Evidence map›Paper›PMID 27846817›Full record

ArticleBMC genomics2016

MicroRNAs regulate gene plasticity during cold shock in zebrafish larvae.

I-Chen Hung, Yu-Chuan Hsiao, H Sunny Sun, Tsung-Ming Chen, Shyh-Jye Lee

Open access · goldAbstract read
In one paragraph

Article in BMC genomics, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
2.2field-weighted citation impact, top 13% 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

15 citing papers in PubMed, 45 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

5 authors at 4 institutions in 1 country.

I-Chen HungDepartment of Life Science, National Taiwan University, Taipei, 10617, Taiwan.
Yu-Chuan HsiaoDepartment of Life Science, National Taiwan University, Taipei, 10617, Taiwan.
H Sunny SunInstitute of Molecular Medicine, College of Medicine, National Cheng Kung University, Tainan, 70456, Taiwan.
Tsung-Ming ChenDepartment and Graduate Institute of Aquaculture, National Kaohsiung Marine University, Kaohsiung 81157, Taiwan. tmtonychen@webmail.nkmu.edu.tw.
Shyh-Jye LeeDepartment of Life Science, National Taiwan University, Taipei, 10617, Taiwan. jefflee@ntu.edu.tw.ORCID 0000-0001-8452-9152
National Taiwan University · TWNational Cheng Kung University · TWNational Kaohsiung Marine University · TWNational Taiwan University of Science and Technology · TW

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundMicroRNAs (miRNAs) are critical regulators responding to acute environmental stresses in both plants and animals. By modulating gene expression, miRNAs either restore or reconstitute a new expression program to enhance cell tolerance to stresses. Cold shock is one of the stresses that can induce acute physiological responses and transcriptional changes in aquatic creatures. Previous genomic studies have revealed many cold-affected genes in fish larvae and adults, however, the role of miRNAs in acute cold response is still ambiguous. To elucidate the regulatory roles of miRNAs in the cold-inducible responses, we performed small RNA-seq and RNA-seq analyses and found potential cold regulatory miRNAs and genes. We further investigated their interactions and involvements in cold tolerance.

resultsSmall RNA-seq and RNA-seq identified 29 up-/26 down-regulated miRNAs and 908 up-/468 down-regulated genes, respectively, in responding to cold shock for 4 h at 18 °C. miRNA and transcriptomic analyses showed these miRNAs and mRNAs are involved in similar biological processes and pathways. Gene ontology enrichment analyses revealed the cold-induced genes were enriched in pathways, including melanogenesis, GnRH pathway, circadian rhythm, etc. We were particularly interested in the changes in circadian clock genes that affect daily metabolism. The enrichment of circadian clock genes was also observed in previous fish cold acclimation studies, but have not been characterized. To characterize the functional roles of circadian clock genes in cold tolerance, we individually overexpressed selected clock genes in zebrafish larvae and found one of the core clock genes per2 resulted in better recovery from cold shock. In addition, we validated the interaction of per2 with its associate miRNA, dre-mir-29b, which is also cold-inducible. It suggests the transcription of per2 can be modulated by miRNA upon cold shock.

conclusionsCollectively, our observations suggest that miRNAs are fine turners for regulating genomic plasticity against cold shock. We further showed that the fine tuning of core clock gene per2 via its associated miRNA, dre-mir-29b, can enhance the cold tolerance of zebrafish larvae.

Indexed as

Gene Expression RegulationTranscriptomeAnimalsCircadian ClocksCold-Shock ResponseComputational BiologyGene Expression ProfilingGenetic Association StudiesHigh-Throughput Nucleotide SequencingLarvaMicroRNAsMolecular Sequence AnnotationPhenotypeReproducibility of ResultsStress, PhysiologicalZebrafishMicroRNAsClock genesCold stressDeep sequencingEmbryonic developmentmiRNAZebrafish

Identifiers

PMID27846817
PMCPMC5111229
OpenAlexW2550861558

What OpenQuestion holds

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LicenceCC BY
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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.