| dc.contributor.author | Segel, Michael | |
| dc.contributor.author | Lash, Blake | |
| dc.contributor.author | Song, Jingwei | |
| dc.contributor.author | Ladha, Alim | |
| dc.contributor.author | Liu, Catherine C | |
| dc.contributor.author | Jin, Xin | |
| dc.contributor.author | Mekhedov, Sergei L | |
| dc.contributor.author | Macrae, Rhiannon K | |
| dc.contributor.author | Koonin, Eugene V | |
| dc.contributor.author | Zhang, Feng | |
| dc.date.accessioned | 2022-03-04T19:31:02Z | |
| dc.date.available | 2022-03-04T19:31:02Z | |
| dc.date.issued | 2021-08-20 | |
| dc.identifier.uri | https://hdl.handle.net/1721.1/141023 | |
| dc.description.abstract | Hitching a ride with a retroelement
Retroviruses and retroelements have inserted their genetic code into mammalian genomes throughout evolution. Although many of these integrated virus-like sequences pose a threat to genomic integrity, some have been retooled by mammalian cells to perform essential roles in development. Segel
<jats:italic>et al</jats:italic>
. found that one of these retroviral-like proteins, PEG10, directly binds to and secretes its own mRNA in extracellular virus–like capsids. These virus-like particles were then pseudotyped with fusogens to deliver functional mRNA cargos to mammalian cells. This potentially provides an endogenous vector for RNA-based gene therapy. —DJ | en_US |
| dc.language.iso | en | |
| dc.publisher | American Association for the Advancement of Science (AAAS) | en_US |
| dc.relation.isversionof | 10.1126/science.abg6155 | en_US |
| dc.rights | Creative Commons Attribution-Noncommercial-Share Alike | en_US |
| dc.rights.uri | http://creativecommons.org/licenses/by-nc-sa/4.0/ | en_US |
| dc.source | PMC | en_US |
| dc.title | Mammalian retrovirus-like protein PEG10 packages its own mRNA and can be pseudotyped for mRNA delivery | en_US |
| dc.type | Article | en_US |
| dc.identifier.citation | Segel, Michael, Lash, Blake, Song, Jingwei, Ladha, Alim, Liu, Catherine C et al. 2021. "Mammalian retrovirus-like protein PEG10 packages its own mRNA and can be pseudotyped for mRNA delivery." Science, 373 (6557). | |
| dc.contributor.department | Howard Hughes Medical Institute | |
| dc.contributor.department | McGovern Institute for Brain Research at MIT | |
| dc.contributor.department | Massachusetts Institute of Technology. Department of Brain and Cognitive Sciences | |
| dc.contributor.department | Massachusetts Institute of Technology. Department of Biological Engineering | |
| dc.contributor.department | Massachusetts Institute of Technology. Department of Biology | |
| dc.relation.journal | Science | en_US |
| dc.eprint.version | Author's final manuscript | en_US |
| dc.type.uri | http://purl.org/eprint/type/JournalArticle | en_US |
| eprint.status | http://purl.org/eprint/status/PeerReviewed | en_US |
| dc.date.updated | 2022-03-04T18:50:37Z | |
| dspace.orderedauthors | Segel, M; Lash, B; Song, J; Ladha, A; Liu, CC; Jin, X; Mekhedov, SL; Macrae, RK; Koonin, EV; Zhang, F | en_US |
| dspace.date.submission | 2022-03-04T18:50:38Z | |
| mit.journal.volume | 373 | en_US |
| mit.journal.issue | 6557 | en_US |
| mit.license | OPEN_ACCESS_POLICY | |
| mit.metadata.status | Authority Work and Publication Information Needed | en_US |