TransgeneOmics Unit, Max Planck Institute of Molecular Cell Biology and Genetics, Dresden 01307, Germany.
Cell. 2012 Aug 17;150(4):855-66. doi: 10.1016/j.cell.2012.08.001.
Understanding the in vivo dynamics of protein localization and their physical interactions is important for many problems in biology. To enable systematic protein function interrogation in a multicellular context, we built a genome-scale transgenic platform for in vivo expression of fluorescent- and affinity-tagged proteins in Caenorhabditis elegans under endogenous cis regulatory control. The platform combines computer-assisted transgene design, massively parallel DNA engineering, and next-generation sequencing to generate a resource of 14,637 genomic DNA transgenes, which covers 73% of the proteome. The multipurpose tag used allows any protein of interest to be localized in vivo or affinity purified using standard tag-based assays. We illustrate the utility of the resource by systematic chromatin immunopurification and automated 4D imaging, which produced detailed DNA binding and cell/tissue distribution maps for key transcription factor proteins.
了解蛋白质定位的体内动力学及其物理相互作用对于生物学中的许多问题都很重要。为了能够在多细胞环境中系统地进行蛋白质功能研究,我们构建了一个基于基因组规模的转基因平台,用于在秀丽隐杆线虫中,以内源顺式调控控制下,体内表达荧光标记和亲和标记的蛋白质。该平台结合了计算机辅助转基因设计、大规模平行 DNA 工程和下一代测序技术,生成了一个包含 14637 个基因组 DNA 转基因的资源,涵盖了 73%的蛋白质组。使用的多用途标签允许使用标准的基于标签的测定法,对任何感兴趣的蛋白质进行体内定位或亲和纯化。我们通过系统的染色质免疫沉淀和自动化的 4D 成像,说明了该资源的实用性,这些方法为关键转录因子蛋白质产生了详细的 DNA 结合和细胞/组织分布图谱。