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Cockayne syndrome group B protein has novel strand annealing and exchange activities

8 Jan 2006

Abstract excerpt

Cockayne syndrome (CS) is a rare inherited human genetic disorder characterized by UV sensitivity, severe neurological abnormalities and prageroid symptoms. The CS complementation group B (CSB) protein is involved in UV-induced transcription coupled repair (TCR), base excision repair and general transcription. CSB also has a DNA-dependent ATPase activity that may play a role in remodeling chromatin in vivo. This...

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PMID: 16410611
DOI: 10.1093/nar/gkj410

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