Abstract
The spatiotemporal organization of multiple components within biomolecular condensates helps coordinate gene expression. Mitochondria separate transcription and RNA processing into two distinct condensates: mt-nucleoids and mtRNA granules (MRGs), respectively. However, how mtRNA transcripts are transferred from mt-nucleoids to distant MRGs was unclear. With high-resolution imaging, we examined the steady-state organization of mt-condensates in human cells. We identified a wide distribution of distances between centroids of mt-condensates, from roughly a micron apart to within 100 nm of each other. Live imaging revealed that such organization was dynamic: mt-condensates frequently underwent cycles of mixing and demixing. Indeed, mtRNA transcripts and the mtRNA polymerase co-localized within mixed mt-condensates, while transcription inhibition led to complete dissolution of MRGs, supporting that nascently transcribed mtRNA is a key driver of mt-condensate organization. Together, our results show that active transcription sustains the phase coexistence between mt-nucleoids and MRGs, with implications for transcriptional condensates more broadly.
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Abstract
The spatiotemporal organization of multiple components within biomolecular condensates helps coordinate gene expression. Mitochondria separate transcription and RNA processing into two distinct condensates: mt-nucleoids and mtRNA granules (MRGs), respectively. However, how mtRNA transcripts are transferred from mt-nucleoids to distant MRGs was unclear. With high-resolution imaging, we examined the steady-state organization of mt-condensates in human cells. We identified a wide distribution of distances between centroids of mt-condensates, from roughly a micron apart to within 100 nm of each other. Live imaging revealed that such organization was dynamic: mt-condensates frequently underwent cycles of mixing and demixing. Indeed, mtRNA transcripts and the mtRNA polymerase co-localized within mixed mt-condensates, while transcription inhibition led to complete dissolution of MRGs, supporting that nascently transcribed mtRNA is a key driver of mt-condensate organization. Together, our results show that active transcription sustains the phase coexistence between mt-nucleoids and MRGs, with implications for transcriptional condensates more broadly.
Competing Interest Statement
The authors have declared no competing interest.
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