numerous ancestral mitochondrial features. Collectively these data contribute to untangling the early evolution of euglenozoan mitochondria.

Indexed as

EuglenidaGenome, MitochondrialDNA, MitochondrialEuglenozoaEuropiumGenomicsPhylogenyRNA, TransferDNA, MitochondrialEuropiumRNA, TransferEvolutionMitochondrial ribosomePhylogenySingle-cell amplified genome

Identifiers

PMID34001130
PMCPMC8130358
OpenAlexW3160045500

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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.