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Peer-reviewedCC BY 4.0PLoS Genetics

PLoS Genetics Issue Image | Vol. 22(1) October 2026

Abstract

Local heterogeneity of ATP levels within a heteroplasmic yeast zygote: A widefield fluorescence microscopy image of a heteroplasmic Saccharomyces cerevisiae zygote with its emerging daughter cell, expressing the mitochondrially targeted ratiometric ATP sensor mtQUEEN-2m, displayed as the pixel-wise 400 nm/480 nm excitation ratio. The wild-type parental cell was identified by cell-wall staining with concanavalin A–Alexa 633 prior to mating with a partner carrying mutant mtDNA. Although the parental mitochondrial networks fuse, ATP levels remain locally higher in the wild-type-derived network, suggesting that mitochondrial bioenergetics are not fully equilibrated and may locally reflect the quality of the underlying mitochondrial genome. Thoma et al. 2026

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BibTeX
@article{anon2026plos,
  title = {{PLoS Genetics Issue Image | Vol. 22(1) October 2026}},
  journal = {PLoS Genetics},
  year = {2026},
  month = oct,
  doi = {10.1371/image.pgen.v22.i01},
  url = {https://doi.org/10.1371/image.pgen.v22.i01},
  note = {CC BY 4.0},
}
RIS
TY  - JOUR
TI  - PLoS Genetics Issue Image | Vol. 22(1) October 2026
PY  - 2026
DA  - 2026/10/27
JO  - PLoS Genetics
DO  - 10.1371/image.pgen.v22.i01
UR  - https://doi.org/10.1371/image.pgen.v22.i01
AB  - Local heterogeneity of ATP levels within a heteroplasmic yeast zygote: A widefield fluorescence microscopy image of a heteroplasmic Saccharomyces cerevisiae zygote with its emerging daughter cell, expressing the mitochondrially targeted ratiometric ATP sensor mtQUEEN-2m, displayed as the pixel-wise 400 nm/480 nm excitation ratio. The wild-type parental cell was identified by cell-wall staining with concanavalin A–Alexa 633 prior to mating with a partner carrying mutant mtDNA. Although the parental mitochondrial networks fuse, ATP levels remain locally higher in the wild-type-derived network, suggesting that mitochondrial bioenergetics are not fully equilibrated and may locally reflect the quality of the underlying mitochondrial genome. Thoma et al. 2026
SN  - 1553-7404
ER  -