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Record W7057421043

Human adenovirus type 5 E4orf4 interacts wih the nucleopore component nup205 to regulate viral gene expression and replication

2013· other· en· W7057421043 on OpenAlexvenueno aff

Bibliographic record

VenueLibrary and Archives Canada (Government of Canada) · 2013
Typeother
Languageen
FieldPhysics and Astronomy
TopicMagnetic confinement fusion research
Canadian institutionsnot available
Fundersnot available
KeywordsViral replicationGeneViral structural proteinTranscription (linguistics)Transcription factorImmunoprecipitationViral proteinNuclear proteinZinc fingerRNA splicing
DOInot available

Abstract

fetched live from OpenAlex

The Adenovirus type 5 E4orf4 protein (E4orf4) is a multifunctional protein that regulates viral transcription and splicing. Much of the activity of E4orf4 is thought to be mediated through binding of the Protein Phosphatase 2A (PP2A). E4orf4 recruits target phosphoproteins into complexes with PP2A resulting in dephosphorylation of host factors, such as SR splicing factors and the AP-1 transcription factor. However, the full complement of cellular factors that interact with E4orf4, and the molecular mechanisms that E4orf4 utilizes during replication to regulate gene expression remain poorly understood. In the following study, we utilized immunoprecipitation followed by mass spectrometry to identify novel interacting proteins with E4orf4. Interestingly, we identified a nucleoporin, Nup 205, a component of the nuclear pore complex as an interacting partner. We show that the Arginine Rich Motif (ARM) of E4orf4 is required for interaction with Nup 205 and for nuclear localization of E4orf4. ARMs are commonly found on many viral nuclear proteins. Interestingly, we observed that Nup 205 interacts with three different viral nuclear proteins containing ARMs. In each case, viral ARM proteins also bound to the same region on Nup 205. Point mutations of the ARM sequence on each of the three viral proteins resulted in loss of interaction with Nup 205 and loss of nuclear localization of the viral protein. Nup 205 may therefore represent a common cellular target for viruses encoding ARM containing proteins. We have further tested the role of E4orf4 and Nup 205 in adenovirus replication and gene expression. Previous studies have shown that compared to wild type adenovirus, E4orf4 deficient adenovirus (Orf4-) have elevated E1A and E4orf6 expressions and reduced late protein production. Such effects are phenotypically copied by the loss of Nup 205, where wild type adenovirus infecting H1299 cells with reduced level of Nup 205 also results in elevated E1A and E4orf6 and reduced late protein production. Furthermore, knockdown of Nup 205 resulted in reduced cytopathic effect and a more than four-fold reduction in the replication of wild type adenovirus. Taken together, these data suggest Nup 205 is required by adenovirus for proper regulation of gene expressions and viral replication, and that interaction with E4orf4 may mediate these effects. Since E4orf4 is known to deregulate phosphorylation of its target proteins, our future studies will focus on identifying phosphorylation sites on Nup 205 and determining the effect of E4orf4 on such sites and nucleopore structure and function.

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 score0.001
Threshold uncertainty score0.003

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)0.0010.000

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 head0.005
GPT teacher head0.181
Teacher spread0.177 · 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
Published2013
Admission routes1
Has abstractyes

Explore more

Same venueLibrary and Archives Canada (Government of Canada)→Same topicMagnetic confinement fusion research→French-language works237,207→