RNAi knockdown of hPrp31 leads to an accumulation of U4/U6 di-snRNPs in Cajal bodies
about
A novel EB-1/AIDA-1 isoform, AIDA-1c, interacts with the Cajal body protein coilin.Identification, cloning, and functional analysis of the human U6 snRNA-specific terminal uridylyl transferaseCTNNBL1 is a novel nuclear localization sequence-binding protein that recognizes RNA-splicing factors CDC5L and Prp31RNA structural requirements for the association of the spliceosomal hPrp31 protein with the U4 and U4atac small nuclear ribonucleoproteinsThe human U5 snRNP 52K protein (CD2BP2) interacts with U5-102K (hPrp6), a U4/U6.U5 tri-snRNP bridging protein, but dissociates upon tri-snRNP formation.An architectural role for a nuclear noncoding RNA: NEAT1 RNA is essential for the structure of paraspecklesA dynamic scaffold of pre-snoRNP factors facilitates human box C/D snoRNP assemblyOngoing U snRNP biogenesis is required for the integrity of Cajal bodiesHuman splicing factor SF3a, but not SF1, is essential for pre-mRNA splicing in vivoThe network of protein-protein interactions within the human U4/U6.U5 tri-snRNPThe Cajal body and histone locus bodyCajal-body formation correlates with differential coilin phosphorylation in primary and transformed cell linesA stochastic view of spliceosome assembly and recycling in the nucleusStructural basis for dual roles of Aar2p in U5 snRNP assemblyCoilin: The first 25 yearsSplicing factor SPF30 bridges an interaction between the prespliceosome protein U2AF35 and tri-small nuclear ribonucleoprotein protein hPrp3Splicing of a rare class of introns by the U12-dependent spliceosomeSMN in spinal muscular atrophy and snRNP biogenesisDynamic control of Cajal body number during zebrafish embryogenesis.In vivo kinetics of U4/U6·U5 tri-snRNP formation in Cajal bodies.Reduced viability, fertility and fecundity in mice lacking the cajal body marker protein, coilin.USP15 regulates dynamic protein-protein interactions of the spliceosome through deubiquitination of PRP31.Mutation analysis of pre-mRNA splicing genes in Chinese families with retinitis pigmentosa.The N-terminus of Prp1 (Prp6/U5-102 K) is essential for spliceosome activation in vivo.Mutations in spliceosomal proteins and retina degenerationMutational screening of splicing factor genes in cases with autosomal dominant retinitis pigmentosaThree gene-targeted mouse models of RNA splicing factor RP show late-onset RPE and retinal degeneration.An integrative analysis of colon cancer identifies an essential function for PRPF6 in tumor growthDominant PRPF31 mutations are hypostatic to a recessive CNOT3 polymorphism in retinitis pigmentosa: a novel phenomenon of "linked trans-acting epistasis".PRPF mutations are associated with generalized defects in spliceosome formation and pre-mRNA splicing in patients with retinitis pigmentosa.Nuclear bodies: random aggregates of sticky proteins or crucibles of macromolecular assembly?A missense mutation in PRPF6 causes impairment of pre-mRNA splicing and autosomal-dominant retinitis pigmentosaPoly(A) RNAs including coding proteins RNAs occur in plant Cajal bodies.A quantitative high-throughput in vitro splicing assay identifies inhibitors of spliceosome catalysis.The Drosophila melanogaster Cajal bodyNUFIP and the HSP90/R2TP chaperone bind the SMN complex and facilitate assembly of U4-specific proteins.Premature termination codons in PRPF31 cause retinitis pigmentosa via haploinsufficiency due to nonsense-mediated mRNA decay.Pearls are novel Cajal body-like structures in the Xenopus germinal vesicle that are dependent on RNA pol III transcription.Pre-mRNA splicing and retinitis pigmentosaThe assembly of a spliceosomal small nuclear ribonucleoprotein particle.
P2860
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P248
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P2860
RNAi knockdown of hPrp31 leads to an accumulation of U4/U6 di-snRNPs in Cajal bodies
description
2004 nî lūn-bûn
@nan
2004 թուականի Օգոստոսին հրատարակուած գիտական յօդուած
@hyw
2004 թվականի օգոստոսին հրատարակված գիտական հոդված
@hy
2004年の論文
@ja
2004年論文
@yue
2004年論文
@zh-hant
2004年論文
@zh-hk
2004年論文
@zh-mo
2004年論文
@zh-tw
2004年论文
@wuu
name
RNAi knockdown of hPrp31 leads to an accumulation of U4/U6 di-snRNPs in Cajal bodies
@ast
RNAi knockdown of hPrp31 leads to an accumulation of U4/U6 di-snRNPs in Cajal bodies
@en
RNAi knockdown of hPrp31 leads to an accumulation of U4/U6 di-snRNPs in Cajal bodies
@en-gb
RNAi knockdown of hPrp31 leads to an accumulation of U4/U6 di-snRNPs in Cajal bodies
@nl
type
label
RNAi knockdown of hPrp31 leads to an accumulation of U4/U6 di-snRNPs in Cajal bodies
@ast
RNAi knockdown of hPrp31 leads to an accumulation of U4/U6 di-snRNPs in Cajal bodies
@en
RNAi knockdown of hPrp31 leads to an accumulation of U4/U6 di-snRNPs in Cajal bodies
@en-gb
RNAi knockdown of hPrp31 leads to an accumulation of U4/U6 di-snRNPs in Cajal bodies
@nl
prefLabel
RNAi knockdown of hPrp31 leads to an accumulation of U4/U6 di-snRNPs in Cajal bodies
@ast
RNAi knockdown of hPrp31 leads to an accumulation of U4/U6 di-snRNPs in Cajal bodies
@en
RNAi knockdown of hPrp31 leads to an accumulation of U4/U6 di-snRNPs in Cajal bodies
@en-gb
RNAi knockdown of hPrp31 leads to an accumulation of U4/U6 di-snRNPs in Cajal bodies
@nl
P2093
P2860
P921
P356
P1433
P1476
RNAi knockdown of hPrp31 leads to an accumulation of U4/U6 di-snRNPs in Cajal bodies
@en
P2093
Markus Hossbach
Rainer Heintzmann
Tilmann Achsel
P2860
P304
P356
10.1038/SJ.EMBOJ.7600296
P407
P577
2004-08-04T00:00:00Z