Evidence map›Paper›PMID 34996453›Full record

ArticleBMC biology2022

Fragmentation in mitochondrial genomes in relation to elevated sequence divergence and extreme rearrangements.

Shiqian Feng, Andrea Pozzi, Vaclav Stejskal, George Opit, Qianqian Yang, Renfu Shao, Damian K Dowling, Zhihong Li

Open access · goldAbstract read
In one paragraph

Article in BMC biology, 2022. 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
1.6field-weighted citation impact, top 18% 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, 20 citations in OpenAlex.

  1. Article
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  5. Review
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  10. Article
  11. A Novel Mitochondrial Genome Fragmentation Pattern in the Buffalo LouseInternational journal of molecular sciences · 2022
    Article
  12. Human pediculosis, a global public health problem.Infectious diseases of poverty · 2022
    Review
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 6 institutions in 4 countries.

Shiqian Feng *Department of Plant Biosecurity, College of Plant Protection, China Agricultural University, Beijing, 100193, China.
Andrea Pozzi *School of Biological Sciences, Monash University, Clayton, VIC, 3800, Australia.
Vaclav StejskalCrop Research Institute, Drnovská 507, 161 06, Prague, Czech Republic.
George OpitDepartment of Entomology and Plant Pathology, Oklahoma State University, Oklahoma, 74078, USA.
Qianqian YangZhejiang Provincial Key Laboratory of Biometrology and Inspection & Quarantine, College of Life Sciences, China Jiliang University, Hangzhou, 310018, China.
Renfu ShaoGeneCology Research Centre, Centre for Animal Health Innovation, School of Science and Engineering, University of the Sunshine Coast, Maroochydore DC, Queensland, 4556, Australia.
Damian K Dowling *School of Biological Sciences, Monash University, Clayton, VIC, 3800, Australia.
Zhihong Li *Department of Plant Biosecurity, College of Plant Protection, China Agricultural University, Beijing, 100193, China. lizh@cau.edu.cn.ORCID 0000-0002-1281-2108
China Agricultural University · CNMonash University · AUChina Jiliang University · CNCzech Agrifood Research Center · CZOklahoma State University · USUniversity of the Sunshine Coast · AU

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundA single circular mitochondrial (mt) genome is a common feature across most metazoans. The mt-genome includes protein-coding genes involved in oxidative phosphorylation, as well as RNAs necessary for translation of mt-RNAs, whose order and number are highly conserved across animal clades, with few known exceptions of alternative mt-gene order or mt-genome architectures. One such exception consists of the fragmented mitochondrial genome, a type of genome architecture where mt-genes are split across two or more mt-chromosomes. However, the origins of mt-genome fragmentation and its effects on mt-genome evolution are unknown. Here, we investigate these origin and potential mechanisms underlying mt-genome fragmentation, focusing on a genus of booklice, Liposcelis, which exhibits elevated sequence divergence, frequent rearrangement of mt-gene order, and fragmentation of the mt genome, and compare them to other Metazoan clades.

resultsWe found this genus Liposcelis exhibits very low conservation of mt-gene order across species, relative to other metazoans. Levels of gene order rearrangement were, however, unrelated to whether or not mt-genomes were fragmented or intact, suggesting mitochondrial genome fragmentation is not affecting mt-gene order directly. We further investigated possible mechanisms underpinning these patterns and revealed very high conservation of non-coding sequences at the edges of multiple recombination regions across populations of one particular Liposcelis species, supportive of a hypothesis that mt-fragmentation arises from recombination errors between mt-genome copies. We propose these errors may arise as a consequence of a heightened mutation rate in clades exhibiting mt-fragmentation. Consistent with this, we observed a striking pattern across three Metazoan phyla (Arthropoda, Nematoda, Cnidaria) characterised by members exhibiting high levels of mt-gene order rearrangement and cases of mt-fragmentation, whereby the mt-genomes of species more closely related to species with fragmented mt-genomes diverge more rapidly despite experiencing strong purifying selection.

conclusionsWe showed that contrary to expectations, mt-genome fragmentation is not correlated with the increase in mt-genome rearrangements. Furthermore, we present evidence that fragmentation of the mt-genome may be part of a general relaxation of a natural selection on the mt-genome, thus providing new insights into the origins of mt-genome fragmentation and evolution.

Indexed as

Genome, MitochondrialAnimalsEvolution, MolecularGene OrderGene RearrangementGenes, MitochondrialPhylogenyBookliceEvolutionFragmentationMitochondrial genomeRearrangementRecombination

Identifiers

PMID34996453
PMCPMC8742463
OpenAlexW4205734308

What OpenQuestion holds

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LicenceCC BY
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Registered trials

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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.