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Sirey, T. M.

Publications and source records attributed to Sirey, T. M..

2 recordsLinked to original sources

Systematic morphological profiling of human and mouse miRNAs in 24M single cells

MicroRNAs (miRNAs) are post-transcriptional regulators of gene expression whose contributions to cell biology remain underexplored. Here, we used Cell Painting to quantify the morphological effect of 2,565 human and 1,900 mouse miRNA mimics on 24 million cells across five cell lines. To do so, we developed a novel single-cell morphological profiling analysis framework, involving stringent batch correction, feature selection, and hit calling. With this, we discovered that 9% of human and 15% of mouse miRNA mimics significantly alter cell morphology in at least one cell line. Eighteen miRNAs caused significant changes in multiple cell lines, including eight orthologous miRNAs that altered morphology in both human and mouse cells. Among the replicating miRNAs were human and mouse miR-155-5p, which affected morphology in at least one replicate of four cell lines. As expected, miRNAs with identical seed sequences induced more similar morphological changes than miRNAs with different seeds. Also, morphological changes were associated with cytotoxicity and annotation confidence. This comprehensive single-cell morphological resource will help elucidate the cellular functions of human and mouse miRNAs.

genomics↗

Cerox1 and microRNA-488-3p noncoding RNAs jointly regulate mitochondrial complex I catalytic activity

To generate energy efficiently, the cell is uniquely challenged to co-ordinate the abundance of electron transport chain protein subunits expressed from both nuclear and mitochondrial genomes. How an effective stoichiometry of this many constituent subunits is co-ordinated post-transcriptionally remains poorly understood. Here we show that Cerox1, an unusually abundant cytoplasmic long noncoding RNA (lncRNA), modulates the levels of mitochondrial complex I subunit transcripts in a manner that requires binding to microRNA-488-3p. Increased abundance of Cerox1 cooperatively elevates complex I subunit protein abundance and enzymatic activity, decreases reactive oxygen species production, and protects against the complex I inhibitor rotenone. Cerox1 function is conserved across placental mammals: human and mouse orthologues effectively modulate complex I enzymatic activity in mouse and human cells, respectively. Cerox1 is the first lncRNA demonstrated, to our knowledge, to regulate mitochondrial oxidative phosphorylation (OXPHOS) and, with miR-488-3p, represent novel targets for the modulation of complex I activity.

biochemistry↗