JCB logo
  Home | Help | Feedback | Subscriptions | Archive | Search | Table of Contents

Published online 2 June 2003. doi:10.1083/jcb1615rr5
This Article
Right arrow Full Text (PDF, 695K)
Right arrow PPT slides of all figures
Right arrow Alert me when this article is cited
Services
Right arrow Email this article
Right arrow Similar articles in this journal
Right arrow Alert me to new content in the JCB
Right arrow Download to citation manager
Citing Articles
Right arrow Citing Articles via CrossRef
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by LeBrasseur, N.
Right arrow Search for Related Content
PubMed
Right arrow Articles by LeBrasseur, N.
Social Bookmarking
 Add to CiteULike   Add to Complore   Add to Connotea   Add to Del.icio.us   Add to Digg   Add to Facebook   Add to Reddit   Add to Technorati   Add to Twitter  
What's this?

© The Rockefeller University Press, 0021-9525/2003/6/835-b $5.00
The Journal of Cell Biology, Volume 161, Number 5, 835-b-835


Research Roundup

Cyclin B knows its place



Though normally cytoplasmic (left), cyclin B (red) targeted to the nucleus (right) can start S phase.

Hunt/AAAS

In mammalian cells the work of the cell cycle is divided between two workhorses: Cdk2/cyclin E for S phase and Cdk1/cyclin B for mitosis. Now, Jonathan Moore, Jane Kirk, and Tim Hunt (Cancer Research UK London Research Institute, London, UK) show that this apparent specificity is achieved by limiting access to substrates. By denying entrance to the nucleus, cells prevent Cdk1–cyclin B from jumpstarting S phase at inopportune times.

In frog egg extracts, S phase is induced in nuclei by Cdk2–cyclin E, but not by Cdk1–cyclin B. This difference has often been construed as specificity in cyclin substrate preferences, but the new results show that cyclin/Cdk pairs are in fact surprisingly promiscuous enzymes. Hunt's group simply replaced the nuclear export signal from cyclin B with a nuclear localization signal and found that this altered Cdk1–cyclin B promoted both DNA replication and mitosis."I'm a biochemist," says Hunt. "I tend to think in terms of specificity between substrate and enzyme. So it was a shock to find the different [CDKs] might not discriminate their substrates." Vertebrate cells apparently avoid the danger that cyclin B might initiate S phase via its cytoplasmic localization and low levels during G1. In yeast, a single cyclin can, under some circumstances, promote both S phase and mitosis. Yeast may not have as severe a need to restrict cyclin activities because the G2 to M transition is less clear than in higher eukaryotes. "Maybe it's okay to start mitosis early in yeast because chromosomes are still able to replicate as they are set on the metaphase plate," Hunt suggests. {blacksquare}

Reference:

Moore, J., et al. 2003. Science. 300:987–990.[Abstract/Free Full Text]



Nicole LeBrasseur

lebrasn{at}rockefeller.edu


Add to CiteULike CiteULike   Add to Complore Complore   Add to Connotea Connotea   Add to Del.icio.us Del.icio.us   Add to Digg Digg   Add to Facebook Facebook   Add to Reddit Reddit   Add to Technorati Technorati   Add to Twitter Twitter    What's this?



This Article
Right arrow Full Text (PDF, 695K)
Right arrow PPT slides of all figures
Right arrow Alert me when this article is cited
Services
Right arrow Email this article
Right arrow Similar articles in this journal
Right arrow Alert me to new content in the JCB
Right arrow Download to citation manager
Citing Articles
Right arrow Citing Articles via CrossRef
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by LeBrasseur, N.
Right arrow Search for Related Content
PubMed
Right arrow Articles by LeBrasseur, N.
Social Bookmarking
 Add to CiteULike   Add to Complore   Add to Connotea   Add to Del.icio.us   Add to Digg   Add to Facebook   Add to Reddit   Add to Technorati   Add to Twitter  
What's this?


  Home | Help | Feedback | Subscriptions | Archive | Search | Table of Contents