Cook April, Mieczkowski Jakub, Tolstorukov Michael Y
Department of Molecular Biology, Massachusetts General Hospital and Harvard Medical School, Boston, Massachusetts.
Current address: Dana-Farber Cancer Institute, Boston, Massachusetts.
Curr Protoc Mol Biol. 2017 Oct 2;120:21.34.1-21.34.18. doi: 10.1002/cpmb.45.
This unit describes a method for determining the accessibility of chromatinized DNA and nucleosome occupancy in the same assay. Enzymatic digestion of chromatin using micrococcal nuclease (MNase) is optimized for liberation, retrieval, and characterization of DNA fragments from chromatin. MNase digestion is performed in a titration series, and the DNA fragments are isolated and sequenced for each individual digest independently. These sequenced fragments are then collectively analyzed in a novel bioinformatics pipeline to produce a metric describing MNase accessibility of chromatin (MACC) and nucleosome occupancy. This approach allows profiling of the entire genome including regions of open and closed chromatin. Moreover, the MACC protocol can be supplemented with a histone immunoprecipitation step to estimate and compare both histone and non-histone DNA protection components. © 2017 by John Wiley & Sons, Inc.
本单元描述了一种在同一测定中确定染色质化DNA的可及性和核小体占有率的方法。使用微球菌核酸酶(MNase)对染色质进行酶切消化,以优化从染色质中释放、回收和鉴定DNA片段的过程。MNase消化以滴定系列进行,每个单独消化的DNA片段都被分离并独立测序。然后,这些测序片段在一个新颖的生物信息学流程中进行综合分析,以生成一个描述染色质MNase可及性(MACC)和核小体占有率的指标。这种方法能够对包括开放和封闭染色质区域在内的整个基因组进行分析。此外,MACC方案可以补充一个组蛋白免疫沉淀步骤,以估计和比较组蛋白和非组蛋白DNA保护成分。© 2017约翰威立国际出版公司。