Human Molecular Genetics · 2017 · 29 citations · 36 references
Life SciencesGeneticsMolecular BiologyCraniofacial GeneticsGene ExpressionTranscriptionCraniofacial Developmental GeneticsDevelopmental MutationsPolymerase Chain ReactionRna Polymerase Iii TranscriptionRna Polymerase RegulationRna Polymerase StructureCraniofacial DysmorphogenesisCraniofacial Malformation MutationsFacial BonesRna Polymerase I ActivityRna Polymerase I Complex StructureRna Polymerase I FunctionRna Polymerase I Regulation
Treacher Collins syndrome (TCS) is a craniofacial disorder that is characterized by the malformation of the facial bones. Mutations in three genes (TCOF1, POLR1C and POLR1D) involved in RNA polymerase I (Pol I) transcription account for more than 90% of disease cases. Two of these TCS-associated genes, POLR1C and POLR1D, encode for essential Pol I/III subunits that form a heterodimer necessary for Pol I/III assembly, and many TCS mutations lie along their evolutionarily conserved dimerization interface. Here we elucidate the molecular basis of TCS mutations in Saccharomyces cerevisiae, and present a new model for how TCS mutations may disrupt Pol I and III complex integrity.
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