Evidence map›Paper›PMID 31721105›Full record

ArticleGenes & genomics2020

Expression analysis of LTR-derived miR-1269a and target gene, KSR2 in Sebastes schlegelii.

Jennifer Im, Woo Ryung Kim, Hee-Eun Lee, Ahran Kim, Do-Hyung Kim, Yung Hyun Choi, Hee-Jae Cha, Suhkmann Kim, Heui-Soo Kim

Abstract read
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In one paragraph

Article in Genes & genomics, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
0.2field-weighted citation impact, top 49% 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

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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

1 citing paper in PubMed, 3 citations in OpenAlex.

  1. 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

9 authors at 4 institutions in 1 country.

Jennifer ImDepartment of Biological Sciences, College of Natural Sciences, Pusan National University, Busan, 46241, Republic of Korea.
Woo Ryung KimDepartment of Biological Sciences, College of Natural Sciences, Pusan National University, Busan, 46241, Republic of Korea.
Hee-Eun LeeDepartment of Biological Sciences, College of Natural Sciences, Pusan National University, Busan, 46241, Republic of Korea.
Ahran KimDepartment of Aquatic Life Medicine, College of Fisheries Sciences, Pukyong National University, Busan, 48513, Republic of Korea.
Do-Hyung KimDepartment of Aquatic Life Medicine, College of Fisheries Sciences, Pukyong National University, Busan, 48513, Republic of Korea.
Yung Hyun ChoiDepartment of Biochemistry, College of Korean Medicine, Dong-eui University, Busan, 47340, Republic of Korea.
Hee-Jae ChaDepartment of Parasitology and Genetics, College of Medicine, Kosin University, Busan, 49267, Republic of Korea.
Suhkmann KimDepartment of Chemistry, College of Natural Sciences, Pusan National University, Busan, 46241, Republic of Korea.
Heui-Soo KimDepartment of Biological Sciences, College of Natural Sciences, Pusan National University, Busan, 46241, Republic of Korea. khs307@pusan.ac.kr.ORCID 0000-0002-5226-6594
Pusan National University · KRPukyong National University · KRDong-Eui University · KRKosin University · KR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundSebastes schlegelii are an important species of fish found in the coastal areas of the Korea with significant commercial importance. Most studies thus far have been primarily focused on environmental factors; behavioural patterns, aquaculture, diseases and limited genetic studies with little to none related to either microRNAs (miRNAs) or transposable elements (TE).

objectivesIn order to understand biological roles of TE-derived miR-1269a, we examined expression pattern for miR-1269a and its target gene, KSR2, in various tissues of Sebastes schlegelii. Also, we performed luciferase reporter assay in HINAE cells.

methodsUCSC Genome Browser (https://genome.ucsc.edu/) was used to examine which TE is associated with miR-1269a. For the target genes for miR-1269a, the target genes associated with the miRNA were identified using miRDB (http://www.mirdb.org/) and TargetScan 7.1 (http://www.targetscan.org/vert_71/). A two-step miRNA kit, HB miR Multi Assay Kit™ System. I was used for the analysis of TE-derived miRNA expression patterns. The 3'UTR of KSR2 gene was cloned into the psiCHECK-2 vector. Subsequently co-transfected with miR-1269a mimics to HINAE cells for luciferase reporter assay.

resultsMiR-1269a was found to be derived from LTR retrotransposon, MLT2B. LTR-derived miR-1269a was highly expressed in the muscle, liver and gonad tissues of Sebastes schlegelii, but KSR2 revealed high expression in the brain. Co-transfection of KSR2 and miR-1269a mimic to HINAE cells showed high activity of miR-1269a in relation to KSR2.

conclusionLTR-derived miR-1269a showed enhancer activity with relation to KSR2 in Sebastes schlegelii. The data may be used as a foundation for further investigation regarding correlation of miRNA and target genes in addition to other functional studies of biological significance in Sebastes schlegelii.

Indexed as

3' Untranslated RegionsAnimalsBase SequenceComputational BiologyFish ProteinsGene Expression ProfilingGene Expression RegulationMicroRNAsPerciformesProtein Serine-Threonine KinasesRetroelementsSequence HomologyTerminal Repeat Sequences3' Untranslated RegionsFish ProteinsMicroRNAsProtein Serine-Threonine KinasesRetroelementsKSR2miR-1269aMLT2BSebastes schlegeliiTransposable element

Identifiers

PMID31721105
OpenAlexW2986251685

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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.