دورية أكاديمية

Dynamics of SIN asymmetry establishment.

التفاصيل البيبلوغرافية
العنوان: Dynamics of SIN asymmetry establishment.
المؤلفون: Archana Bajpai, Anna Feoktistova, Jun-Song Chen, Dannel McCollum, Masamitsu Sato, Rafael E Carazo-Salas, Kathleen L Gould, Attila Csikász-Nagy
المصدر: PLoS Computational Biology, Vol 9, Iss 7, p e1003147 (2013)
بيانات النشر: Public Library of Science (PLoS)
سنة النشر: 2013
المجموعة: Directory of Open Access Journals: DOAJ Articles
مصطلحات موضوعية: Biology (General), QH301-705.5
الوصف: Timing of cell division is coordinated by the Septation Initiation Network (SIN) in fission yeast. SIN activation is initiated at the two spindle pole bodies (SPB) of the cell in metaphase, but only one of these SPBs contains an active SIN in anaphase, while SIN is inactivated in the other by the Cdc16-Byr4 GAP complex. Most of the factors that are needed for such asymmetry establishment have been already characterized, but we lack the molecular details that drive such quick asymmetric distribution of molecules at the two SPBs. Here we investigate the problem by computational modeling and, after establishing a minimal system with two antagonists that can drive reliable asymmetry establishment, we incorporate the current knowledge on the basic SIN regulators into an extended model with molecular details of the key regulators. The model can capture several peculiar earlier experimental findings and also predicts the behavior of double and triple SIN mutants. We experimentally tested one prediction, that phosphorylation of the scaffold protein Cdc11 by a SIN kinase and the core cell cycle regulatory Cyclin dependent kinase (Cdk) can compensate for mutations in the SIN inhibitor Cdc16 with different efficiencies. One aspect of the prediction failed, highlighting a potential hole in our current knowledge. Further experimental tests revealed that SIN induced Cdc11 phosphorylation might have two separate effects. We conclude that SIN asymmetry is established by the antagonistic interactions between SIN and its inhibitor Cdc16-Byr4, partially through the regulation of Cdc11 phosphorylation states.
نوع الوثيقة: article in journal/newspaper
اللغة: English
تدمد: 1553-734X
1553-7358
العلاقة: https://www.ncbi.nlm.nih.gov/pmc/articles/pmid/23874188/pdf/?tool=EBITest; https://doaj.org/toc/1553-734XTest; https://doaj.org/toc/1553-7358Test; https://doaj.org/article/629c65f6069d401386dd6545a9c7f988Test
DOI: 10.1371/journal.pcbi.1003147
الإتاحة: https://doi.org/10.1371/journal.pcbi.1003147Test
https://doaj.org/article/629c65f6069d401386dd6545a9c7f988Test
رقم الانضمام: edsbas.67A20830
قاعدة البيانات: BASE
الوصف
تدمد:1553734X
15537358
DOI:10.1371/journal.pcbi.1003147