Evidence map›Paper›PMID 35130952›Full record

ArticleGenome biology2022

Accurate identification of circRNA landscape and complexity reveals their pivotal roles in human oligodendroglia differentiation.

Yangping Li, Feng Wang, Peng Teng, Li Ku, Li Chen, Yue Feng, Bing Yao

Open access · goldAbstract read
In one paragraph

Article in Genome biology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed
2.5field-weighted citation impact, top 10% 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

20 citing papers in PubMed, 29 citations in OpenAlex.

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  9. NewmedRxiv : the preprint server for health sciences · 2024
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  14. The epigenetic landscape of oligodendrocyte lineage cells.Annals of the New York Academy of Sciences · 2023
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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.

Yangping Li *Department of Human Genetics, Emory University School of Medicine, Atlanta, GA, 30322, USA.
Feng Wang *Department of Human Genetics, Emory University School of Medicine, Atlanta, GA, 30322, USA.
Peng Teng *Department of Pharmacology and Chemical Biology, Emory University School of Medicine, Atlanta, GA, 30322, USA.
Li KuDepartment of Pharmacology and Chemical Biology, Emory University School of Medicine, Atlanta, GA, 30322, USA.
Li ChenDepartment of Biostatistics and Health Data Science, Center for Computational Biology and Bioinformatics, Indiana University School of Medicine, Indianapolis, IN, 46202, USA.
Yue FengDepartment of Pharmacology and Chemical Biology, Emory University School of Medicine, Atlanta, GA, 30322, USA. yfeng@emory.edu.
Bing YaoDepartment of Human Genetics, Emory University School of Medicine, Atlanta, GA, 30322, USA. bing.yao@emory.edu.ORCID 0000-0002-3205-8130
Emory University · USIndiana University School of Medicine

Funding

Genome-wide mapping and integrative analysis of DNA 6mA methylome in human AD brainR01AG064786 · NIA · UNIVERSITY OF FLORIDA · PI BENNETT, DAVID ALAN, YAO, BING · 2019 to 2023
$3.3M
Novel Regulation and Function of the lncRNA Gomafu in Human NeuronsR01NS110110 · NINDS · EMORY UNIVERSITY · PI FENG, YUE · 2019 to 2023
$2.9M
Regulation and function of human neural circular RNAsR01NS118819 · NINDS · EMORY UNIVERSITY · PI FENG, YUE, YAO, BING · 2021 to 2025
$2.7M
Epigenetic roles of DNA adenine methylation in stress responseR01MH117122 · NIMH · EMORY UNIVERSITY · PI YAO, BING · 2019 to 2023
$2.0M
Epigenetic roles of DNA adenine methylation in Alzheimer's DiseaseR01AG062577 · NIA · EMORY UNIVERSITY · PI YAO, BING · 2019 to 2023
$2.0M
Computational modeling of genetic variations by multi-omics integration todecipher personal genomeR35GM142701 · NIGMS · UNIVERSITY OF FLORIDA · PI CHEN, LI · 2021 to 2025
$1.8M
Novel control of CDK5 function in the brainR01NS093016 · NINDS · EMORY UNIVERSITY · PI FENG, YUE · 2015 to 2019
$1.7M
Use of CRISPR/Cas9 to Treat Huntington DiseaseR33NS106120 · NINDS · EMORY UNIVERSITY · PI YAO, BING · 2021 to 2022
$778k
NIA NIH HHS R01 AG062577NIA NIH HHS R01 AG064786NIGMS NIH HHS R35 GM142701NIMH NIH HHS R01 MH117122NINDS NIH HHS R01 NS093016NINDS NIH HHS R01 NS110110NINDS NIH HHS R01 NS118819NINDS NIH HHS R33 NS106120
6 · The paper itself

Abstract

backgroundCircular RNAs (circRNAs), a novel class of poorly conserved non-coding RNAs that regulate gene expression, are highly enriched in the human brain. Despite increasing discoveries of circRNA function in human neurons, the circRNA landscape and function in developing human oligodendroglia, the myelinating cells that govern neuronal conductance, remains unexplored. Meanwhile, improved experimental and computational tools for the accurate identification of circRNAs are needed.

resultsWe adopt a published experimental approach for circRNA enrichment and develop CARP (CircRNA identification using A-tailing RNase R approach and Pseudo-reference alignment), a comprehensive 21-module computational framework for accurate circRNA identification and quantification. Using CARP, we identify developmentally programmed human oligodendroglia circRNA landscapes in the HOG oligodendroglioma cell line, distinct from neuronal circRNA landscapes. Numerous circRNAs display oligodendroglia-specific regulation upon differentiation, among which a subclass is regulated independently from their parental mRNAs. We find that circRNA flanking introns often contain cis-regulatory elements for RNA editing and are predicted to bind differentiation-regulated splicing factors. In addition, we discover novel oligodendroglia-specific circRNAs that are predicted to sponge microRNAs, which co-operatively promote oligodendroglia development. Furthermore, we identify circRNA clusters derived from differentiation-regulated alternative circularization events within the same gene, each containing a common circular exon, achieving additive sponging effects that promote human oligodendroglia differentiation.

conclusionsOur results reveal dynamic regulation of human oligodendroglia circRNA landscapes during early differentiation and suggest critical roles of the circRNA-miRNA-mRNA axis in advancing human oligodendroglia development.

Indexed as

MicroRNAsRNA, CircularCell DifferentiationHumansOligodendrogliaRNARNA, MessengerMicroRNAsRNARNA, CircularRNA, MessengerCircRNAsMicroRNAsOL DifferentiationOligodendroglia

Identifiers

PMID35130952
PMCPMC8819885
OpenAlexW4210854459

What OpenQuestion holds

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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.