Components required for in vitro cleavage and polyadenylation of eukaryotic mRNA.

scientific article

Components required for in vitro cleavage and polyadenylation of eukaryotic mRNA. is …
instance of (P31):
scholarly articleQ13442814

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P356DOI10.1093/NAR/16.12.5323
P932PMC publication ID336770
P698PubMed publication ID2898767
P5875ResearchGate publication ID20257026

P2093author name stringMoore CL
Clements JB
Simpson S
McLauchlan J
P2860cites workAccurate transcription initiation by RNA polymerase II in a soluble extract from isolated mammalian nucleiQ27860728
3' non-coding region sequences in eukaryotic messenger RNAQ27860858
Accurate cleavage and polyadenylation of exogenous RNA substrateQ28646786
Cleavage and polyadenylation of messenger RNA precursors in vitro occurs within large and specific 3' processing complexes.Q33930140
Steps in the processing of Ad2 mRNA: poly(A)+ nuclear sequences are conserved and poly(A) addition precedes splicingQ34057240
The consensus sequence YGTGTTYY located downstream from the AATAAA signal is required for efficient formation of mRNA 3' terminiQ36136653
Sedimentation analysis of polyadenylation-specific complexesQ36780246
Requirements for accurate and efficient mRNA 3' end cleavage and polyadenylation of a simian virus 40 early pre-RNA in vitroQ36834250
Identification of a sequence element on the 3' side of AAUAAA which is necessary for simian virus 40 late mRNA 3'-end processing.Q36894844
Fine-structure analysis of the processing and polyadenylation region of the herpes simplex virus type 1 thymidine kinase gene by using linker scanning, internal deletion, and insertion mutationsQ36902305
The AAUAAA sequence is required both for cleavage and for polyadenylation of simian virus 40 pre-mRNA in vitroQ36916774
Identification of a complex associated with processing and polyadenylation in vitro of herpes simplex virus type 1 thymidine kinase precursor RNAQ36921323
Sequences on the 3' side of hexanucleotide AAUAAA affect efficiency of cleavage at the polyadenylation site.Q36946265
A sequence downstream of A-A-U-A-A-A is required for formation of simian virus 40 late mRNA 3' termini in frog oocytesQ37691120
A modular system for the assay of transcription regulatory signals: the sequence TAATGARAT is required for herpes simplex virus immediate early gene activation.Q40472440
Formation of mRNA 3' termini: stability and dissociation of a complex involving the AAUAAA sequenceQ41330964
Specific pre-cleavage and post-cleavage complexes involved in the formation of SV40 late mRNA 3' termini in vitroQ41360882
Analysis of RNA cleavage at the adenovirus-2 L3 polyadenylation siteQ42572169
Sequences capable of restoring poly(A) site function define two distinct downstream elements.Q42574256
The sequence 5'-AAUAAA-3'forms parts of the recognition site for polyadenylation of late SV40 mRNAsQ48410195
Poly(A) site cleavage in a HeLa nuclear extract is dependent on downstream sequences.Q55060176
Recognition of cap structure in splicing in vitro of mRNA precursors.Q55062652
Alpha-thalassaemia caused by a polyadenylation signal mutation.Q55062701
Inhibition of RNA cleavage but not polyadenylation by a point mutation in mRNA 3′ consensus sequence AAUAAAQ58451156
A sequence downstream of AAUAAA is required for rabbit β-globin mRNA 3′-end formationQ59058833
Regulation of adenovirus-2 gene expression at the level of transcriptional termination and RNA processingQ59098268
Electrophoretic separation of polyadenylation-specific complexesQ64379710
Requirement of a downstream sequence for generation of a poly(A) addition siteQ64380598
Site-specific polyadenylation in a cell-free reactionQ64380699
Position-dependent sequence elements downstream of AAUAAA are required for efficient rabbit beta-globin mRNA 3' end formationQ68985721
Normal and mutant human β-globin pre-mRNAs are faithfully and efficiently spliced in vitroQ70196254
Role of the Conserved AAUAAA Sequence: Four AAUAAA Point Mutants Prevent Messenger RNA 3′ End FormationQ72749074
P433issue12
P407language of work or nameEnglishQ1860
P304page(s)5323-5344
P577publication date1988-06-01
P1433published inNucleic Acids ResearchQ135122
P1476titleComponents required for in vitro cleavage and polyadenylation of eukaryotic mRNA.
P478volume16

Reverse relations

cites work (P2860)
Q28776198A multicomponent complex is required for the AAUAAA-dependent cross-linking of a 64-kilodalton protein to polyadenylation substrates
Q40060352A negative regulatory element in the human papillomavirus type 16 genome acts at the level of late mRNA stability
Q45002161A simple procedure for isolation of eukaryotic mRNA polyadenylation factors
Q40108584Analysis of human papillomavirus type 16 late mRNA 3' processing signals in vitro and in vivo
Q41505232Approaches to maximizing stable expression of alpha 1-antitrypsin in transformed CHO cells
Q38434984Optimizing In Vitro Pre-mRNA 3' Cleavage Efficiency: Reconstitution from Anion-Exchange Separated HeLa Cleavage Factors and from Adherent HeLa Cell Nuclear Extract
Q40530952Potential role of poly(A) polymerase in the assembly of polyadenylation-specific RNP complexes
Q36763488Role of poly(A) polymerase in the cleavage and polyadenylation of mRNA precursor
Q42823824Sumoylation modulates the assembly and activity of the pre-mRNA 3' processing complex
Q40473966Transcription of the Herpes Simplex Virus Genome during Productive and Latent Infection
Q43256728Transcriptional termination sequences in the mouse serum albumin gene.
Q42941845Unusual aspects of in vitro RNA processing in the 3' regions of the GAL1, GAL7, and GAL10 genes in Saccharomyces cerevisiae

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