Evidence map›Paper›PMID 29758057›Full record

ArticlePloS one2018

ANKK1 is found in myogenic precursors and muscle fibers subtypes with glycolytic metabolism.

Estrella Rubio-Solsona, Salvador Martí, Juan J Vílchez, Francesc Palau, Janet Hoenicka

Erratum issuedOpen access · goldAbstract read
In one paragraph

Article in PloS one, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 7 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed, 1 pooled it
0.3field-weighted citation impact, top 49% 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, 1 synthesis or guideline pooled it, 8 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. ANKK1 Is a Wnt/PCP Scaffold Protein for Neural F-ACTIN Assembly.International journal of molecular sciences · 2024
    Article
  4. Frontiers in neuroscience · 2022
    Article
  5. Review
  6. Article
  7. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

5 authors at 3 institutions in 1 country.

Estrella Rubio-SolsonaCIBERER Biobank, Centro de Investigación Biomédica en Red de Enfermedades Raras (CIBERER), Valencia, Spain.ORCID 0000-0003-1274-4819
Salvador MartíCIBERER Biobank, Centro de Investigación Biomédica en Red de Enfermedades Raras (CIBERER), Valencia, Spain.
Juan J VílchezCIBERER Biobank, Centro de Investigación Biomédica en Red de Enfermedades Raras (CIBERER), Valencia, Spain.
Francesc PalauCIBERER Biobank, Centro de Investigación Biomédica en Red de Enfermedades Raras (CIBERER), Valencia, Spain.
Janet HoenickaCentro de Investigación Príncipe Felipe, Valencia, Spain.
Centre for Biomedical Network Research on Rare Diseases · ESHospital Sant Joan de Déu Barcelona · ESUniversitat de València · ES

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Ankyrin repeat and kinase domain containing 1 (ANKK1) gene has been widely related to neuropsychiatry disorders. The localization of ANKK1 in neural progenitors and its correlation with the cell cycle has suggested its participation in development. However, ANKK1 functions still need to be identified. Here, we have further characterized the ANKK1 localization in vivo and in vitro, by using immunolabeling, quantitative real-time PCR and Western blot in the myogenic lineage. Histologic investigations in mice and humans revealed that ANKK1 is expressed in precursors of embryonic and adult muscles. In mice embryos, ANKK1 was found in migrating myotubes where it shows a polarized cytoplasmic distribution, while proliferative myoblasts and satellite cells show different isoforms in their nuclei and cytoplasm. In vitro studies of ANKK1 protein isoforms along the myogenic progression showed the decline of nuclear ANKK1-kinase until its total exclusion in myotubes. In adult mice, ANKK1 was expressed exclusively in the Fast-Twitch muscles fibers subtype. The induction of glycolytic metabolism in C2C12 cells with high glucose concentration or treatment with berberine caused a significant increase in the ANKK1 mRNA. Similarly, C2C12 cells under hypoxic conditions caused the increase of nuclear ANKK1. These results altogether show a relationship between ANKK1 gene regulation and the metabolism of muscles during development and in adulthood. Finally, we found ANKK1 expression in regenerative fibers of muscles from dystrophic patients. Future studies in ANKK1 biology and the pathological response of muscles will reveal whether this protein is a novel muscle disease biomarker.

Indexed as

AdultAnimalsCell HypoxiaCell LineCell NucleusCell ProliferationChildCytoplasmFemaleHumansInfantMaleMice, Inbred BALB CMice, Inbred C57BLMiddle AgedMuscle CellsANKK1 protein, humanANKK1 protein, mouseProtein Serine-Threonine Kinases

Identifiers

PMID29758057
PMCPMC5951577
OpenAlexW2799379656

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.