| Literature DB >> 28973381 |
Nancy Walker-Kopp1, Ashleigh J Jackobel1, Gianno N Pannafino1, Paola A Morocho1,2, Xia Xu1, Bruce A Knutson1.
Abstract
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.Entities:
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Year: 2017 PMID: 28973381 PMCID: PMC6251613 DOI: 10.1093/hmg/ddx317
Source DB: PubMed Journal: Hum Mol Genet ISSN: 0964-6906 Impact factor: 6.150