期刊论文详细信息
BMC Biology
Fragmentation in mitochondrial genomes in relation to elevated sequence divergence and extreme rearrangements
Vaclav Stejskal1  George Opit2  Zhihong Li3  Shiqian Feng4  Renfu Shao5  Damian K. Dowling6  Andrea Pozzi6  Qianqian Yang7 
[1] Crop Research Institute, Drnovská 507, 161 06, Prague, Czech Republic;Faculty of Agrobiology, Food and Natural Resources, Czech University of Life Sciences, Kamycka 129, 165 00, Prague, Czech Republic;Department of Entomology and Plant Pathology, Oklahoma State University, 74078, Oklahoma, USA;Department of Plant Biosecurity, College of Plant Protection, China Agricultural University, 100193, Beijing, China;Department of Plant Biosecurity, College of Plant Protection, China Agricultural University, 100193, Beijing, China;School of Biological Sciences, Monash University, 3800, Clayton, VIC, Australia;GeneCology Research Centre, Centre for Animal Health Innovation, School of Science and Engineering, University of the Sunshine Coast, 4556, Maroochydore DC, Queensland, Australia;School of Biological Sciences, Monash University, 3800, Clayton, VIC, Australia;Zhejiang Provincial Key Laboratory of Biometrology and Inspection & Quarantine, College of Life Sciences, China Jiliang University, 310018, Hangzhou, China;
关键词: Mitochondrial genome;    Booklice;    Fragmentation;    Rearrangement;    Recombination;    Evolution;   
DOI  :  10.1186/s12915-021-01218-7
来源: Springer
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【 摘 要 】

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.

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