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Recent advances in isolating cells based on visual phenotypes have transformed our ability to identify the mechanisms and consequences of complex traits. Micronucleus (MN) formation is a frequent outcome of genome instability, triggers extensive changes in genome structure and signaling coincident with MN rupture, and is almost exclusively defined by visual analysis. Automated MN detection in microscopy images has proved challenging, limiting discovery of the mechanisms and consequences of MN. In this study we describe two new MN segmentation modules: a rapid model for classifying micronucleated cells and their rupture status (VCS MN), and a robust model for accurate MN segmentation (MNFinder) from a broad range of cell lines. As proof-of-concept, we define the transcriptome of non-transformed human cells with intact or ruptured MN after chromosome missegregation by combining VCS MN with photoactivation-based cell isolation and RNASeq. Surprisingly, we find that neither MN formation nor rupture triggers a strong unique transcriptional response. Instead, transcriptional changes appear correlated with small increases in aneuploidy in these cell classes. Our MN segmentation modules overcome a significant challenge with reproducible MN quantification, and, joined with visual cell sorting, enable the application of powerful functional genomics assays to a wide-range of questions in MN biology.
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http://dx.doi.org/10.7554/eLife.101579 | DOI Listing |
Methods Mol Biol
August 2025
Institute of Molecular Biology, Mainz, Germany.
A hallmark consequence of errors in mitosis is the generation of aberrant nuclear structures, such as micronuclei and chromosome bridges, which have long been associated with disease like cancer. Groundbreaking recent work showed that whole chromosomes or chromosome segments that transit through such structures can accumulate severe rearrangements and thus contribute to the evolution of complex genetic structural events, collectively called "chromoanagenesis". Despite strong interest in the field of genomic instability, a detailed mechanistic understanding of the choreography of transgenerational events that lead to chromoanagenesis is lacking.
View Article and Find Full Text PDFMethods Mol Biol
August 2025
Department of Toxicology, Institute of Pharmacology and Toxicology, University of Würzburg, Würzburg, Germany.
This chapter provides a brief overview about micronuclei and their postmitotic fate. Micronuclei are small chromatin-containing bodies formed during mitosis and located in the cytoplasm. Micronuclei have been known for more than 100 years and used as biomarkers for decades, but their fate after formation and with that their biological relevance for the organism has only been addressed in recent years.
View Article and Find Full Text PDFJ Oral Pathol Med
August 2025
Department of Biology, Hacettepe University, Faculty of Science, Ankara, Türkiye.
Background: Despite its widespread use in acne vulgaris treatment, the potential cytological and genotoxic effects of systemic isotretinoin on oral mucosal cells remain poorly understood. This study aimed to investigate the cytological and genotoxic effects of systemic isotretinoin on oral mucosal cells.
Methods: Buccal smear samples were collected from isotretinoin users (n = 20) and controls (n = 20).
Mutat Res Genet Toxicol Environ Mutagen
July 2025
Aydın Adnan Menderes University, Faculty of Science, Department of Biology, B Block, Central Campus, Aydın 09010, Türkiye. Electronic address:
Objective: This study aimed to assess the genotoxic effects of chronic occupational exposure to low-dose ionizing radiation among healthcare professionals employed at three hospitals in Aydın, Turkey: Aydın Adnan Menderes University Research and Application Hospital (ADU-UAH), Atatürk State Hospital, and Aydın State Hospital. The exposed group comprised 27 healthcare workers routinely operating in radiation-related departments, while 27 matched individuals with no known exposure constituted the control group.
Methods: Genetic damage was evaluated using the exfoliated buccal micronucleus cytome (BMCyt) assay, a validated and non-invasive method for human biomonitoring.
Nature
August 2025
Computational Oncology, Department of Epidemiology and Biostatistics, Memorial Sloan Kettering Cancer Center, New York, NY, USA.
Whole-genome doubling (WGD) is a common feature of human cancers and is linked to tumour progression, drug resistance, and metastasis. Here we examine the impact of WGD on somatic evolution and immune evasion at single-cell resolution in patient tumours. Using single-cell whole-genome sequencing, we analysed 70 high-grade serous ovarian cancer samples from 41 patients (30,260 tumour genomes) and observed near-ubiquitous evidence that WGD is an ongoing mutational process.
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