Evidence map›Paper›PMID 37315088›Full record

ArticlePLoS genetics2023

Development of AlissAID system targeting GFP or mCherry fusion protein.

Yoshitaka Ogawa, Kohei Nishimura, Keisuke Obara, Takumi Kamura

Open access · goldAbstract read
In one paragraph

Article in PLoS genetics, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
1.7field-weighted citation impact, top 16% 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

7 citing papers in PubMed, 11 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

4 authors at 1 institution in 1 country.

Yoshitaka OgawaDepartment of Biological Science, Division of Natural Science, Graduate School of Science, Nagoya University, Nagoya, Japan.
Kohei NishimuraDepartment of Biological Science, Division of Natural Science, Graduate School of Science, Nagoya University, Nagoya, Japan.ORCID 0000-0003-3299-9499
Keisuke ObaraDepartment of Biological Science, Division of Natural Science, Graduate School of Science, Nagoya University, Nagoya, Japan.ORCID 0000-0002-2441-0907
Takumi KamuraDepartment of Biological Science, Division of Natural Science, Graduate School of Science, Nagoya University, Nagoya, Japan.ORCID 0000-0001-8541-447X
Nagoya University · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Conditional control of target proteins using the auxin-inducible degron (AID) system provides a powerful tool for investigating protein function in eukaryotes. Here, we established an Affinity-linker based super-sensitive auxin-inducible degron (AlissAID) system in budding yeast by using a single domain antibody (a nanobody). In this system, target proteins fused with GFP or mCherry were degraded depending on a synthetic auxin, 5-Adamantyl-IAA (5-Ad-IAA). In AlissAID system, nanomolar concentration of 5-Ad-IAA induces target degradation, thus minimizing the side effects from chemical compounds. In addition, in AlissAID system, we observed few basal degradations which was observed in other AID systems including ssAID system. Furthermore, AlissAID based conditional knockdown cell lines are easily generated by using budding yeast GFP Clone Collection. Target protein, which has antigen recognition sites exposed in cytosol or nucleus, can be degraded by the AlissAID system. From these advantages, the AlissAID system would be an ideal protein-knockdown system in budding yeast cells.

Indexed as

Drug-Related Side Effects and Adverse ReactionsSaccharomycetalesCell LineCell NucleusCytosolIndoleacetic AcidsIndoleacetic Acids

Identifiers

PMID37315088
PMCPMC10266622
OpenAlexW4380628393

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.