Evidence map›Paper›PMID 39148092›Full record

ArticleMolecular brain2024

Comprehensive identification of ubiquitin-like 3 (UBL3)-interacting proteins in the mouse brain.

Hiroshi Ageta, Tomoki Nishioka, Hisateru Yamaguchi, Kunihiro Tsuchida, Natsumi Ageta-Ishihara

Abstract read
In one paragraph

Article in Molecular brain, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. 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

5 authors.

Hiroshi AgetaDivision for Therapies Against Intractable Diseases, Center for Medical Science, Fujita Health University, 1-98 Dengakugakubo, Kutsukake-cho, Toyoake, Aichi, 470-1192, Japan. hiage@fujita-hu.ac.jp.
Tomoki NishiokaOpen Facility Center, Research Promotion Headquarters, Fujita Health University, Toyoake, Aichi, 470-1192, Japan.
Hisateru YamaguchiDepartment of Medical Technology, Yokkaichi Nursing and Medical Care University, Yokkaichi, 512-8045, Japan.
Kunihiro TsuchidaDivision for Therapies Against Intractable Diseases, Center for Medical Science, Fujita Health University, 1-98 Dengakugakubo, Kutsukake-cho, Toyoake, Aichi, 470-1192, Japan. tsuchida@fujita-hu.ac.jp.
Natsumi Ageta-IshiharaDepartment of Biomolecular Science, Faculty of Science, Toho University, 2-2-1 Miyama, Funabashi, Chiba, 274-8510, Japan. natsumi.ageta-ishihara@sci.toho-u.ac.jp.ORCID 0000-0003-2543-4828

Funding

Amgen Astellas Biopharma Astellas Foundation for Research on Metabolic DisordersChugai Foundation for Innovative Drug Discovery Science Chugai Foundation for Innovative Drug Discovery ScienceFujita Health University Fujita Health UniversityJapan Agency for Medical Research and Development AMED 22wm0525011h0002 and 23wm0525011h0002Japan Society for the Promotion of Science JSPS KAKENHI Grant Number 23K06394Japan Society for the Promotion of Science JSPS KAKENHI Grant Number JP21K07159 and 21H00293Koyanagi-Foundation Koyanagi-FoundationNational Center of Neurology and Psychiatry Intramural Research Grant (5-6) for Neurological and Psychiatric DisordersPrecursory Research for Embryonic Science and Technology JST, PRESTO Grant Number JPMJPR21E1Research Foundation for Opto-Science and Technology Research Foundation for Opto-Science and TechnologyToho University TUGRIP
6 · The paper itself

Abstract

Discovery of novel post-translational modifications provides new insights into changes in protein function, localization, and stability. They are also key elements in understanding disease mechanisms and developing therapeutic strategies. We have previously reported that ubiquitin-like 3 (UBL3) serves as a novel post-translational modifier that is highly expressed in the cerebral cortex and hippocampus, in addition to various other organs, and that 60% of proteins contained in small extracellular vesicles (sEVs), including exosomes, are influenced by UBL3. In this study, we generated transgenic mice expressing biotinylated UBL3 in the forebrain under control of the alpha-CaMKII promoter (Ubl3

Indexed as

BrainUbiquitinsAnimalsCerebral CortexExosomesGene OntologyMiceMice, Inbred C57BLMice, TransgenicProtein BindingUbiquitinsNeurodegenerative diseasesPost-translational modificationProteomicsRNA binding proteinsSmall extracellular vesicles (sEVs)Ubiquitin-like 3 (UBL3)

Identifiers

PMID39148092
PMCPMC11325695

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Registered trials

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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.