Genome-Wide Profiling of Transcription Factor Binding and Epigenetic Marks in Adipocytes by ChIP-seq

被引:20
|
作者
Nielsen, Ronni [1 ]
Mandrup, Susanne [1 ]
机构
[1] Univ Southern Denmark, Dept Biochem & Mol Biol, Odense, Denmark
来源
关键词
ACTIVATED RECEPTOR-GAMMA; PROTEIN-DNA INTERACTIONS; PPAR-GAMMA; CHROMATIN IMMUNOPRECIPITATION; ADIPOGENESIS; DIFFERENTIATION; RESOLUTION; CELLS;
D O I
10.1016/B978-0-12-411619-1.00014-8
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
The recent advances in high-throughput sequencing combined with various other technologies have allowed detailed and genome-wide insight into the transcriptional networks that control adipogenesis. Chromatin immunoprecipitation (ChIP) combined with high-throughput sequencing (ChIP-seq) is one of the most widely used of these technologies. Using these methods, association of transcription factors, cofactors, and epigenetic marks can be mapped to DNA in a genome-wide manner. Here, we provide a detailed protocol for performing ChIP-seq analyses in preadipocytes and adipocytes. We have focused mainly on critical points, limitations of the assay, and quality controls required in order to obtain reproducible ChIP-seq data.
引用
收藏
页码:261 / 279
页数:19
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