|
|
|
|
A more recent version of this article appeared on July 1, 2008
| ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Submitted on June 4, 2007
Revised on March 27, 2008
Accepted on April 9, 2008
Departments of *Cellular and Molecular Medicine and
Pathology, and
Ludwig Institute for Cancer Research, University of California San Diego, La Jolla, CA 92093
Monitoring Editor: Yixian Zheng
Numerous proteins involved in endocytosis at the plasma membrane have been shown to be present at novel intracellular locations and to have previously unrecognized functions. ARH (Autosomal Recessive Hypercholesterolemia) is an endocytic clathrin-associated adaptor protein that sorts members of the LDL receptor superfamily (LDLR, megalin, LRP). We report here that ARH also associates with centrosomes in several cell types. ARH interacts with centrosomal (
-tubulin and GPC2 and GPC3) and motor proteins (dynein heavy and intermediate chains). ARH cofractionates with
-tubulin on isolated centrosomes, and
-tubulin and ARH interact on isolated membrane vesicles. During mitosis, ARH sequentially localizes to the nuclear membrane, kinetochores, spindle poles and the midbody. ARH-/- embryonic fibroblasts (MEFs) show smaller or absent centrosomes suggesting ARH plays a role in centrosome assembly. Rat-1 fibroblasts depleted of ARH by siRNA and ARH-/- MEFs exhibit a slower rate of growth and prolonged cytokinesis. Taken together the data suggest that the defects in centrosome assembly in ARH depleted cells may give rise to cell cycle and mitotic/cytokinesis defects. We propose that ARH participates in centrosomal and mitotic dynamics by interacting with centrosomal proteins. Whether the centrosomal and mitotic functions of ARH are related to its endocytic role remains to be established.
These authors contributed equally to this work.
Address correspondence to:
Marilyn G. Farquhar (mfarquhar{at}ucsd.edu)