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Intersection of Small RNA Pathways in Arabidopsis thaliana Sub-Nuclear Domains
Authors:Olga Pontes  Alexa Vitins  Thomas S. Ream  Evelyn Hong  Craig S. Pikaard  Pedro Costa-Nunes
Affiliation:1. Department of Biology, University of New Mexico, Albuquerque, New Mexico, United States of America.; 2. Biology Department, Washington University in St. Louis, St. Louis, Missouri, United States of America.; 3. Department of Biology and Department of Molecular and Cellular Biochemistry, Indiana University, Bloomington, Indiana, United States of America.; University of British Columbia, Canada,
Abstract:In Arabidopsis thaliana, functionally diverse small RNA (smRNA) pathways bring about decreased RNA accumulation of target genes via several different mechanisms. Cytological experiments have suggested that the processing of microRNAs (miRNAs) and heterochromatic small interfering RNAs (hc-siRNAs) occurs within a specific nuclear domain that can present Cajal Body (CB) characteristics. It is unclear whether single or multiple smRNA-related domains are found within the same CB and how specialization of the smRNA pathways is determined within this specific sub-compartment. To ascertain whether nuclear smRNA centers are spatially related, we localized key proteins required for siRNA or miRNA biogenesis by immunofluorescence analysis. The intranuclear distribution of the proteins revealed that hc-siRNA, miRNA and trans-acting siRNA (ta-siRNA) pathway proteins accumulate and colocalize within a sub-nuclear structure in the nucleolar periphery. Furthermore, colocalization of miRNA- and siRNA-pathway members with CB markers, and reduced wild-type localization patterns in CB mutants indicates that proper nuclear localization of these proteins requires CB integrity. We hypothesize that these nuclear domains could be important for RNA silencing and may partially explain the functional redundancies and interactions among components of the same protein family. The CB may be the place in the nucleus where Dicer-generated smRNA precursors are processed and assigned to a specific pathway, and where storage, recycling or assembly of RNA interference components takes place.
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