Specificity of RNA maturation pathways: RNAs transcribed by RNA polymerase III are not substrates for splicing or polyadenylation.
about
A serine/arginine-rich nuclear matrix cyclophilin interacts with the C-terminal domain of RNA polymerase IIEpigenetics in alternative pre-mRNA splicingInfluence of Friedreich ataxia GAA noncoding repeat expansions on pre-mRNA processingMammalian capping enzyme complements mutant Saccharomyces cerevisiae lacking mRNA guanylyltransferase and selectively binds the elongating form of RNA polymerase IIRNA polymerase II localizes at sites of human cytomegalovirus immediate-early RNA synthesis and processingA nuclear matrix protein interacts with the phosphorylated C-terminal domain of RNA polymerase II.The C-terminal domain of the largest subunit of RNA polymerase II interacts with a novel set of serine/arginine-rich proteinsFormation of mRNA 3' ends in eukaryotes: mechanism, regulation, and interrelationships with other steps in mRNA synthesisAn optimized RNA amplification method for prokaryotic expression profiling analysis.Introduction and expression of the 400 kilobase amyloid precursor protein gene in transgenic mice [corrected]T7 RNA polymerase-directed transcripts are processed in yeast and link 3' end formation to mRNA nuclear export.LINEs, SINEs and processed pseudogenes: parasitic strategies for genome modeling.Assembly and functional organization of the nucleolus: ultrastructural analysis of Saccharomyces cerevisiae mutantsRegulation of mouse thymidylate synthase gene expression in growth-stimulated cells: upstream S phase control elements are indistinguishable from the essential promoter elements.Coupling mRNA processing with transcription in time and space.FUS functions in coupling transcription to splicing by mediating an interaction between RNAP II and U1 snRNPDNA template effect on RNA splicing: two copies of the same gene in the same nucleus are processed differently.RNA polymerase III transcripts and the PTB protein are essential for the integrity of the perinucleolar compartment.Splicing of the U6 RNA precursor is impaired in fission yeast pre-mRNA splicing mutants.Co-transcriptional regulation of alternative pre-mRNA splicingOrigins of mRNA identity: capping enzymes bind to the phosphorylated C-terminal domain of RNA polymerase IIIn vivo transcriptional pausing and cap formation on three Drosophila heat shock genes.Discrete nuclear domains of poly(A) RNA and their relationship to the functional organization of the nucleus.Introns are essential for growth-regulated expression of the mouse thymidylate synthase geneThe 5'-flanking region of the mouse thymidylate synthase gene is necessary but not sufficient for normal regulation in growth-stimulated cells.Synthesis of functional mRNA in mammalian cells by bacteriophage T3 RNA polymerase.XPB, a subunit of TFIIH, is a target of the natural product triptolide.Expression of chimeric tRNA-driven antisense transcripts renders NIH 3T3 cells highly resistant to Moloney murine leukemia virus replication.Activity of chimeric U small nuclear RNA (snRNA)/mRNA genes in transfected protoplasts of Nicotiana plumbaginifolia: U snRNA 3'-end formation and transcription initiation can occur independently in plants.The Carboxyl-terminal Domain of RNA Polymerase II Is Not Sufficient to Enhance the Efficiency of Pre-mRNA Capping or Splicing in the Context of a Different Polymerase"Cotranscriptionality": the transcription elongation complex as a nexus for nuclear transactions.A Tetrahymena thermophila ribozyme-based indicator gene to detect transposition of marked retroelements in mammalian cells.Functional mRNA can be generated by RNA polymerase III.Regulation of poly(A) site selection in adenovirus.A sequence motif in the simian virus 40 (SV40) early core promoter affects alternative splicing of transcribed mRNA.Human retroelements may introduce intragenic polyadenylation signals.The most abundant nascent poly(A) + RNAs are transcribed by RNA polymerase III in murine tumor cells.Cis requirements for alternative splicing of the cardiac troponin T pre-mRNA.Posttranscriptional regulation of thymidylate synthase gene expression.Messenger RNAs that are not synthesized by RNA polymerase II can be 3' end cleaved and polyadenylated.
P2860
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P2860
Specificity of RNA maturation pathways: RNAs transcribed by RNA polymerase III are not substrates for splicing or polyadenylation.
description
1987 nî lūn-bûn
@nan
1987年の論文
@ja
1987年論文
@yue
1987年論文
@zh-hant
1987年論文
@zh-hk
1987年論文
@zh-mo
1987年論文
@zh-tw
1987年论文
@wuu
1987年论文
@zh
1987年论文
@zh-cn
name
Specificity of RNA maturation ...... r splicing or polyadenylation.
@en
type
label
Specificity of RNA maturation ...... r splicing or polyadenylation.
@en
prefLabel
Specificity of RNA maturation ...... r splicing or polyadenylation.
@en
P2093
P2860
P356
P1476
Specificity of RNA maturation ...... r splicing or polyadenylation.
@en
P2093
B Sollner-Webb
D W Cleveland
S S Sisodia
P2860
P304
P356
10.1128/MCB.7.10.3602
P407
P577
1987-10-01T00:00:00Z