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Hum Mol Genet ; 26(21): 4290-4300, 2017 11 01.
Artigo em Inglês | MEDLINE | ID: mdl-28973381

RESUMO

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.


Assuntos
RNA Polimerases Dirigidas por DNA/genética , Disostose Mandibulofacial/genética , RNA Polimerase III/genética , RNA Polimerase I/genética , RNA Polimerases Dirigidas por DNA/metabolismo , Genes Reguladores , Humanos , Disostose Mandibulofacial/metabolismo , Mutação , RNA Polimerase I/metabolismo , RNA Polimerase III/metabolismo , Saccharomyces cerevisiae/genética , Saccharomyces cerevisiae/metabolismo , Proteínas de Saccharomyces cerevisiae/genética , Proteínas de Saccharomyces cerevisiae/metabolismo
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