The severe hereditary progeroid disorder Cockayne syndrome is a consequence of a defective transcription-coupled repair (TCR) pathway. This special mode of DNA repair aids a RNA polymerase that is stalled by a DNA lesion in the template and ensures efficient DNA repair to permit resumption of transcription and prevent cell death. Although some key players in TCR, such as the Cockayne syndrome A (CSA) and B (CSB) proteins have been identified, the exact molecular mechanism still remains illusive. A recent report provides new unexpected insights into TCR in yeast. The identification and characterisation of a novel protein co-purifying with the yeast homologue of CSB (Rad26) imposes reassessment of our current understanding of TCR in yeast. What about humans?

doi.org/10.1002/bies.10150, hdl.handle.net/1765/54746
BioEssays
Department of Molecular Genetics

van den Boom, V., Jaspers, N., & Vermeulen, W. (2002). When machines get stuck - Obstructed RNA polymerase II: Displacement, degradation or suicide. BioEssays, 24(9), 780–784. doi:10.1002/bies.10150