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通过果蝇多线染色体上的双分子荧光互补分析对特定多蛋白复合物结合的基因组位点进行可视化。

Visualization of the Genomic Loci That Are Bound by Specific Multiprotein Complexes by Bimolecular Fluorescence Complementation Analysis on Drosophila Polytene Chromosomes.

作者信息

Deng Huai, Kerppola Tom K

机构信息

University of Michigan, Ann Arbor, MI, United States.

University of Michigan, Ann Arbor, MI, United States.

出版信息

Methods Enzymol. 2017;589:429-455. doi: 10.1016/bs.mie.2017.02.003. Epub 2017 Mar 11.

Abstract

We have developed a procedure that enables visualization of the genomic loci that are bound by complexes formed by a specific combination of chromatin-binding proteins. This procedure is based on imaging bimolecular fluorescence complementation (BiFC) complexes on Drosophila polytene chromosomes. BiFC complexes are formed by the facilitated association of two fluorescent protein fragments that are fused to proteins that interact with, or are in close proximity to, each other. The intensity of BiFC complex fluorescence at individual genomic loci is greatly enhanced by the parallel alignment of hundreds of chromatids within the polytene chromosomes. The loci that are bound by the complexes are mapped by comparing the locations of BiFC complex fluorescence with the stereotypical banding patterns of the chromosomes. We describe strategies for the design, expression, and validation of fusion proteins for the analysis of BiFC complex binding on polytene chromosomes. We detail protocols for the preparation of polytene chromosome spreads that have been optimized for the purpose of BiFC complex visualization. Finally, we provide guidance for the interpretation of results from studies of BiFC complex binding on polytene chromosomes and for comparison of the genomic loci that are bound by BiFC complexes with those that are bound by subunits of the corresponding endogenous complexes. The visualization of BiFC complex binding on polytene chromosomes provides a unique method to visualize multiprotein complex binding at specific loci, throughout the genome, in individual cells.

摘要

我们开发了一种程序,可实现对由特定组合的染色质结合蛋白形成的复合物所结合的基因组位点的可视化。该程序基于对果蝇多线染色体上的双分子荧光互补(BiFC)复合物进行成像。BiFC复合物由两个荧光蛋白片段的促进结合形成,这两个片段分别与相互作用或紧密相邻的蛋白质融合。多线染色体中数百条染色单体的平行排列极大地增强了单个基因组位点处BiFC复合物荧光的强度。通过将BiFC复合物荧光的位置与染色体的典型带型模式进行比较,来绘制复合物所结合的位点。我们描述了用于设计、表达和验证融合蛋白以分析多线染色体上BiFC复合物结合的策略。我们详细介绍了为BiFC复合物可视化目的而优化的多线染色体铺片制备方案。最后,我们为解释多线染色体上BiFC复合物结合研究的结果以及将BiFC复合物所结合的基因组位点与相应内源性复合物亚基所结合的位点进行比较提供指导。多线染色体上BiFC复合物结合的可视化提供了一种独特的方法,可在单个细胞的整个基因组中可视化特定位点处的多蛋白复合物结合。

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