A mitochondrion-like ribosome in an insect endosymbiont

Abstract

Understanding how the mitochondrion evolved from a bacterial endosymbiont to an organelle is obscured by time and a lack of comparative examples. It is clear that mitochondrial ribosomes are derived from bacterial ribosomes, but it is unclear whether the baroque and idiosyncratic structural changes seen in mitochondrial ribosomes are specifically driven by mitochondrial evolution or simply reflect the syndrome of being a long-term endosymbiont. Here we show that two of the most characteristic features of mitochondrial ribosomes--the acquisition of host proteins and alterations to specific structural regions--are shared by Hodgkinia, an ancient bacterial endosymbiont of cicadas. These results imply that many of the striking changes observed in mitochondrial ribosomes result from their common ancestry as bacterial endosymbionts rather than their uniqueness as mitochondria.

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BibTeX

@misc{fernandez2026mitochondrionlike,
  title = {{A mitochondrion-like ribosome in an insect endosymbiont}},
  author = {Israel S Fernandez and Jessica Warren and Justs Nwachukwu and Dewight Williams and Amaia Gonzalez-Magana and Noa Spencer and John McCutcheon},
  howpublished = {bioRxiv},
  year = {2026},
  month = oct,
  doi = {10.64898/2026.10.18.759926},
  url = {https://www.biorxiv.org/content/10.64898/2026.10.18.759926v1},
  note = {CC BY},
}

RIS

TY  - UNPB
TI  - A mitochondrion-like ribosome in an insect endosymbiont
AU  - Israel S Fernandez
AU  - Jessica Warren
AU  - Justs Nwachukwu
AU  - Dewight Williams
AU  - Amaia Gonzalez-Magana
AU  - Noa Spencer
AU  - John McCutcheon
PY  - 2026
DA  - 2026/10/18
PB  - bioRxiv
DO  - 10.64898/2026.10.18.759926
UR  - https://www.biorxiv.org/content/10.64898/2026.10.18.759926v1
AB  - Understanding how the mitochondrion evolved from a bacterial endosymbiont to an organelle is obscured by time and a lack of comparative examples. It is clear that mitochondrial ribosomes are derived from bacterial ribosomes, but it is unclear whether the baroque and idiosyncratic structural changes seen in mitochondrial ribosomes are specifically driven by mitochondrial evolution or simply reflect the syndrome of being a long-term endosymbiont. Here we show that two of the most characteristic features of mitochondrial ribosomes--the acquisition of host proteins and alterations to specific structural regions--are shared by Hodgkinia, an ancient bacterial endosymbiont of cicadas. These results imply that many of the striking changes observed in mitochondrial ribosomes result from their common ancestry as bacterial endosymbionts rather than their uniqueness as mitochondria.
SN  - 2692-8205
ER  -

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