Protocol

Mapping Chromatin Features of Xenopus Embryos

  1. James C. Smith1,2
  1. 1Developmental Biology Laboratory, The Francis Crick Institute, London NW1 1AT, United Kingdom
  1. 2Correspondence: george.gentsch{at}crick.ac.uk; jim.smith{at}crick.ac.uk

Abstract

Chromatin immunoprecipitation (ChIP) combined with genomic analysis provides a global snapshot of protein–DNA interactions in the context of chromatin, yielding insights into which genome loci might be regulated by the DNA-associated protein under investigation. This protocol is an update of a previous version and describes how to perform ChIP on intact or dissected Xenopus embryos. The ChIP-isolated DNA fragments are suitable for both deep sequencing (ChIP-Seq) and quantitative polymerase chain reaction (ChIP-qPCR). General advice for qPCR and for making ChIP-Seq libraries is offered, and approaches for analyzing ChIP-Seq data are outlined.

Footnotes

  • From the Xenopus collection, edited by Hazel L. Sive.

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