Overexpression of Arabidopsis thaliana ERI, the homolog of C. elegans Enhancer of RNAinterference, leads to enhanced growth
Identifieur interne : 001635 ( Main/Curation ); précédent : 001634; suivant : 001636Overexpression of Arabidopsis thaliana ERI, the homolog of C. elegans Enhancer of RNAinterference, leads to enhanced growth
Auteurs : Rhonda C. Meyer [Allemagne] ; Gunnar Hönig [Allemagne] ; Ronny Brandt [Allemagne] ; Fernando Arana-Ceballos [Allemagne] ; Cathleen Neitsch [Allemagne] ; Gunter Reuter [Allemagne] ; Thomas Altmann [Allemagne] ; Markus Kuhlmann [Allemagne]Source :
- Frontiers in Plant Science [ 1664-462X ] ; 2015.
Abstract
Organisms adopt a wide range of strategies to adapt to change. Gene silencing describes the ability of organisms to modulate the expression of susceptible genes at certain times at the transcriptional or the translational level. In all known eukaryotic organisms 21-nt long short interfering RNAs (siRNAs) are the effector molecules of post-transcriptional gene silencing (PTGS), while 24-nt long siRNAs are involved in PTGS in plants. Mutant studies in
Url:
DOI: 10.3389/fpls.2015.00531
PubMed: 26257748
PubMed Central: 4510415
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Meyer</name><affiliation wicri:level="1"><nlm:aff id="aff1"><institution>Department of Molecular Genetics, Leibniz Institute of Plant Genetics and Crop Plant Research (IPK Gatersleben)</institution>,<country>Stadt Seeland, Germany</country></nlm:aff><country xml:lang="fr">Allemagne</country><wicri:regionArea></wicri:regionArea></affiliation></author><author><name sortKey="Honig, Gunnar" sort="Honig, Gunnar" uniqKey="Honig G" first="Gunnar" last="Hönig">Gunnar Hönig</name><affiliation wicri:level="1"><nlm:aff id="aff2"><institution>Department of Developmental Genetics, Institute of Biology, Martin Luther University Halle-Wittenberg</institution>,<country>Halle (Saale), Germany</country></nlm:aff><country xml:lang="fr">Allemagne</country><wicri:regionArea></wicri:regionArea></affiliation></author><author><name sortKey="Brandt, Ronny" sort="Brandt, Ronny" uniqKey="Brandt R" first="Ronny" last="Brandt">Ronny Brandt</name><affiliation wicri:level="1"><nlm:aff id="aff1"><institution>Department of Molecular Genetics, Leibniz Institute of Plant Genetics and Crop Plant Research (IPK Gatersleben)</institution>,<country>Stadt Seeland, Germany</country></nlm:aff><country xml:lang="fr">Allemagne</country><wicri:regionArea></wicri:regionArea></affiliation></author><author><name sortKey="Arana Ceballos, Fernando" sort="Arana Ceballos, Fernando" uniqKey="Arana Ceballos F" first="Fernando" last="Arana-Ceballos">Fernando Arana-Ceballos</name><affiliation wicri:level="1"><nlm:aff id="aff1"><institution>Department of Molecular Genetics, Leibniz Institute of Plant Genetics and Crop Plant Research (IPK Gatersleben)</institution>,<country>Stadt Seeland, Germany</country></nlm:aff><country xml:lang="fr">Allemagne</country><wicri:regionArea></wicri:regionArea></affiliation></author><author><name sortKey="Neitsch, Cathleen" sort="Neitsch, Cathleen" uniqKey="Neitsch C" first="Cathleen" last="Neitsch">Cathleen Neitsch</name><affiliation wicri:level="1"><nlm:aff id="aff1"><institution>Department of Molecular Genetics, Leibniz Institute of Plant Genetics and Crop Plant Research (IPK Gatersleben)</institution>,<country>Stadt Seeland, Germany</country></nlm:aff><country xml:lang="fr">Allemagne</country><wicri:regionArea></wicri:regionArea></affiliation></author><author><name sortKey="Reuter, Gunter" sort="Reuter, Gunter" uniqKey="Reuter G" first="Gunter" last="Reuter">Gunter Reuter</name><affiliation wicri:level="1"><nlm:aff id="aff2"><institution>Department of Developmental Genetics, Institute of Biology, Martin Luther University Halle-Wittenberg</institution>,<country>Halle (Saale), Germany</country></nlm:aff><country xml:lang="fr">Allemagne</country><wicri:regionArea></wicri:regionArea></affiliation></author><author><name sortKey="Altmann, Thomas" sort="Altmann, Thomas" uniqKey="Altmann T" first="Thomas" last="Altmann">Thomas Altmann</name><affiliation wicri:level="1"><nlm:aff id="aff1"><institution>Department of Molecular Genetics, Leibniz Institute of Plant Genetics and Crop Plant Research (IPK Gatersleben)</institution>,<country>Stadt Seeland, Germany</country></nlm:aff><country xml:lang="fr">Allemagne</country><wicri:regionArea></wicri:regionArea></affiliation></author><author><name sortKey="Kuhlmann, Markus" sort="Kuhlmann, Markus" uniqKey="Kuhlmann M" first="Markus" last="Kuhlmann">Markus Kuhlmann</name><affiliation wicri:level="1"><nlm:aff id="aff1"><institution>Department of Molecular Genetics, Leibniz Institute of Plant Genetics and Crop Plant Research (IPK Gatersleben)</institution>,<country>Stadt Seeland, Germany</country></nlm:aff><country xml:lang="fr">Allemagne</country><wicri:regionArea></wicri:regionArea></affiliation></author></analytic><series><title level="j">Frontiers in Plant Science</title><idno type="eISSN">1664-462X</idno><imprint><date when="2015">2015</date></imprint></series></biblStruct></sourceDesc></fileDesc><profileDesc><textClass></textClass></profileDesc></teiHeader><front><div type="abstract" xml:lang="en"><p>Organisms adopt a wide range of strategies to adapt to change. Gene silencing describes the ability of organisms to modulate the expression of susceptible genes at certain times at the transcriptional or the translational level. In all known eukaryotic organisms 21-nt long short interfering RNAs (siRNAs) are the effector molecules of post-transcriptional gene silencing (PTGS), while 24-nt long siRNAs are involved in PTGS in plants. Mutant studies in <italic>Caenorhabditis elegans</italic> lead to the identification of the enzyme ERI (Enhancer of RNAinterference) with enhanced PTGS. Although the genes involved in growth vigor and growth rate are still unknown, it becomes clearer that the population of small RNAs plays a role in the very early phase of plant development. To pinpoint the link between growth and siRNAs, the expression of <italic>Arabidopsis</italic> uni-gene <italic>Enhancer of RNAi</italic> (<italic>ERI</italic>) homolog from <italic>C. elegans</italic> was modulated. Increased degradation of small RNAs was achieved by ectopic <italic>AtERI</italic> overexpression <italic>in planta</italic>. Based on global small RNA analysis, <italic>AtERI</italic> overexpression affects mainly the population of 21 mers, excluding miRNAs. To identify target genes, AtERI gain-of-function mutants were analyzed, and differentially abundant small RNAs were identified. Plants with an elevated level of <italic>AtERI</italic> were bigger in all three light intensities analyzed, indicating an inhibitory function of particular small RNAs in plant growth, with differences in relative growth rates depending on developmental stage and light intensity. Understanding the role of these siRNAs could open new avenues for enhancing plant growth.</p></div></front><back><div1 type="bibliography"><listBibl><biblStruct><analytic><author><name sortKey="Aravind, L" uniqKey="Aravind L">L. Aravind</name></author><author><name sortKey="Koonin, E V" uniqKey="Koonin E">E. V. 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