Evidence map›Paper›PMID 24440912›Full record

ArticleCell death and differentiation2014

ADAR1 deaminase contributes to scheduled skeletal myogenesis progression via stage-specific functions.

C-L Hsieh, H Liu, Y Huang, L Kang, H-W Chen, Y-T Chen, Y-R Wee, S-J Chen, B C-M Tan

Open access · bronzeAbstract read
In one paragraph

Article in Cell death and differentiation, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 27 papers.

0numbers the graph read from it
0cells of the map it votes in
27citing papers in PubMed
0.7field-weighted citation impact, top 31% 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

27 citing papers in PubMed, 39 citations in OpenAlex.

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  13. IFN-I inducibleFrontiers in immunology · 2022
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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 at 3 institutions in 2 countries.

C-L HsiehDepartment of Biomedical Sciences, Graduate Institute of Biomedical Sciences, College of Medicine, Tao-Yuan, Taiwan.
H LiuMolecular Medicine Research Center, Chang Gung University, Tao-Yuan, Taiwan.
Y HuangMolecular Medicine Research Center, Chang Gung University, Tao-Yuan, Taiwan.
L KangBGI-Shenzhen, Shenzhen, China.
H-W ChenDepartment of Biomedical Sciences, Graduate Institute of Biomedical Sciences, College of Medicine, Tao-Yuan, Taiwan.
Y-T Chen1] Department of Biomedical Sciences, Graduate Institute of Biomedical Sciences, College of Medicine, Tao-Yuan, Taiwan [2] Molecular Medicine Research Center, Chang Gung University, Tao-Yuan, Taiwan.
Y-R WeeDepartment of Biomedical Sciences, Graduate Institute of Biomedical Sciences, College of Medicine, Tao-Yuan, Taiwan.
S-J Chen1] Department of Biomedical Sciences, Graduate Institute of Biomedical Sciences, College of Medicine, Tao-Yuan, Taiwan [2] Molecular Medicine Research Center, Chang Gung University, Tao-Yuan, Taiwan.
B C-M Tan1] Department of Biomedical Sciences, Graduate Institute of Biomedical Sciences, College of Medicine, Tao-Yuan, Taiwan [2] Molecular Medicine Research Center, Chang Gung University, Tao-Yuan, Taiwan.
Chang Gung University · TWInstitute of Biomedical Sciences, Academia Sinica · TWBGI Group (China) · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Adenosine deaminases acting on RNA 1 (ADAR1) catalyzes cellular RNA adenosine-to-inosine editing events on structured RNA molecules. In line with this critical role, ADAR1 exhibits ubiquitous expression and is essential for embryonic development. However, regulation and developmental significance of this RNA editor in a spatiotemporal context are largely elusive. Here we unveil a novel tissue-specific role of ADAR1 in skeletal myogenesis. ADAR1 expression displayed programmed alteration that is coordinated with differentiation cues, and mediated negatively by miRNA-1/206. Coincidently, ADAR1 exerts stage-dependent functions-suppression of apoptosis at the onset of differentiation and preservation of timely myotube formation through later phase. Furthermore, the post-transcriptional aspect of its myogenic role was illustrated by the spectrum of binding RNAs, as revealed by high-throughput approach, as well as by direct regulation of myogenesis-associated targets such as dynamin 1/2 (Dnm1/2) and annexin A4. Consequently, maintenance of target gene expression profiles likely contributes to a state of cytoskeleton and membrane dynamics that is amenable to myoblast morphogenesis. Collectively, these findings uncover a critical link of ADAR1 to myogenesis, and further highlight an epigenetic mechanism by which ADAR1 and miR-1/206 interplay to control scheduled myoblast-myotube transition.

Indexed as

Adenosine DeaminaseAnimalsApoptosisCell DifferentiationCell Growth ProcessesHeLa CellsHumansMiceMice, TransgenicMuscle, SkeletalRNA-Binding ProteinsADARB1 protein, humanAdenosine DeaminaseRNA-Binding Proteins

Identifiers

PMID24440912
PMCPMC3978302
OpenAlexW2014008375

What OpenQuestion holds

Textmetadata
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.