Literature DB >> 6245233

Order of polyadenylic acid addition and splicing events in early adenovirus mRNA formation.

J Weber, J M Blanchard, H Ginsberg, J E Darnell.   

Abstract

A study of the processing of mRNA from two early adenovirus type 2 transcription units (regions 2 and 4 of adenovirus type 2 genome; [J. Flint, Cell 10:153--166, 1977]) revealed that polyadenylic acid [poly(A)] was added in most if not all cases to an unspliced nuclear RNA molecule whose coordinates extended from the apparent initiation site for RNA synthesis to the single poly(A) site in each transcription unit. An intermediate RNA molecule in the processing of the mRNA for the 72,000-M, single-stranded DNA binding protein showed that the first of the two intervening sequences, the one closest to the 5' end of the molecule, was removed first at least in the majority of the processed molecules. Finally, in cells labeled for 10 min and then treated with actinomycin D to stop further RNA synthesis, the majority, if not all, of the poly(A)-terminated nuclear RNA specific for region 2 was successfully processed and transported to the cytoplasm.

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Year:  1980        PMID: 6245233      PMCID: PMC288545     

Source DB:  PubMed          Journal:  J Virol        ISSN: 0022-538X            Impact factor:   5.103


  27 in total

1.  Mapping of adenovirus 2 RNA sequences in lytically infected cells and transformed cell lines.

Authors:  P A Sharp; P H Gallimore; S J Flint
Journal:  Cold Spring Harb Symp Quant Biol       Date:  1975

Review 2.  Characteristics and significance of the polyadenylate sequence in mammalian messenger RNA.

Authors:  G Brawerman
Journal:  Prog Nucleic Acid Res Mol Biol       Date:  1976

3.  Location and identification of the genes for adenovirus type 2 early polypeptides.

Authors:  J B Lewis; J F Atkins; P R Baum; R Solem; R F Gesteland; C W Anderson
Journal:  Cell       Date:  1976-01       Impact factor: 41.582

4.  Presence of cell and virus specific sequences in the same molecules of nuclear RNA from virus transformed cells.

Authors:  R Wall; J E Darnell
Journal:  Nat New Biol       Date:  1971-07-21

5.  Addition of polyadenylate sequences to virus-specific RNA during adenovirus replication.

Authors:  L Philipson; R Wall; G Glickman; J E Darnell
Journal:  Proc Natl Acad Sci U S A       Date:  1971-11       Impact factor: 11.205

6.  Competition hybridization by "pre-saturation" of HeLa cell DNA.

Authors:  R Soeiro; J E Darnell
Journal:  J Mol Biol       Date:  1969-09-28       Impact factor: 5.469

7.  The topography and transcription of the adenovirus genome.

Authors:  J Flint
Journal:  Cell       Date:  1977-02       Impact factor: 41.582

8.  Thermolabile DNA binding proteins from cells infected with a temperature-sensitive mutant of adenovrius defective in viral DNA synthesis.

Authors:  P C Van Der Vliet; A J Levine; M J Ensinger; H S Ginsberg
Journal:  J Virol       Date:  1975-02       Impact factor: 5.103

9.  Nuclear transcripts larger than the cytoplasmic mRNAs are specified by segments of the adenovirus genome coding for early functions.

Authors:  E A Craig; H J Raskas
Journal:  Cell       Date:  1976-06       Impact factor: 41.582

10.  Short-lived messenger RNA in HeLa cells and its impace on the kinetics of accumulation of cytoplasmic polyadenylate.

Authors:  L Puckett; S Chambers; J E Darnell
Journal:  Proc Natl Acad Sci U S A       Date:  1975-01       Impact factor: 11.205

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  10 in total

Review 1.  Formation of mRNA 3' ends in eukaryotes: mechanism, regulation, and interrelationships with other steps in mRNA synthesis.

Authors:  J Zhao; L Hyman; C Moore
Journal:  Microbiol Mol Biol Rev       Date:  1999-06       Impact factor: 11.056

2.  Nuclei of adenovirus 2-infected cells contain an RNA species that corresponds to an intron excised intact from mRNA precursors.

Authors:  R Rosenthal; H J Raskas
Journal:  Mol Cell Biol       Date:  1985-05       Impact factor: 4.272

Review 3.  Reflections on the history of pre-mRNA processing and highlights of current knowledge: a unified picture.

Authors:  James E Darnell
Journal:  RNA       Date:  2013-02-25       Impact factor: 4.942

4.  Splicing kinetics and transcript release from the chromatin compartment limit the rate of Lipid A-induced gene expression.

Authors:  Amy Pandya-Jones; Dev M Bhatt; Chia-Ho Lin; Ann-Jay Tong; Stephen T Smale; Douglas L Black
Journal:  RNA       Date:  2013-04-24       Impact factor: 4.942

5.  Large heterogeneous nuclear ribonucleic acid has three times as many 5' caps as polyadenylic acid segments, and most caps do not enter polyribosomes.

Authors:  M Salditt-Georgieff; M M Harpold; M C Wilson; J E Darnell
Journal:  Mol Cell Biol       Date:  1981-02       Impact factor: 4.272

6.  Different mRNAs have different nuclear transit times in Dictyostelium discoideum aggregates.

Authors:  G Mangiarotti; C Zuker; R L Chisholm; H F Lodish
Journal:  Mol Cell Biol       Date:  1983-08       Impact factor: 4.272

7.  The orderly splicing of the first three leaders of the adenovirus-2 major late transcript.

Authors:  P Keohavong; R Gattoni; J M LeMoullec; M Jacob; J Stévenin
Journal:  Nucleic Acids Res       Date:  1982-02-25       Impact factor: 16.971

8.  A small nuclear ribonucleoprotein is required for splicing of adenoviral early RNA sequences.

Authors:  V W Yang; M R Lerner; J A Steitz; S J Flint
Journal:  Proc Natl Acad Sci U S A       Date:  1981-03       Impact factor: 11.205

9.  Splicing precedes polyadenylation during Drosophila E74A transcription.

Authors:  M F LeMaire; C S Thummel
Journal:  Mol Cell Biol       Date:  1990-11       Impact factor: 4.272

10.  Addition of poly(A) to nuclear RNA occurs soon after RNA synthesis.

Authors:  M Salditt-Georgieff; M Harpold; S Sawicki; J Nevins; J E Darnell
Journal:  J Cell Biol       Date:  1980-09       Impact factor: 10.539

  10 in total

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