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Nucleic Acids Research, 1993, Vol. 21, No. 25 5890-5895
© 1993


MOLECULAR BIOLOGY

Deficient repair of the transcribed strand of active genes in Cockayne's syndrome cells

Anneke van Hoffen1, A.T. Natarajan1,2, Lynne V. Mayne3, Albert A.van Zeeland1,2, Leon H.F. Mullenders1,2,* and Jaap Venema1,+

1MGC – Department of Radiation Genetics and Chemical Mutagenesis, State University of Leiden, Wassenaarseweg 72, 2333 AL Leiden 2J.A.Cohen Institute, Interuniversity Research Institute for Radiation Protection and Radiopathology Leiden, The Netherlands 3The Trafford Centre for Medical Research, University of Sussex, Falmer Brighton BN1 9RY, UK

*Department of Radiation Genetics and Chemical Mutagenesis, State University of Leiden, Wassenaarseweg, 72, 2333 AL Leiden, The Netherlands

Received September 20, 1993. Revised November 22, 1993. Accepted November 22, 1993.

Removal of ultraviolet light induced cyclobutane pyrimidine dimers (CPD) from active and inactive genes was analyzed in cells derived from patients suffering from the hereditary disease Cockayne's syndrome (CS) using strand specific probes. The results indicate that the defect in CS cells affects two levels of repair of lesions in active genes. Firstly, CS cells are deficient in selective repair of the transcribed strand of active genes. In these cells the rate and efficiency of repair of CPD are equal for the transcribed and the nontranscribed strand of the active ADA and DHFR genes. In normal cells on the other hand, the transcribed strand of these genes is repaired faster than the nontranscribed strand. However, the nontranscribed strand is still repaired more efficiently than the inactive 754 gene and the gene coding for coagulation factor IX. Secondly, the repair level of active genes in CS cells exceeds that of inactive loci but is slower than the nontranscribed strand of active genes in normal cells. Our results support the model that CS cells lack a factor which is involved in targeting repair enzymes specifically towards DNA damage located in (potentially) active DNA.


+Department of Biochemistry and Molecular Biology, Vrije Universiteit, de Boelelaan 1083, 1081 HV Amsterdam, The Netherlands


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