Evidence map›Paper›PMID 39215947›Full record

ArticleGenes & genomics2024

Genomic analyses of intricate interaction of TE-lncRNA overlapping genes with miRNAs in human diseases.

Du Hyeong Lee, Eun Gyung Park, Jung-Min Kim, Hae Jin Shin, Yun Ju Lee, Hyeon-Su Jeong, Hyun-Young Roh, Woo Ryung Kim, Hongseok Ha, Sang-Woo Kim and 2 more

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Article in Genes & genomics, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
–field-weighted citation impact
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

2 citing papers in PubMed.

  1. Article
  2. Metamorphosis and lncRNAs: A Close Relationship.Genesis (New York, N.Y. : 2000) · 2026
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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

12 authors.

Du Hyeong LeeDepartment of Integrated Biological Sciences, Pusan National University, Busan, 46241, Republic of Korea.
Eun Gyung ParkDepartment of Integrated Biological Sciences, Pusan National University, Busan, 46241, Republic of Korea.
Jung-Min KimDepartment of Integrated Biological Sciences, Pusan National University, Busan, 46241, Republic of Korea.
Hae Jin ShinDepartment of Integrated Biological Sciences, Pusan National University, Busan, 46241, Republic of Korea.
Yun Ju LeeDepartment of Integrated Biological Sciences, Pusan National University, Busan, 46241, Republic of Korea.
Hyeon-Su JeongDepartment of Integrated Biological Sciences, Pusan National University, Busan, 46241, Republic of Korea.
Hyun-Young RohInstitute of Systems Biology, Pusan National University, Busan, 46241, Republic of Korea.
Woo Ryung KimDepartment of Integrated Biological Sciences, Pusan National University, Busan, 46241, Republic of Korea.
Hongseok HaInstitute of Endemic Disease, Medical Research Center, Seoul National University, Seoul, 03080, Republic of Korea.
Sang-Woo KimDepartment of Integrated Biological Sciences, Pusan National University, Busan, 46241, Republic of Korea.
Yung Hyun ChoiDepartment of Biochemistry, College of Oriental Medicine, Dong-Eui University, Busan, 47227, Republic of Korea.
Heui-Soo KimInstitute of Systems Biology, Pusan National University, Busan, 46241, Republic of Korea. khs307@pusan.ac.kr.ORCID 0000-0002-5226-6594

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundTransposable elements (TEs) are known to be inserted into genome to create transcript isoforms or to generate long non-coding RNA (lncRNA) sequences. The insertion of TEs generates a gene protein sequence within the genome, but also provides a microRNA (miRNA) regulatory region.

objectiveTo determine the effect of gene sequence changes caused by TE insertion on miRNA binding and to investigate the formation of an overlapping lncRNA that represses it.

methodsThe distribution of overlapping regions between exons and TE regions with lncRNA was examined using the Bedtools. miRNAs that can bind to those overlapping regions were identified through the miRDB web program. For TE-lncRNA overlapping genes, bioinformatic analysis was conducted using DAVID web database. Differential expression analysis was conducted using data from the GEO dataset and TCGA.

resultsMost TEs were distributed more frequently in untranslated regions than open reading frames. There were 30 annotated TE-lncRNA overlapping genes with same strand that could bind to the same miRNA. As a result of identifying the association between these 30 genes and diseases, TGFB2, FCGR2A, DCTN5, and IFI6 were associated with breast cancer, and HMGCS1, FRMD4A, EDNRB, and SNCA were associated with Alzheimer's disease. Analysis of the GEO and TCGA data showed that the relevant expression of miR-891a and miR-28, which bind to the TE overlapping region of DCTN5 and HMGCS1, decreased.

conclusionThis study indicates that the interaction between TE-lncRNA overlapping genes and miRNAs can affect disease progression.

Indexed as

DNA Transposable ElementsMicroRNAsRNA, Long NoncodingAlzheimer DiseaseBreast NeoplasmsGenes, OverlappingHumansDNA Transposable ElementsMicroRNAsRNA, Long NoncodingBioinformaticsHuman diseaselong non-coding RNAmicroRNATransposable elements

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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 Socratic graph.