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- W2885287988 abstract "Understanding chromatin dynamics is essential to define the contribution of chromatin to heritable gene silencing and the long-term maintenance of gene expression. Here we present a detailed protocol for time-ChIP, a novel method to measure histone turnover at high resolution across long timescales. This method is based on the SNAP-tag, a self-labeling enzyme that can be pulse labeled with small molecules in cells. Upon pulse biotinylation of a cohort of SNAP-tagged histones we can determine their abundance and fate across a chase period using a biotin-specific chromatin pulldown followed by DNA sequencing or quantitative PCR. This method is unique in its ability to trace the long-term fate of a chromatin bound histone pool, genome wide. In addition to a step by step protocol, we outline advantages and limitations of the method in relation to other existing techniques. time-ChIP can define regions of high and low histone turnover and identify the location of pools of long lived histones." @default.
- W2885287988 created "2018-08-22" @default.
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- W2885287988 date "2018-01-01" @default.
- W2885287988 modified "2023-09-27" @default.
- W2885287988 title "time-ChIP: A Method to Determine Long-Term Locus-Specific Nucleosome Inheritance" @default.
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- W2885287988 doi "https://doi.org/10.1007/978-1-4939-8663-7_7" @default.
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