Evidence map›Paper›PMID 32375827›Full record

ArticleRetrovirology2020

Identification of the distribution of human endogenous retroviruses K (HML-2) by PCR-based target enrichment sequencing.

Bei Xue, Tiansheng Zeng, Lisha Jia, Dongsheng Yang, Stanley L Lin, Leonardo A Sechi, David J Kelvin

Open access · goldAbstract read
In one paragraph

Article in Retrovirology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
9.7field-weighted citation impact, top 2% 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

16 citing papers in PubMed, 32 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

7 authors at 3 institutions in 3 countries.

Bei XueDivision of Immunology, Shantou University Medical College, Shantou, China.
Tiansheng ZengDivision of Immunology, Shantou University Medical College, Shantou, China.
Lisha JiaDivision of Immunology, Shantou University Medical College, Shantou, China.ORCID 0000-0001-7757-9493
Dongsheng YangDivision of Immunology, Shantou University Medical College, Shantou, China.
Stanley L LinDivision of Immunology, Shantou University Medical College, Shantou, China.
Leonardo A SechiDepartment of Biomedical Sciences, University of Sassari, Sassari, Italy. sechila@uniss.it.
David J KelvinDivision of Immunology, Shantou University Medical College, Shantou, China. dkelvin@jidc.org.
Shantou University · CNDalhousie University · CAUniversity of Sassari · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundHuman endogenous retroviruses (HERVs), suspected to be transposition-defective, may reshape the transcriptional network of the human genome by regulatory elements distributed in their long terminal repeats (LTRs). HERV-K (HML-2), the most preserved group with the least number of accumulated of mutations, has been associated with aberrant gene expression in tumorigenesis and autoimmune diseases. Because of the high sequence similarity between different HERV-Ks, current methods have limitations in providing genome-wide mapping specific for individual HERV-K (HML-2) members, a major barrier in delineating HERV-K (HML-2) function.

resultsIn an attempt to obtain detailed distribution information of HERV-K (HML-2), we utilized a PCR-based target enrichment sequencing protocol for HERV-K (HML-2) (PTESHK) loci, which not only maps the presence of reference loci, but also identifies non-reference loci, enabling determination of the genome-wide distribution of HERV-K (HML-2) loci. Here we report on the genomic data obtained from three individuals. We identified a total of 978 loci using this method, including 30 new reference loci and 5 non-reference loci. Among the 3 individuals in our study, 14 polymorphic HERV-K (HML-2) loci were identified, and solo-LTR330 and N6p21.32 were identified as polymorphic for the first time.

conclusionsInterestingly, PTESHK provides an approach for the identification of the genome-wide distribution of HERV-K (HML-2) and can be used for the identification of polymorphic loci. Since polymorphic HERV-K (HML-2) integrations are suspected to be related to various diseases, PTESHK can supplement other emerging techniques in accessing polymorphic HERV-K (HML-2) elements in cancer and autoimmune diseases.

Indexed as

Genome, HumanEndogenous RetrovirusesHumansPolymerase Chain ReactionProvirusesSequence Analysis, DNATerminal Repeat SequencesGenome-wide distributionHERV-K (HML-2)Polymorphic lociPTESHK

Identifiers

PMID32375827
PMCPMC7201656
OpenAlexW3023706196

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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.