Splicing speckles are not reservoirs of RNA polymerase II, but contain an inactive form, phosphorylated on serine2 residues of the C-terminal domain.
about
N6-methyladenosine in nuclear RNA is a major substrate of the obesity-associated FTOAn architectural role for a nuclear noncoding RNA: NEAT1 RNA is essential for the structure of paraspecklesThe chromatin remodeling factor CHD8 interacts with elongating RNA polymerase II and controls expression of the cyclin E2 geneSubnuclear localization and dynamics of the Pre-mRNA 3' end processing factor mammalian cleavage factor I 68-kDa subunitRNA Polymerase II C-Terminal Domain: Tethering Transcription to Transcript and TemplateCancer biomarker discovery: the entropic hallmark.Intermingling of chromosome territories in interphase suggests role in translocations and transcription-dependent associationsMyc dynamically and preferentially relocates to a transcription factory occupied by IghMaintenance of long-range DNA interactions after inhibition of ongoing RNA polymerase II transcription.Poised transcription factories prime silent uPA gene prior to activation.Inhibition of U4 snRNA in human cells causes the stable retention of polyadenylated pre-mRNA in the nucleus.Changes in histone H3 lysine 36 methylation in porcine oocytes and preimplantation embryos.Gene positioning.Phosphorylation Status of RNA Polymerase II Carboxyl-terminal Domain in Porcine Oocytes and Early Embryos.FUS immunogold labeling TEM analysis of the neuronal cytoplasmic inclusions of neuronal intermediate filament inclusion disease: a frontotemporal lobar degeneration with FUS proteinopathy.T-loop phosphorylated Cdk9 localizes to nuclear speckle domains which may serve as sites of active P-TEFb function and exchange between the Brd4 and 7SK/HEXIM1 regulatory complexes.Paraspeckles.Hierarchical molecular events driven by oocyte-specific factors lead to rapid and extensive reprogrammingProteomic analysis of mitotic RNA polymerase II reveals novel interactors and association with proteins dysfunctional in disease.Subnuclear compartmentalization of transiently expressed polyadenylated pri-microRNAs: processing at transcription sites or accumulation in SC35 foci.RNAP-II molecules participate in the anchoring of the ORC to rDNA replication origins.A human artificial chromosome recapitulates the metabolism of native telomeres in mammalian cellsRNA-related nuclear functions of human Pat1b, the P-body mRNA decay factor.Subcellular distribution of human RDM1 protein isoforms and their nucleolar accumulation in response to heat shock and proteotoxic stressTranscription of hepatitis delta virus RNA by RNA polymerase II.Transcription and chromatin organization of a housekeeping gene cluster containing an integrated beta-globin locus control region.Methylation of RNA polymerase II non-consensus Lysine residues marks early transcription in mammalian cells.Similar active genes cluster in specialized transcription factories.The long non-coding RNA nuclear-enriched abundant transcript 1_2 induces paraspeckle formation in the motor neuron during the early phase of amyotrophic lateral sclerosisParaspeckles: nuclear bodies built on long noncoding RNAModifications of RNA polymerase II are pivotal in regulating gene expression states.Spatial Organization and Dynamics of Transcription Elongation and Pre-mRNA Processing in Live Cells.Nuclear organization of RNA polymerase II transcription.RNA Pol II accumulates at promoters of growth genes during developmental arrest.Splicing in immune cells-mechanistic insights and emerging topics.Localization of heat shock protein HSPA6 (HSP70B') to sites of transcription in cultured differentiated human neuronal cells following thermal stress.Pin1 modulates RNA polymerase II activity during the transcription cycle.Inhibition of P-TEFb disrupts global transcription, oocyte maturation, and embryo development in the mouse.Stress-induced expression of p53 target genes is insensitive to SNW1/SKIP downregulation.Promoter chromatin remodeling of immediate-early genes is mediated through H3 phosphorylation at either serine 28 or 10 by the MSK1 multi-protein complex.
P2860
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P2860
Splicing speckles are not reservoirs of RNA polymerase II, but contain an inactive form, phosphorylated on serine2 residues of the C-terminal domain.
description
2006 nî lūn-bûn
@nan
2006 թուականի Փետրուարին հրատարակուած գիտական յօդուած
@hyw
2006 թվականի փետրվարին հրատարակված գիտական հոդված
@hy
2006年の論文
@ja
2006年論文
@yue
2006年論文
@zh-hant
2006年論文
@zh-hk
2006年論文
@zh-mo
2006年論文
@zh-tw
2006年论文
@wuu
name
Splicing speckles are not rese ...... dues of the C-terminal domain.
@ast
Splicing speckles are not rese ...... dues of the C-terminal domain.
@en
Splicing speckles are not rese ...... dues of the C-terminal domain.
@nl
type
label
Splicing speckles are not rese ...... dues of the C-terminal domain.
@ast
Splicing speckles are not rese ...... dues of the C-terminal domain.
@en
Splicing speckles are not rese ...... dues of the C-terminal domain.
@nl
prefLabel
Splicing speckles are not rese ...... dues of the C-terminal domain.
@ast
Splicing speckles are not rese ...... dues of the C-terminal domain.
@en
Splicing speckles are not rese ...... dues of the C-terminal domain.
@nl
P2860
P50
P356
P1476
Splicing speckles are not rese ...... dues of the C-terminal domain.
@en
P2093
Sheila Q Xie
Sonya Martin
P2860
P304
P356
10.1091/MBC.E05-08-0726
P577
2006-02-08T00:00:00Z