Evidence map›Paper›PMID 28106162›Full record

ArticleScientific reports2017

Heterogeneous nuclear ribonucleoprotein M associates with mTORC2 and regulates muscle differentiation.

Wei-Yen Chen, Chia-Lung Lin, Jen-Hua Chuang, Fu-Yu Chiu, Yun-Ya Sun, Mei-Chih Liang, Yenshou Lin

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
0.7field-weighted citation impact, top 32% 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

12 citing papers in PubMed, 21 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

7 authors at 2 institutions in 1 country.

Wei-Yen ChenDepartment of Life Science, National Taiwan Normal University, Taipei 116, Taiwan.
Chia-Lung LinDepartment of Life Science, National Taiwan Normal University, Taipei 116, Taiwan.
Jen-Hua ChuangDepartment of Life Science, National Taiwan Normal University, Taipei 116, Taiwan.
Fu-Yu ChiuDepartment of Life Science, National Taiwan Normal University, Taipei 116, Taiwan.
Yun-Ya SunDepartment of Life Science, National Taiwan Normal University, Taipei 116, Taiwan.
Mei-Chih LiangDepartment of Biological Science and Technology, National Chiao Tung University, Hsinchu 300, Taiwan.
Yenshou LinDepartment of Life Science, National Taiwan Normal University, Taipei 116, Taiwan.
National Taiwan Normal University · TWNational Yang Ming Chiao Tung University · TW

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Mammalian target of rapamycin (mTOR) plays a range of crucial roles in cell survival, growth, proliferation, metabolism, and morphology. However, mTOR forms two distinct complexes, mTOR complex 1 and mTOR complex 2 (mTORC1 and mTORC2), via association with a series of different components; this allows the complexes to execute their wide range of functions. This study explores further the composition of the mTORC2 complex. Utilizing Rictor knock-out cells, immunoprecipitation and mass spectrometry, a novel Rictor associated protein, heterogeneous nuclear ribonucleoprotein M (hnRNP M), was identified. The association between hnRNP M and Rictor was verified using recombinant and endogenous protein and the binding site was found to be within aa 1~532 of hnRNP M. The presence of hnRNP M significantly affects phosphorylation of SGK1 S422, but not of Akt S473, PKCα S657 and PKCζ T560. Furthermore, hnRNP M also plays a critical role in muscle differentiation because knock-down of either hnRNP M or Rictor in C2C12 myoblasts reduced differentiation. This decrease is able to be rescued by overexpression SGK S422D in hnRNP M knockdown C2C12 myoblasts. Taken together, we have identified a novel Rictor/mTOR binding molecule, hnRNP M, that allows mTORC2 signaling to phosphorylate SGK1 thus regulating muscle differentiation.

Indexed as

AnimalsBinding SitesCell DifferentiationCell LineGene Knockout TechniquesHEK293 CellsHeterogeneous-Nuclear Ribonucleoprotein Group MHumansImmediate-Early ProteinsMiceMyoblastsPhosphorylationProtein BindingProtein Kinase C-alphaProtein Serine-Threonine KinasesRapamycin-Insensitive Companion of mTOR ProteinHeterogeneous-Nuclear Ribonucleoprotein Group MImmediate-Early ProteinsPrkca protein, mouseProtein Kinase C-alphaProtein Serine-Threonine KinasesRapamycin-Insensitive Companion of mTOR Proteinrictor protein, mouseSerum-Glucocorticoid Regulated Kinases

Identifiers

PMID28106162
PMCPMC5247691
OpenAlexW2575859089

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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.