Evidence map›Paper›PMID 36903960›Full record

ReviewPlants (Basel, Switzerland)2023

Miniature Inverted-Repeat Transposable Elements: Small DNA Transposons That Have Contributed to Plant

Joseph L Pegler, Jackson M J Oultram, Christopher W G Mann, Bernard J Carroll, Christopher P L Grof, Andrew L Eamens

Full text readReview
In one paragraph

Review in Plants (Basel, Switzerland), 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing 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

12 citing papers in PubMed.

  1. Article
  2. Review
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  4. Article
  5. Review
  6. Article
  7. New Sights into Bioinformatics of Gene Regulations and Structure.International journal of molecular sciences · 2025
    Article
  8. Article
  9. Article
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  11. Review
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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

6 authors.

Joseph L PeglerCentre for Plant Science, School of Environmental and Life Sciences, College of Engineering, Science and Environment, University of Newcastle, Callaghan, NSW 2308, Australia.ORCID 0000-0001-7353-3850
Jackson M J OultramCentre for Plant Science, School of Environmental and Life Sciences, College of Engineering, Science and Environment, University of Newcastle, Callaghan, NSW 2308, Australia.ORCID 0000-0003-0734-9574
Christopher W G MannSchool of Chemistry and Molecular Biosciences, The University of Queensland, St. Lucia, QLD 4072, Australia.ORCID 0000-0001-8431-6317
Bernard J CarrollSchool of Chemistry and Molecular Biosciences, The University of Queensland, St. Lucia, QLD 4072, Australia.ORCID 0000-0002-1976-8269
Christopher P L GrofCentre for Plant Science, School of Environmental and Life Sciences, College of Engineering, Science and Environment, University of Newcastle, Callaghan, NSW 2308, Australia.ORCID 0000-0003-1968-5401
Andrew L EamensSchool of Health, University of the Sunshine Coast, Maroochydore, QLD 4558, Australia.ORCID 0000-0002-6327-3618

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Angiosperms form the largest phylum within the Plantae kingdom and show remarkable genetic variation due to the considerable difference in the nuclear genome size of each species. Transposable elements (TEs), mobile DNA sequences that can amplify and change their chromosome position, account for much of the difference in nuclear genome size between individual angiosperm species. Considering the dramatic consequences of TE movement, including the complete loss of gene function, it is unsurprising that the angiosperms have developed elegant molecular strategies to control TE amplification and movement. Specifically, the RNA-directed DNA methylation (RdDM) pathway, directed by the repeat-associated small-interfering RNA (rasiRNA) class of small regulatory RNA, forms the primary line of defense to control TE activity in the angiosperms. However, the miniature inverted-repeat transposable element (MITE) species of TE has at times avoided the repressive effects imposed by the rasiRNA-directed RdDM pathway. MITE proliferation in angiosperm nuclear genomes is due to their preference to transpose within gene-rich regions, a pattern of transposition that has enabled MITEs to gain further transcriptional activity. The sequence-based properties of a MITE results in the synthesis of a noncoding RNA (ncRNA), which, after transcription, folds to form a structure that closely resembles those of the precursor transcripts of the microRNA (miRNA) class of small regulatory RNA. This shared folding structure results in a MITE-derived miRNA being processed from the MITE-transcribed ncRNA, and post-maturation, the MITE-derived miRNA can be used by the core protein machinery of the miRNA pathway to regulate the expression of protein-coding genes that harbor homologous MITE insertions. Here, we outline the considerable contribution that the MITE species of TE have made to expanding the miRNA repertoire of the angiosperms.

Indexed as

angiospermsMICRORNA (MIR) gene evolutionmicroRNA (miRNA)miniature inverted-repeat transposable element (MITE)repeat-associated small-interfering RNA (rasiRNA)RNA-directed DNA methylation (RdDM)transposable element (TE)

Identifiers

PMID36903960
PMCPMC10004981

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measurements read51
Read underepoch 390

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.