Reconstituted mammalian U4/U6 snRNP complements splicing: a mutational analysis.
about
p110, a novel human U6 snRNP protein and U4/U6 snRNP recycling factorIn vitro reconstitution of mammalian U1 snRNPs active in splicing: the U1-C protein enhances the formation of early (E) spliceosomal complexesNS1-Binding protein (NS1-BP): a novel human protein that interacts with the influenza A virus nonstructural NS1 protein is relocalized in the nuclei of infected cellsSMNrp is an essential pre-mRNA splicing factor required for the formation of the mature spliceosome.NMR structure of the 3' stem-loop from human U4 snRNA.Conservation of functional features of U6atac and U12 snRNAs between vertebrates and higher plantsThe 5' and 3' domains of yeast U6 snRNA: Lsm proteins facilitate binding of Prp24 protein to the U6 telestem regionEvidence for a Prp24 binding site in U6 snRNA and in a putative intermediate in the annealing of U6 and U4 snRNAsA composite double-/single-stranded RNA-binding region in protein Prp3 supports tri-snRNP stability and splicing.Site-specific deoxynucleotide substitutions in yeast U6 snRNA block splicing of pre-mRNA in vitro.RNA modifications: a mechanism that modulates gene expression.A tertiary interaction detected in a human U2-U6 snRNA complex assembled in vitro resembles a genetically proven interaction in yeast.Modified nucleotides at the 5' end of human U2 snRNA are required for spliceosomal E-complex formation.Characterization of the catalytic activity of U2 and U6 snRNAsA discrete 3' region of U6 small nuclear RNA modulates the phosphorylation cycle of the C1 heterogeneous nuclear ribonucleoprotein particle protein.Mammalian U6 small nuclear RNA undergoes 3' end modifications within the spliceosome.Uncoupling two functions of the U1 small nuclear ribonucleoprotein particle during in vitro splicingSplicing function of mammalian U6 small nuclear RNA: conserved positions in central domain and helix I are essential during the first and second step of pre-mRNA splicing.Antisense probes targeted to an internal domain in U2 snRNP specifically inhibit the second step of pre-mRNA splicing.Reconstitution of functional mammalian U4 small nuclear ribonucleoprotein: Sm protein binding is not essential for splicing in vitro.In vitro reconstitution of mammalian U2 and U5 snRNPs active in splicing: Sm proteins are functionally interchangeable and are essential for the formation of functional U2 and U5 snRNPs.The phylogenetically invariant ACAGAGA and AGC sequences of U6 small nuclear RNA are more tolerant of mutation in human cells than in Saccharomyces cerevisiaeIn vitro reconstitution of yeast splicing with U4 snRNA reveals multiple roles for the 3' stem-loopMultiple functional domains of human U2 small nuclear RNA: strengthening conserved stem I can block splicingModifications of U2 snRNA are required for snRNP assembly and pre-mRNA splicing.Functional spliceosomal A complexes can be assembled in vitro in the absence of a penta-snRNP.An mRNA-type intron is present in the Rhodotorula hasegawae U2 small nuclear RNA gene.
P2860
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P2860
Reconstituted mammalian U4/U6 snRNP complements splicing: a mutational analysis.
description
1992 nî lūn-bûn
@nan
1992年の論文
@ja
1992年論文
@yue
1992年論文
@zh-hant
1992年論文
@zh-hk
1992年論文
@zh-mo
1992年論文
@zh-tw
1992年论文
@wuu
1992年论文
@zh
1992年论文
@zh-cn
name
Reconstituted mammalian U4/U6 snRNP complements splicing: a mutational analysis.
@en
type
label
Reconstituted mammalian U4/U6 snRNP complements splicing: a mutational analysis.
@en
prefLabel
Reconstituted mammalian U4/U6 snRNP complements splicing: a mutational analysis.
@en
P2860
P1433
P1476
Reconstituted mammalian U4/U6 snRNP complements splicing: a mutational analysis
@en
P2093
P2860
P304
P356
10.1002/J.1460-2075.1992.TB05057.X
P407
P577
1992-01-01T00:00:00Z