Specific and stable intron-factor interactions are established early during in vitro pre-mRNA splicing.
about
Identification, purification, and biochemical characterization of U2 small nuclear ribonucleoprotein auxiliary factorN-myc mRNA forms an RNA-RNA duplex with endogenous antisense transcriptsYeast U1 snRNP-pre-mRNA complex formation without U1snRNA-pre-mRNA base pairing.Noncoding region between the env and src genes of Rous sarcoma virus influences splicing efficiency at the src gene 3' splice site.Regulation of alternative splicing in the generation of isoforms of the mouse Ly-5 (CD45) glycoprotein.Electron microscopy of small nuclear ribonucleoprotein (snRNP) particles U2 and U5: evidence for a common structure-determining principle in the major U snRNP familyUACUAAC is the preferred branch site for mammalian mRNA splicingThe accumulation of mature RNA for the Xenopus laevis ribosomal protein L1 is controlled at the level of splicing and turnover of the precursor RNA.A conformational rearrangement in the spliceosome is dependent on PRP16 and ATP hydrolysis3' splice site recognition in nematode trans-splicing involves enhancer-dependent recruitment of U2 snRNPA new natural hGH variant--17.5 kd--produced by alternative splicing. An additional consensus sequence which might play a role in branchpoint selection.Formation of the yeast splicing complex A1 and association of the splicing factor PRP19 with the pre-mRNA are independent of the 3' region of the intron.Splice site consensus sequences are preferentially accessible to nucleases in isolated adenovirus RNA.Branch point selection in alternative splicing of tropomyosin pre-mRNAs.Nucleotide sequences of mRNAs encoding Epstein-Barr virus nuclear proteins: a probable transcriptional initiation siteRole of the branch site/3'-splice site region in adenovirus-2 E1A pre-mRNA alternative splicing: evidence for 5'- and 3'-splice site co-operation.Inhibition of SV40 gene expression by microinjected small antisense RNA and DNA molecules.Requirements for U2 snRNP addition to yeast pre-mRNA.Interaction of hnRNP A1 with snRNPs and pre-mRNAs: evidence for a possible role of A1 RNA annealing activity in the first steps of spliceosome assembly.Nucleotide substitutions within the cardiac troponin T alternative exon disrupt pre-mRNA alternative splicing.Plant intron sequences: evidence for distinct groups of introns.Antisense RNA inhibits splicing of pre-mRNA in vitro.A 5' exo-ribonuclease and RNA ligase of T. brucei.Three distinct activities possibly involved in mRNA splicing are found in a nuclear fraction lacking U1 and U2 RNA.Evidence that the 60-kDa protein of 17S U2 small nuclear ribonucleoprotein is immunologically and functionally related to the yeast PRP9 splicing factor and is required for the efficient formation of prespliceosomes.Accumulation of a novel spliceosomal complex on pre-mRNAs containing branch site mutations.Direct interactions between pre-mRNA and six U2 small nuclear ribonucleoproteins during spliceosome assemblySmall nuclear ribonucleoprotein (RNP) U2 contains numerous additional proteins and has a bipartite RNP structure under splicing conditionsIdentification and characterization by antisense oligonucleotides of exon and intron sequences required for splicingExon definition may facilitate splice site selection in RNAs with multiple exons.Polyadenylation-specific complexes undergo a transition early in the polymerization of a poly(A) tailSplice site choice in a complex transcription unit containing multiple inefficient polyadenylation signalsMapping of branch sites in trans-spliced pre-mRNAs of Trypanosoma brucei.Factor interactions with the simian virus 40 early pre-mRNA influence branch site selection and alternative splicing.Gel electrophoretic isolation of splicing complexes containing U1 small nuclear ribonucleoprotein particles.The length of the downstream exon and the substitution of specific sequences affect pre-mRNA splicing in vitro.Competition between splicing and polyadenylation reactions determines which adenovirus region E3 mRNAs are synthesizedThe 216-nucleotide intron of the E1A pre-mRNA contains a hairpin structure that permits utilization of unusually distant branch acceptors.Multiple interactions between the splicing substrate and small nuclear ribonucleoproteins in spliceosomesMultiple cis-acting sequence elements are required for efficient splicing of simian virus 40 small-t antigen pre-mRNA
P2860
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P2860
Specific and stable intron-factor interactions are established early during in vitro pre-mRNA splicing.
description
1985 nî lūn-bûn
@nan
1985年の論文
@ja
1985年学术文章
@wuu
1985年学术文章
@zh
1985年学术文章
@zh-cn
1985年学术文章
@zh-hans
1985年学术文章
@zh-my
1985年学术文章
@zh-sg
1985年學術文章
@yue
1985年學術文章
@zh-hant
name
Specific and stable intron-fac ...... ng in vitro pre-mRNA splicing.
@en
Specific and stable intron-fac ...... ng in vitro pre-mRNA splicing.
@nl
type
label
Specific and stable intron-fac ...... ng in vitro pre-mRNA splicing.
@en
Specific and stable intron-fac ...... ng in vitro pre-mRNA splicing.
@nl
prefLabel
Specific and stable intron-fac ...... ng in vitro pre-mRNA splicing.
@en
Specific and stable intron-fac ...... ng in vitro pre-mRNA splicing.
@nl
P1433
P1476
Specific and stable intron-fac ...... ng in vitro pre-mRNA splicing.
@en
P2093
P304
P356
10.1016/0092-8674(85)90018-2
P407
P577
1985-11-01T00:00:00Z