UVSSA and USP7: new players regulating transcription-coupled nucleotide excision repair in human cells

作者：Sarasin Alain^*

来源：Genome Medicine, 2012, 4: 44.

DOI：10.1186/gm343

• DNA repair-deficient diseases
• transcription-coupled repair
• stalled RNA polymerase
• UV sensitivity

Transcription-coupled nucleotide excision repair (TC-NER) specifically removes DNA damage located in actively transcribed genes. Defects in TC-NER are associated with several human disorders, including Cockayne syndrome (CS) and ultraviolet (UV)-sensitive syndrome (UVSS). Using exome sequencing, and genetic and proteomic approaches, three recent studies have identified mutations in the UVSSA gene as being responsible for UVSS-A. These findings suggest a new mechanistic model involving UV-stimulated scaffold protein A (UVSSA) and the ubiquitin-specific protease 7 (USP7) in the fate of stalled RNA polymerase II during TC-NER, and provide insights into the diverse clinical features of CS and (UVS)-S-S.

• 出版日期2012-5-23