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Quantitative sequential chromatin immunoprecipitation a method for analyzing co-occupancy of proteins at genomic regions in vivo

机译:定量顺序染色质免疫沉淀一种分析体内基因组区域蛋白质共存的方法

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摘要

Sequential chromatin immunoprecipitation (SeqChIP) is a procedure in which formaldehyde-crosslinked, protein–DNA complexes from living cells are subjected to two sequential immunoprecipitations with antibodies of different specificity. SeqChIP has been used to address, in a qualitative manner, whether two proteins can simultaneously co-occupy a stretch of DNA in vivo. Here, we expand on our earlier work and describe theoretical and practical considerations for performing and interpreting SeqChIP experiments in a quantitative manner. We provide a detailed experimental procedure for designing and performing SeqChIP experiments as well as experimental examples of the three possible outcomes: full co-occupancy, no co-occupancy and partial co-occupancy. In some cases of partial co-occupancy, the order of immunoprecipitations in SeqChIP can strongly influence the outcome. We experimentally confirm a quantitative parameter that provides a measure of co-occupancy of two proteins on a given region of DNA and provide information on how to interpret the results of SeqChIP experiments. Our quantitative treatment of SeqChIP data substantially expands the usefulness of the technique for elucidating molecular mechanisms in vivo.
机译:顺序染色质免疫沉淀(SeqChIP)是一种程序,其中将来自活细胞的甲醛交联的蛋白质-DNA复合物用不同特异性的抗体进行两次连续免疫沉淀。 SeqChIP已用于定性分析两种蛋白质是否可以同时在体内共同占据一段DNA。在这里,我们扩展了我们的早期工作,并描述了以定量方式执行和解释SeqChIP实验的理论和实践考虑。我们为设计和执行SeqChIP实验提供了详细的实验程序,并提供了三种可能结果的实验​​示例:完全同居,无同居和部分同居。在部分同居的某些情况下,SeqChIP中免疫沉淀的顺序会强烈影响结果。我们通过实验确定了定量参数,该参数提供了在给定DNA区域上两种蛋白质共存的度量,并提供了有关如何解释SeqChIP实验结果的信息。我们对SeqChIP数据的定量处理大大扩展了该技术在体内阐明分子机制的用途。

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