TChIP-Seq: Cell-Type-Specific Epigenome Profiling

被引:1
|
作者
Mito, Mari [1 ,2 ]
Kadota, Mitsutaka [3 ]
Nakagawa, Shinichi [1 ,4 ]
Iwasaki, Shintaro [2 ,5 ]
机构
[1] RIKEN, RNA Biol Lab, Wako, Saitama, Japan
[2] RIKEN, Cluster Pioneering Res, RNA Syst Biochem Lab, Wako, Saitama, Japan
[3] RIKEN, Ctr Biosystems Dynam Res, Lab Phyloinformat, Wako, Saitama, Japan
[4] Hokkaido Univ, Fac Pharmaceut Sci, RNA Biol Lab, Sapporo, Hokkaido, Japan
[5] Univ Tokyo, Grad Sch Frontier Sci, Dept Computat Biol & Med Sci, Tokyo, Japan
来源
关键词
Biology; Issue; 143; ChIP-Seq; cell-type-specific gene expression; epigenetics; histone modification; next-generation sequencing; histone H2B;
D O I
10.3791/58298
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Epigenetic regulation plays central roles in gene expression. Since histone modification was discovered in the 1960s, its physiological and pathological functions have been extensively studied. Indeed, the advent of next-generation deep sequencing and chromatin immunoprecipitation (ChIP) via specific histone modification antibodies has revolutionized our view of epigenetic regulation across the genome. Conversely, tissues typically consist of diverse cell types, and their complex mixture poses analytic challenges to investigating the epigenome in a particular cell type. To address the cell type-specific chromatin state in a genome-wide manner, we recently developed tandem chromatin immunoprecipitation sequencing (tChIP-Seq), which is based on the selective purification of chromatin by tagged core histone proteins from cell types of interest, followed by ChIP-Seq. The goal of this protocol is the introduction of best practices of tChIP-Seq. This technique provides a versatile tool for tissue-specific epigenome investigation in diverse histone modifications and model organisms.
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页数:8
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