Xu X, Schloissnig S, Murray JI, Teichgraber T, Angermann K, Janosch S, Rupprecht M, Preston E, Hasse S, Waterston RH, Ejsmont RK, Snyder M, Tinney M, Reis K, Vinis E, Reinke V, Hyman AA, Janette J, Schanze K, Pozniakovski A, Slightam C, Stewart AF, Kim SK, Enst S, Sarov M, Niu W, Zinke A
[
Cell,
2012]
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.