We TFIIH consists of nine subunits, and one of them, Cdk7, possesses kinase activity. Transcription factor IIH (TFIIH) is a multiprotein complex involved in both eukaryotic transcription and DNA repair, revealing a tight connection between these two processes. Its activities include DNA-dependent ATPase helicase, C-terminal domain kinase, catalyzation of promoter escape, and participation in NER. TAF7 inhibited the phosphorylation of the Pol II CTD by the CAK complex, demonstrating that TAF7 acts directly on CAK ( Fig. TFIIH consists of a complex of 10 subunits, 3 of which including the CDK7 kinase form a subcomplex called CAK ( 28 ). TFIIH transcriptional activity and TFIIH-associated CTD kinase activity are repressed in the mitotic extract. Here the substrate specicities (A) Transcription of the CMV MIEP or the HIV-1 promoter was monitored (as The columns enzyme activities of TFIIH contribute to transcrip-tion has remained elusive. TFIIE stimulates the TFIIH-dependent kinase activity that phosphorylates the carboxy-terminal domain of the largest subunit of RNA polymerase II 6, and possesses a Inhibition of CAK prevents cell cycle from progressing. The kinase activity of TFIIH displayed stronger substrate preference for Cdk4 than did CAK. Kin28, the TFIIH kinase subunit, is important for promoter escape not elongation Kin28 depletion dramatically increases Mediator occupancy at the core promoter Stronger defects in promoter escape are linked to stronger transcriptional effects TFIIH phosphorylation of the CTD causes Mediator dissociation and promoter escape Summary These sections were identical in different eukaryotic organisms from yeast to humans, suggesting that these regions may be important for tuning or controlling the activity Three subunits of TFIIH, cdk7, cyclin H and MAT1, form a ternary complex, cdk-activating kinase (CAK), found either on its own or as part of TFIIH. Here the substrate specificities of TFIIH and two forms of the Cdk7-containing kinase complex are These and other observations to be discussed below strongly suggest that the loss of Kin28 kinase, rather than the TFIIH complex, results in a defect in promoter escape, such that Pol II spends relatively more time at or near the PIC in the Kin28-depleted strain than in the control strain. Concomitant with the open complex The discrepancy between mRNA level and Pol II density is attributed to the defective 5-capping, which results in the destabilization of mRNAs. TFIIH, a 10-subunit complex with many resident enzymatic activities, is essential for transcription by RNA polymerase II (Pol II) ( 1 5 ). A subunit of TFIIH with helicase activity unwinds DNA and promotes the formation of a transcriptionally competent open complex (510). [1] TFIIH is also part of the DNA repair machinery and phosphorylates both cdc2 and cdk2 (Shiekhattar et al. Transcription factor II Human is an important protein complex, having roles in transcription of various protein-coding genes and DNA nucleotide excision repair pathways. Requirement for TFIIH kinase activity in transcription by RNA polymerase II Sasha Akoulitchev, Tomi P. Mkel, Robert A. Weinberg & Danny Reinberg Nature 377 , TFIIH consists of nine subunits, and one of them, Cdk7, possesses kinase activity. During transcription of protein coding genes, the ATP-dependent helicase activity of XPB is required for promoter opening, and the cyclin-dependent kinase 7 (CDK7) kinase Both roles are TFIIH, a large protein complex consisting of 10 subunits, is functionally divided into two subcomplexes ( Table 1) [99]: the seven-subunit core, which contains three disease-related gene products, XPB ( ERCC3 ), XPD ( ERCC2 ), and TTDA ( GTF2H5) [100102]; and the CDK-activating kinase (CAK) module, composed of CDK7, cyclin H, and MAT1 [103,104]. The general transcription factor TFIIH plays important roles in initiation and the transition to 1994; Shiekhattar et al. Repression of TFIIH Transcriptional Activity and TFIIH-Associated cdk7 Kinase Activity at Mitosis TFIIH consists of two subcomplexes: the core complex, comprising ATP-dependent helicases, and the CAK complex, which harbours the kinase activity of CDK7 [ 8 ]. TAF7 inhibited the CTD kinase activities of TFIIH ( Fig. Download : Download high-res image (444KB) This mechanism ensures the fidelity of chromosome transmission. Surprisingly, inhibition of TFIIH kinase activity only partially affected both Pol II density and Ser-2 phosphorylation level. 1 B ). These results suggest that the TFIIH kinase activity is essential for CDK7 is the serine/threonine kinase of the basal transcription factor TFIIH. Background The general transcription factor TFIIH plays important roles in initiation and the transition to elongation steps of transcription by RNA polymerase II (PolII). The kinase subunit (Kin28 in S. cerevisiae or Cdk7 in humans) marks the transcriptionally active polymerase by hyperphosphorylating the C-terminal domain (CTD) of its largest subunit ( Lee and Young, 2000, Liu et al., 2013, Roeder, 1996 ). A kinase activity specific for CTD is a component of the general transcription factor TFIIH. chemical genetics CTD kinase TFIIH disassembly T FIIH, a 10-subunit complex with many resident enzymatic activities,isessentialfortranscriptionbyRNApolymeraseII (Pol II) (15). 1995). for the genes transcribed by rna polymerase iii (pol iii) (such as 5s rrna and trna genes), previous studies have documented that the activity of the general class iii transcription factor tfiiib is greatly diminished in extracts from synchronized mitotic cells (49) or by the conversion of an interphase xenopusegg extract to the mitotic state by HeLa nuclear extract was fractionated on equivalent GST-VP16 or control GST affinity columns. 1995). TFIIH is a eukaryotic complex composed of two subcomplexes, the CAK (Cdk Activating Kinase) and the core-TFIIH. TFIIH first came to For an activated promoter, targets of repression are TFIID and TFIIH, while for a basal promoter, TFIIH is the major target for mitotic inactivation of transcription. the kinase activity, are critical for global gene transcription. Additionally, this heterotrimer is part of a larger complex termed general transcription factor TFIIH that contains the major RNA polymerase II C-terminal domain kinase activity (22, 23). Here we show that human TFIIH has DNA-dependent ATPase activity and we characterize the stimulatory effect of TFIIE on both the ATPase and kinase activities. TFIIH along with Pol II and several Recently, a cyclin-dependent kinase-activator kinase (MO15 and cyclin H) was The transcription/DNA repair factor TFIIH consists of nine subunits, several exhibiting known functions: helicase/ATPase, kinase activity and DNA binding. We also show that transcription requires CTD kinase activity provided by the CDK7 subunit of TFIIH17-19. Moreover, TFIIH-phosphorylated CTD stimulated SETD1A/B activity toward nucleosomes, revealing a mechanistic basis for CDK7 regulation of H3K4me3 spreading. Cdk7 is the kinase catalytic subunit of CAK, the Cdc2 activating kinase complex, consisting of Cdk7, cyclin H and MAT-1 (19-21). Figure 1: TFIIH(CAK) CTD kinase activity binds to the VP16 activation domain. The substrate specificities ofTFIIH and two forms of the Cdk7containing kinase complex are compared, and the relationship between transcription activity and the TFIIHdependent phosphorylation of the carboxy terminal domain of the largest subunit of PolII (CTD) is studied. TFIIH contains a DNA-dependent ATPase activity, two ATP-dependent DNA helicase activities, and a kinase activity specific for the CTD of RNAPII ( Drapkin and Reinberg 1994; During the transcription, TFIIH enters the RNA It is a member of the Transcription Factor IIH (TFIIH) complex and has been shown to be essential for phosphorylation of the C-terminal Domain of RNA polymerase II (Feaver et al. 1 A ). We observed a strong negative correlation between the gene-expression ratio and transcription rate. [1] The activity of CAK associated with TFIIH decreases when DNA is damaged by UV irradiation. Decreased CAK activity creates a feedback loop, which turns off TFIIH activity. TFIIH along with Pol II and several other multisubunit complexes assembles into a preinitiation complex CAK also plays a role in DNA damage response. It is shown that the CTD, but not its phosphoryla-tion, is required for initiation of
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