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Immediate chromatin immunoprecipitation and on-bead quantitative PCR analysis: a versatile and rapid ChIP procedure

机译:立即染色质免疫沉淀和珠上定量PCR分析:通用且快速的ChIP程序

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Genome-wide chromatin immunoprecipitation (ChIP) studies have brought significant insight into the genomic localization of chromatin-associated proteins and histone modifications. The large amount of data generated by these analyses, however, require approaches that enable rapid validation and analysis of biological relevance. Furthermore, there are still protein and modification targets that are difficult to detect using standard ChIP methods. To address these issues, we developed an immediate chromatin immunoprecipitation procedure which we call ZipChip. ZipChip significantly reduces the time and increases sensitivity allowing for rapid screening of multiple loci. Here we describe how ZipChIP enables detection of histone modifications (H3K4 mono-and trimethylation) and two yeast histone demethylases, Jhd2 and Rph1, which were previously difficult to detect using standard methods. Furthermore, we demonstrate the versatility of ZipChIP by analyzing the enrichment of the histone deacetylase Sir2 at heterochromatin in yeast and enrichment of the chromatin remodeler, PICKLE, at euchromatin in Ara-bidopsis thaliana.
机译:全基因组染色质免疫沉淀(ChIP)研究为染色质相关蛋白的基因组定位和组蛋白修饰带来了重要见识。但是,这些分析所产生的大量数据需要能够快速验证和分析生物学相关性的方法。此外,仍然存在使用标准ChIP方法难以检测的蛋白质和修饰靶标。为了解决这些问题,我们开发了一种即时染色质免疫沉淀程序,称为ZipChip。 ZipChip可显着减少时间并提高灵敏度,从而可以快速筛选多个基因座。在这里,我们描述ZipChIP如何实现组蛋白修饰(H3K4单和三甲基化)和两种酵母组蛋白脱甲基酶Jhd2和Rph1的检测,这以前很难用标准方法检测到。此外,我们通过分析组蛋白脱乙酰基酶Sir2在酵母异染色质中的富集和染色质重塑剂PICKLE在拟南芥中的常染色质的富集来证明ZipChIP的多功能性。

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