Literature DB >> 27730588

Chromatin Immunoprecipitation for Analyzing Transcription Factor Binding and Histone Modifications in Drosophila.

Yad Ghavi-Helm1, Bingqing Zhao1, Eileen E M Furlong2.   

Abstract

Chromatin immunoprecipitation followed by next-generation sequencing (ChIP-seq) is an invaluable technique to assess transcription factor binding and histone modifications in a genome-wide manner, an essential step towards understanding the mechanisms that govern embryonic development. Here, we provide a detailed protocol for all steps involved in generating a ChIP-seq library, starting from embryo collection, fixation, chromatin preparation, immunoprecipitation, and finally library preparation. The protocol is optimized for Drosophila embryos, but can be easily adapted for any model organism. The resulting library is suitable for sequencing on an Illumina HiSeq or MiSeq platform.

Entities:  

Keywords:  ChIP-seq; Chromatin immunoprecipitation; Development; Drosophila; Next-generation sequencing; Transcription

Mesh:

Substances:

Year:  2016        PMID: 27730588     DOI: 10.1007/978-1-4939-6371-3_16

Source DB:  PubMed          Journal:  Methods Mol Biol        ISSN: 1064-3745


  3 in total

1.  Divergent expression of paralogous genes by modification of shared enhancer activity through a promoter-proximal silencer.

Authors:  Ryan Loker; Richard S Mann
Journal:  Curr Biol       Date:  2022-07-18       Impact factor: 10.900

2.  ChIP-Seq from Limited Starting Material of K562 Cells and Drosophila Neuroblasts Using Tagmentation Assisted Fragmentation Approach.

Authors:  Junaid Akhtar; Piyush More; Steffen Albrecht
Journal:  Bio Protoc       Date:  2020-02-20

3.  Cell-type-specific Hox regulatory strategies orchestrate tissue identity.

Authors:  Ryan Loker; Jordyn E Sanner; Richard S Mann
Journal:  Curr Biol       Date:  2021-08-05       Impact factor: 10.900

  3 in total

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