Wake-sleep cycles are severely disrupted by diseases affecting cytoplasmic homeostasis
DC Field | Value | Language |
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dc.contributor.author | Beesley, Stephen | - |
dc.contributor.author | Kim, Dae Wook | - |
dc.contributor.author | D'Alessandroa, Matthew | - |
dc.contributor.author | Jin, Yuanhu | - |
dc.contributor.author | Lee, Kwangjun | - |
dc.contributor.author | Joo, Hyunjeong | - |
dc.contributor.author | Young, Yang | - |
dc.contributor.author | Tomko, Robert J., Jr. | - |
dc.contributor.author | Faulkner, John | - |
dc.contributor.author | Gamsby, Joshua | - |
dc.contributor.author | Kim, Jae Kyoung | - |
dc.contributor.author | Lee, Choogon | - |
dc.date.available | 2021-02-22T05:21:24Z | - |
dc.date.issued | 2020-11 | - |
dc.identifier.issn | 0027-8424 | - |
dc.identifier.issn | 1091-6490 | - |
dc.identifier.uri | https://scholarworks.sookmyung.ac.kr/handle/2020.sw.sookmyung/1077 | - |
dc.description.abstract | The circadian clock is based on a transcriptional feedback loop with an essential time delay before feedback inhibition. Previous work has shown that PERIOD (PER) proteins generate circadian time cues through rhythmic nuclear accumulation of the inhibitor complex and subsequent interaction with the activator complex in the feedback loop. Although this temporal manifestation of the feedback inhibition is the direct consequence of PER's cytoplasmic trafficking before nuclear entry, how this spatial regulation of the pacemaker affects circadian timing has been largely unexplored. Here we show that circadian rhythms, including wake-sleep cycles, are lengthened and severely unstable if the cytoplasmic trafficking of PER is disrupted by any disease condition that leads to increased congestion in the cytoplasm. Furthermore, we found that the time delay and robustness in the circadian clock are seamlessly gener-ated by delayed and collective phosphorylation of PER molecules, followed by synchronous nuclear entry. These results provide clear mechanistic insight into why circadian and sleep disorders arise in such clinical conditions as metabolic and neurodegenerative diseases and aging, in which the cytoplasm is congested. | - |
dc.format.extent | 10 | - |
dc.language | 영어 | - |
dc.language.iso | ENG | - |
dc.publisher | NATL ACAD SCIENCES | - |
dc.title | Wake-sleep cycles are severely disrupted by diseases affecting cytoplasmic homeostasis | - |
dc.type | Article | - |
dc.publisher.location | United States | - |
dc.identifier.doi | 10.1073/pnas.2003524117 | - |
dc.identifier.scopusid | 2-s2.0-85096080106 | - |
dc.identifier.wosid | 000591072400001 | - |
dc.identifier.bibliographicCitation | PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, v.117, no.45, pp 28402 - 28411 | - |
dc.citation.title | PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA | - |
dc.citation.volume | 117 | - |
dc.citation.number | 45 | - |
dc.citation.startPage | 28402 | - |
dc.citation.endPage | 28411 | - |
dc.description.isOpenAccess | N | - |
dc.description.journalRegisteredClass | scie | - |
dc.description.journalRegisteredClass | scopus | - |
dc.identifier.url | https://www.pnas.org/content/117/45/28402 | - |
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