Discover Community Create You

Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Article

Efficiency of a programmed -1 ribosomal frameshift in the different subtypes of the human immunodeficiency virus type 1 group M.

RNA (New York, N.Y.) - 1 Oct 2003

Baril Martin, Dulude Dominic, Gendron Karine, Lemay Guy, Brakier-Gingras Léa

Abstract excerpt

The synthesis of the Gag-Pol polyprotein, the precursor of the enzymes of the human immunodeficiency virus type 1 (HIV-1), requires a programmed -1 ribosomal frameshift. This frameshift has been investigated so far only for subtype B of HIV-1 group M. In this subtype, the frameshift stimulatory signal was found to be a two-stem helix, in which a three-purine bulge interrupts the two stems. In this study, using a...

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Share to Conserved Sequence
Share to Frameshifting, Ribosomal

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Gene Expression Regulation, Viral

Share to Genes, Reporter

Share to Luciferases

Share to Nucleic Acid Conformation

Share to Protein Biosynthesis

Share to Sequence Homology, Nucleic Acid

Source

Open in PubMed Open full text

Identifiers

PMID: 13130138
DOI: 10.1261/rna.5113603
PMCID: PMC1370488

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Efficiency of a programmed -1 ribosomal frameshift in the different subtypes of the human immunodeficiency virus type 1 group M.PMID 13130138Read ↗

A reassessment of the response of the bacterial ribosome to the frameshift stimulatory signal of the human immunodeficiency virus type 1.Semantic proximity Read ↗

Characterization of the frameshift stimulatory signal controlling a programmed -1 ribosomal frameshift in the human immunodeficiency virus type 1.Semantic proximity Read ↗

A review on architecture of the gag-pol ribosomal frameshifting RNA in human immunodeficiency virus: a variability survey of virus genotypes.Semantic proximity Read ↗

The many paths to frameshifting: kinetic modelling and analysis of the effects of different elongation steps on programmed –1 ribosomal frameshiftingSemantic proximity Read ↗

Stability of HIV Frameshift Site RNA Correlates with Frameshift Efficiency and Decreased Virus InfectivitySemantic proximity Read ↗

The three transfer RNAs occupying the A, P and E sites on the ribosome are involved in viral programmed -1 ribosomal frameshift.Semantic proximity Read ↗

The human immunodeficiency virus type 1 ribosomal frameshifting site is an invariant sequence determinant and an important target for antiviral therapy.Semantic proximity Read ↗

Comparative mutational analysis of cis-acting RNA signals for translational frameshifting in HIV-1 and HTLV-2.Semantic proximity Read ↗

High-throughput interrogation of programmed ribosomal frameshifting in human cellsSemantic proximity Read ↗

High-throughput interrogation of programmed ribosomal frameshifting in human cells.Semantic proximity Read ↗

Programmed ribosomal frameshifting in HIV-1 and the SARS–CoVSemantic proximity Read ↗

Comparative study of the effects of heptameric slippery site composition on −1 frameshifting among different eukaryotic systemsSemantic proximity Read ↗

⌁Select a neighboring publication to make it the new centre.