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

Published online
doi:10.1083/jcb.1793rr3
The Journal of Cell Biology, Vol. 179, No. 3, 363-
The Rockefeller University Press, 0021-9525 $30.00
© Sedwick
This Article
Right arrow Full Text (PDF, 1065K)
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 Sedwick, C.
Right arrow Search for Related Content
PubMed
Right arrow Articles by Sedwick, C.
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?

Research Roundup

Structure of the meiotic spindle



Figure 1
Fluorescently labeled tubulin monomers within meiotic spindle filaments are seen as speckles whose motion can be tracked.

KAPOOR/MACMILLAN

The meiotic spindle is made up of shorter microtubules than previously believed, suggest results from Ge Yang, Gaudenz Danuser (Scripps Research Institute, La Jolla, CA), Ben Houghtaling, Tarun Kapoor (Rockefeller University, New York, NY), and colleagues. Current models of the spindle, as a bipolar array of overlapping filaments extending from opposite spindle poles, will require revision.

To get a closer look at the architecture of the meiotic spindle, Yang et al. incorporated labeled tubulin subunits into the spindle in a cell-free system. By refining their fluorescent speckle microscopy techniques, the authors were able for the first time to track individual tubulin subunits (seen as speckles) in a single tubulin polymer.

The authors identified pairs of speckles representing subunits on the same filament. Speckle separation supplied them with the minimum length of that filament. They then fitted a mathematical model to these observed lengths to predict overall filament lengths: most filaments were only ~40% of the total spindle length. The short filaments were also scattered throughout the spindle. The researchers now propose that the spindle is a tiled array of overlapping short filaments.

The group next examined how spindle-associated proteins might control filament and spindle size. By inhibiting microtubule motor proteins, they found that dynein–dynactin limited individual fiber lengths and thus overall spindle length. Kinesin 5 activity limited the overlap between fibers by sliding them apart. "Our work suggests the spindle is a self-organizing system, whose stability and functional characteristics are built on these kind of local interactions," says Kapoor. Formula

Reference:

Yang, G., et al. 2007. Nat. Cell Biol. doi:10.1038/ncb1643.[CrossRef][Medline]



Caitlin Sedwick

csedwick{at}gmail.com


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, 1065K)
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 Sedwick, C.
Right arrow Search for Related Content
PubMed
Right arrow Articles by Sedwick, C.
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