Evidence map›Paper›PMID 34337357›Full record

ArticleiScience2021

Microscopic image-based covariation network analysis for actin scaffold-modified insulin signaling.

Yoshiyuki Noguchi, Fumi Kano, Nobuhiko Maiya, Chisako Iwamoto, Shoko Yamasaki, Yosuke Otsubo, Daiki Nakatsu, Rina Kunishige, Masayuki Murata

Abstract read
In one paragraph

Article in iScience, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing 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

4 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
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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

9 authors.

Yoshiyuki NoguchiDepartment of Life Sciences, Graduate School of Arts and Sciences, The University of Tokyo, 3-8-1 Komaba, Meguro-ku, Tokyo 153-8902, Japan.
Fumi KanoCell Biology Center, Institute of Innovative Research, Tokyo Institute of Technology, 4259 Nagatsuta, Midori-ku, Yokohama, Kanagawa 226-8503, Japan.
Nobuhiko MaiyaSystem Development Department, Technology Solutions Sector, Healthcare Business Unit, NIKON CORPORATION, 471, Nagaodai-cho, Sakae-ku, Yokohama, Kanagawa 244-8533, Japan.
Chisako IwamotoSystem Development Department, Technology Solutions Sector, Healthcare Business Unit, NIKON CORPORATION, 471, Nagaodai-cho, Sakae-ku, Yokohama, Kanagawa 244-8533, Japan.
Shoko YamasakiMathematical Sciences Research Laboratory, Research & Development Division, NIKON CORPORATION, 471, Nagaodai-cho, Sakae-ku, Yokohama, Kanagawa 244-8533, Japan.
Yosuke OtsuboMathematical Sciences Research Laboratory, Research & Development Division, NIKON CORPORATION, 471, Nagaodai-cho, Sakae-ku, Yokohama, Kanagawa 244-8533, Japan.
Daiki NakatsuCell Biology Center, Institute of Innovative Research, Tokyo Institute of Technology, 4259 Nagatsuta, Midori-ku, Yokohama, Kanagawa 226-8503, Japan.
Rina KunishigeDepartment of Life Sciences, Graduate School of Arts and Sciences, The University of Tokyo, 3-8-1 Komaba, Meguro-ku, Tokyo 153-8902, Japan.
Masayuki MurataDepartment of Life Sciences, Graduate School of Arts and Sciences, The University of Tokyo, 3-8-1 Komaba, Meguro-ku, Tokyo 153-8902, Japan.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

To infer a "live" protein network in single cells, we developed a novel Protein Localization and Modification-based Covariation Network (PLOM-CON) analysis method using a large set of quantitative data on the abundance (quantity), post-translational modification state (quality), and localization/morphological information of target proteins from microscope immunostained images. The generated network exhibited synchronized time-dependent behaviors of the target proteins to visualize how a live protein network develops or changes in cells under specific experimental conditions. As a proof of concept for PLOM-CON analysis, we applied this method to elucidate the role of actin scaffolds, in which actin fibers and signaling molecules accumulate and form membrane-associated protein condensates, in insulin signaling in rat hepatoma cells. We found that the actin scaffold in cells may function as a platform for glycogenesis and protein synthesis upon insulin stimulation.

Indexed as

BioinformaticsMolecular networkSystems biology

Identifiers

PMID34337357
PMCPMC8324808

What Socratic holds

Textmetadata
LicenceCC BY-NC-ND
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 Socratic graph.