Evidence map›Paper›PMID 25190459›Full record

ArticleNucleic acids research2014

Gammaretrovirus mRNA expression is mediated by a novel, bipartite post-transcriptional regulatory element.

Guy R Pilkington, Katarzyna J Purzycka, Jenifer Bear, Stuart F J Le Grice, Barbara K Felber

Open access · goldAbstract read
In one paragraph

Article in Nucleic acids research, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
1.1field-weighted citation impact, top 22% 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

10 citing papers in PubMed, 14 citations in OpenAlex.

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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

5 authors at 4 institutions in 2 countries.

Guy R PilkingtonHuman Retrovirus Pathogenesis Section, Vaccine Branch, Center for Cancer Research, National Cancer Institute at Frederick, Frederick, MD 21702, USA.
Katarzyna J PurzyckaRT Biochemistry Section, Drug Resistance Program, National Cancer Institute at Frederick, Frederick, MD 21702, USA Institute of Bioorganic Chemistry, Polish Academy of Sciences, Poznan, 61-704, Poland.
Jenifer BearHuman Retrovirus Pathogenesis Section, Vaccine Branch, Center for Cancer Research, National Cancer Institute at Frederick, Frederick, MD 21702, USA.
Stuart F J Le GriceRT Biochemistry Section, Drug Resistance Program, National Cancer Institute at Frederick, Frederick, MD 21702, USA legrices@mail.nih.gov.
Barbara K FelberHuman Retrovirus Pathogenesis Section, Vaccine Branch, Center for Cancer Research, National Cancer Institute at Frederick, Frederick, MD 21702, USA Barbara.felber@nih.gov.
Center for Cancer Research · USFrederick National Laboratory for Cancer Research · USInstitute of Bioorganic Chemistry, Polish Academy of Sciences · PLNational Cancer Institute · US

Funding

Posttranscriptional control of gene expressionZIABC010334 · NCI · DIVISION OF BASIC SCIENCES - NCI · PI FELBER, BARBARA K · 2009 to 2025
$15.1M
Intramural NIH HHS
6 · The paper itself

Abstract

Post-transcriptional regulatory mechanisms of several complex and simple retroviruses and retroelements have been elucidated, with the exception of the gammaretrovirus family. We found that, similar to the other retroviruses, gag gene expression of MuLV and XMRV depends on post-transcriptional regulation mediated via an RNA sequence overlapping the pro-pol open reading frame, termed the Post-Transcriptional Element (PTE). PTE function can be replaced by heterologous RNA export elements, e.g. CTE of simian type D retroviruses. Alternatively, Gag particle production is achieved using an RNA/codon optimized gag gene. PTE function is transferable and can replace HIV Rev-RRE-regulated expression of HIV gag. Analysis of PTE by SHAPE revealed a highly structured RNA comprising seven stem-loop structures, with the 5' and 3' stem-loops forming an essential bipartite signal. MuLV and XMRV PTE share 98% identity and have highly similar RNA structures, with changes mostly located to single-stranded regions. PTE identification strongly suggests that all retroviruses and retroelements share common strategies of post-transcriptional gene regulation to produce Gag. Expression depends on complex RNA structures embedded within retroviral mRNA, in coding regions or the 3' untranslated region. These specific structures serve as recognition signals for either cellular or viral proteins.

Indexed as

Gene Expression Regulation, ViralRegulatory Sequences, Ribonucleic Acidgag Gene Products, Human Immunodeficiency VirusGene Products, gagHEK293 CellsHeLa CellsHumansMoloney murine leukemia virusNucleic Acid ConformationRNA, MessengerRNA, ViralXenotropic murine leukemia virus-related virusgag Gene Products, Human Immunodeficiency VirusGene Products, gagRegulatory Sequences, Ribonucleic AcidRNA, MessengerRNA, Viral

Identifiers

PMID25190459
PMCPMC4176177
OpenAlexW2108630434

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.