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121
Cytoplasmic mRNA decay represses RNA polymerase II transcription during early apoptosis
Published 2021-06-01Subjects: Get full text
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122
Condensin II Counteracts Cohesin and RNA Polymerase II in the Establishment of 3D Chromatin Organization
Published 2019-03-01Get full text
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123
Repression of RNA polymerase II elongation in vivo is critically dependent on the C-terminus of Spt5.
Published 2009-09-01“…The stalling of RNA polymerase II (RNAPII) at the promoters of many genes, including developmental regulators, stress-responsive genes, and HIVLTR, suggests transcription elongation as a critical regulatory step in addition to initiation. …”
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124
BRCA2 Regulates Transcription Elongation by RNA Polymerase II to Prevent R-Loop Accumulation
Published 2018-01-01Subjects: Get full text
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125
Structural basis of RNA polymerase II transcription on the chromatosome containing linker histone H1
Published 2022-11-01Get full text
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126
Condensin controls recruitment of RNA polymerase II to achieve nematode X-chromosome dosage compensation
Published 2013-06-01“…Here we define TSSs and the distribution of transcriptionally engaged RNA polymerase II (Pol II) genome-wide in wild-type and dosage-compensation-defective animals to dissect this regulatory mechanism. …”
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127
Maintenance of long-range DNA interactions after inhibition of ongoing RNA polymerase II transcription.
Published 2008-01-01“…We demonstrate that upon transcription inhibition binding of RNA polymerase II to gene regulatory elements is severely reduced. …”
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128
Autophagy receptor NDP52 alters DNA conformation to modulate RNA polymerase II transcription
Published 2023-05-01“…We find that NDP52 clusters with RNA Polymerase II (RNAPII) at transcription initiation sites and that its overexpression promotes the formation of additional transcriptional clusters. …”
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129
Prdm5 regulates collagen gene transcription by association with RNA polymerase II in developing bone.
Published 2012-01-01“…In particular, we show that Prdm5 controls both Collagen I transcription and fibrillogenesis by binding inside the Col1a1 gene body and maintaining RNA polymerase II occupancy. In vivo, Prdm5 loss results in delayed ossification involving a pronounced impairment in the assembly of fibrillar collagens. …”
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130
A DNA damage response system associated with the phosphoCTD of elongating RNA polymerase II.
Published 2013-01-01“…RNA polymerase II translocates across much of the genome and since it can be blocked by many kinds of DNA lesions, detects DNA damage proficiently; it thereby contributes to DNA repair and to normal levels of DNA damage resistance. …”
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131
Poised RNA Polymerase II Changes over Developmental Time and Prepares Genes for Future Expression
Published 2012-12-01“…Poised RNA polymerase II (Pol II) is predominantly found at developmental control genes and is thought to allow their rapid and synchronous induction in response to extracellular signals. …”
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132
Recruitment of TREX to the transcription machinery by its direct binding to the phospho-CTD of RNA polymerase II.
Published 2013-11-01“…Here, we show that TREX is recruited to the transcription machinery by direct interaction of its subcomplex THO with the serine 2-serine 5 (S2/S5) diphosphorylated CTD of RNA polymerase II. S2 and/or tyrosine 1 (Y1) phosphorylation of the CTD is required for TREX occupancy in vivo, establishing a second interaction platform necessary for TREX recruitment in addition to RNA. …”
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133
Distinct Cdk9-phosphatase switches act at the beginning and end of elongation by RNA polymerase II
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134
Phosphorylation Status of RNA Polymerase II Carboxyl-terminal Domain in Porcine Oocytes and Early Embryos
Published 2012-06-01Subjects: “…RNA Polymerase II…”
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135
Sensitivity of mitochondrial transcription and resistance of RNA polymerase II dependent nuclear transcription to antiviral ribonucleosides.
Published 2012-01-01“…We show that all of the anti-HCV ribonucleoside analogues are substrates for human mitochondrial RNA polymerase (POLRMT) and eukaryotic core RNA polymerase II (Pol II) in vitro. Unexpectedly, analogues containing 2'-C-methyl, 4'-methyl and 4'-azido substituents were inhibitors of POLRMT and Pol II. …”
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136
The host RNA polymerase II C-terminal domain is the anchor for replication of the influenza virus genome
Published 2024-02-01“…Abstract The current model is that the influenza virus polymerase (FluPol) binds either to host RNA polymerase II (RNAP II) or to the acidic nuclear phosphoprotein 32 (ANP32), which drives its conformation and activity towards transcription or replication of the viral genome, respectively. …”
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137
The nucleosomal barrier to promoter escape by RNA polymerase II is overcome by the chromatin remodeler Chd1
Published 2014-04-01Subjects: Get full text
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138
GRANT Motif Regulates CENP-A Incorporation and Restricts RNA Polymerase II Accessibility at Centromere
Published 2022-09-01Subjects: Get full text
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139
The RNA Polymerase II Factor RPAP1 Is Critical for Mediator-Driven Transcription and Cell Identity
Published 2018-01-01“…Keywords: transcription, RNA polymerase II, Mediator, cell identity, differentiation, interactome, enhancer…”
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140
Striatal NELF-mediated RNA polymerase II stalling controls l-dopa induced dyskinesia
Published 2016-01-01“…Their rapid transcription involves the stalling of RNA polymerase II on IEG promoters, a mechanism that critically depends on the presence of the negative elongation factor (NELF) protein complex. …”
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