Evidence map›Paper›PMID 35676699›Full record

ArticleRetrovirology2022

Comprehensive identification and characterization of the HERV-K (HML-9) group in the human genome.

Lei Jia, Mengying Liu, Caiqin Yang, Hanping Li, Yongjian Liu, Jingwan Han, Xiuli Zhai, Xiaolin Wang, Tianyi Li, Jingyun Li and 3 more

Open access · goldAbstract read
In one paragraph

Article in Retrovirology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
3.4field-weighted citation impact, top 8% 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

13 citing papers in PubMed, 17 citations in OpenAlex.

  1. Article
  2. Review
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  5. Article
  6. Functional Bidirectionality of ERV-Derived Long Non-Coding RNAs in Humans.International journal of molecular sciences · 2024
    Review
  7. Article
  8. Article
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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

13 authors at 2 institutions in 1 country.

Lei Jia *Department of Virology, Beijing Institute of Microbiology and Epidemiology, Beijing, 100071, China.
Mengying Liu *College of Life Science and Technology, Beijing University of Chemical Technology, Beijing, 100029, China.
Caiqin YangDepartment of Virology, Beijing Institute of Microbiology and Epidemiology, Beijing, 100071, China.
Hanping LiDepartment of Virology, Beijing Institute of Microbiology and Epidemiology, Beijing, 100071, China.
Yongjian LiuDepartment of Virology, Beijing Institute of Microbiology and Epidemiology, Beijing, 100071, China.
Jingwan HanDepartment of Virology, Beijing Institute of Microbiology and Epidemiology, Beijing, 100071, China.
Xiuli ZhaiDepartment of Virology, Beijing Institute of Microbiology and Epidemiology, Beijing, 100071, China.
Xiaolin WangDepartment of Virology, Beijing Institute of Microbiology and Epidemiology, Beijing, 100071, China.
Tianyi LiDepartment of Virology, Beijing Institute of Microbiology and Epidemiology, Beijing, 100071, China.
Jingyun LiDepartment of Virology, Beijing Institute of Microbiology and Epidemiology, Beijing, 100071, China.
Bohan ZhangDepartment of Virology, Beijing Institute of Microbiology and Epidemiology, Beijing, 100071, China.
Changyuan YuCollege of Life Science and Technology, Beijing University of Chemical Technology, Beijing, 100029, China. yucy@mail.buct.edu.cn.
Lin LiDepartment of Virology, Beijing Institute of Microbiology and Epidemiology, Beijing, 100071, China. dearwood@sina.com.
Institute of Microbiology · CNBeijing University of Chemical Technology · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundHuman endogenous retroviruses (HERVs) result from ancestral infections caused by exogenous retroviruses that became incorporated into the germline DNA and evolutionarily fixed in the human genome. HERVs can be transmitted vertically in a Mendelian fashion and be stably maintained in the human genome, of which they are estimated to comprise approximately 8%. HERV-K (HML1-10) transcription has been confirmed to be associated with a variety of diseases, such as breast cancer, lung cancer, prostate cancer, melanoma, rheumatoid arthritis, and amyotrophic lateral sclerosis. However, the poor characterization of HML-9 prevents a detailed understanding of the regulation of the expression of this family in humans and its impact on the host genome. In light of this, a precise and updated HERV-K HML-9 genomic map is urgently needed to better evaluate the role of these elements in human health.

resultsWe report a comprehensive analysis of the presence and distribution of HERV-K HML-9 elements within the human genome, with a detailed characterization of the structural and phylogenetic properties of the group. A total of 23 proviruses and 47 solo LTR elements were characterized, with a detailed description of the provirus structure, integration time, potential regulated genes, transcription factor binding sites (TFBS), and primer binding site (PBS) features. The integration time results showed that the HML-9 elements found in the human genome integrated into the primate lineage between 17.5 and 48.5 million years ago (mya).

conclusionThe results provide a clear characterization of HML-9 and a comprehensive background for subsequent functional studies.

Indexed as

Endogenous RetrovirusesAnimalsChromosome MappingGenome, HumanHumansPhylogenyProvirusesBLATGene regulationGRCh38/hg38HML-9Human endogenous retrovirus

Identifiers

PMID35676699
PMCPMC9178832
OpenAlexW4282925067

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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.