Hansen Katja G, Baxter-Koenigs Autum, Weiss Caroline Am, McShane Erik, Churchman L Stirling
Department of Genetics, Blavatnik Institute, Harvard Medical School, Boston, MA, USA.
Department of Genetics, Blavatnik Institute, Harvard Medical School, Boston, MA, USA
Life Sci Alliance. 2025 Jun 16;8(9). doi: 10.26508/lsa.202403082. Print 2025 Sep.
Mitochondrial gene expression regulation is required for the biogenesis of oxidative phosphorylation (OXPHOS) complexes, yet the spatial organization of mitochondrial RNAs (mt-RNAs) remains unknown. Here, we investigated the spatial distribution of mt-RNAs during various cellular stresses using single-molecule RNA-FISH. We discovered that transcription inhibition leads to the formation of distinct RNA granules within mitochondria, which we term inhibition granules. These structures differ from canonical mitochondrial RNA granules and form in response to multiple transcription arrest conditions, including ethidium bromide treatment, specific inhibition or stalling of the mitochondrial RNA polymerase, and depletion of the SUV3 helicase. Inhibition granules appear to stabilize certain mt-mRNAs during prolonged transcription inhibition. This phenomenon coincides with an imbalance in OXPHOS complex expression, where mitochondrial-encoded transcripts decrease while nuclear-encoded subunits remain stable. We found that cells recover from transcription inhibition via resolving the granules, restarting transcription, and repopulating the mitochondrial network with mt-mRNAs within hours. We suggest that inhibition granules may act as a reservoir to help overcome OXPHOS imbalance during recovery from transcription arrest.
线粒体基因表达调控是氧化磷酸化(OXPHOS)复合体生物发生所必需的,但线粒体RNA(mt-RNA)的空间组织仍不清楚。在这里,我们使用单分子RNA-FISH研究了各种细胞应激过程中mt-RNA的空间分布。我们发现转录抑制会导致线粒体内形成独特的RNA颗粒,我们将其称为抑制颗粒。这些结构不同于典型的线粒体RNA颗粒,并且在多种转录停滞条件下形成,包括溴化乙锭处理、线粒体RNA聚合酶的特异性抑制或停滞以及SUV3解旋酶的耗竭。抑制颗粒似乎在长时间转录抑制期间稳定某些mt-mRNA。这种现象与OXPHOS复合体表达的失衡同时出现,即线粒体编码的转录本减少而核编码的亚基保持稳定。我们发现细胞通过在数小时内分解颗粒、重新启动转录并用mt-mRNA重新填充线粒体网络,从转录抑制中恢复。我们认为抑制颗粒可能作为一种储存库,有助于在从转录停滞中恢复的过程中克服OXPHOS失衡。