Literature DB >> 8617234

MAT1, cdk7 and cyclin H form a kinase complex which is UV light-sensitive upon association with TFIIH.

J P Adamczewski1, M Rossignol, J P Tassan, E A Nigg, V Moncollin, J M Egly.   

Abstract

MAT1, cyclin H and cdk7 are part of TFIIH, a class II transcription factor which possesses numerous subunits of which several have been shown to be involved in processes other than transcription. Two of them, XPD (ERCC2) and XPB (ERCC3), are helicases involved in nucleotide excision repair (NER), whereas cdk7, cyclin H and MAT1 are thought to participate in cell cycle regulation. MAT1, cyclin H and cdk7 exist as a ternary complex either free or associated with TFIIH from which the latter can be dissociated at high salt concentration. MAT1 is strongly associated with cdk7 and cyclin H. Although not strictly required for the formation and activity of the complex, it stimulates its kinase activity. The kinase activity of TFIIH, which is constant during the cell cycle, is reduced after UV light irradiation.

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Year:  1996        PMID: 8617234      PMCID: PMC450106     

Source DB:  PubMed          Journal:  EMBO J        ISSN: 0261-4189            Impact factor:   11.598


  41 in total

1.  The cellular responses to DNA damage.

Authors:  A M Carr; M F Hoekstra
Journal:  Trends Cell Biol       Date:  1995-01       Impact factor: 20.808

2.  Mitotic regulation of a TATA-binding-protein-containing complex.

Authors:  R J White; T M Gottlieb; C S Downes; S P Jackson
Journal:  Mol Cell Biol       Date:  1995-04       Impact factor: 4.272

Review 3.  Transcription by RNA polymerase II: a process linked to DNA repair.

Authors:  C Chalut; V Moncollin; J M Egly
Journal:  Bioessays       Date:  1994-09       Impact factor: 4.345

4.  Phosphorylation of C-terminal domain of RNA polymerase II is not required in basal transcription.

Authors:  H Serizawa; J W Conaway; R C Conaway
Journal:  Nature       Date:  1993-05-27       Impact factor: 49.962

5.  Mitotic repression of RNA polymerase III transcription in vitro mediated by phosphorylation of a TFIIIB component.

Authors:  J M Gottesfeld; V J Wolf; T Dang; D J Forbes; P Hartl
Journal:  Science       Date:  1994-01-07       Impact factor: 47.728

6.  Production of large numbers of mitotic mammalian cells by use of the reversible microtubule inhibitor nocodazole. Nocodazole accumulated mitotic cells.

Authors:  G W Zieve; D Turnbull; J M Mullins; J R McIntosh
Journal:  Exp Cell Res       Date:  1980-04       Impact factor: 3.905

7.  Three unusual repair deficiencies associated with transcription factor BTF2(TFIIH): evidence for the existence of a transcription syndrome.

Authors:  W Vermeulen; A J van Vuuren; M Chipoulet; L Schaeffer; E Appeldoorn; G Weeda; N G Jaspers; A Priestley; C F Arlett; A R Lehmann
Journal:  Cold Spring Harb Symp Quant Biol       Date:  1994

8.  Human general transcription factor IIH phosphorylates the C-terminal domain of RNA polymerase II.

Authors:  H Lu; L Zawel; L Fisher; J M Egly; D Reinberg
Journal:  Nature       Date:  1992-08-20       Impact factor: 49.962

9.  Relationship of CDK-activating kinase and RNA polymerase II CTD kinase TFIIH/TFIIK.

Authors:  W J Feaver; J Q Svejstrup; N L Henry; R D Kornberg
Journal:  Cell       Date:  1994-12-16       Impact factor: 41.582

10.  p44 and p34 subunits of the BTF2/TFIIH transcription factor have homologies with SSL1, a yeast protein involved in DNA repair.

Authors:  S Humbert; H van Vuuren; Y Lutz; J H Hoeijmakers; J M Egly; V Moncollin
Journal:  EMBO J       Date:  1994-05-15       Impact factor: 11.598

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  46 in total

Review 1.  Phosphorylation in transcription: the CTD and more.

Authors:  T Riedl; J M Egly
Journal:  Gene Expr       Date:  2000

Review 2.  Dial 9-1-1 for p53: mechanisms of p53 activation by cellular stress.

Authors:  M Ljungman
Journal:  Neoplasia       Date:  2000 May-Jun       Impact factor: 5.715

3.  CAK-independent activation of CDK6 by a viral cyclin.

Authors:  P Kaldis; P M Ojala; L Tong; T P Mäkelä; M J Solomon
Journal:  Mol Biol Cell       Date:  2001-12       Impact factor: 4.138

4.  Substrate specificity of the cdk-activating kinase (CAK) is altered upon association with TFIIH.

Authors:  M Rossignol; I Kolb-Cheynel; J M Egly
Journal:  EMBO J       Date:  1997-04-01       Impact factor: 11.598

5.  Regulation of CDK7 substrate specificity by MAT1 and TFIIH.

Authors:  K Y Yankulov; D L Bentley
Journal:  EMBO J       Date:  1997-04-01       Impact factor: 11.598

6.  Phosphorylation of XPB helicase regulates TFIIH nucleotide excision repair activity.

Authors:  Frédéric Coin; Jérome Auriol; Angel Tapias; Pascale Clivio; Wim Vermeulen; Jean-Marc Egly
Journal:  EMBO J       Date:  2004-11-18       Impact factor: 11.598

7.  T-loop phosphorylation stabilizes the CDK7-cyclin H-MAT1 complex in vivo and regulates its CTD kinase activity.

Authors:  S Larochelle; J Chen; R Knights; J Pandur; P Morcillo; H Erdjument-Bromage; P Tempst; B Suter; R P Fisher
Journal:  EMBO J       Date:  2001-07-16       Impact factor: 11.598

Review 8.  TFIIH: when transcription met DNA repair.

Authors:  Emmanuel Compe; Jean-Marc Egly
Journal:  Nat Rev Mol Cell Biol       Date:  2012-05-10       Impact factor: 94.444

9.  Human and yeast cdk-activating kinases (CAKs) display distinct substrate specificities.

Authors:  P Kaldis; A A Russo; H S Chou; N P Pavletich; M J Solomon
Journal:  Mol Biol Cell       Date:  1998-09       Impact factor: 4.138

10.  Mat1 inhibits peroxisome proliferator-activated receptor gamma-mediated adipocyte differentiation.

Authors:  Katja Helenius; Ying Yang; Jukka Alasaari; Tomi P Mäkelä
Journal:  Mol Cell Biol       Date:  2008-11-03       Impact factor: 4.272

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