Evidence map›Paper›PMID 24563702›Full record

ReviewCommunicative & integrative biology2013

Phenotypic diversification by gene silencing in Phytophthora plant pathogens.

Ramesh R Vetukuri, Anna Km Asman, Sultana N Jahan, Anna O Avrova, Stephen C Whisson, Christina Dixelius

Open access · goldAbstract readReview
In one paragraph

Review in Communicative & integrative biology, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
2.8field-weighted citation impact, top 10% 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

6 citing papers in PubMed, 12 citations in OpenAlex.

  1. Article
  2. Evolutionary origins and impacts of genome architecture in ciliates.Annals of the New York Academy of Sciences · 2019
    Review
  3. Article
  4. Review
  5. Article
  6. Epigenetic control of effectors in plant pathogens.Frontiers in plant science · 2014
    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

6 authors at 4 institutions in 4 countries.

Ramesh R VetukuriDepartment of Plant Biology and Forest Genetics; Uppsala BioCenter; Swedish University of Agricultural Sciences and Linnean Center for Plant Biology; Uppsala, Sweden.
Anna Km AsmanDepartment of Plant Biology and Forest Genetics; Uppsala BioCenter; Swedish University of Agricultural Sciences and Linnean Center for Plant Biology; Uppsala, Sweden.
Sultana N JahanDepartment of Plant Biology and Forest Genetics; Uppsala BioCenter; Swedish University of Agricultural Sciences and Linnean Center for Plant Biology; Uppsala, Sweden.
Anna O AvrovaCell and Molecular Sciences; The James Hutton Institute; Invergowrie; Dundee, UK.
Stephen C WhissonCell and Molecular Sciences; The James Hutton Institute; Invergowrie; Dundee, UK.
Christina DixeliusDepartment of Plant Biology and Forest Genetics; Uppsala BioCenter; Swedish University of Agricultural Sciences and Linnean Center for Plant Biology; Uppsala, Sweden.
Swedish University of Agricultural Sciences · SETataa Biocenter (Sweden) · SEInstitute of Molecular and Cell Biology · RUJames Hutton Institute · GB

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Advances in genome sequencing technologies have enabled generation of unprecedented information on genome content and organization. Eukaryote genomes in particular may contain large populations of transposable elements (TEs) and other repeated sequences. Active TEs can result in insertional mutations, altered transcription levels and ectopic recombination of DNA. The genome of the oomycete plant pathogen, Phytophthora infestans, contains vast numbers of TE sequences. There are also hundreds of predicted disease-promoting effector proteins, predominantly located in TE-rich genomic regions. Expansion of effector gene families is also a genomic signature of related oomycetes such as P. sojae. Deep sequencing of small RNAs (sRNAs) from P. infestans has identified sRNAs derived from all families of transposons, highlighting the importance of RNA silencing for maintaining these genomic invaders in an inactive form. Small RNAs were also identified from specific effector encoding genes, possibly leading to RNA silencing of these genes and variation in pathogenicity and virulence toward plant resistance genes. Similar findings have also recently been made for the distantly related species, P. sojae. Small RNA "hotspots" originating from arrays of amplified gene sequences, or from genes displaying overlapping antisense transcription, were also identified in P. infestans. These findings suggest a major role for RNA silencing processes in the adaptability and diversification of these economically important plant pathogens. Here we review the latest progress and understanding of gene silencing in oomycetes with emphasis on transposable elements and sRNA-associated events.

Indexed as

effectorsoomycetePhytophthorasmall RNAstransposable element

Identifiers

PMID24563702
PMCPMC3917941
OpenAlexW2003984381

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.