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General transcription factor

General transcription factors (GTFs) are a set of proteins and protein complexes that are essential for the accurate initiation of transcription by RNA polymerase II in eukaryotic cells, enabling the synthesis of messenger RNA (mRNA) from protein-coding genes.^[1] These factors assemble sequentially at core promoter elements, such as the TATA box or initiator sequence, to form the pre-initiation complex (PIC), which recruits and positions RNA polymerase II at the transcription start site (TSS).^[2] By stabilizing polymerase binding, promoting DNA unwinding, and facilitating promoter clearance, GTFs ensure basal levels of transcription and serve as a scaffold for gene-specific regulatory factors.^[1] The core GTFs for RNA polymerase II transcription include TFIID, TFIIA, TFIIB, TFIIE, TFIIF, and TFIIH, each contributing distinct functions to PIC assembly and activation.^[2] TFIID, composed of the TATA-binding protein (TBP) and TBP-associated factors (TAFs), initiates the process by recognizing and binding the TATA box, inducing a sharp DNA bend to recruit subsequent factors.^[1] TFIIA stabilizes this TBP-DNA interaction, while TFIIB bridges TFIID to the RNA polymerase II-TFIIF complex, precisely positioning the polymerase over the TSS.^[2] TFIIF aids in polymerase recruitment and stabilizes the complex during early elongation, whereas TFIIE and TFIIH complete PIC formation; TFIIE supports DNA melting, and TFIIH uses its ATPase/helicase activity to unwind promoter DNA while phosphorylating the carboxyl-terminal domain (CTD) of RNA polymerase II via its CDK7 subunit, promoting transcription initiation and escape.^[1]^[2] GTFs are conserved across eukaryotes, though variations exist, such as multigene families in plants that allow nuanced responses to developmental cues and stress.^[2] Notably, TBP is a universal component also required for transcription by RNA polymerases I and III, underscoring the foundational role of GTFs in cellular gene expression.^[1] Disruptions in GTF function can lead to impaired transcription, highlighting their critical importance in maintaining genomic regulation and cellular homeostasis.^[2]

Overview

Definition and role

General transcription factors (GTFs) constitute a class of proteins essential for the basal transcription of protein-coding genes in eukaryotes, functioning to assemble RNA polymerase II at core promoter sequences and form the preinitiation complex (PIC) required for transcription initiation. These factors enable the recognition of promoter elements without conferring sequence-specific regulation, supporting the constitutive expression of genes at minimal levels.^[3]^[4] In eukaryotes, multiple GTFs—including TFIIA, TFIIB, TFIID (comprising TBP and TAFs), TFIIE, TFIIF, and TFIIH—cooperatively assemble with RNA polymerase II at core promoters, where TFIID's TBP subunit binds the TATA box to nucleate PIC formation and subsequent recruitment of other components. This assembly positions RNA polymerase II at the transcription start site, facilitating promoter melting and the escape into productive elongation.^[5]^[6]^[4] GTFs are indispensable for cellular viability, as their disruption halts essential transcription; for instance, conditional knockouts of TFIIB in yeast (Saccharomyces cerevisiae) result in cell lethality by impairing PIC assembly and basal transcription. Their universal conservation underscores their fundamental role in sustaining life processes. GTFs were first identified in the 1980s through pioneering in vitro reconstitution experiments, which demonstrated that purified RNA polymerase alone was insufficient for accurate promoter-dependent transcription, necessitating these accessory factors for PIC formation.^[7]

Distinction from specific factors

General transcription factors (GTFs) are a class of ubiquitous proteins that assemble on the core promoters of all genes transcribed by RNA polymerase II, enabling the constitutive, basal level of transcription essential for housekeeping functions across all protein-coding genes.^[1] Unlike sequence-specific transcription factors (sTFs), GTFs do not recognize unique DNA sequences but instead bind promoter-proximal elements such as the TATA box in a relatively non-specific manner to position RNA polymerase II for initiation.^[8] In contrast, sTFs are diverse, low-abundance proteins that bind to specific DNA motifs in enhancers or silencers, often located distantly from the promoter, to modulate gene expression in response to cellular signals, developmental cues, or environmental stimuli.^[8] For example, the tumor suppressor p53 acts as an sTF by binding to consensus response elements in target gene promoters to activate transcription of genes involved in cell cycle arrest and apoptosis following DNA damage.^[9] Similarly, NF-κB functions as an sTF that recognizes κB sites in regulatory regions to drive expression of inflammatory and immune response genes upon activation by pathogens or stress.^[10] While GTFs form the core preinitiation complex that serves as the foundational platform for transcription, sTFs exert regulatory control by recruiting, stabilizing, or modifying this complex to achieve gene-selective fine-tuning of expression levels.^[8] This functional overlap underscores the hierarchical nature of transcription regulation, where GTFs provide the universal machinery and sTFs impose specificity.^[1]

Classification

Prokaryotic types

In prokaryotes, general transcription factors (GTFs) are notably simpler than their eukaryotic counterparts, typically involving fewer components to facilitate promoter recognition and transcription initiation by RNA polymerase.^[11] In bacteria, the primary GTF is the sigma (σ) factor, a dissociable subunit of RNA polymerase that confers promoter specificity.^[12] The housekeeping σ70 factor, prevalent in species like Escherichia coli, recognizes conserved promoter elements such as the -10 box (TATAAT) and -35 box (TTGACA), enabling the recruitment of the core RNA polymerase holoenzyme.^[12] Alternative sigma factors, such as σS for stationary phase or σE for heat stress, direct transcription to specific gene sets under environmental challenges, allowing adaptive responses without the need for additional GTFs.^[12] Unlike eukaryotic GTFs, bacterial sigma factors associate transiently with RNA polymerase and dissociate shortly after initiation, recycling for subsequent rounds of transcription.^[12] Archaea employ a more eukaryote-like but still streamlined set of GTFs, primarily TATA-binding protein (TBP) and transcription factor B (TFB), which together with RNA polymerase suffice for basal transcription from TATA-box promoters.^[13] TBP binds the TATA box to bend DNA and recruit the polymerase, while TFB, homologous to eukaryotic TFIIB, stabilizes this complex and positions the start site, often interacting with a BRE (TFB recognition element) upstream.^[13] Some archaea also utilize TFE (a TFIIE α homolog) to enhance open complex formation, resulting in typically 3-4 GTF components overall, reflecting an evolutionary intermediate between bacterial simplicity and eukaryotic complexity.^[14] In contrast to the full eukaryotic TFII suite required for RNA polymerase II, archaea lack factors like TFIIA, TFIIE (beyond TFE), TFIIF, and TFIIH.^[13] Prokaryotic GTFs represent evolutionary precursors to the more numerous and stably associated eukaryotic factors, with archaeal TBP and TFB sharing direct homology that underscores the archaeal origin of eukaryotic basal transcription machinery.^[11]

Eukaryotic types

In eukaryotes, general transcription factors (GTFs) are essential multi-subunit complexes that facilitate the assembly of the preinitiation complex (PIC) for the three major RNA polymerases, with the TFII family primarily supporting RNA polymerase II (Pol II) for mRNA synthesis.^[2] Unlike the simpler prokaryotic systems, eukaryotic GTFs exhibit greater complexity, involving up to 14 subunits in some cases, to accommodate diverse core promoter elements and regulatory needs.^[15] For Pol II transcription, the core GTFs include TFIIA, TFIIB, TFIID, TFIIE, TFIIF, and TFIIH, each with distinct roles in promoter recognition and PIC formation. TFIIA is a multi-subunit protein (comprising α, β, and γ subunits in higher eukaryotes) that stabilizes the binding of TFIID to the TATA box and enhances promoter specificity by interacting with upstream elements.^[2] TFIIB, a single polypeptide, bridges the TFIID-DNA complex to Pol II and TFIIF, positioning the polymerase at the start site while recognizing BRE (TFIIB recognition element) sequences.^[2] TFIID is a large complex consisting of the TATA-binding protein (TBP) and 13-14 TBP-associated factors (TAFs), responsible for core promoter recognition, including TATA, initiator (INR), and downstream promoter elements (DPE); TAFs provide additional DNA-binding specificity beyond TBP's bending activity.^[15] TFIIE, a heterotetrameric complex (α and β subunits), recruits TFIIH to the PIC and stabilizes promoter opening.^[2] TFIIF, also heterotetrameric (including RAP30 and RAP74 subunits), associates with Pol II to deliver it to the promoter and aids in the initial RNA synthesis steps.^[2] TFIIH is a 10-subunit complex with helicase (XPB, XPD) and kinase (CDK7) activities, essential for DNA melting at the transcription start site and phosphorylation of Pol II's C-terminal domain.^[2] Beyond Pol II, eukaryotes employ specialized GTFs for the other polymerases. For RNA polymerase I (Pol I), which transcribes ribosomal RNA, SL1 (selectivity factor 1) is a multi-subunit complex containing TBP and TAFs that recruits Pol I to rDNA promoters in cooperation with upstream binding factor (UBF).^[1] For RNA polymerase III (Pol III), responsible for tRNA and 5S rRNA genes, TFIIIB is a multi-subunit assembly including TBP that directs Pol III to internal promoters like A-box and B-box elements.^[1] These GTFs are indispensable for all cellular mRNA, rRNA, and small RNA production, underscoring their universal role in gene expression.^[2] Eukaryotic GTFs also display variations through tissue-specific isoforms, particularly TBP-related factors (TRFs) that can substitute for or complement TBP in developmental contexts. TRF1, found in Drosophila, supports Pol III transcription and select Pol II promoters.^[16] TRF2 is testis-specific in mammals, aiding spermiogenesis by promoting chromatin compaction during meiosis.^[16] TRF3 (TBPL2) drives mesendoderm specification and muscle differentiation in vertebrates, replacing TBP in certain lineages.^[16] TRF4, identified in Drosophila, functions in cytoplasmic roles but influences developmental transcription programs.^[17] These TRFs enable specialized PIC assembly in tissues like gonads and embryos, enhancing regulatory flexibility.^[16]

Structural features

Core domains and motifs

General transcription factors (GTFs) possess conserved domains and motifs that facilitate their interactions with DNA and other proteins during transcription initiation. In prokaryotes, sigma factors, which serve as the primary GTF, feature helix-turn-helix (HTH) motifs in their region 4 for sequence-specific DNA recognition at the -35 promoter element. These HTH motifs consist of two alpha helices connected by a short turn, with the recognition helix inserting into the major groove of DNA to contact bases. In archaea and eukaryotes, transcription factor B (TFB or TFIIB) contains an HTH motif in its C-terminal core domain that recognizes the BRE (TFB recognition element) upstream of the TATA box. Meanwhile, the TATA-binding protein (TBP), a universal GTF subunit, adopts a saddle-shaped structure formed by a curved antiparallel beta-sheet, enabling it to bind the minor groove of the TATA box and induce significant DNA distortion.^[18]^[19]^[20] Protein-protein interaction domains in GTFs are equally critical for assembling the pre-initiation complex (PIC). In TFIIB, the B-reader domain, a flexible loop near the N-terminus, and the B-linker, an alpha-helical extension, interact with the RNA polymerase II (Pol II) dock region to position the enzyme correctly over the promoter. These elements stabilize early transcription intermediates by contacting the nascent RNA chain. In eukaryotes, TFIIE includes a zinc-finger motif in its alpha subunit (TFIIEα) that coordinates a zinc ion to maintain structural integrity and facilitate binding to TFIIH and Pol II. TFIIH, in turn, features coiled-coil domains in its core subunits, such as the p62 subunit in humans, which mediate dimerization and interactions with TFIIE to anchor the helicase modules for DNA unwinding.^[21]^[22]^[23] High-resolution structural studies, particularly cryo-electron microscopy (cryo-EM) of the eukaryotic PIC from 2017 to 2023, have revealed the precise architecture of these domains at resolutions of 2.5–3.8 Å, showing TBP's saddle-shaped beta-sheet inserting into the minor groove and bending promoter DNA by approximately 80°. These structures highlight how the HTH in TFIIB/TFB orients the complex asymmetrically on DNA. The archaeal TBP-TFB complex serves as a minimalist model, with crystal structures at 2.1–2.4 Å resolution demonstrating conserved interactions where TFB's core domain wraps around TBP-bound DNA, facilitating polymerase recruitment without additional factors.00629-2)^[24] A distinctive feature of eukaryotic TFIID, which includes TBP and TBP-associated factors (TAFs), lies in the histone-fold domains of certain TAF subunits, such as TAF6-9 and TAF10-11 heterodimers, that mimic the structure of core histones H3/H4 and H2A/H2B. These histone-like motifs enable TFIID to engage promoter-proximal nucleosomes, promoting their displacement or remodeling to expose the core promoter for PIC assembly.45003-4/fulltext)^[25]

Assembly interfaces

Assembly interfaces in general transcription factors (GTFs) refer to the specific protein-protein contact surfaces that enable the ordered assembly of the pre-initiation complex (PIC) by facilitating interactions among GTFs and RNA polymerase II (Pol II) in eukaryotes, or their homologs in prokaryotes and archaea. These interfaces, often built upon core domains such as zinc ribbons and helix-turn-helix motifs, ensure stable docking and positional accuracy during transcription initiation.^[26] In eukaryotes, a prominent interface involves the TFIIB core domain, which docks adjacent to the Pol II dock region, stabilizing the PIC through the TFIIB N-terminal zinc-ribbon domain binding directly to the dock.^[26] Another critical contact is the TFIID-TFIIA interface, where TFIIA's β-barrel and four-helix bundle motifs extend the TBP β-sheet and interact with the upstream DNA, stabilizing the sharply bent TBP-DNA complex via hydrogen bonds and electrostatic interactions with the DNA backbone.^[27] In bacterial and archaeal systems, analogous interfaces support promoter recognition. The sigma factor's region 4, featuring a helix-turn-helix motif, binds the -35 promoter element by inserting into the DNA major groove, forming hydrogen bonds with conserved guanines at positions -35 and -34 to ensure specific recognition without significant DNA bending.^[28] In archaea, the saddle-shaped TBP interacts with its TFIIB homolog TFB at the convex surface opposite the DNA-binding saddle, facilitating promoter element recognition and complex stability through conserved hydrophobic and electrostatic contacts.^[29] Dynamic conformational changes at these interfaces drive PIC maturation. For instance, in the eukaryotic TFIIH complex, the XPB subunit undergoes a rotational conformational switch, powered by ATP hydrolysis, to load and unwind promoter DNA, as resolved in cryo-EM structures at approximately 4 Å resolution.^[30] While the Mediator complex serves as a bridge between GTFs and specific transcription factors to integrate regulatory signals, GTF-Pol II interfaces remain basal and constitutive; for example, the TFIIF subunit RAP30 (RAP30) binds the mobile clamp domain of Pol II via its C-terminal domain, suppressing non-specific DNA interactions and stabilizing the core PIC.^[31]^[32]

Mechanisms of action

Initiation in prokaryotes

In bacterial transcription initiation, the RNA polymerase (RNAP) core enzyme associates with a sigma (σ) factor to form the holoenzyme, which specifically recognizes promoter sequences. The primary housekeeping σ factor, such as σ⁷⁰ in Escherichia coli, directs the holoenzyme to the promoter's conserved -35 (TTGACA) and -10 (TATAAT) boxes via its region 4 and 2 domains, respectively, enabling initial closed complex formation.^[33]^[12] Following binding, the holoenzyme undergoes isomerization, driven by interactions between σ region 2.4 and the -10 box, leading to DNA melting and formation of the open complex with a transcription bubble of approximately 13-14 base pairs from -11 to +3 relative to the transcription start site (+1).^[34]^[33] Transcription then initiates at +1 upon incorporation of the first nucleotide triphosphate (NTP), with the σ factor remaining associated until promoter clearance, after which it typically dissociates to allow elongation.^[12]^[35] In archaea, transcription initiation involves TATA-binding protein (TBP) and transcription factor B (TFB) as the core general transcription factors, which recruit the multi-subunit RNAP to promoters lacking bacterial-like σ-dependent elements. TBP initially binds the TATA box (consensus sequence such as TTTWWWW or YTTATATA depending on the archaeal group, located approximately 25 bp upstream of +1), bending the DNA and creating a platform that recruits TFB via its B-reader and B-linker domains, forming a TBP-TFB complex.^[36]^[37]^[38] This scaffold then engages the RNAP dock domain, positioning the catalytic cleft over the promoter without a dedicated helicase; DNA melting (~13 bp bubble) is instead facilitated by RNAP's clamp domain dynamics and initial NTP incorporation.^[36]^[39] A hallmark of prokaryotic initiation in both bacteria and archaea is abortive initiation, where RNAP synthesizes short RNA oligomers (typically 2-10 nucleotides) that are repeatedly released without promoter escape, allowing promoter clearance only upon productive elongation after ~10-15 nt synthesis; this process is powered solely by NTP hydrolysis, without requiring ATP-dependent remodeling.^[35]^[40] In vitro reconstitution assays demonstrate σ⁷⁰'s specificity for housekeeping promoters, such as those driving ribosomal RNA operons, where open complex formation rates exceed 0.1 min^-1 at physiological salt concentrations, underscoring its role in constitutive gene expression.^[41]^[42]

Initiation in eukaryotes

In eukaryotic transcription initiation, the preinitiation complex (PIC) assembles sequentially on the core promoter to position RNA polymerase II (Pol II) at the transcription start site (TSS), enabling the synthesis of messenger RNA. This process requires the coordinated action of general transcription factors (GTFs), including TFIID, TFIIA, TFIIB, TFIIF, TFIIE, and TFIIH, which overcome chromatin barriers and facilitate DNA unwinding in an ATP-dependent manner. Unlike prokaryotic initiation, eukaryotic assembly is ordered and multi-step, ensuring precise TSS selection and promoter recognition.^[43] The assembly begins with TFIID binding to the core promoter, where the TATA-box-binding protein (TBP) subunit inserts into the minor groove of the TATA box, bending the DNA by approximately 80 degrees, while TBP-associated factors (TAFs) recognize additional elements such as the initiator (Inr) sequence surrounding the TSS and the downstream promoter element (DPE) located 28-34 base pairs downstream. The Inr, often consisting of a pyrimidine-rich motif like YYANWYY in mammals, and the DPE, such as RGWYVT in Drosophila, are directly contacted by specific TAFs, enhancing promoter specificity particularly in TATA-less promoters. TFIIA and TFIIB then stabilize this initial complex: TFIIA reinforces TBP-DNA interactions to prevent dissociation, while TFIIB bridges TFIID to the incoming Pol II, orienting it via its B-reader and B-linker domains.^[44]^[45] Next, the TFIIF-Pol II module joins the growing complex, with TFIIF's RAP30 and RAP74 subunits loading Pol II onto the promoter and stabilizing its clamp domain for DNA engagement. TFIIE is subsequently recruited by TFIIB and TFIIF, forming a platform that allosterically activates TFIIH through interactions with its core and kinase modules. Finally, TFIIH binds and initiates DNA melting primarily using its XPB helicase subunit, which translocates along the DNA to unwind the double helix, generating a transcription bubble of approximately 15 base pairs centered near the TSS. This unwinding, powered by ATP hydrolysis, exposes the template strand for initial nucleotide incorporation by Pol II.^[43]^[46]^[47] Following open complex formation, promoter clearance occurs as Pol II escapes the promoter to enter early elongation, driven by TFIIH's kinase subunit (CDK7 in humans) phosphorylating the C-terminal domain (CTD) of Pol II at serine 5, which promotes the release of GTFs like TFIIB and TFIIE while facilitating the recruitment of elongation factors. TBP often remains associated with the promoter post-initiation, enabling GTF recycling for subsequent rounds of transcription and maintaining promoter accessibility in chromatin contexts. Recent cryo-electron microscopy (cryo-EM) structures from the 2020s have revealed dynamic PIC configurations, showing how TFIIH kinase activity resolves promoter-proximal pausing of Pol II by phosphorylating the CTD and coordinating with the Mediator complex to transition to productive elongation.^[48]^[49]

Regulation and significance

Modulatory mechanisms

General transcription factors (GTFs) are subject to post-translational modifications that fine-tune their activity and integration into the pre-initiation complex (PIC). Phosphorylation by the TFIIH-associated kinase CDK7 targets the C-terminal domain (CTD) of RNA polymerase II, specifically the heptad repeats YSPTSPS, to promote promoter clearance and elongation. Acetylation of TBP by histone acetyltransferases such as p300 and PCAF enhances its DNA-binding affinity and stability within the TFIID complex, facilitating promoter recognition. GTF function is further modulated through protein-protein interactions with co-activators and repressors. The Mediator co-activator complex bridges sequence-specific activators and the PIC, enhancing recruitment of GTFs like TFIID and TFIIH to promoters and stimulating basal transcription rates. Conversely, the repressor NC2 (negative cofactor 2) binds to the underside of the TBP-DNA complex, inhibiting TBP association with promoters and preventing PIC assembly. Environmental cues influence GTF activity via alternative factors and chromatin dynamics. The TBP-related factor 2 (TRF2) regulates neuronal gene expression during differentiation through alternative splicing, acting as a TBP family member that can form transcription complexes on certain promoters.^[50] Chromatin remodeling complexes like SWI/SNF facilitate GTF access to nucleosomal DNA by evicting or repositioning nucleosomes at promoters, thereby enabling TFIID binding and PIC formation.^[51] The stoichiometry of GTFs imposes quantitative limits on transcription efficiency. TFIID, as the rate-limiting GTF due to its low cellular abundance relative to other components, controls the overall rate of PIC assembly and thus global transcription output.^[52]

Role in disease and evolution

Mutations in subunits of the general transcription factor TFIIH, particularly the helicase components XPB and XPD, are a primary cause of xeroderma pigmentosum, a rare genetic disorder characterized by defective nucleotide excision repair of DNA damage, leading to extreme sensitivity to ultraviolet light and a markedly elevated risk of skin cancer.^[53] These mutations impair TFIIH's dual role in transcription initiation and DNA repair, resulting in reduced transcriptional activity and accumulation of DNA lesions that promote carcinogenesis.^[54] Similarly, variants in TFIID subunits, such as missense mutations in TAF1, have been linked to X-linked developmental disorders including intellectual disability, dystonia, and dysmorphic features, often presenting with global developmental delay and neurological symptoms like hypotonia.^[55]^[56] These TAF1 alterations disrupt TFIID assembly and promoter recognition, underscoring GTFs' critical involvement in neurodevelopment.^[57] Therapeutically, GTFs represent promising targets in oncology, where inhibitors of CDK7—a kinase subunit of TFIIH—block phosphorylation of the RNA polymerase II C-terminal domain, thereby suppressing aberrant transcription in cancer cells and inducing selective tumor cell death.^[58] Compounds like THZ1 exemplify this approach, demonstrating efficacy against transcriptionally addicted cancers such as MYC-driven malignancies by globally reducing Pol II processivity without broadly affecting normal cells.^[59] Evolutionarily, GTFs trace their origins to archaea, where TBP and TFB serve as foundational "ur-GTFs" for basal transcription initiation, binding TATA-like promoters to recruit RNA polymerase in a simplified machinery conserved across domains of life.^[60] In eukaryotes, this system expanded through gene duplications, notably of TAF subunits in TFIID, which evolved histone-like folds to integrate chromatin remodeling into transcription, enabling regulation of the ~80% of the human genome transcribed by RNA polymerase II.^[61]^[62] Key innovations include the TFIIH helicase modules (XPB/XPD), which likely arose to resolve chromatin barriers during transcription, facilitating the transition from prokaryotic-like systems to complex eukaryotic gene expression.^[63]

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TFIID, a megadalton-sized multiprotein complex comprising 20 subunits, is among the first GTFs to bind the core promoter. TFIID assists in nucleating PIC ...
[50]
Mutations in XPB and XPD helicases found in xeroderma ...
As part of TFIIH, XPB and XPD helicases have been shown to play a role in nucleotide excision repair (NER). Mutations in these subunits are associated with ...
[51]
Mutations in XPB and XPD helicases found in xeroderma ... - PubMed
As part of TFIIH, XPB and XPD helicases have been shown to play a role in nucleotide excision repair (NER). Mutations in these subunits are ...
[52]
Missense variants in TAF1 and developmental phenotypes
We recently identified individuals from nine families in which missense or splice-site variants in the X-linked gene TAF1 were associated with hypotonia, ...
[53]
TAF1 Variants Are Associated with Dysmorphic Features, Intellectual ...
We describe an X-linked genetic syndrome associated with mutations in TAF1 and manifesting with global developmental delay, intellectual disability (ID), ...
[54]
The roles of TAF1 in neuroscience and beyond - PubMed
Sep 25, 2024 · TAF1 is dysregulated in X-linked dystonia-parkinsonism and congenital mutations in the gene are causative for neurodevelopmental phenotypes; ...
[55]
Cdk7: a kinase at the core of transcription and in the crosshairs ... - NIH
Cdk7, associated with the transcription initiation factor TFIIH, is both an effector CDK that phosphorylates Pol II and other targets within the ...
[56]
Inhibit Globally, Act Locally: CDK7 Inhibitors in Cancer Therapy
Aug 11, 2014 · GTFs such as TFIID and ... THZ1 Inhibits the CDK7 Kinase Activity, Pol II CTD Phosphorylation, and Global Transcription in Cancer Cells.
[57]
Gene regulation technologies for gene and cell therapy
May 7, 2025 · This review highlights next-generation technologies under development to expand the reach of gene therapies by enabling precise modulation of gene expression.
[58]
The evolution of TBP in archaea and their eukaryotic offspring - NIH
TBP binding to the promoter is essential for the recruitment of the second conserved basal transcription factor termed TFB (transcription factor B) in archaea ...
[59]
Histone-like TAFs Are Essential for Transcription In Vivo - Cell Press
In yeast, the TBP-associated factors (TAFs) Taf17, Taf60, and Taf61(68) resemble histones H3, H4, and H2B, respectively. To analyze their roles in vivo, ...<|separator|>
[60]
ATAC-king the complexity of SAGA during evolution
During evolution, gene duplications have occurred for TAF5, TAF6, TAF9, TAF10, GCN5, and ADA2. In yeast, the Taf5 and Taf6 proteins are part of SAGA but ...
[61]
Envisioning how the prototypic molecular machine TFIIH functions in ...
Sep 17, 2020 · We provocatively consider that TFIIH may have first evolved from evolutionary pressure for TCR to resolve arrested transcription blocks to DNA ...
[62]
Evolutionarily recent transcription factors partake in human cell cycle ...
Aug 13, 2025 · Here, we systematically map the influence of evolutionarily recent transcription factors (TFs) on human cell cycle progression. We find that the ...