Evidence map›Paper›PMID 2841471›Full record

ArticleJournal of virology1988

Translational control of synthesis of simian virus 40 late proteins from polycistronic 19S late mRNA.

C Dabrowski, J C Alwine

Open access · bronzeAbstract read
In one paragraph

Article in Journal of virology, 1988. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
5.1field-weighted citation impact, top 5% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

11 citing papers in PubMed, 19 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. The 5'-untranslated region of picornaviral genomes.Advances in virus research · 1991
    Review
  9. Article
  10. The scanning model for translation: an update.The Journal of cell biology · 1989
    Review
  11. Polycistronic animal virus mRNAs.Progress in nucleic acid research and molecular biology · 1989
    Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

2 authors at 1 institution in 1 country.

C DabrowskiGraduate Group of Molecular Biology, School of Medicine, University of Pennsylvania, Philadelphia 19104-6076.
J C Alwine
University of Pennsylvania · US

Funding

REGULATION OF DNA TUMOR VIRUS GENE EXPRESSIONR01CA028379 · NCI · UNIVERSITY OF PENNSYLVANIA · PI ALWINE, JAMES C · 1985 to 2009
$4.5M
NCI NIH HHS CA28379
6 · The paper itself

Abstract

The simian virus 40 (SV40) 19S late mRNA is polycistronic, encoding multiple late proteins: agnoprotein, VP2, and VP3. We constructed a chloramphenicol acetyltransferase (CAT) transient expression vector in which the SV40 sequences between nucleotides 5171 and 1046 (via the SV40 origin of replication and including the late promoter) were inserted 5' to the cat gene; therefore, the AUG for CAT expression occurs after the AUGs for agnoprotein, VP2, and VP3. CAT enzyme activity assayed after transfection of these constructions indicates the level of CAT AUG utilization and, therefore, can be used as a measure of the ability of prior AUGs to intercept scanning ribosomes. Specifically, deletions and point mutations of the viral AUGs resulted in increased CAT enzyme activity owing to increased utilization of the downstream CAT AUG. To compare a variety of mutants, we used the levels of increase to calculate the translational efficiency of the viral AUGs. Some of our data agree with predictions of the modified scanning model (MSM). Little variation in downstream CAT AUG utilization was noted regardless of whether the VP2 AUG (in a weak MSM sequence context) was intact or removed. Hence, a scanning ribosome may easily bypass it. Similar analysis of the VP3 AUG (in a favorable MSM sequence context) demonstrated that it could efficiently intercept ribosomes prior to the downstream AUG. Overall, these data indicate that the structure of the 19S late mRNA and the relative efficiency of translational start codon utilization can account for the VP3/VP2 ratio found in infected cells. The agnoprotein reading frame, depending on how the mRNA precursor is spliced, is either not contained in the mRNA or is terminated near the VP2 AUG. Under these conditions, the ability of the agnoprotein AUG to block downstream CAT AUG utilization was found to be minimal in our assay. However, we directly tested the blocking ability of the agnoprotein AUG under conditions in which the reading frame terminated well after the CAT AUG. Although the agnoprotein AUG lies in a very good sequence context, this direct analysis showed that it interfered minimally with utilization of the CAT AUG when under the control of the SV40 late promoter. However, expected high levels of interference were regained when the late promoter was replaced with the Rous sarcoma virus long terminal repeat.(ABSTRACT TRUNCATED AT 400 WORDS)

Indexed as

Protein BiosynthesisAcetyltransferasesAnimalsCell Line, TransformedChloramphenicol O-AcetyltransferaseCodonDNA Restriction EnzymesEndonucleasesGene Expression RegulationGenetic VectorsMutationNucleic Acid HybridizationPlasmidsPromoter Regions, GeneticRNA, MessengerSimian virus 40Acetyltransferasesagnoprotein, polyomavirusChloramphenicol O-AcetyltransferaseCodonDNA Restriction EnzymesEndonucleasesRNA, MessengerSingle-Strand Specific DNA and RNA EndonucleasesViral ProteinsViral Regulatory and Accessory ProteinsViroporin Proteins

Identifiers

PMID2841471
PMCPMC253436
OpenAlexW1510051622

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.