Evidence map›Paper›PMID 19853618›Full record

ArticleJournal of molecular biology2009

Factors that determine the efficiency of HIV-1 strand transfer initiated at a specific site.

Sean T Rigby, Keith P Van Nostrand, April E Rose, Robert J Gorelick, David H Mathews, Robert A Bambara

Abstract read
In one paragraph

Article in Journal of molecular biology, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
–field-weighted citation impact
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

3 citing papers in PubMed.

  1. Host SAMHD1 protein promotes HIV-1 recombination in macrophages.The Journal of biological chemistry · 2014
    Article
  2. Article
  3. Article
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

6 authors.

Sean T RigbyDepartment of Biochemistry and Biophysics, University of Rochester School of Medicine and Dentistry, Rochester, NY 14642, USA.
Keith P Van Nostrand
April E Rose
Robert J Gorelick
David H Mathews
Robert A Bambara

Funding

Supporting RNAstructure: Software for RNA AnalysisR01GM076485 · NIGMS · UNIVERSITY OF ROCHESTER · PI MATHEWS, DAVID H. · 2006 to 2021
$4.7M
DNA SYNTHESIS AND RECOMBINATION BY HIV DNA POYLMERASER01GM049573 · NIGMS · UNIVERSITY OF ROCHESTER · PI BAMBARA, ROBERT A · 1993 to 2011
$4.0M
Training in HIV Replication and PathogenesisT32AI049815 · NIAID · UNIVERSITY OF ROCHESTER · PI WEDEKIND, JOSEPH E · 2001 to 2020
$3.5M
Innovations in RNA Structure PredictionR01HG004002 · NHGRI · UNIVERSITY OF ROCHESTER · PI MATHEWS, DAVID H. · 2007 to 2011
$1.7M
NCI NIH HHS N01 CO012400NCI NIH HHS N01-CO-12400NHGRI NIH HHS HG 004002NIAID NIH HHS 5T32 AI 049815NIAID NIH HHS T32 AI049815NIGMS NIH HHS GM 049573NIGMS NIH HHS R01 GM049573NIGMS NIH HHS R01 GM076485
6 · The paper itself

Abstract

Human immunodeficiency virus-1 employs strand transfer for recombination between two viral genomes. We have previously provided evidence that strand transfer proceeds by an invasion-mediated mechanism in which a DNA segment on the original RNA template is invaded by a second RNA template at a gap site. The initial RNA-DNA hybrid then expands until the DNA is fully transferred. Ribonuclease H (RNase H) cleavages and nucleocapsid protein (NC) were required for long-distance propagation of the hybrid. Evaluation was performed on a unique substrate, with a short gap serving as a precreated invasion site. In our current work, this substrate provided an opportunity for us to test what factors influence a specific invasion site to support transfer, and to distinguish factors that influence invasion site creation from those that impact later steps. RNase H can act in a polymerization-dependent or polymerization-independent mode. Polymerization-dependent and polymerization-independent RNase H were found to be important in creating efficiently used invasion sites in the primer-donor complex, with or without NC. Propagation and terminus transfer steps, emanating from a precreated invasion site in the presence of NC, were stimulated by polymerization-dependent, but not polymerization-independent, RNase H. RNase H can carry out primary and secondary cleavages during synthesis. While both modes of cleavage promoted invasion, only primary cleavage promoted propagation in the presence of NC in our system. These observations suggest that once invasion is initiated at a short gap, it can propagate through an adjacent region interrupted only by nicks, with help by NC. We considered the possibility that propagation solely by strand exchange was a significant contributor to transfers. However, it did not promote transfer even if synthetic progress of reverse transcriptase was intentionally slowed, consistent with strand exchange by random walk in which rate declines precipitously with distance.

Indexed as

Recombination, GeneticDNA, ViralHIV-1HumansModels, BiologicalNucleocapsid ProteinsRibonuclease HRNA, ViralDNA, ViralNucleocapsid ProteinsRibonuclease HRNA, Viral

Identifiers

PMID19853618
PMCPMC2860860

What OpenQuestion holds

Textmetadata
LicenceTDM
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.