Transcription without XPB Establishes a Unified Helicase-Independent Mechanism of Promoter Opening in Eukaryotic Gene Expression

被引:56
作者
Alekseev, Sergey [1 ,2 ,3 ,4 ]
Nagy, Zita [1 ,2 ,3 ,4 ]
Sandoz, Jeremy [1 ,2 ,3 ,4 ]
Weiss, Amelie [1 ,2 ,3 ,4 ]
Egly, Jean-Marc [1 ,2 ,3 ,4 ]
Le May, Nicolas [1 ,2 ,3 ,4 ]
Coin, Frederic [1 ,2 ,3 ,4 ]
机构
[1] Univ Strasbourg, Dept Funct Genom & Canc, Equipe Labellisee Ligue 2014, CNRS,INSERM,IGBMC, BP 163, F-67404 Illkirch Graffenstaden, Cu Strasbourg, France
[2] Ctr Natl Rech Sci, UMR7104, F-67404 Illkirch Graffenstaden, France
[3] Inst Natl Sante & Rech Med, U964, F-67404 Illkirch Graffenstaden, France
[4] Univ Strasbourg, F-67404 Illkirch Graffenstaden, France
关键词
RNA-POLYMERASE-II; NUCLEOTIDE EXCISION-REPAIR; DNA-REPAIR; PREINITIATION COMPLEX; FACTOR TFIIH; DAMAGED DNA; IN-VIVO; INITIATION; ATP; MUTATIONS;
D O I
10.1016/j.molcel.2017.01.012
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Transcription starts with the assembly of pre-initiation complexes on promoters followed by their opening. Current models suggest that class II gene transcription requires ATP and the TFIIH XPB subunit to open a promoter. Here, we observe that XPB depletion surprisingly leaves transcription virtually intact. In contrast, inhibition of XPB ATPase activity affects transcription, revealing that mRNA expression paradoxically accommodates the absence of XPB while being sensitive to the inhibition of its ATPase activity. The XPB-depleted TFIIH complex is recruited to active promoters and contributes to transcription. We finally demonstrate that the XPB ATPase activity is only used to relieve a transcription initiation block imposed by XPB itself. In the absence of this block, transcription initiation can take place without XPB ATPase activity. These results suggest that a helicase is dispensable for mRNA transcription, thereby unifying the mechanism of promoter DNA opening for the three eukaryotic RNA polymerases.
引用
收藏
页码:504 / +
页数:15
相关论文
共 42 条
[1]   A Small Molecule Screen Identifies an Inhibitor of DNA Repair Inducing the Degradation of TFIIH and the Chemosensitization of Tumor Cells to Platinum [J].
Alekseev, Sergey ;
Ayadi, Meriam ;
Brino, Laurent ;
Egly, Jean-Marc ;
Larsen, Annette K. ;
Coin, Frederic .
CHEMISTRY & BIOLOGY, 2014, 21 (03) :398-407
[2]  
Araújo SJ, 2000, GENE DEV, V14, P349
[3]   Mutations in the XPD helicase gene result in XP and TTD phenotypes, preventing interaction between XPD and the p44 subunit of TFIIH [J].
Coin, F ;
Marinoni, JC ;
Rodolfo, C ;
Fribourg, S ;
Pedrini, AM ;
Egly, JM .
NATURE GENETICS, 1998, 20 (02) :184-188
[4]   Nucleotide excision repair driven by the dissociation of CAK from TFIIH [J].
Coin, Frederic ;
Oksenych, Valentyn ;
Mocquet, Vincent ;
Groh, Stefanie ;
Blattner, Christine ;
Egly, Jean Marc .
MOLECULAR CELL, 2008, 31 (01) :9-20
[5]   Distinct roles for the XPB/p52 and XPD/p44 subcomplexes of TFIIH in damaged DNA opening during nucleotide excision repair [J].
Coin, Frederic ;
Oksenych, Valentyn ;
Egly, Jean-Marc .
MOLECULAR CELL, 2007, 26 (02) :245-256
[6]   Nucleotide Excision Repair and Transcriptional Regulation: TFIIH and Beyond [J].
Compe, Emmanuel ;
Egly, Jean-Marc .
ANNUAL REVIEW OF BIOCHEMISTRY, VOL 85, 2016, 85 :265-290
[7]   DUAL ROLE OF TFIIH IN DNA EXCISION-REPAIR AND IN TRANSCRIPTION BY RNA-POLYMERASE-II [J].
DRAPKIN, R ;
REARDON, JT ;
ANSARI, A ;
HUANG, JC ;
ZAWEL, L ;
AHN, KJ ;
SANCAR, A ;
REINBERG, D .
NATURE, 1994, 368 (6473) :769-772
[8]   XPB: An unconventional SF2 DNA helicase [J].
Fan, Li ;
DuPrez, Kevin T. .
PROGRESS IN BIOPHYSICS & MOLECULAR BIOLOGY, 2015, 117 (2-3) :174-181
[9]   DUAL ROLES OF A MULTIPROTEIN COMPLEX FROM SACCHAROMYCES-CEREVISIAE IN TRANSCRIPTION AND DNA-REPAIR [J].
FEAVER, WJ ;
SVEJSTRUP, JQ ;
BARDWELL, L ;
BARDWELL, AJ ;
BURATOWSKI, S ;
GULYAS, KD ;
DONAHUE, TF ;
FRIEDBERG, EC ;
KORNBERG, RD .
CELL, 1993, 75 (07) :1379-1387
[10]   Structural Basis for Promoter-10 Element Recognition by the Bacterial RNA Polymerase σ Subunit [J].
Feklistov, Andrey ;
Darst, Seth A. .
CELL, 2011, 147 (06) :1257-1269