An Efficient Chromatin Immunoprecipitation Protocol for the Analysis of Histone Modification Distributions in the Brown Alga Ectocarpus

被引:2
|
作者
Bourdareau, Simon [1 ,3 ]
Godfroy, Olivier [1 ]
Gueno, Josselin [1 ]
Scornet, Delphine [1 ]
Coelho, Susana M. [1 ,4 ]
Tirichine, Leila [2 ]
Cock, J. Mark [1 ]
机构
[1] Sorbonne Univ, Integrat Biol Marine Models Lab, Stn Biol Roscoff, Algal Genet Grp,CNRS, CS 90074, F-29688 Roscoff, France
[2] Nantes Univ, US2B, CNRS, UMR 6286, F-44000 Nantes, France
[3] Stowers Inst Med Res, 1000 E 50th St, Kansas City, MO 64110 USA
[4] Max Planck Inst Dev Biol, Max Planck Ring 5, D-72076 Tubingen, Germany
基金
欧洲研究理事会;
关键词
brown algae; chromatin; chromatin immunoprecipitation; ChIP-seq; Ectocarpus; Phaeophyceae; MULTICELLULARITY; EVOLUTION; GENOME;
D O I
10.3390/mps5030036
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
The brown algae are an important but understudied group of multicellular marine organisms. A number of genetic and genomic tools have been developed for the model brown alga Ectocarpus; this includes, most recently, chromatin immunoprecipitation methodology, which allows genome-wide detection and analysis of histone post-translational modifications. Post-translational modifications of histone molecules have been shown to play an important role in gene regulation in organisms from other major eukaryotic lineages, and this methodology will therefore be a very useful tool to investigate genome function in the brown algae. This article provides a detailed, step-by-step description of the Ectocarpus ChIP protocol, which effectively addresses the difficult problem of efficiently extracting chromatin from cells protected by a highly resistant cell wall. The protocol described here will be an essential tool for the future application of chromatin analysis methodologies in brown algal research.
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页数:12
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