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

Published online 16 October 2006. doi:10.1083/jcb.1752iti4
The Rockefeller University Press, 0021-9525 $8.00
JCB, Volume 175, Number 2, 195-195
This Article
Right arrow Full Text (PDF, 1670K)
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 Leslie, M.
Right arrow Search for Related Content
PubMed
Right arrow Articles by Leslie, M.
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 Facebook   Add to Reddit   Add to Technorati   Add to Twitter  
What's this?

In This Issue

Melanin's backups



Figure 1
Tyrosinase dispersal (top) requires Rab32 (bottom).

Sports teams and melanin-making cells follow the same strategy: they have substitutes in case a regular can't perform. The cells rely on redundant proteins to deliver enzymes for pigment production, as Wasmeier et al. report on page 271. The results might clarify researchers' understanding of an enigmatic class of cell organelles that participate in everything from immunity to blood clotting.

The melanosomes that manufacture melanin are lysosome-related organelles (LROs), which store and synthesize molecules in many cell types. In platelets, for example, LROs house coagulation factors. Researchers are still working out the details of LRO formation. One mystery is how melanosomes stock up on the enzymes tyrosinase and tyrosinase-related protein-1 (Tyrp1), which are essential for making melanin. Wasmeier et al. investigated one protein that might have a role in the process, Rab38.

Mice with a faulty version of Rab38 are less dark than usual, but they are not albinos, suggesting that another protein picks up the pigmentation slack. The team identified the backup as Rab38's relative, Rab32. Cells lacking both proteins are pale, and their melanosomes show scant tyrosinase and Tyrp1.

The researchers tracked Rab38 and Rab32 to vesicles that often harbored tyrosinase or Tyrp1. Wasmeier et al. conclude that the two proteins somehow help pick up freshly minted enzymes from the Golgi apparatus and bundle them into endosomes for shipment to the melanosomes. How Rab38 and Rab32 work together and whether they help fashion other LROs remain open questions. Formula



Mitch Leslie

mitchleslie{at}comcast.net


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?

Related Article

Rab38 and Rab32 control post-Golgi trafficking of melanogenic enzymes
Christina Wasmeier, Maryse Romao, Lynn Plowright, Dorothy C. Bennett, Graça Raposo, and Miguel C. Seabra
J. Cell Biol. 2006 175: 271-281. [Abstract] [Full Text] [PDF]




This Article
Right arrow Full Text (PDF, 1670K)
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 Leslie, M.
Right arrow Search for Related Content
PubMed
Right arrow Articles by Leslie, M.
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 Facebook   Add to Reddit   Add to Technorati   Add to Twitter  
What's this?


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