Evidence map›Paper›PMID 25949793›Full record

ReviewCell & bioscience2014

Functional Impact of RNA editing and ADARs on regulation of gene expression: perspectives from deep sequencing studies.

Hsuan Liu, Chung-Pei Ma, Yi-Tung Chen, Scott C Schuyler, Kai-Ping Chang, Bertrand Chin-Ming Tan

Open access · goldAbstract readReview
In one paragraph

Review in Cell & bioscience, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
1.0field-weighted citation impact, top 24% 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

19 citing papers in PubMed, 46 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Alternative splicing of transposable elements in human breast cancer.bioRxiv : the preprint server for biology · 2024
    Article
  5. Article
  6. RBPs: an RNA editor's choice.Frontiers in molecular biosciences · 2024
    Review
  7. Article
  8. Article
  9. Article
  10. Article
  11. Review
  12. Article
  13. Review
  14. Adar3 Is Involved in Learning and Memory in Mice.Frontiers in neuroscience · 2018
    Article
  15. Article
  16. Article
  17. Article
  18. Article
  19. 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

6 authors at 3 institutions in 1 country.

Hsuan LiuGraduate Institute of Biomedical Sciences, Tao-Yuan, Taiwan ; Department of Biochemistry, Tao-Yuan, Taiwan ; Molecular Medicine Research Center, Chang Gung University, Tao-Yuan, Taiwan.
Chung-Pei MaGraduate Institute of Biomedical Sciences, Tao-Yuan, Taiwan.
Yi-Tung ChenGraduate Institute of Biomedical Sciences, Tao-Yuan, Taiwan.
Scott C SchuylerGraduate Institute of Biomedical Sciences, Tao-Yuan, Taiwan ; Department of Biomedical Sciences, College of Medicine, Tao-Yuan, Taiwan.
Kai-Ping ChangMolecular Medicine Research Center, Chang Gung University, Tao-Yuan, Taiwan ; Department of Otolaryngology, Chang Gung Memorial Hospital at Lin-Kuo, Tao-Yuan, Taiwan.
Bertrand Chin-Ming TanGraduate Institute of Biomedical Sciences, Tao-Yuan, Taiwan ; Department of Biomedical Sciences, College of Medicine, Tao-Yuan, Taiwan ; Molecular Medicine Research Center, Chang Gung University, Tao-Yuan, Taiwan.
Institute of Biomedical Sciences, Academia Sinica · TWChang Gung University · TWTao Yuan General Hospital · TW

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Cells regulate gene expression at multiple levels leading to a balance between robustness and complexity within their proteome. One core molecular step contributing to this important balance during metazoan gene expression is RNA editing, such as the co-transcriptional recoding of RNA transcripts catalyzed by the adenosine deaminse acting on RNA (ADAR) family of enzymes. Understanding of the adenosine-to-inosine RNA editing process has been broadened considerably by the next generation sequencing (NGS) technology, which allows for in-depth demarcation of an RNA editome at nucleotide resolution. However, critical issues remain unresolved with regard to how RNA editing cooperates with other transcript-associated events to underpin regulated gene expression. Here we review the growing body of evidence, provided by recent NGS-based studies, that links RNA editing to other mechanisms of post-transcriptional RNA processing and gene expression regulation including alternative splicing, transcript stability and localization, and the biogenesis and function of microRNAs (miRNAs). We also discuss the possibility that systematic integration of NGS data may be employed to establish the rules of an "RNA editing code", which may give us new insights into the functional consequences of RNA editing.

Indexed as

ADARAlternative splicingGene regulationMicroRNANext generation sequencing (NGS)RNA editingRNA-seqSmall RNA-seqTranscriptional regulation

Identifiers

PMID25949793
PMCPMC4422215
OpenAlexW2163805752

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.