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PMID: 9326587 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, P.H.S.

Cockayne syndrome group B protein enhances elongation by RNA polymerase II.

Selby CP, Sancar A

Abstract

Cockayne syndrome (CS) is characterized by impaired physical and mental development. Two complementation groups, CSA and CSB, have been identified. Here we report that the CSB gene product enhances elongation by RNA polymerase II. CSB stimulated the rate of elongation on an undamaged template by a factor of about 3. A thymine-thymine cyclobutane dimer located in the template strand is known to be a strong block to transcription. Addition of CSB to the blocked polymerase resulted in addition of one nucleotide to the nascent transcript. Finally, addition of transcription factor IIS is known to cause polymerase blocked at a thymine-thymine cyclobutane dimer to digest its nascent transcript, and CSB counteracted this transcript shortening action of transcription factor IIS. Thus a deficiency in transcription elongation may contribute to the CS phenotype.

MeSH Terms
Base Sequence Cockayne Syndrome/genetics DNA/chemistry,metabolism DNA Helicases/genetics,metabolism DNA Repair Enzymes Enzyme Activation Humans Poly-ADP-Ribose Binding Proteins Pyrimidine Dimers RNA/chemistry RNA Polymerase II/metabolism Substrate Specificity Templates, Genetic Transcription Factors/metabolism Transcription Factors, General Transcription, Genetic Transcriptional Elongation Factors
Chemicals
Poly-ADP-Ribose Binding Proteins Pyrimidine Dimers Transcription Factors Transcription Factors, General Transcriptional Elongation Factors transcription factor S-II RNA DNA RNA Polymerase II DNA Helicases ERCC6 protein, human DNA Repair Enzymes
Authors & Affiliations
2 authors, click to expand affiliations / ORCID
Selby C P
Department of Biochemistry and Biophysics, University of North Carolina School of Medicine, Chapel Hill, NC 27599-7260, USA.
Sancar A
References (33)
33 references, click to expand
  1. Three unusual repair deficiencies associated with transcription factor BTF2(TFIIH): evidence for the existence of a transcription syndrome.
    Cold Spring Harb Symp Quant Biol. 1994;59:317-29 PMID: 7587084
  2. Reduced RNA polymerase II transcription in intact and permeabilized Cockayne syndrome group B cells.
    Proc Natl Acad Sci U S A. 1997 Apr 29;94(9):4306-11 PMID: 9113985
  3. Double mutants of Saccharomyces cerevisiae with alterations in global genome and transcription-coupled repair.
    Mol Cell Biol. 1996 Feb;16(2):496-502 PMID: 8552076
  4. Interactions involving the human RNA polymerase II transcription/nucleotide excision repair complex TFIIH, the nucleotide excision repair protein XPG, and Cockayne syndrome group B (CSB) protein.
    Biochemistry. 1996 Feb 20;35(7):2157-67 PMID: 8652557
  5. DNA excision repair.
    Annu Rev Biochem. 1996;65:43-81 PMID: 8811174
  6. Cockayne syndrome--a primary defect in DNA repair, transcription, both or neither?
    Bioessays. 1996 Sep;18(9):731-8 PMID: 8831289
  7. The RNA polymerase II general elongation factors.
    Trends Biochem Sci. 1996 Sep;21(9):351-5 PMID: 8870500
  8. Genetic complementation groups in cockayne syndrome.
    Somatic Cell Genet. 1981 Jul;7(4):445-55 PMID: 7280930
  9. Failure of RNA synthesis to recover after UV irradiation: an early defect in cells from individuals with Cockayne's syndrome and xeroderma pigmentosum.
    Cancer Res. 1982 Apr;42(4):1473-8 PMID: 6174225
  10. Studies of in vitro transcription by calf thymus RNA polymerase II using a novel duplex DNA template.
    J Biol Chem. 1982 May 10;257(9):5286-95 PMID: 7068686
  11. Three complementation groups in Cockayne syndrome.
    Mutat Res. 1982 Dec;106(2):347-56 PMID: 6185841
  12. DNA repair in an active gene: removal of pyrimidine dimers from the DHFR gene of CHO cells is much more efficient than in the genome overall.
    Cell. 1985 Feb;40(2):359-69 PMID: 3838150
  13. Selective removal of transcription-blocking DNA damage from the transcribed strand of the mammalian DHFR gene.
    Cell. 1987 Oct 23;51(2):241-9 PMID: 3664636
  14. The genetic defect in Cockayne syndrome is associated with a defect in repair of UV-induced DNA damage in transcriptionally active DNA.
    Proc Natl Acad Sci U S A. 1990 Jun;87(12):4707-11 PMID: 2352945
  15. An RNA polymerase II transcription factor shares functional properties with Escherichia coli sigma 70.
    Science. 1990 Jun 22;248(4962):1550-3 PMID: 2193400
  16. Nucleotide excision repair of DNA by human cell extracts is suppressed in reconstituted nucleosomes.
    J Biol Chem. 1991 Nov 25;266(33):22472-8 PMID: 1939267
  17. Mechanistic studies of transcription arrest at the adenovirus major late attenuation site. Comparison of purified RNA polymerase II and washed elongation complexes.
    J Biol Chem. 1992 Apr 15;267(11):7733-44 PMID: 1373137
  18. ERCC6, a member of a subfamily of putative helicases, is involved in Cockayne's syndrome and preferential repair of active genes.
    Cell. 1992 Dec 11;71(6):939-53 PMID: 1339317
  19. Molecular mechanism of transcription-repair coupling.
    Science. 1993 Apr 2;260(5104):53-8 PMID: 8465200
  20. Cell-free repair of UV-damaged simian virus 40 chromosomes in human cell extracts. I. Development of a cell-free system detecting excision repair of UV-irradiated SV40 chromosomes.
    J Biol Chem. 1993 Apr 25;268(12):9098-104 PMID: 8386176
  21. DNA repair. Engagement with transcription.
    Nature. 1993 May 13;363(6425):114-5 PMID: 8483493
  22. Cockayne syndrome: review of 140 cases.
    Am J Med Genet. 1992 Jan 1;42(1):68-84 PMID: 1308368
  23. Dual role of TFIIH in DNA excision repair and in transcription by RNA polymerase II.
    Nature. 1994 Apr 21;368(6473):769-72 PMID: 8152490
  24. Transcript cleavage by RNA polymerase II arrested by a cyclobutane pyrimidine dimer in the DNA template.
    Proc Natl Acad Sci U S A. 1994 Aug 30;91(18):8502-6 PMID: 8078911
  25. The ancient regulatory-protein family of WD-repeat proteins.
    Nature. 1994 Sep 22;371(6495):297-300 PMID: 8090199
  26. RAD26, the functional S. cerevisiae homolog of the Cockayne syndrome B gene ERCC6.
    EMBO J. 1994 Nov 15;13(22):5361-9 PMID: 7957102
  27. Transcription-coupled repair and human disease.
    Science. 1994 Dec 23;266(5193):1957-8 PMID: 7801121
  28. Recycling of the general transcription factors during RNA polymerase II transcription.
    Genes Dev. 1995 Jun 15;9(12):1479-90 PMID: 7601352
  29. The Cockayne syndrome group A gene encodes a WD repeat protein that interacts with CSB protein and a subunit of RNA polymerase II TFIIH.
    Cell. 1995 Aug 25;82(4):555-64 PMID: 7664335
  30. Human transcription-repair coupling factor CSB/ERCC6 is a DNA-stimulated ATPase but is not a helicase and does not disrupt the ternary transcription complex of stalled RNA polymerase II.
    J Biol Chem. 1997 Jan 17;272(3):1885-90 PMID: 8999876
  31. RNA polymerase II stalled at a thymine dimer: footprint and effect on excision repair.
    Nucleic Acids Res. 1997 Feb 15;25(4):787-93 PMID: 9016630
  32. Defective transcription-coupled repair of oxidative base damage in Cockayne syndrome patients from XP group G.
    Science. 1997 Feb 14;275(5302):990-3 PMID: 9020084
  33. The RNA polymerase II elongation complex.
    FASEB J. 1995 Nov;9(14):1419-28 PMID: 7589983
Article Info
Journal
Proceedings of the National Academy of Sciences of the United States of America
Abbr.
Proc Natl Acad Sci U S A
ISSN
0027-8424
Published
1997-10-14
Pages
11205-9
Language
English
Region
United States
NLM ID
7505876
PMCID
PMC23417
Subset
IM
Grants
NIGMS NIH HHS · R01 GM032833 · United States
NIGMS NIH HHS · GM32833 · United States
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