Systematic identification of interchromosomal interaction networks supports the existence of specialized RNA factories.

Most studies of genome organization have focused on intrachromosomal () contacts because they harbor key features such as DNA loops and topologically associating domains. Interchromosomal () contacts have received much less attention, and tools for interrogating potential biologically relevant structures are lacking. Here, we develop a computational framework that uses Hi-C data to identify sets of loci that jointly interact in This method, trans-C, initiates probabilistic random walks with restarts from a set of seed loci to traverse an input Hi-C contact network, thereby identifying sets of -contacting loci. We validate trans-C in three increasingly complex models of established contacts: the genes, the mouse olfactory receptor "Greek islands," and the human RBM20 cardiac splicing factory. We then apply trans-C to systematically test the hypothesis that genes coregulated by the same -acting element (i.e., a transcription or splicing factor) colocalize in three dimensions to form "RNA factories" that maximize the efficiency and accuracy of RNA biogenesis. We find that many loci with multiple binding sites of the same DNA-binding proteins interact with one another in , especially those bound by factors with intrinsically disordered domains. Similarly, clustered binding of a subset of RNA-binding proteins correlates with interaction of the encoding loci. We observe that these -interacting loci are close to nuclear speckles. These findings support the existence of interacting chromatin domains (TIDs) driven by RNA biogenesis. Trans-C provides an efficient computational framework for studying these and other types of interactions, empowering studies of a poorly understood aspect of genome architecture.