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dc.contributor.authorMetkar, Mihir
dc.contributor.authorOzadam, Hakan
dc.contributor.authorLajoie, Bryan R.
dc.contributor.authorImakaev, Maxim
dc.contributor.authorMirny, Leonid A.
dc.contributor.authorDekker, Job
dc.contributor.authorMoore, Melissa J.
dc.date2022-08-11T08:10:59.000
dc.date.accessioned2022-08-23T17:27:30Z
dc.date.available2022-08-23T17:27:30Z
dc.date.issued2018-11-15
dc.date.submitted2018-12-06
dc.identifier.citation<p>Mol Cell. 2018 Nov 15;72(4):715-726.e3. doi: 10.1016/j.molcel.2018.09.012. Epub 2018 Nov 8. <a href="https://doi.org/10.1016/j.molcel.2018.09.012">Link to article on publisher's site</a></p>
dc.identifier.issn1097-2765 (Linking)
dc.identifier.doi10.1016/j.molcel.2018.09.012
dc.identifier.pmid30415953
dc.identifier.urihttp://hdl.handle.net/20.500.14038/49880
dc.description.abstractCompared to noncoding RNAs (ncRNAs), such as rRNAs and ribozymes, for which high-resolution structures abound, little is known about the tertiary structures of mRNAs. In eukaryotic cells, newly made mRNAs are packaged with proteins in highly compacted mRNA particles (mRNPs), but the manner of this mRNA compaction is unknown. Here, we developed and implemented RIPPLiT (RNA immunoprecipitation and proximity ligation in tandem), a transcriptome-wide method for probing the 3D conformations of RNAs stably associated with defined proteins, in this case, exon junction complex (EJC) core factors. EJCs multimerize with other mRNP components to form megadalton-sized complexes that protect large swaths of newly synthesized mRNAs from endonuclease digestion. Unlike ncRNPs, wherein strong locus-specific structures predominate, mRNPs behave more like flexible polymers. Polymer analysis of proximity ligation data for hundreds of mRNA species demonstrates that nascent and pre-translational mammalian mRNAs are compacted by their associated proteins into linear rod-like structures.
dc.language.isoen_US
dc.relation<p><a href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=pubmed&cmd=Retrieve&list_uids=30415953&dopt=Abstract">Link to Article in PubMed</a></p>
dc.relation.urlhttps://doi.org/10.1016/j.molcel.2018.09.012
dc.subjectAmino Acids, Peptides, and Proteins
dc.subjectBioinformatics
dc.subjectCell Biology
dc.subjectCells
dc.subjectComputational Biology
dc.subjectEnzymes and Coenzymes
dc.subjectMolecular Biology
dc.subjectNucleic Acids, Nucleotides, and Nucleosides
dc.subjectStructural Biology
dc.subjectSystems Biology
dc.titleHigher-Order Organization Principles of Pre-translational mRNPs
dc.typeJournal Article
dc.source.journaltitleMolecular cell
dc.source.volume72
dc.source.issue4
dc.identifier.legacycoverpagehttps://escholarship.umassmed.edu/sysbio_pubs/151
dc.identifier.contextkey13437624
html.description.abstract<p>Compared to noncoding RNAs (ncRNAs), such as rRNAs and ribozymes, for which high-resolution structures abound, little is known about the tertiary structures of mRNAs. In eukaryotic cells, newly made mRNAs are packaged with proteins in highly compacted mRNA particles (mRNPs), but the manner of this mRNA compaction is unknown. Here, we developed and implemented RIPPLiT (RNA immunoprecipitation and proximity ligation in tandem), a transcriptome-wide method for probing the 3D conformations of RNAs stably associated with defined proteins, in this case, exon junction complex (EJC) core factors. EJCs multimerize with other mRNP components to form megadalton-sized complexes that protect large swaths of newly synthesized mRNAs from endonuclease digestion. Unlike ncRNPs, wherein strong locus-specific structures predominate, mRNPs behave more like flexible polymers. Polymer analysis of proximity ligation data for hundreds of mRNA species demonstrates that nascent and pre-translational mammalian mRNAs are compacted by their associated proteins into linear rod-like structures.</p>
dc.identifier.submissionpathsysbio_pubs/151
dc.contributor.departmentGraduate School of Biomedical Sciences
dc.contributor.departmentDepartment of Biochemistry and Molecular Pharmacology
dc.contributor.departmentProgram in Systems Biology
dc.contributor.departmentRNA Therapeutics Institute
dc.source.pages715-726.e3


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