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dc.contributor.authorDiAndreth, Breanna
dc.contributor.authorWauford, Noreen
dc.contributor.authorHu, Eileen
dc.contributor.authorPalacios, Sebastian
dc.contributor.authorWeiss, Ron
dc.date.accessioned2023-02-07T18:24:32Z
dc.date.available2023-02-07T18:24:32Z
dc.date.issued2022-05-11
dc.identifier.urihttps://hdl.handle.net/1721.1/147940
dc.description.abstract<jats:title>Abstract</jats:title><jats:p>Regulated transgene expression is an integral component of gene therapies, cell therapies and biomanufacturing. However, transcription factor-based regulation, upon which most applications are based, suffers from complications such as epigenetic silencing that limit expression longevity and reliability. Constitutive transgene transcription paired with post-transcriptional gene regulation could combat silencing, but few such RNA- or protein-level platforms exist. Here we develop an RNA-regulation platform we call “PERSIST" which consists of nine CRISPR-specific endoRNases as RNA-level activators and repressors as well as modular OFF- and ON-switch regulatory motifs. We show that PERSIST-regulated transgenes exhibit strong OFF and ON responses, resist silencing for at least two months, and can be readily layered to construct cascades, logic functions, switches and other sophisticated circuit topologies. The orthogonal, modular and composable nature of this platform as well as the ease in constructing robust and predictable gene circuits promises myriad applications in gene and cell therapies.</jats:p>en_US
dc.language.isoen
dc.publisherSpringer Science and Business Media LLCen_US
dc.relation.isversionof10.1038/s41467-022-30172-3en_US
dc.rightsCreative Commons Attribution 4.0 International licenseen_US
dc.rights.urihttps://creativecommons.org/licenses/by/4.0/en_US
dc.sourceNatureen_US
dc.titlePERSIST platform provides programmable RNA regulation using CRISPR endoRNasesen_US
dc.typeArticleen_US
dc.identifier.citationDiAndreth, Breanna, Wauford, Noreen, Hu, Eileen, Palacios, Sebastian and Weiss, Ron. 2022. "PERSIST platform provides programmable RNA regulation using CRISPR endoRNases." Nature Communications, 13 (1).
dc.contributor.departmentMassachusetts Institute of Technology. Department of Biological Engineeringen_US
dc.relation.journalNature Communicationsen_US
dc.eprint.versionFinal published versionen_US
dc.type.urihttp://purl.org/eprint/type/JournalArticleen_US
eprint.statushttp://purl.org/eprint/status/PeerRevieweden_US
dc.date.updated2023-02-07T18:19:52Z
dspace.orderedauthorsDiAndreth, B; Wauford, N; Hu, E; Palacios, S; Weiss, Ren_US
dspace.date.submission2023-02-07T18:19:54Z
mit.journal.volume13en_US
mit.journal.issue1en_US
mit.licensePUBLISHER_CC
mit.metadata.statusAuthority Work and Publication Information Neededen_US


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