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Record W2790863169 · doi:10.1093/jcag/gwy008.179

A178 ARGONAUTE 2 IS DISPENSABLE FOR EFFICIENT HEPATITIS C VIRUS REPLICATION IN HUH 7.5 CELLS.

2018· article· en· W2790863169 on OpenAlexafffundabout
Yalena Amador, Joyce A. Wilson

Bibliographic record

VenueJournal of the Canadian Association of Gastroenterology · 2018
Typearticle
Languageen
FieldMedicine
TopicHepatitis C virus research
Canadian institutionsUniversity of Saskatchewan
FundersSaskatchewan Health Research Foundation
KeywordsArgonauteGene silencingBiologySmall interfering RNAGene knockdownRNA interferenceViral replicationmicroRNAVirologyCell biologyHepatitis C virusNS2-3 proteaseMolecular biologyRNAVirusGeneGenetics

Abstract

fetched live from OpenAlex

A liver-specific microRNA, miR-122, protects the Hepatitis C virus (HCV) genome from degradation and promotes its replication. Therefore, the virus is deemed highly dependent on this miRNA. This makes it a very attractive therapeutic target that has shown promise in the clinical setting. Nevertheless, the underlying mechanism and the potential role of other host factors are still poorly understood. Argonaute (Ago) proteins are host multifunctional proteins that can be found at the heart of the RNA-Induced Silencing Complex. Humans express 4 Ago isoforms (Ago1-4) and Ago2, the only human Ago capable of endonucleolytic cleavage, has generally been viewed as the primary Ago involved in the HCV life cycle. This work aimed to investigate the specific role of Ago2 and to determine the impact of the other Ago isoforms in the HCV life cycle. To fulfill this objective we made use of the CRISPR/Cas9 technology to generate hepatoma-derived Ago2 knockout Huh7.5 cells. We have generated two cell lines with confirmed biallelic indel mutations in the Ago2 gene and both showed undetectable levels of Ago2 expression by Western blot. We also confirmed that the Ago2 knockout cells were devoid of knockdown activity by assaying for small interfering RNA (siRNA) directed cleavage activity. Somewhat unexpectedly, Ago2 knockout cells are able to support HCV replication, albeit to lower levels (50–70%) than the wild-type cells. Importantly, in the absence of Ago2, two siRNAs targeting miR-122 binding site 1 rescue HCV replication that had been inhibited by blocking the activity of miR-122. These results indicate that the other human Ago isoforms (Ago1, 3 and/or 4) are able to sustain HCV replication in the absence of Ago2, and that at least one, but potentially all, of the other Ago proteins can mediate miR-122 promotion of the HCV life cycle. Additionally, our data suggest that Ago2’s endonucleolytic cleavage activity is not required for miR-122 promotion of HCV replication. At present, we are generating cell lines in which combinations of all 4 Ago isoforms are knocked out in order to assess the roles of each Ago isoform in the HCV life cycle, and generate an Ago null cell line to be used for trans-complementation assays to investigate the mechanism by which Ago and miR-122 promote the HCV life cycle. These novel cell lines constitute valuable tools in the field of HCV research. They will allow the identification of other host factors for the design of multi-target therapeutic approaches, with potentially reduced long-term side effects and higher barriers to resistance compared to single target approaches. Saskatchewan Health Research Foundation and the Canadian Network on Hepatitis C

Fetched live from OpenAlex and de-inverted. Abstracts are not stored in this database: the inverted indexes are 8.6 GB of the frame’s 9.3 GB of text, and the host has 13 GB free.

How this classification was reachedexpand

Full frame machine prediction

Teacher imitation

Not calibrated prevalence, not ground truth. Human validation pending. The Gemma side is a direct model label for every work in the frame, read from the title-only record. The Codex side is a classifier learned from the 10,348 direct Codex labels and calibrated to design-weighted sample rates; fields without enough sample support carry no Codex call. Candidate is the union of the two sides; consensus is their intersection. These outputs are machine_predicted_unvalidated and are not human labels.

metaresearch head score (Codex)0.000
metaresearch head score (Gemma)0.000
Version: metacan-v3-hybrid-931329e0061cValidation status: machine_predicted_unvalidated
Candidate categoriesnone
Consensus categoriesnone
DomainCandidate signal: none · Consensus signal: none
Study designCandidate signal: Bench or experimental · Consensus signal: Bench or experimental
GenreCandidate signal: Empirical · Consensus signal: Empirical
Teacher disagreement score0.003
Threshold uncertainty score0.009

Distilled classifier scores by category (both heads)

CategoryCodexGemma
Metaresearch0.0000.000
Meta-epidemiology (narrow)0.0000.000
Meta-epidemiology (broad)0.0000.000
Bibliometrics0.0000.000
Science and technology studies0.0000.000
Scholarly communication0.0000.000
Open science0.0000.000
Research integrity0.0000.000
Insufficient payload (model declined to judge)0.0030.001

Machine scores (provisional)

The two teacher heads of the student model, read on this work. A score orders the frame for review; it never asserts a category, and the validation status ships verbatim with every row.

Baseline scores from an immature model (maturity gate not passed, 7 training rounds). Scores rank; they never assert a category.

Opus teacher head0.017
GPT teacher head0.289
Teacher spread0.272 · how far apart the two teachers sit on this one work
Validation statusscore_only:v0-immature-baseline · verbatim from the scoring run: score_only means the number may rank works, and no category label ships from it

Classification

machine, unvalidated

Machine predicted; a candidate call from one source (direct Gemma or distilled Codex), not a consensus.

The models applied no category: nothing in the taxonomy fit this work.
Study designBench or experimental
Domainnot available
GenreEmpirical

How this classification was reached, model by model and score by score, is at the end of the page under "How this classification was reached".

Quick stats

Citations0
Published2018
Admission routes3
Has abstractyes

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