Identical components of yeast transcription factor IIIB are required and sufficient for transcription of TATA box-containing and TATA-less genes.
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RNA polymerase III transcription from the human U6 and adenovirus type 2 VAI promoters has different requirements for human BRF, a subunit of human TFIIIBCloning and characterization of SNAP50, a subunit of the snRNA-activating protein complex SNAPcDifferent human TFIIIB activities direct RNA polymerase III transcription from TATA-containing and TATA-less promotersAlternatively spliced hBRF variants function at different RNA polymerase III promotersA novel upstream RNA polymerase III promoter element becomes essential when the chromatin structure of the yeast U6 RNA gene is altered.A cryptic DNA binding domain at the COOH terminus of TFIIIB70 affects formation, stability, and function of preinitiation complexes.High-mobility-group proteins NHP6A and NHP6B participate in activation of the RNA polymerase III SNR6 gene.The RNA polymerase III transcription initiation factor TFIIIB participates in two steps of promoter opening.The Brf and TATA-binding protein subunits of the RNA polymerase III transcription factor IIIB mediate position-specific integration of the gypsy-like element, Ty3.A post-recruitment function for the RNA polymerase III transcription-initiation factor IIIBA subunit of yeast TFIIIC participates in the recruitment of TATA-binding proteinA novel subunit of yeast RNA polymerase III interacts with the TFIIB-related domain of TFIIIB70.Cloning, expression, and function of TFC5, the gene encoding the B" component of the Saccharomyces cerevisiae RNA polymerase III transcription factor TFIIIB.Cloning and functional characterization of the gene encoding the TFIIIB90 subunit of RNA polymerase III transcription factor TFIIIB.Functional and structural organization of Brf, the TFIIB-related component of the RNA polymerase III transcription initiation complex.Survey and summary: transcription by RNA polymerases I and III.RNA polymerase II/III transcription specificity determined by TATA box orientation.Kinetic trapping of DNA by transcription factor IIIBComparison of the RNA polymerase III transcription machinery in Schizosaccharomyces pombe, Saccharomyces cerevisiae and human.Role of TATA box sequence and orientation in determining RNA polymerase II/III transcription specificity.RNA polymerase III transcription: its control by tumor suppressors and its deregulation by transforming agents.Small nuclear RNA genes: a model system to study fundamental mechanisms of transcription.The fission yeast TFIIB-related factor limits RNA polymerase III to a TATA-dependent pathway of TBP recruitment.The Saccharomyces cerevisiae RNA polymerase III recruitment factor subunits Brf1 and Bdp1 impose a strict sequence preference for the downstream half of the TATA box.Use of a macromolecular crowding agent to dissect interactions and define functions in transcriptional activation by a DNA-tracking protein: bacteriophage T4 gene 45 protein and late transcription.A common site on TBP for transcription by RNA polymerases II and IIITFIIIB placement on a yeast U6 RNA gene in vivo is directed primarily by TFIIIC rather than by sequence-specific DNA contactsSilkworm TFIIIB binds both constitutive and silk gland-specific tRNA Ala promoters but protects only the constitutive promoter from DNase I cleavage.Functional dissection of the B" component of RNA polymerase III transcription factor IIIB: a scaffolding protein with multiple roles in assembly and initiation of transcriptionDistinct roles of transcription factors TFIIIB and TFIIIC in RNA polymerase III transcription reinitiation.Genome-wide occupancy profile of the RNA polymerase III machinery in Saccharomyces cerevisiae reveals loci with incomplete transcription complexes.A TATA element is required for tRNA promoter activity and confers TATA-binding protein responsiveness in Drosophila Schneider-2 cells.TATA-Binding protein-TATA interaction is a key determinant of differential transcription of silkworm constitutive and silk gland-specific tRNA(Ala) genes.Architecture of protein and DNA contacts within the TFIIIB-DNA complex.Polymerase (Pol) III TATA box-binding protein (TBP)-associated factor Brf binds to a surface on TBP also required for activated Pol II transcription.Marking the start site of RNA polymerase III transcription: the role of constraint, compaction and continuity of the transcribed DNA strand.Multiple roles of the tau131 subunit of yeast transcription factor IIIC (TFIIIC) in TFIIIB assemblyA differential response of wild type and mutant promoters to TFIIIB70 overexpression in vivo and in vitro.A tetratricopeptide repeat mutation in yeast transcription factor IIIC131 (TFIIIC131) facilitates recruitment of TFIIB-related factor TFIIIB70.Interactions between yeast TFIIIB components.
P2860
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P2860
Identical components of yeast transcription factor IIIB are required and sufficient for transcription of TATA box-containing and TATA-less genes.
description
1994 nî lūn-bûn
@nan
1994年の論文
@ja
1994年論文
@yue
1994年論文
@zh-hant
1994年論文
@zh-hk
1994年論文
@zh-mo
1994年論文
@zh-tw
1994年论文
@wuu
1994年论文
@zh
1994年论文
@zh-cn
name
Identical components of yeast ...... ontaining and TATA-less genes.
@en
type
label
Identical components of yeast ...... ontaining and TATA-less genes.
@en
prefLabel
Identical components of yeast ...... ontaining and TATA-less genes.
@en
P2093
P2860
P356
P1476
Identical components of yeast ...... ontaining and TATA-less genes.
@en
P2093
C A Joazeiro
E P Geiduschek
G A Kassavetis
P2860
P304
P356
10.1128/MCB.14.4.2798
P407
P577
1994-04-01T00:00:00Z