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Evidence for Large Complex Networks of Plant Short Silencing RNAs

BACKGROUND: In plants and animals there are many classes of short RNAs that carry out a wide range of functions within the cell; short silencing RNAs (ssRNAs) of 21–25 nucleotides in length are produced from double-stranded RNA precursors by the protein Dicer and guide nucleases and other proteins t...

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Autores principales: MacLean, Daniel, Elina, Nataliya, Havecker, Ericka R., Heimstaedt, Susanne B., Studholme, David J., Baulcombe, David C.
Formato: Texto
Lenguaje:English
Publicado: Public Library of Science 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2845630/
https://www.ncbi.nlm.nih.gov/pubmed/20360863
http://dx.doi.org/10.1371/journal.pone.0009901
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author MacLean, Daniel
Elina, Nataliya
Havecker, Ericka R.
Heimstaedt, Susanne B.
Studholme, David J.
Baulcombe, David C.
author_facet MacLean, Daniel
Elina, Nataliya
Havecker, Ericka R.
Heimstaedt, Susanne B.
Studholme, David J.
Baulcombe, David C.
author_sort MacLean, Daniel
collection PubMed
description BACKGROUND: In plants and animals there are many classes of short RNAs that carry out a wide range of functions within the cell; short silencing RNAs (ssRNAs) of 21–25 nucleotides in length are produced from double-stranded RNA precursors by the protein Dicer and guide nucleases and other proteins to their RNA targets through base pairing interactions. The consequence of this process is degradation of the targeted RNA, suppression of its translation or initiation of secondary ssRNA production. The secondary ssRNAs in turn could then initiate further layers of ssRNA production to form extensive cascades and networks of interacting RNA [1]. Previous empirical analysis in plants established the existence of small secondary ssRNA cascade [2], in which a single instance of this event occurred but it was not known whether there are other more extensive networks of secondary sRNA production. METHODOLOGY/PRINCIPAL FINDINGS: We generated a network by predicting targets of ssRNA populations obtained from high-throughput sequencing experiments. The topology of the network shows it to have power law connectivity distribution, to be dissortative, highly clustered and composed of multiple components. We also identify protein families, PPR and ULP1, that act as hubs within the network. Comparison of the repetition of genomic sub-sequences of ssRNA length between Arabidopsis and E.coli suggest that the network structure is made possible by the underlying repetitiveness in the genome sequence. CONCLUSIONS/SIGNIFICANCE: Together our results provide good evidence for the existence of a large, robust ssRNA interaction network with distinct regulatory function. Such a network could have a massive effect on the regulation of gene expression via mediation of transcript levels.
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spelling pubmed-28456302010-04-02 Evidence for Large Complex Networks of Plant Short Silencing RNAs MacLean, Daniel Elina, Nataliya Havecker, Ericka R. Heimstaedt, Susanne B. Studholme, David J. Baulcombe, David C. PLoS One Research Article BACKGROUND: In plants and animals there are many classes of short RNAs that carry out a wide range of functions within the cell; short silencing RNAs (ssRNAs) of 21–25 nucleotides in length are produced from double-stranded RNA precursors by the protein Dicer and guide nucleases and other proteins to their RNA targets through base pairing interactions. The consequence of this process is degradation of the targeted RNA, suppression of its translation or initiation of secondary ssRNA production. The secondary ssRNAs in turn could then initiate further layers of ssRNA production to form extensive cascades and networks of interacting RNA [1]. Previous empirical analysis in plants established the existence of small secondary ssRNA cascade [2], in which a single instance of this event occurred but it was not known whether there are other more extensive networks of secondary sRNA production. METHODOLOGY/PRINCIPAL FINDINGS: We generated a network by predicting targets of ssRNA populations obtained from high-throughput sequencing experiments. The topology of the network shows it to have power law connectivity distribution, to be dissortative, highly clustered and composed of multiple components. We also identify protein families, PPR and ULP1, that act as hubs within the network. Comparison of the repetition of genomic sub-sequences of ssRNA length between Arabidopsis and E.coli suggest that the network structure is made possible by the underlying repetitiveness in the genome sequence. CONCLUSIONS/SIGNIFICANCE: Together our results provide good evidence for the existence of a large, robust ssRNA interaction network with distinct regulatory function. Such a network could have a massive effect on the regulation of gene expression via mediation of transcript levels. Public Library of Science 2010-03-26 /pmc/articles/PMC2845630/ /pubmed/20360863 http://dx.doi.org/10.1371/journal.pone.0009901 Text en MacLean et al. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
MacLean, Daniel
Elina, Nataliya
Havecker, Ericka R.
Heimstaedt, Susanne B.
Studholme, David J.
Baulcombe, David C.
Evidence for Large Complex Networks of Plant Short Silencing RNAs
title Evidence for Large Complex Networks of Plant Short Silencing RNAs
title_full Evidence for Large Complex Networks of Plant Short Silencing RNAs
title_fullStr Evidence for Large Complex Networks of Plant Short Silencing RNAs
title_full_unstemmed Evidence for Large Complex Networks of Plant Short Silencing RNAs
title_short Evidence for Large Complex Networks of Plant Short Silencing RNAs
title_sort evidence for large complex networks of plant short silencing rnas
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2845630/
https://www.ncbi.nlm.nih.gov/pubmed/20360863
http://dx.doi.org/10.1371/journal.pone.0009901
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