4.8 Article

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

期刊

BMC BIOLOGY
卷 19, 期 1, 页码 -

出版社

BMC
DOI: 10.1186/s12915-021-01035-y

关键词

Single-cell amplified genome; Evolution; Mitochondrial ribosome; Phylogeny

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资金

  1. Czech Grant Agency [20-07186S]
  2. ERC CZ [LL1601]
  3. ERD funds of the Czech Ministry of Education [16_019/0000759]
  4. Royal Society University Research Fellowship [URF\R\191005]
  5. project e-Infrastruktura CZ [LM2018140]

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The study sequenced and assembled 20 euglenozoan single-cell amplified genomes, identifying three in kinetoplastids, 14 in diplonemids, one in euglenids, and two potentially branching as early-branching euglenozoans. Notably, two of the genomes contained unique features such as full-length rns and rnl genes, multiple mitoribosomal genes, and nad11, suggesting ancestral mitochondrial characteristics.
Background The 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. Results We 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. Conclusions Our 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.

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