dc.contributor.author | Bury, Leah | |
dc.contributor.author | Moodie, Brittania | |
dc.contributor.author | Ly, Jimmy | |
dc.contributor.author | McKay, Liliana S | |
dc.contributor.author | Miga, Karen HH | |
dc.contributor.author | Cheeseman, Iain M | |
dc.date.accessioned | 2021-10-27T19:58:18Z | |
dc.date.available | 2021-10-27T19:58:18Z | |
dc.date.issued | 2020 | |
dc.identifier.uri | https://hdl.handle.net/1721.1/134140 | |
dc.description.abstract | © Bury et al. Although originally thought to be silent chromosomal regions, centromeres are instead actively transcribed. However, the behavior and contributions of centromere-derived RNAs have remained unclear. Here, we used single-molecule fluorescence in-situ hybridization (smFISH) to detect alpha-satellite RNA transcripts in intact human cells. We find that alpha-satellite RNA-smFISH foci levels vary across cell lines and over the cell cycle, but do not remain associated with centromeres, displaying localization consistent with other long non-coding RNAs. Alpha-satellite expression occurs through RNA polymerase II-dependent transcription, but does not require established centromere or cell division components. Instead, our work implicates centromere– nucleolar interactions as repressing alpha-satellite expression. The fraction of nucleolar-localized centromeres inversely correlates with alpha-satellite transcripts levels across cell lines and transcript levels increase substantially when the nucleolus is disrupted. The control of alpha-satellite transcripts by centromere-nucleolar contacts provides a mechanism to modulate centromere transcription and chromatin dynamics across diverse cell states and conditions. | |
dc.language.iso | en | |
dc.publisher | eLife Sciences Publications, Ltd | |
dc.relation.isversionof | 10.7554/eLife.59770 | |
dc.rights | Creative Commons Attribution 4.0 International license | |
dc.rights.uri | https://creativecommons.org/licenses/by/4.0/ | |
dc.source | eLife | |
dc.title | Alpha-satellite RNA transcripts are repressed by centromere–nucleolus associations | |
dc.type | Article | |
dc.contributor.department | Whitehead Institute for Biomedical Research | |
dc.contributor.department | Massachusetts Institute of Technology. Department of Biology | |
dc.relation.journal | eLife | |
dc.eprint.version | Final published version | |
dc.type.uri | http://purl.org/eprint/type/JournalArticle | |
eprint.status | http://purl.org/eprint/status/PeerReviewed | |
dc.date.updated | 2021-07-14T17:34:50Z | |
dspace.orderedauthors | Bury, L; Moodie, B; Ly, J; McKay, LS; Miga, KHH; Cheeseman, IM | |
dspace.date.submission | 2021-07-14T17:34:52Z | |
mit.journal.volume | 9 | |
mit.license | PUBLISHER_CC | |
mit.metadata.status | Authority Work and Publication Information Needed | |