E. Friedberg, W. Walker, R. Siede, R. Wood, A. Schultz et al., DNA repair and mutagenesis, 2006.

M. Zurita and C. Merino, The transcriptional complexity of the TFIIH complex, Trends in Genetics, vol.19, issue.10, pp.578-584, 2003.
DOI : 10.1016/j.tig.2003.08.005

G. Giglia-mari, F. Coin, J. Ranish, D. Hoogstraten, and A. Theil, A new, tenth subunit of TFIIH is responsible for the DNA repair syndrome trichothiodystrophy group A, Nature Genetics, vol.54, issue.7, pp.714-719, 2004.
DOI : 10.1093/emboj/cdg489

Y. Takagi, C. Masuda, W. Chang, H. Komori, and D. Wang, Ubiquitin Ligase Activity of TFIIH and the Transcriptional Response to DNA Damage, Molecular Cell, vol.18, issue.2, pp.237-243, 2005.
DOI : 10.1016/j.molcel.2005.03.007

A. Lehmann, Dual functions of DNA repair genes: molecular, cellular, and clinical implications, BioEssays, vol.16, issue.2, pp.146-155, 1998.
DOI : 10.1002/(SICI)1521-1878(199802)20:2<146::AID-BIES7>3.0.CO;2-R

A. Lehmann, DNA repair-deficient diseases, xeroderma pigmentosum, Cockayne syndrome and trichothiodystrophy, Biochimie, vol.85, issue.11, pp.1101-1111, 2003.
DOI : 10.1016/j.biochi.2003.09.010

J. Ranish, S. Hahn, Y. Lu, E. Yi, X. Li et al., Identification of TFB5, a new component of general transcription and DNA repair factor IIH, Nature Genetics, vol.266, issue.7, pp.707-713, 2004.
DOI : 10.1016/0092-8674(91)90168-X

F. Coin, P. De-santis, L. Nardo, T. Zlobinskaya, and O. , p8/TTD-A as a Repair-Specific TFIIH Subunit, Molecular Cell, vol.21, issue.2, pp.215-226, 2006.
DOI : 10.1016/j.molcel.2005.10.024
URL : https://hal.archives-ouvertes.fr/hal-00187863

Y. Zhou, H. Kou, and Z. Wang, Tfb5 interacts with Tfb2 and facilitates nucleotide excision repair in yeast, Nucleic Acids Research, vol.35, issue.3, pp.861-871, 2007.
DOI : 10.1093/nar/gkl1085

F. Coin, F. Oksenych, and J. Egly, Distinct Roles for the XPB/p52 and XPD/p44 Subcomplexes of TFIIH in Damaged DNA Opening during Nucleotide Excision Repair, Molecular Cell, vol.26, issue.2, pp.245-256, 2007.
DOI : 10.1016/j.molcel.2007.03.009
URL : https://hal.archives-ouvertes.fr/hal-00190901

G. Giglia-mari, C. Miquel, A. Theil, P. Mari, and D. Hoogstraten, Dynamic Interaction of TTDA with TFIIH Is Stabilized by Nucleotide Excision Repair in Living Cells, PLoS Biology, vol.115, issue.6, pp.156-166, 2006.
DOI : 10.1371/journal.pbio.0040156.sg003

J. Jung and N. Bonini, CREB-Binding Protein Modulates Repeat Instability in a Drosophila Model for PolyQ Disease, Science, vol.315, issue.5820, pp.1857-1859, 2007.
DOI : 10.1126/science.1139517

P. Auluck, H. Chan, J. Trsjanowski, V. Lee, and N. Bonini, Chaperone Suppression of alpha -Synuclein Toxicity in a Drosophila Model for Parkinson's Disease, Science, vol.295, issue.5556, pp.865-868, 2002.
DOI : 10.1126/science.1067389

L. Mounkes, R. Jones, L. Bee-choo, W. Gelbart, and M. Fuller, A Drosophila model for xeroderma pigmentosum and Cockayne's syndrome: haywire encodes the fly homolog of ERCC3, a human excision repair gene, Cell, vol.71, issue.6, pp.925-937, 1992.
DOI : 10.1016/0092-8674(92)90389-T

C. Merino, E. Reynaud, M. Vazquez, and M. Zurita, DNA Repair and Transcriptional Effects of Mutations in TFIIH in Drosophila Development, Molecular Biology of the Cell, vol.13, issue.9, pp.3246-3256, 2002.
DOI : 10.1091/mbc.E02-02-0087

M. Fregoso, J. Lainé, J. Aguilar-fuentes, and V. Mocquet, DNA Repair and Transcriptional Deficiencies Caused by Mutations in the Drosophila p52 Subunit of TFIIH Generate Developmental Defects and Chromosome Fragility, Molecular and Cellular Biology, vol.27, issue.10, pp.3640-3650, 2007.
DOI : 10.1128/MCB.00030-07
URL : https://hal.archives-ouvertes.fr/hal-00189989

L. Mounkes and M. Fuller, Molecular characterization of mutant alleles of the DNA repair/basal transcription factor haywire/ERCC3 in Drosophila, Genetics, vol.152, pp.291-297, 1999.

E. Botta, T. Nardo, A. Lehmann, J. Egly, A. Pedrini et al., Reduced level of the repair/transcription factor TFIIH in trichothiodystrophy, Human Molecular Genetics, vol.11, issue.23, pp.2919-2928, 2002.
DOI : 10.1093/hmg/11.23.2919

A. Jawhari, J. Lainé, S. Dubaele, V. Lamour, and A. Poterszman, p52 Mediates XPB Function within the Transcription/Repair Factor TFIIH, Journal of Biological Chemistry, vol.277, issue.35, pp.31761-31767, 2002.
DOI : 10.1074/jbc.M203792200

M. Shivji, J. Moggs, I. Kuraoka, and R. Wood, Dual-incision assays for nucleotide excision repair using DNA with a lesion at a specific site, Met Mol Biol, vol.113, pp.373-392, 1999.

T. Riedl, F. Hanoaka, and J. Egly, The comings and goings of nucleotide excision repair factors on damaged DNA, The EMBO Journal, vol.22, issue.19, pp.5293-5303, 2003.
DOI : 10.1093/emboj/cdg489

J. Lainé and J. Egly, When transcription and repair meet: a complex system, Trends in Genetics, vol.22, issue.8, pp.430-436, 2006.
DOI : 10.1016/j.tig.2006.06.006

N. Kobayashi, S. Katsumi, K. Imoto, A. Nakagawa, and S. Miyagawa, Quantitation and Visualization of Ultraviolet-Induced DNA Damage Using Specific Antibodies: Application to Pigment Cell Biology, Pigment Cell Research, vol.14, issue.2, pp.94-102, 2001.
DOI : 10.1034/j.1600-0749.2001.140204.x

V. Bohr, C. Smith, D. Okumoto, and P. Hanawalt, 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, vol.40, issue.2, pp.359-369, 1985.
DOI : 10.1016/0092-8674(85)90150-3

Y. You, D. Lee, J. Yoon, S. Nakajima, and A. Yasui, Cyclobutane Pyrimidine Dimers Are Responsible for the Vast Majority of Mutations Induced by UVB Irradiation in Mammalian Cells, Journal of Biological Chemistry, vol.276, issue.48, pp.44688-44694, 2001.
DOI : 10.1074/jbc.M107696200

L. Riou, E. Eveno, A. Van-hoffen, A. Van-zeeland, and A. Sarasin, Differential Repair of the Two Major UV-Induced Photolesions in Trichothiodystrophy Fibroblasts, Cancer Research, vol.64, issue.3, pp.889-894, 2004.
DOI : 10.1158/0008-5472.CAN-03-2070

J. Cock-de, A. Van-hoffen, J. Wijnands, G. Molenaar, and P. Lohman, Repair of UV induced (6-4)photoproducts measured in individual genes in the Drosophila embryonic Kc cell line. Nuc Acid Res, pp.4789-4793, 1992.

S. Ito, I. Kuraoka, P. Chymkowitch, E. Compe, and A. Takedachi, XPG Stabilizes TFIIH, Allowing Transactivation of Nuclear Receptors: Implications for Cockayne Syndrome in XP-G/CS Patients, Molecular Cell, vol.26, issue.2, pp.231-243, 2007.
DOI : 10.1016/j.molcel.2007.03.013
URL : https://hal.archives-ouvertes.fr/hal-00189983

O. Schä-rer, The molecular basis for different disease states caused by mutations in TFIIH and XPG, DNA Repair, vol.7, issue.2, pp.339-344, 2008.
DOI : 10.1016/j.dnarep.2007.10.007

Y. Hirose and Y. Ohkuma, Phosphorylation of the C-terminal Domain of RNA Polymerase II Plays Central Roles in the Integrated Events of Eucaryotic Gene Expression, Journal of Biochemistry, vol.141, issue.5, pp.601-608, 2007.
DOI : 10.1093/jb/mvm090

S. Macneill, S. Moreno, N. Reynolds, P. Nurse, and P. Fantes, The fission yeast Cdc1 protein, a homologue of the small subunit of DNA polymerase delta, binds to Pol3 and Cdc27, EMBO J, vol.15, pp.4613-4618, 1996.

C. Wilkinson, K. Ferrell, M. Penney, M. Wallace, and W. Dubiel, Analysis of a Gene Encoding Rpn10 of the Fission Yeast Proteasome Reveals That the Polyubiquitin-binding Site of This Subunit Is Essential When Rpn12/Mts3 Activity Is Compromised, Journal of Biological Chemistry, vol.275, issue.20, pp.15182-15192, 2000.
DOI : 10.1074/jbc.275.20.15182

J. Offman, J. N. Theron, T. Pallas, J. Hubank, and M. , Transcriptional changes in trichothiodystrophy cells, DNA Repair, vol.7, issue.8, 2008.
DOI : 10.1016/j.dnarep.2008.05.002

D. Kainov, M. Vitorino, J. Cavarelli, A. Porterszman, and J. Egly, Structural basis for group A trichothiodystrophy, Nature Structural & Molecular Biology, vol.276, issue.9, 2008.
DOI : 10.1038/nsmb.1478
URL : https://hal.archives-ouvertes.fr/inserm-00357162

J. De-boer, J. De-wit, H. Van-steeg, R. Berg, and H. Morreau, A Mouse Model for the Basal Transcription/DNA Repair Syndrome Trichothiodystrophy, Molecular Cell, vol.1, issue.7, pp.981-990, 1998.
DOI : 10.1016/S1097-2765(00)80098-2

J. De-boer, H. Van-steeg, R. Berg, J. Garssen, and J. De-wit, Mouse model for the DNA repair/basal transcription disorder trichothiodystrophy reveals cancer predisposition, Cancer Res, vol.59, pp.3489-3494, 1999.