Evidence map›Paper›PMID 17517142›Full record

ArticleBMC plant biology2007

Endogenous pararetroviral sequences in tomato (Solanum lycopersicum) and related species.

Christina Staginnus, Wolfgang Gregor, M Florian Mette, Chee How Teo, Eduviges Glenda Borroto-Fernández, Margit Laimer da Câmara Machado, Marjori Matzke, Trude Schwarzacher

Open access · goldAbstract read
In one paragraph

Article in BMC plant biology, 2007. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 37 papers.

0numbers the graph read from it
0cells of the map it votes in
37citing papers in PubMed
5.5field-weighted citation impact, top 5% 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

37 citing papers in PubMed, 99 citations in OpenAlex.

  1. Article
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  6. Review
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  8. The nature and organization of satellite DNAs inFrontiers in plant science · 2023
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  9. Plant Cytogenetics: From Chromosomes to Cytogenomics.Methods in molecular biology (Clifton, N.J.) · 2023
    Article
  10. Article
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  15. Article
  16. Review
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  18. Article
  19. Virus Latency and the Impact on Plants.Frontiers in microbiology · 2019
    Review
  20. Article
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

8 authors at 5 institutions in 3 countries.

Christina StaginnusGregor Mendel Institute of Plant Molecular Biology (GMI), Wien, Austria. christina.staginnus@gmi.oeaw.ac.at
Wolfgang Gregor
M Florian Mette
Chee How Teo
Eduviges Glenda Borroto-Fernández
Margit Laimer da Câmara Machado
Marjori Matzke
Trude Schwarzacher
BOKU University · ATUniversity of Leicester · GBGregor Mendel Institute of Molecular Plant Biology · ATLeibniz Institute of Plant Genetics and Crop Plant Research · DEUniversity of Veterinary Medicine Vienna · AT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundEndogenous pararetroviral sequences (EPRVs) are a recently discovered class of repetitive sequences that is broadly distributed in the plant kingdom. The potential contribution of EPRVs to plant pathogenicity or, conversely, to virus resistance is just beginning to be explored. Some members of the family Solanaceae are particularly rich in EPRVs. In previous work, EPRVs have been characterized molecularly in various species of Nicotiana including N.tabacum (tobacco) and Solanum tuberosum (potato). Here we describe a family of EPRVs in cultivated tomato (Solanum lycopersicum L.) and a wild relative (S.habrochaites).

resultsMolecular cloning and DNA sequence analysis revealed that tomato EPRVs (named LycEPRVs) are most closely related to those in tobacco. The sequence similarity of LycEPRVs in S.lycopersicum and S.habrochaites indicates they are potentially derived from the same pararetrovirus. DNA blot analysis revealed a similar genomic organization in the two species, but also some independent excision or insertion events after species separation, or flanking sequence divergence. LycEPRVs share with the tobacco elements a disrupted genomic structure and frequent association with retrotransposons. Fluorescence in situ hybridization revealed that copies of LycEPRV are dispersed on all chromosomes in predominantly heterochromatic regions. Methylation of LycEPRVs was detected in CHG and asymmetric CHH nucleotide groups. Although normally quiescent EPRVs can be reactivated and produce symptoms of infection in some Nicotiana interspecific hybrids, a similar pathogenicity of LycEPRVs could not be demonstrated in Solanum L. section Lycopersicon [Mill.] hybrids. Even in healthy plants, however, transcripts derived from multiple LycEPRV loci and short RNAs complementary to LycEPRVs were detected and were elevated upon infection with heterologous viruses encoding suppressors of PTGS.

conclusionThe analysis of LycEPRVs provides further evidence for the extensive invasion of pararetroviral sequences into the genomes of solanaceous plants. The detection of asymmetric CHH methylation and short RNAs, which are hallmarks of RNAi in plants, suggests that LycEPRVs are controlled by an RNA-mediated silencing mechanism.

Indexed as

Base SequenceCaulimoviridaeChromosomes, PlantCloning, MolecularGene Expression Regulation, PlantGene Expression Regulation, ViralGenome, PlantIn Situ Hybridization, FluorescenceMolecular Sequence DataNicotianaPhylogenyRetroelementsReverse Transcriptase Polymerase Chain ReactionSequence Analysis, DNASequence Homology, Nucleic AcidSolanaceaeRetroelements

Identifiers

PMID17517142
PMCPMC1899175
OpenAlexW2005166015

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

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.