Evidence map›Paper›PMID 37501164›Full record

ArticleBMC genomics2023

Lineage-specific amplification and epigenetic regulation of LTR-retrotransposons contribute to the structure, evolution, and function of Fabaceae species.

Long-Long Yang, Xin-Yu Zhang, Li-Ying Wang, Yan-Ge Li, Xiao-Ting Li, Yi Yang, Qing Su, Ning Chen, Yu-Lan Zhang, Ning Li and 3 more

Open access · goldAbstract read
In one paragraph

Article in BMC genomics, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
7.9field-weighted citation impact, top 3% of its field
1 · What the graph read from it

What it found

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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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3 · Its place in the literature

Who cites it

10 citing papers in PubMed, 20 citations in OpenAlex.

  1. Article
  2. Article
  3. Genome-Wide Identification and Analysis of Plant Cysteine Oxidase (International journal of molecular sciences · 2026
    Article
  4. Genome-wide in-silico identification and characterization of LTR retrotransposons in domestic goat (Capra hircus).Mammalian genome : official journal of the International Mammalian Genome Society · 2026
    Article
  5. Article
  6. Article
  7. Review
  8. Article
  9. Article
  10. Article
4 · The record

Corrections and comments

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5 · Who and what money

Authors and funding

13 authors at 1 institution in 1 country.

Long-Long YangCollege of Life Sciences, Henan Normal University, Xinxiang, 453007, P. R. China.
Xin-Yu ZhangCollege of Life Sciences, Henan Normal University, Xinxiang, 453007, P. R. China.
Li-Ying WangCollege of Life Sciences, Henan Normal University, Xinxiang, 453007, P. R. China.
Yan-Ge LiCollege of Life Sciences, Henan Normal University, Xinxiang, 453007, P. R. China.
Xiao-Ting LiCollege of Life Sciences, Henan Normal University, Xinxiang, 453007, P. R. China.
Yi YangCollege of Life Sciences, Henan Normal University, Xinxiang, 453007, P. R. China.
Qing SuCollege of Life Sciences, Henan Normal University, Xinxiang, 453007, P. R. China.
Ning ChenCollege of Life Sciences, Henan Normal University, Xinxiang, 453007, P. R. China.
Yu-Lan ZhangCollege of Life Sciences, Henan Normal University, Xinxiang, 453007, P. R. China.
Ning LiCollege of Life Sciences, Henan Normal University, Xinxiang, 453007, P. R. China.
Chuan-Liang DengCollege of Life Sciences, Henan Normal University, Xinxiang, 453007, P. R. China.
Shu-Fen LiCollege of Life Sciences, Henan Normal University, Xinxiang, 453007, P. R. China. lishufen83@163.com.
Wu-Jun GaoCollege of Life Sciences, Henan Normal University, Xinxiang, 453007, P. R. China. gaowujun@htu.cn.
Henan Normal University · CN

Funding

National Natural Science Foundation of China 31970240
6 · The paper itself

Abstract

backgroundLong terminal repeat (LTR)-retrotransposons (LTR-RTs) are ubiquitous and make up the majority of nearly all sequenced plant genomes, whereas their pivotal roles in genome evolution, gene expression regulation as well as their epigenetic regulation are still not well understood, especially in a large number of closely related species.

resultsHere, we analyzed the abundance and dynamic evolution of LTR-RTs in 54 species from an economically and agronomically important family, Fabaceae, and also selected two representative species for further analysis in expression of associated genes, transcriptional activity and DNA methylation patterns of LTR-RTs. Annotation results revealed highly varied proportions of LTR-RTs in these genomes (5.1%~68.4%) and their correlation with genome size was highly positive, and they were significantly contributed to the variance in genome size through species-specific unique amplifications. Almost all of the intact LTR-RTs were inserted into the genomes 4 Mya (million years ago), and more than 50% of them were inserted in the last 0.5 million years, suggesting that recent amplifications of LTR-RTs were an important force driving genome evolution. In addition, expression levels of genes with intronic, promoter, and downstream LTR-RT insertions of Glycine max and Vigna radiata, two agronomically important crops in Fabaceae, showed that the LTR-RTs located in promoter or downstream regions suppressed associated gene expression. However, the LTR-RTs within introns promoted gene expression or had no contribution to gene expression. Additionally, shorter and younger LTR-RTs maintained higher mobility and transpositional potential. Compared with the transcriptionally silent LTR-RTs, the active elements showed significantly lower DNA methylation levels in all three contexts. The distributions of transcriptionally active and silent LTR-RT methylation varied across different lineages due to the position of LTR-RTs located or potentially epigenetic regulation.

conclusionLineage-specific amplification patterns were observed and higher methylation level may repress the activity of LTR-RTs, further influence evolution in Fabaceae species. This study offers valuable clues into the evolution, function, transcriptional activity and epigenetic regulation of LTR-RTs in Fabaceae genomes.

Indexed as

FabaceaeRetroelementsEpigenesis, GeneticEvolution, MolecularGenome, PlantPhylogenyTerminal Repeat SequencesRetroelementsDNA methylationFabaceae speciesGenome evolutionLTR-RT insertionLTR-RTsTranscriptional activity

Identifiers

PMID37501164
PMCPMC10373317
OpenAlexW4385330109

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LicenceCC BY
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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.