Johansen Kristen M, Cai Weili, Deng Huai, Bao Xiaomin, Zhang Weiguo, Girton Jack, Johansen Jørgen
Department of Biochemistry, Biophysics, and Molecular Biology, Iowa State University, 3154 Molecular Biology Building, Ames, IA 50011, USA.
Methods. 2009 Aug;48(4):387-97. doi: 10.1016/j.ymeth.2009.02.019. Epub 2009 Mar 9.
The giant polytene chromosomes from Drosophila third instar larval salivary glands provide an important model system for studying the architectural changes in chromatin morphology associated with the process of transcription initiation and elongation. Especially, analysis of the heat shock response has proved useful in correlating chromatin structure remodeling with transcriptional activity. An important tool for such studies is the labeling of polytene chromosome squash preparations with antibodies to the enzymes, transcription factors, or histone modifications of interest. However, in any immunohistochemical experiment there will be advantages and disadvantages to different methods of fixation and sample preparation, the relative merits of which must be balanced. Here we provide detailed protocols for polytene chromosome squash preparation and discuss their relative pros and cons in terms of suitability for reliable antibody labeling and preservation of high resolution chromatin structure.
果蝇三龄幼虫唾液腺中的巨大多线染色体为研究与转录起始和延伸过程相关的染色质形态结构变化提供了一个重要的模型系统。特别是,热休克反应分析已被证明有助于将染色质结构重塑与转录活性联系起来。此类研究的一个重要工具是用针对感兴趣的酶、转录因子或组蛋白修饰的抗体标记多线染色体压片标本。然而,在任何免疫组织化学实验中,不同的固定和样品制备方法都有其优缺点,必须权衡其相对优点。在这里,我们提供了多线染色体压片制备的详细方案,并根据对可靠抗体标记的适用性和高分辨率染色质结构的保存情况讨论了它们的相对优缺点。