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

Published online 12 June 2006. doi:10.1083/jcb.1736iti4
The Rockefeller University Press, 0021-9525 $8.00
JCB, Volume 173, Number 6, 825-825
This Article
Right arrow PDF (Full Text)
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 Wells, W. A.
Right arrow Search for Related Content
PubMed
Right arrow Articles by Wells, W. A.
Related Collections
Right arrowRelated Article
Social Bookmarking
 Add to CiteULike   Add to Complore   Add to Connotea   Add to Del.icio.us   Add to Digg   Add to Reddit   Add to Technorati  
What's this?

In This Issue

Biased spindle formation


Figure 1
HURP (green) is localized close to chromosomes (blue).

A microtubule-stabilizing protein called HURP forms a gradient around chromosomes that stabilizes spindles, say Wong and Fang (page 879).

HURP was previously associated with hepatocellular carcinoma, but Wong and Fang picked it out as being induced during mitosis and showing covariation with known mitotic regulators. Almost half of all HURP-depleted cells had one or more unaligned chromosome during metaphase. The kinetochores of these chromosomes were not attached to microtubules, and even attached kinetochores were under less tension than in a normal spindle.

HURP has also shown up recently as part of a complex from frog egg extracts that is required for the conversion of aster-like to spindle-like structures (Koffa, M.D., et al. 2006. Curr. Biol. 16:743-754). The complex consists of two characterized microtubule-associated proteins (TPX2 and XMAP215), a plus end-directed microtubule motor (Eg5), a mitotic kinase (Aurora A), and HURP. This complex is dependent on the activity of chromatin-localized Ran-GTP, thus helping to focus the spindle around chromosomes.

This is consistent with Wong and Fang's finding that HURP is found on microtubules and in a gradient that peaks around chromosomes. They also found that HURP binds to and stabilizes microtubules. HURP's activity may be needed as, based on mathematical modeling, unbiased microtubule growth is too inefficient for kinetochore capture given the time constraints of mitosis.

The HeLa cells depleted of HURP eventually escaped from their cell cycle arrest induced by unattached chromosomes. The same was true if the cells were treated with low levels of microtubule depolymerizing drugs that induced some chromosome detachment. This suggests that the mitotic checkpoint is weak in certain tumor-derived cells, which would promote genomic instability. Formula



William A. Wells

wellsw{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 Reddit Reddit   Add to Technorati Technorati    What's this?

Related Article

HURP controls spindle dynamics to promote proper interkinetochore tension and efficient kinetochore capture
Jim Wong and Guowei Fang
J. Cell Biol. 2006 173: 879-891. [Abstract] [Full Text] [PDF]




This Article
Right arrow PDF (Full Text)
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 Wells, W. A.
Right arrow Search for Related Content
PubMed
Right arrow Articles by Wells, W. A.
Related Collections
Right arrowRelated Article
Social Bookmarking
 Add to CiteULike   Add to Complore   Add to Connotea   Add to Del.icio.us   Add to Digg   Add to Reddit   Add to Technorati  
What's this?


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