Adult muscle stem cells (MuSCs), also called satellite cells, are situated under the basal lamina of myofibers in skeletal muscles. MuSCs are instrumental for postnatal muscle growth and regeneration of skeletal muscles. Under physiological conditions, the majority of MuSCs is actively maintained in a quiescent state but becomes rapidly activated during muscle regeneration, which is accompanied with massive changes in the epigenome. Moreover, aging, but also pathological conditions, such as in muscle dystrophy, results in profound changes of the epigenome, which can be monitored with different approaches. However, a better understanding of the role of chromatin dynamics in MuSCs and its function for skeletal muscle physiology and disease has been hampered by technical limitations, mostly due to the relatively low number of MuSCs but also due to the strongly condensed chromatin state of quiescent MuSCs. Traditional chromatin immunoprecipitation (ChIP) usually requires large amounts of cells and has several other shortcomings. Cleavage Under Targets and Release Using Nuclease (CUT&RUN) is a simple alternative to ChIP for chromatin profiling, providing higher efficiency and better resolution at lower costs. CUT&RUN maps genome-wide chromatin features, including genome-wide localization of transcription factor binding in small numbers of freshly isolated MuSCs, facilitating analysis of different subpopulations of MuSCs. Here we describe an optimized protocol to profile global chromatin in freshly isolated MuSCs using CUT&RUN.
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http://dx.doi.org/10.1007/978-1-0716-3036-5_28 | DOI Listing |
New Phytol
January 2025
Leibniz Institute of Plant Genetics and Crop Plant Research Gatersleben, Corrensstrasse 3, 06466, Seeland, Germany.
The epigenetic state of chromatin, gene activity and chromosomal positions are interrelated in plants. In Arabidopsis thaliana, chromosome arms are DNA-hypomethylated and enriched with the euchromatin-specific histone mark H3K4me3, while pericentromeric regions are DNA-hypermethylated and enriched with the heterochromatin-specific mark H3K9me2. We aimed to investigate how the chromosomal location affects epigenetic stability and gene expression by chromosome engineering.
View Article and Find Full Text PDFEpstein-Barr virus (EBV) contributes to ~1.5% of human cancers, including lymphomas, gastric and nasopharyngeal carcinomas. In most of these, nearly 80 viral lytic genes are silenced by incompletely understood epigenetic mechanisms, precluding use of antiviral agents such as ganciclovir to treat the 200,000 EBV-associated cancers/year.
View Article and Find Full Text PDFCommun Biol
January 2025
Université Paris Cité, CNRS, Inserm, Institut Cochin, F-75014, Paris, France.
The H3K79 methyltransferase DOT1L is essential for multiple aspects of mammalian development where it has been shown to regulate gene expression. Here, by producing and integrating epigenomic and spike-in RNA-seq data, we decipher the molecular role of DOT1L during mouse spermatogenesis and show that it has opposite effects on gene expression depending on chromatin environment. On one hand, DOT1L represses autosomal genes that are devoid of H3K79me2 at their bodies and located in H3K27me3-rich/H3K27ac-poor environments.
View Article and Find Full Text PDFLife Med
April 2024
State Key Laboratory of Pharmaceutical Biotechnology, School of Life Sciences, Nanjing University, Nanjing 210023, China.
Awareness of estrogen's effects on health is broadening rapidly. The effects of long-term high levels of estrogen on the body involve multiple organs. Here, we used both single-cell chromatin accessibility and RNA sequencing data to analyze the potential effect of estrogen on major organs.
View Article and Find Full Text PDFAttention-deficit/hyperactivity disorder (ADHD) is a highly heritable neurodevelopmental disorder, but its genetic architecture remains incompletely characterized. Rare coding variants, which can profoundly impact gene function, represent an underexplored dimension of ADHD risk. In this study, we analyzed large-scale DNA sequencing datasets from ancestrally diverse cohorts and observed significant enrichment of rare protein-truncating and deleterious missense variants in highly evolutionarily constrained genes.
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