CSB is a component of RNA pol I transcription

Molecular Cell

Volumn 10, Issue 4, 2002, Pages 819-829

  Bradsher, John ^a   Auriol, Jerome ^a   De Santis, Luca Proietti ^a   Iben, Sebastian ^b   Vonesch, Jean Luc ^a   Grummt, Ingrid ^b   Egly, Jean Marc ^a  

^a INSTITUT DE GÉNÉTIQUE ET DE BIOLOGIE MOLÉCULAIRE ET CELLULAIRE   (France)

^b GERMAN CANCER RESEARCH CENTER DKFZ   (Germany)

Author keywords

[No Author keywords available]

Indexed keywords

RIBOSOME RNA;

ARTICLE; COCKAYNE SYNDROME; CONTROLLED STUDY; CSB GENE; GENE; GENE MUTATION; HUMAN; HUMAN CELL; NUCLEOLUS; PHENOTYPE; RNA SYNTHESIS; RNA TRANSCRIPTION; XPB GENE; XPD GENE;

EID: 0036809114     PISSN: 10972765     EISSN: None     Source Type: Journal    
DOI: 10.1016/S1097-2765(02)00678-0     Document Type: Article

References (46)

1. Araujo S.J., Tirode F., Coin F., Pospiech H., Syvaoja J.E., Stucki M., Hubscher U., Egly J.M., Wood R.D. Nucleotide excision repair of DNA with recombinant human proteins. definition of the minimal set of factors, active forms of TFIIH, and modulation by CAK Genes Dev. 14:2000;349-359.
2. Balajee A.S., May A., Dianov G.L., Friedberg E.C., Bohr V.A. Reduced RNA polymerase II transcription in intact and permeabilized Cockayne syndrome group B cells. Proc. Natl. Acad. Sci. USA. 94:1997;4306-4311.
3. Bengal E., Flores O., Krauskopf A., Reinberg D., Aloni Y. Role of the mammalian transcription factors IIF, IIS, and IIX during elongation by RNA polymerase II. Mol. Cell. Biol. 11:1991;1195-1206.
4. Berneburg M., Lehmann A.R. Xeroderma pigmentosum and related disorders. defects in DNA repair and transcription Adv. Genet. 43:2001;71-102.
5. Bohr V.A., Smith C.A., Okumoto D.S., Hanawalt P.C. 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. 40:1985;359-369.
6. Bradsher J., Coin F., Egly J.M. Distinct roles for the helicases of TFIIH in transcript initiation and promoter escape. J. Biol. Chem. 275:2000;2532-2538.
7. Chao D.M., Gadbois E.L., Murray P.J., Anderson S.F., Sonu M.S., Parvin J.D., Young R.A. A mammalian SRB protein associated with an RNA polymerase II holoenzyme. Nature. 380:1996;82-85.
8. Citterio E., Rademakers S., van der Horst G.T., van Gool A.J., Hoeijmakers J.H., Vermeulen W. Biochemical and biological characterization of wild-type and ATPase-deficient Cockayne syndrome B repair protein. J. Biol. Chem. 273:1998;11844-11851.
9. Citterio E., Van Den Boom V., Schnitzler G., Kanaar R., Bonte E., Kingston R.E., Hoeijmakers J.H., Vermeulen W. ATP-dependent chromatin remodeling by the cockayne syndrome B DNA repair-transcription-coupling factor. Mol. Cell. Biol. 20:2000;7643-7653.
10. Coin F., Marinoni J.C., Egly J.M. Mutations in XPD helicase prevent its interaction and regulation by p44, another subunit of TFIIH, resulting in Xeroderma pigmentosum (XP) and trichothiodystrophy (TTD) phenotypes. Pathol. Biol. (Paris). 46:1998;679-680. a.
11. Coin F., Marinoni J.C., Rodolfo C., Fribourg S., Pedrini A.M., Egly J.M. Mutations in the XPD helicase gene result in XP and TTD phenotypes, preventing interaction between XPD and the p44 subunit of TFIIH. Nat. Genet. 20:1998;184-188. b.
12. Conaway J.W., Conaway R.C. A multisubunit transcription factor essential for accurate initiation by RNA polymerase II. J. Biol. Chem. 264:1989;2357-2362.
13. Conconi A., Bespalov V.A., Smerdon M.J. Transcription-coupled repair in RNA polymerase I-transcribed genes of yeast. Proc. Natl. Acad. Sci. USA. 99:2002;649-654.
14. Dianov G.L., Houle J.F., Iyer N., Bohr V.A., Friedberg E.C. Reduced RNA polymerase II transcription in extracts of cockayne syndrome and xeroderma pigmentosum/Cockayne syndrome cells. Nucleic Acids Res. 25:1997;3636-3642.
15. Drapkin R., Reardon J.T., Ansari A., Huang J.C., Zawel L., Ahn K.J., Sancar A., Reinberg D. Dual role of TFIIH in DNA excision repair and in transcription by RNA polymerase II. Nature. 368:1994;769-772.
16. Draptchinskaia N., Gustavsson P., Andersson B., Pettersson M., Willig T.N., Dianzani I., Ball S., Tchernia G., Klar J., Matsson H.et al. The gene encoding ribosomal protein S19 is mutated in Diamond-Blackfan anaemia. Nat. Genet. 21:1999;169-175.
17. Feaver W.J., Gileadi O., Kornberg R. Purification and characterization of yeast RNA polymerase II transcription factor b. J. Biol. Chem. 266:1991;19000-19005.
18. Flores O., Lu H., Reinberg D. Factors involved in specific transcription by mammalian RNA polymerase II. Identification and characterization of factor IIH. J. Biol. Chem. 267:1992;2786-2793.
19. Gerard M., Fischer L., Moncollin V., Chipoulet J.M., Chambon P., Egly J.M. Purification and interaction properties of the human RNA polymerase B(II) general transcription factor BTF2. J. Biol. Chem. 266:1991;20940-20945.
20. Harlow E., Lane D. Using antibodies. a laboratory manual:1999;Cold Spring Harbor Laboratory Press, Cold Spring Harbor, NY.
21. He D., Jeffrey A., Nickerson J., Penman S. Core Filaments of the Nuclear Matrix. J. Cell Biol. 110:2000;569-580.
22. Henning K.A., Li L., Iyer N., McDaniel L.D., Reagan M.S., Legerski R., Shultz R.A., Stefanini M., Lehmann A.R., Mayne L.V., Friedberg E.C. The Cockayne syndrome group A genes encodes a WD repeat protein that interacts with CSB protein and a subunit of RNA polymerase II TFIIH. Cell. 82:1995;555-564.
23. Hisatake K., Hasegawa S., Takada R., Nakatani Y., Horikoshi M., Roeder R.G. The p250 subunit of native TATA box-binding factor TFIID is the cell- cycle regulatory protein CCG1. Nature. 362:1993;179-181.
24. Iben S., Tschochner H., Bier M., Hoogstraten D., Hozak P., Egly J.M., Grummt I. TFIIH plays an essential role in RNA polymerase I transcription. Cell. 109:2002;297-306.
25. Iyer N., Reagan M.S., Wu K.J., Canagarajah B., Friedberg E.C. 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. 35:1996;2157-2167.
26. Keriel A., Stary A., Sarasin A., Rochette-Egly C., Egly J.M. XPD mutations prevent TFIIH-dependent transactivation by nuclear teceptors and phosphorylation of RARα Cell. 109:2002;125-135.
27. Le Page F., Kwoh E.E., Avrutskaya A., Gentil A., Leadon S.A., Sarasin A., Cooper P.K. Transcription-coupled repair of 8-oxoguanine. requirement for XPG, TFIIH, and CSB and implications for Cockayne syndrome Cell. 101:2000;159-171.
28. Lee S.K., Yu S.L., Prakash L., Prakash S. Requirement of yeast RAD2, a homolog of human XPG gene, for efficient RNA polymerase II transcription. Implications for Cockayne syndrome. Cell. 109:2002;823-834.
29. Liebhaber S., Wolf S., Schlessinger D. Differences in rRNA metabolism of primary and SV40-transformed human fibroblasts. Cell. 13:1978;121-127.
30. Liu J., He L., Collins I., Ge H., Libutti D., Li J., Egly J.-M., Levens D. The FBP interacting repressor targets TFIIH to inhibit activated transcription. Mol. Cell. 5:2000;331-341.
31. Lu Y., Mani S., Kandimalla E., Yu D., Agrawal S., States J., Bregman D. The Cockayne syndrome group B DNA repair protein as an anti-cancer target. Int. J. Oncol. 19:2001;1089-1097.
32. Mellon I., Spivak G., Hanawalt P.C. Selective removal of transcription-blocking DNA damage from the transcribed strand of the mammalian DHFR gene. Cell. 51:1987;241-249.
33. Ossipow V., Tassan J.P., Nigg E.A., Schibler U. A mammalian RNA polymerase II holoenzyme containing all the components required for promoter-specific transcription initiation. Cell. 83:1995;137-146.
34. Pan G., Aso T., Greenblatt J. Interaction of elongation factors TFIIS and elongin A with a human RNA polymerase II holoenzyme capable of promoter-specific initiation and responsive to transcriptional activators. J. Biol. Chem. 272:1997;24563-24571.
35. Ruppert S., Wang E.H., Tjian R. Cloning and expression of human TAFII250. a TBP-associated factor implicated in cell-cycle regulation Nature. 362:1993;175-179.
36. Schaeffer L., Roy R., Humbert S., Moncollin V., Vermeulen W., Hoeijmakers J.H.J., Chambon P., Egly J.M. DNA repair helicase. a component of BTF2 (TFIIH) basic transcription factor Science. 260:1993;58-63.
37. Scully R., Anderson S.F., Chao D.M., Wei W., Ye L., Young R.A., Livingston D.M., Parvin J.D. BRCA1 is a component of the RNA polymerase II holoenzyme. Proc. Natl. Acad. Sci. USA. 94:1997;5605-5610.
38. Selby C.P., Sancar A. 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. 272:1997;1885-1890.
39. Serizawa H., Conaway R.C., Conaway J.W. A carboxyl-terminal-domain kinase associated with RNA polymerase II transcription factor δ from rat liver. Proc. Natl. Acad. Sci. USA. 89:1992;7476-7480.
40. Stefanini M., Fawcett H., Botta E., Nardo T., Lehmann A.R. Genetic analysis of twenty-two patients with Cockayne syndrome. Hum. Genet. 97:1996;418-423.
41. Tantin D. RNA polymerase II elongation complexes containing the Cockayne syndrome group B protein interact with a molecular complex containing the transcription factor IIH components xeroderma pigmentosum B and p62. J. Biol. Chem. 273:1998;27794-27799.
42. Tantin D., Kansal A., Carey M. Recruitment of the putative transcription-repair coupling factor CSB/ERCC6 to RNA polymerase II elongation complexes. Mol. Cell. Biol. 17:1997;6803-6814.
43. Taylor E., Broughton B., Botta E., Stefanini M., Sarasin A., Jaspers N., Fawcett H., Harcourt S., Arlett C., Lehmann A. Xeroderma pigmentosum and trichothiodystrophy are associated with different mutations in the XPD (ERCC2) repair/transcription gene. Proc. Natl. Acad. Sci. USA. 94:1997;8658-8663.
44. Troelstra C., van Gool A., de Wit J., Vermeulen W., Bootsma D., Hoeijmakers J.H. ERCC6, a member of a subfamily of putative helicases, is involved in Cockayne's syndrome and preferential repair of active genes. Cell. 71:1992;939-953.
45. van Gool A.J., Citterio E., Rademakers S., van Os R., Vermeulen W., Constantinou A., Egly J.-M., Bootsma D., Hoeijmakers J.H.J. The Cockayne syndrome B protein, involved in transcription-coupled DNA repair, resides in an RNA polymerase II-containing complex. EMBO J. 16:1997;5955-5965.
46. Yu A., Fan H.Y., Liao D., Bailey A.D., Weiner A.M. Activation of p53 or loss of the Cockayne syndrome group B repair protein causes metaphase fragility of human U1, U2, and 5S genes. Mol. Cell. 5:2000;801-810.