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dc.contributor.authorWest, Jason A.en_US
dc.contributor.authorMito, Marien_US
dc.contributor.authorKurosaka, Satoshien_US
dc.contributor.authorTakumi, Toruen_US
dc.contributor.authorTanegashima, Chiharuen_US
dc.contributor.authorChujo, Takeshien_US
dc.contributor.authorYanaka, Kaorien_US
dc.contributor.authorKingston, Robert E.en_US
dc.contributor.authorHirose, Tetsuroen_US
dc.contributor.authorBond, Charlesen_US
dc.contributor.authorFox, Archaen_US
dc.contributor.authorNakagawa, Shinichien_US
dc.date.accessioned2017-04-06T03:19:30Z
dc.date.issued2016en_US
dc.identifier.citationWest, J. A., M. Mito, S. Kurosaka, T. Takumi, C. Tanegashima, T. Chujo, K. Yanaka, et al. 2016. “Structural, super-resolution microscopy analysis of paraspeckle nuclear body organization.” The Journal of Cell Biology 214 (7): 817-830. doi:10.1083/jcb.201601071. http://dx.doi.org/10.1083/jcb.201601071.en
dc.identifier.issnen
dc.identifier.urihttp://nrs.harvard.edu/urn-3:HUL.InstRepos:32072094
dc.description.abstractParaspeckles are nuclear bodies built on the long noncoding RNA Neat1, which regulates a variety of physiological processes including cancer progression and corpus luteum formation. To obtain further insight into the molecular basis of the function of paraspeckles, we performed fine structural analyses of these nuclear bodies using structural illumination microscopy. Notably, paraspeckle proteins are found within different layers along the radially arranged bundles of Neat1 transcripts, forming a characteristic core-shell spheroidal structure. In cells lacking the RNA binding protein Fus, paraspeckle spheroids are disassembled into smaller particles containing Neat1, which are diffusely distributed in the nucleoplasm. Sequencing analysis of RNAs purified from paraspeckles revealed that AG-rich transcripts associate with Neat1, which are distributed along the shell of the paraspeckle spheroids. We propose that paraspeckles sequester core components inside the spheroids, whereas the outer surface associates with other components in the nucleoplasm to fulfill their function.en
dc.language.isoen_USen
dc.publisherThe Rockefeller University Pressen
dc.relation.isversionofdoi:10.1083/jcb.201601071en
dc.relation.hasversionhttp://www.ncbi.nlm.nih.gov/pmc/articles/PMC5037409/pdf/en
dash.licenseLAAen_US
dc.subjectArticleen
dc.titleStructural, super-resolution microscopy analysis of paraspeckle nuclear body organizationen
dc.typeJournal Articleen_US
dc.description.versionVersion of Recorden
dc.relation.journalThe Journal of Cell Biologyen
dash.depositing.authorKingston, Robert E.en_US
dc.date.available2017-04-06T03:19:30Z
dc.identifier.doi10.1083/jcb.201601071*
dash.authorsorderedfalse
dash.contributor.affiliatedKingston, Robert


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