4.4 Article

Linking cell division to cell growth in a spatiotemporal model of the cell cycle

期刊

JOURNAL OF THEORETICAL BIOLOGY
卷 241, 期 1, 页码 120-133

出版社

ACADEMIC PRESS LTD- ELSEVIER SCIENCE LTD
DOI: 10.1016/j.jtbi.2005.11.020

关键词

protein translocation; cell cycle; cell size; nuclear size; mathematical model

资金

  1. NHLBI NIH HHS [R01 HL070748-03, R01 HL070748] Funding Source: Medline

向作者/读者索取更多资源

Cell division must be tightly coupled to cell growth in order to maintain cell size, yet the mechanisms linking these two processes are unclear. It is known that almost all proteins involved in cell division shuttle between cytoplasm and nucleus during the cell cycle; however, the implications of this process for cell cycle dynamics and its coupling to cell growth remains to be elucidated. We developed mathematical models of the cell cycle which incorporate protein translocation between cytoplasm and nucleus. We show that protein translocation between cytoplasm and nucleus not only modulates temporal cell cycle dynamics, but also provides a natural mechanism coupling cell division to cell growth. This coupling is mediated by the effect of cytoplasmic-to-nuclear size ratio on the activation threshold of critical cell cycle proteins, leading to the size-sensing checkpoint (sizer) and the size-independent clock (timer) observed in many cell cycle experiments. (c) 2005 Elsevier Ltd. All rights reserved.

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