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      A Y2H-seq approach defines the human protein methyltransferase interactome.

      Nature Methods
      Chromatography, Liquid, Escherichia coli, Gene Expression Regulation, Enzymologic, physiology, HEK293 Cells, Humans, Methyltransferases, genetics, metabolism, Protein Interaction Mapping, methods, Sensitivity and Specificity, Sequence Analysis, DNA, Tandem Mass Spectrometry, Two-Hybrid System Techniques

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          Abstract

          To accelerate high-density interactome mapping, we developed a yeast two-hybrid interaction screening approach involving short-read second-generation sequencing (Y2H-seq) with improved sensitivity and a quantitative scoring readout allowing rapid interaction validation. We applied Y2H-seq to investigate enzymes involved in protein methylation, a largely unexplored post-translational modification. The reported network of 523 interactions involving 22 methyltransferases or demethylases is comprehensively annotated and validated through coimmunoprecipitation experiments and defines previously undiscovered cellular roles of nonhistone protein methylation.

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