Systematic proteomics of endogenous human cohesin reveals an interaction with diverse splicing factors and RNA-binding proteins required for mitotic progression

Supporting Information

• Supporting Information - Supporting Information
• Table S2 - Proteins identified by GeLC-MS/MS analysis of dual affinity purifications from epitope-tagged cells.
• Table S3 - Reciprocal identification of known subunits of cohesin via mass spectrometric analysis of dual affinity purifications from epitope-tagged cells.
• Table S5 - Identification of splicing factors and RNA binding proteins by mass spectrometric analysis of dual affinity purifications from epitope-tagged cells.
• Table S6 - Non-cohesin, non-splicing factor/RBP proteins identified by mass spectrometry in affinity purifications from four or more epitope-tagged cell lines.
• Movie S1 - Time lapse imaging of HeLa-H2B-GFP cells transfected with SNRNP200 and PRPF31 splicing factor siRNAs.
• Movie S2 - Time lapse imaging of HeLa-H2B-GFP cells transfected with EFTUD2, SF3B3 and Sororin siRNAs.