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RNA polymerase II phosphorylation

Herpes Simplex Virus Type 1 Infection Leads to Loss of Serine-2 Phosphorylation on the Carboxyl-Terminal Domain of RNA Polymerase II

Herpes Simplex Virus Type 1 Infection Leads to Loss of Serine-2 Phosphorylation on the Carboxyl-Terminal Domain of RNA Polymerase II

... RNAP II to nuclear ...RNAP II decline dra- matically after HSV-1 ...RNAP II or with other LS-specific MAbs (ARNA3, 8WG16, or H14) for ...RNAP II declines significantly after ...RNAP II ...

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Stress Induces Changes in the Phosphorylation of Trypanosoma cruzi RNA Polymerase II, Affecting Its Association with Chromatin and RNA Processing

Stress Induces Changes in the Phosphorylation of Trypanosoma cruzi RNA Polymerase II, Affecting Its Association with Chromatin and RNA Processing

... Pol II and anti- ␤ -tubulin antibodies, as ...Pol II antibodies (E) or permeabilized and incubated with Br-UTP (F), following labeling with anti-BrdU as described in Materials and ...Pol II (green), ...

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Smicl is required for phosphorylation of RNA polymerase II and affects
3′ end processing of RNA at the midblastula transition in
Xenopus

Smicl is required for phosphorylation of RNA polymerase II and affects 3′ end processing of RNA at the midblastula transition in Xenopus

... Smicl is expressed both maternally and zygotically during Xenopus development (Collart et al., 2005b). Direct targets of Smicl are likely to be among the first to be up- or downregulated by loss of Smicl function. To ...

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Schueller, Roland
  

(2013):


	Insights into the RNA Polymerase CTD code.


Dissertation, LMU München: Fakultät für Biologie

Schueller, Roland (2013): Insights into the RNA Polymerase CTD code. Dissertation, LMU München: Fakultät für Biologie

... overall phosphorylation frequency along the whole CTD is different between IIO and IIA forms, as only small CTD fragments, mainly 14 or 21 amino acids long, originating from the same CTD could be ...the ...

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Transcription of Hepatitis Delta Virus RNA by RNA Polymerase II

Transcription of Hepatitis Delta Virus RNA by RNA Polymerase II

... genomic RNA is sensitive to ...antigenomic RNA. In contrast, Macnaughton et al. obtained data that antigenomic RNA syn- thesis seemed resistant to amanitin, but we consider that the signals they ...

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Unusual Properties of Adenovirus E2E Transcription by RNA Polymerase III

Unusual Properties of Adenovirus E2E Transcription by RNA Polymerase III

... eight RNA polymerase II transcription units ...cellular RNA polymerase III, the enzyme responsible for the synthesis of small cellular RNAs that function in such pro- cesses as ...

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RNA polymerase II mediated transcription at active loci does not require
histone H3S10 phosphorylation in Drosophila

RNA polymerase II mediated transcription at active loci does not require histone H3S10 phosphorylation in Drosophila

... H3S10 phosphorylation in transcriptional regulation in Drosophila ...H3S10 phosphorylation levels and ...H3S10 phosphorylation (Wang et ...H3S10 phosphorylation are upregulated on the male X ...

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Phosphorylation of RNA polymerase II is independent of P TEFb in the C  elegans germline

Phosphorylation of RNA polymerase II is independent of P TEFb in the C elegans germline

... ‘paused’ polymerase, i.e. Pol II that has initiated transcription but cannot progress to ...paused polymerase signatures are also largely absent from C. elegans Pol II profiles, excluding a ...

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A Role for Histone Chaperones in Regulating RNA Polymerase II

A Role for Histone Chaperones in Regulating RNA Polymerase II

... RNAPII transcribes mRNA from a DNA template in all protein-encoding genes. Transcription relies on a coor- dinated network of histone modifying enzymes and histone chaperones to allow elongating RNAPII to traverse the ...

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Phosphorylation of Serine 177 of the Small Hepatitis Delta Antigen Regulates Viral Antigenomic RNA Replication by Interacting with the Processive RNA Polymerase II

Phosphorylation of Serine 177 of the Small Hepatitis Delta Antigen Regulates Viral Antigenomic RNA Replication by Interacting with the Processive RNA Polymerase II

... RNAP II during both the initiation and elongation phases of tran- scription (66), the possible interaction of different forms of RNAP II with different isoforms of SHDAg during transcrip- tion has not been ...

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RNA Polymerase II during Transcript Elongation: deaiing with DNA damage and staying phosphorylated

RNA Polymerase II during Transcript Elongation: deaiing with DNA damage and staying phosphorylated

... dependent phosphorylation of Rad53 demonstrates the biochemical potential of the whole cell extract prepared here ...DNA, RNA polymerase II, RNA, and CSB to recruit TFIIH correlates ...

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Bioinformatics resources for deciphering the biogenesis and action pathways of plant small RNAs

Bioinformatics resources for deciphering the biogenesis and action pathways of plant small RNAs

... the Pol IV-, RDR2-, and DCL3-dependent pathway (Zhang et al., 2012). Moreover, in Borsani et al. ’ s study (2005), 21- and 24-nt nat-siRNAs were demonstrated to be produced from a cis -NAT pair through the RDR6- and ...

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The Selenocysteine tRNA Gene in Leishmania major Is Transcribed by both RNA Polymerase II and RNA Polymerase III

The Selenocysteine tRNA Gene in Leishmania major Is Transcribed by both RNA Polymerase II and RNA Polymerase III

... total RNA was hybridized with a tRNA-Sec ...400-base RNA most likely corresponds to the transcript that contains the miniexon and a poly(A) tail of about 130 ...

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α-Amanitin-Resistant Viral RNA Synthesis in Nuclei Isolated from Nuclear Polyhedrosis Virus-Infected Heliothis zea Larvae and Spodoptera frugiperda Cells

α-Amanitin-Resistant Viral RNA Synthesis in Nuclei Isolated from Nuclear Polyhedrosis Virus-Infected Heliothis zea Larvae and Spodoptera frugiperda Cells

... Symbols: *-*, RNA synthesized in infected nuclei minus a-amanitin; polymerase II activity and NPV infection by various concentrations of a-amanitin in the cell culture *---@, RNA synthes[r] ...

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Environmental adaptability and stress tolerance of Laribacter hongkongensis: a genome-wide analysis

Environmental adaptability and stress tolerance of Laribacter hongkongensis: a genome-wide analysis

... (RpoE): RNA polymerase sigma-E factor; σ 28 (FliA): RNA polymerase sigma factor for flagellar operon; σ 32 (RpoH): RNA polymerase sigma-32 factor; σ 38 (RpoS): RNA ...

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A phase I trial of the selective oral cyclin-dependent kinase inhibitor seliciclib (CYC202;R-Roscovitine), administered twice daily for 7-days every 21 days.

A phase I trial of the selective oral cyclin-dependent kinase inhibitor seliciclib (CYC202;R-Roscovitine), administered twice daily for 7-days every 21 days.

... phase II dose in that study was 2500 mg per day for 5 days, although this was reported to be associated with manageable grade 3 hypokalaemia and grade 3 skin ...

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Expression of RNA virus proteins by RNA polymerase II dependent expression plasmids is hindered at multiple steps

Expression of RNA virus proteins by RNA polymerase II dependent expression plasmids is hindered at multiple steps

... cytoplasmic RNA viruses by DNA expression ...intronless RNA was retained and degraded in the nucleus, while the same transcript generated by splic- ing reached the cytoplasm ...

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Interaction of RNA polymerase II and the small RNA machinery affects heterochromatic silencing in Drosophila

Interaction of RNA polymerase II and the small RNA machinery affects heterochromatic silencing in Drosophila

... using RNA Pol II 140 (A5)/+ as a ...analysis, RNA Pol II 140 (A5)/+; dcr-2 (G173E)/+ showed decreased H3K9me2 deposition at the chromocentre compared with the single heterozygote of RNA ...

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Vaccinia virus RNA polymerase associated with nuclei of infected HeLa cells.

Vaccinia virus RNA polymerase associated with nuclei of infected HeLa cells.

... RNA polymerase I and vaccinia RNA polymerase were not distinguished in the intact nuclei, but hybridization of 3% of the RNA synthesized by nuclei from infected cells in the presence of [r] ...

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Cycles of gene expression and genome response during mammalian tissue regeneration

Cycles of gene expression and genome response during mammalian tissue regeneration

... Pol II occupancy within the gene body at 36–72 h post-PH; a pattern consistent with the association of the sole H3K36me3 methyltrans- ferase SetD2 with the traveling Pol II ...

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